Infektsiya - Infection - Wikipedia

Infektsiya
Malaria.jpg
Soxta rang elektron mikrograf ko'rsatish a bezgak sporozoit orqali migratsiya o'rta ichak epiteliy a kalamush
MutaxassisligiYuqumli kasallik
Sabablaribakterial, virusli, parazit, qo'ziqorin

An infektsiya bu organizm tanasining bosib olinishi to'qimalar tomonidan kasallik keltirib chiqaruvchi vositalar, ularning ko'payishi va ning reaktsiyasi mezbon yuqumli moddalarga to'qimalar va toksinlar ular ishlab chiqaradi.[1][2] An yuqumli kasallik, shuningdek, a yuqadigan kasallik yoki yuqumli kasallik, bu kasallik infektsiya natijasida.

Infektsiyani yuqumli kasalliklar keltirib chiqaradi (patogenlar ) jumladan:

Xostlar ularning yordamida yuqumli kasalliklarga qarshi kurashishlari mumkin immunitet tizimi. Sutemizuvchi xostlar infektsiyaga qarshi reaktsiya tug'ma ko'pincha o'z ichiga olgan javob yallig'lanish, keyin an moslashuvchan javob.[7]

Maxsus dorilar infektsiyalarni davolash uchun ishlatiladi antibiotiklar, viruslarga qarshi vositalar, qo'ziqorinlarga qarshi vositalar, antiprotozoidlar va antihelminthics. Yuqumli kasalliklar natijasida 2013 yilda 9,2 million o'lim qayd etildi (barcha o'limlarning taxminan 17%).[8] Ning filiali Dori infektsiyalarga yo'naltirilgan deb ataladi yuqumli kasallik.[9]

Tasnifi

Subklinik va klinik (yashirin va aniq)

Semptomatik infektsiyalar aniq va klinik, ammo faol, ammo sezilarli alomatlarga olib kelmaydigan infektsiyani chaqirish mumkin noo'rin, jim, subklinik, yoki yashirin. Faol bo'lmagan yoki harakatsiz bo'lgan infektsiya a deb ataladi yashirin infektsiya.[10] Yashirin bakterial infeksiya misolidir yashirin sil kasalligi. Ba'zi virusli infektsiyalar ham yashirin bo'lishi mumkin, misollar yashirin virusli infektsiyalar bulardan biri Herpesviridae oila.[11]

So'z infektsiya mumkin belgilash ma'lum bir patogenning har qanday mavjudligi umuman (qancha bo'lmasin), lekin ko'pincha a sezgi nazarda tutgan a klinik jihatdan aniq infektsiya (boshqacha aytganda, yuqumli kasallik holati).[12] Bu haqiqat ba'zida ba'zilarini keltirib chiqaradi noaniqlik yoki ba'zi birlarini so'raydi foydalanish munozara; Buning uchun bu odatiy holdir sog'liqni saqlash mutaxassislari gapirish mustamlaka (dan ko'ra infektsiya) ular patogenlarning bir qismi mavjudligini, ammo klinik ko'rinadigan infektsiya (kasallik yo'q) mavjudligini anglatganda.

Infektsiyalarni ta'riflash uchun turli xil atamalar qo'llaniladi. Birinchisi, o'tkir infektsiya. O'tkir infektsiya - bu alomatlar tez rivojlanib boradigan kasallik; uning yo'nalishi tez yoki cho'zilishi mumkin.[13] Keyingi surunkali infektsiya. Surunkali infeksiya - bu alomatlar asta-sekin, bir necha hafta yoki bir necha oy davomida rivojlanib, sekin kechadi.[14] Subakut infektsiya - bu simptomlarning rivojlanishi o'tkir infektsiyaga qaraganda uzoqroq davom etadigan, ammo surunkali infektsiyaga qaraganda tezroq yuzaga keladigan yuqumli kasallik. Yashirin infektsiya - bu o'tkir epizoddan keyin paydo bo'lishi mumkin bo'lgan infektsiya turi; organizm mavjud, ammo simptomlar mavjud emas; vaqt o'tgach kasallik yana paydo bo'lishi mumkin. Fokusli infeksiya organizmlar qon oqimi orqali tananing boshqa hududiga o'tadigan infektsiyaning boshlang'ich joyi deb ta'riflanadi.[15]

Birlamchi va opportunistik

Ko'p navlari orasida mikroorganizmlar, nisbatan kam odam kasallikka olib keladi, aks holda sog'lom odamlarda.[16] Yuqumli kasallik, bu ozchilikning o'zaro ta'siridan kelib chiqadi patogenlar va ular yuqtirgan xostlarning mudofaasi. Har qanday qo'zg'atuvchidan kelib chiqadigan kasallikning ko'rinishi va zo'ravonligi ushbu patogenning mezbonga zarar etkazish qobiliyatiga, shuningdek patogenga qarshi turish qobiliyatiga bog'liq. Shu bilan birga, mezbonning immuniteti infektsiyani nazorat qilish uchun uy egasining o'ziga zarar etkazishi mumkin. Klinisyenler, shuning uchun yuqumli mikroorganizmlarni yoki mikroblarni mezbon himoya darajasiga ko'ra tasniflashadi - yoki shunday asosiy patogenlar yoki kabi opportunistik patogenlar:

Birlamchi patogenlar

Birlamchi patogenlar odatdagi, sog'lom uy egasi va ularning ichki tarkibidagi mavjudligi yoki faoliyati natijasida kasallikka olib keladi zaharlanish (ular keltirib chiqaradigan kasallikning og'irligi), qisman ularning ko'payishi va tarqalishi zarurligining zaruriy natijasidir. Odamlarning eng keng tarqalgan asosiy qo'zg'atuvchilarining ko'pi faqat odamlarga zarar etkazadi, ammo ko'plab jiddiy kasalliklar atrof-muhitdan olingan yoki odam bo'lmagan xostlarga yuqadigan organizmlar tomonidan kelib chiqadi.

Opportunistik patogenlar

Opportunistik patogenlar depressiyaga chidamli xostda yuqumli kasallikni keltirib chiqarishi mumkin (immunitet tanqisligi ) yoki ular tananing ichki qismiga g'ayrioddiy kirish imkoniga ega bo'lsa (masalan, orqali travma ). Opportunistik infektsiya odatdagidek uy egasi bilan aloqada bo'lgan mikroblardan kelib chiqishi mumkin patogen bakteriyalar yoki zamburug'lar oshqozon-ichak yoki yuqori nafas yo'llari va ular boshqa xostlardan olingan mikroblar (aks holda zararsiz) natijasida ham paydo bo'lishi mumkin Clostridium difficile kolit ) yoki natijasida atrofdan shikast etkazuvchi kirish (kabi) jarrohlik yara infektsiyalari yoki aralash sinish ). Fırsatçı kasallik, xost himoyasi buzilishini talab qiladi, buning natijasida paydo bo'lishi mumkin genetik nuqsonlar (kabi Surunkali granulomatoz kasallik ), himoyasizlik mikroblarga qarshi giyohvand moddalar yoki immunosupressiv kimyoviy moddalar (keyingi sodir bo'lishi mumkin) zaharlanish yoki saraton kimyoviy terapiya ), himoyasizlik ionlashtiruvchi nurlanish, yoki immunosupressiv faollik bilan yuqadigan kasallik natijasida (masalan, bilan qizamiq, bezgak yoki OIV kasalligi ). Boshlang'ich patogenlar, shuningdek, depressiyaga chidamli xostda immunitet kam bo'lgan xostda odatdagidan ko'ra og'irroq kasalliklarni keltirib chiqarishi mumkin.[17]

Ikkilamchi infektsiya

Birlamchi infektsiyani amalda quyidagicha ko'rish mumkin eng boshlang'ich sabab shaxsning sog'lig'ining dolzarb muammolari, ikkilamchi infektsiya a oqibat yoki asorat bu asosiy sabab. Masalan, o'pka sil kasalligi ko'pincha birlamchi infektsiya hisoblanadi, lekin bu faqatgina sodir bo'lgan infektsiya kuyish yoki penetratsion travma (asosiy sabab) chuqur to'qimalarga g'ayritabiiy kirish ikkilamchi infektsiya. Birlamchi patogenlar ko'pincha asosiy infektsiyani keltirib chiqaradi va ko'pincha ikkilamchi infektsiyani keltirib chiqaradi. Odatda, opportunistik infektsiyalar ikkinchi darajali infektsiyalar sifatida qaraladi (chunki immunitet tanqisligi yoki jarohat predispozitsiya qiluvchi omil edi).

Infektsiyaning boshqa turlari

Infektsiyaning boshqa turlari aralash, yatrogen, nozokomial va jamoaviy infeksiyadan iborat. Aralash infektsiya - bu ikki yoki undan ortiq patogen qo'zg'atadigan infektsiya. Bunga Bacteroides fragilis va Escherichia coli sabab bo'lgan appenditsitni misol keltirish mumkin. Ikkinchisi - yatrogen infektsiya. Ushbu turdagi infektsiya tibbiyot xodimidan bemorga yuqadigan kasallikdir. Nozokomial infektsiya, shuningdek, sog'liqni saqlash sharoitida yuzaga keladi. Nozokomial infektsiyalar - kasalxonada yotish paytida yuqadigan kasalliklar. Va nihoyat, jamoat tomonidan yuqtirilgan infektsiya bu infektsiya butun bir jamoadan olingan infektsiya.[15]

Yuqumli yoki yuqtirilmagan

Ushbu kasallik yuqumli ekanligini isbotlash usullaridan biri qondirishdir Koch postulatlari (birinchi tomonidan taklif qilingan Robert Koch ), buni avval talab qiladigan, yuqumli vosita sog'lom nazoratda emas, balki faqat kasallikka chalingan bemorlarda aniqlanishi mumkin, ikkinchidan, yuqumli kasallik bilan kasallangan bemorlarda ham kasallik rivojlanadi. Ushbu postulatlar birinchi marta kashf etishda ishlatilgan Mikobakteriyalar turlari sabab bo'ladi sil kasalligi.

Biroq, odatda Kochning postulatlarini axloqiy sabablarga ko'ra zamonaviy amaliyotda sinab ko'rish mumkin emas. Ularni isbotlash uchun sog'lom odamga a bilan eksperimental yuqtirish kerak patogen sof madaniyat sifatida ishlab chiqarilgan. Aksincha, aniq yuqumli kasalliklar ham har doim ham yuqumli mezonlarga javob bera olmaydi; masalan, Treponema pallidum, sababchi spiroket ning sifiliz bo'lishi mumkin emas madaniyatli in vitro - ammo organizm quyonda o'stirilishi mumkin moyaklar. Plastinka madaniyatidan olingan mikroblardan olinadiganiga qaraganda, sof madaniyat xost sifatida xizmat qiladigan hayvonot manbalaridan kelib chiqishi aniq emas.

Epidemiologiya, yoki kasallik kim, nima uchun va qaerda paydo bo'lishini va turli populyatsiyalarda kasallik bor-yo'qligini aniqlaydigan narsalarni o'rganish va tahlil qilish yuqumli kasallikni tushunishda ishlatiladigan yana bir muhim vositadir. Epidemiologlar populyatsiya tarkibidagi guruhlar o'rtasidagi farqlarni aniqlay olishlari mumkin, masalan, ayrim yosh guruhlarida infektsiyaning ko'pmi yoki kammi; turli xil mahallalarda yashovchi guruhlar yuqtirish ehtimoli ko'proqmi; va boshqa omillar, masalan, jins va irq. Tadqiqotchilar kasallik yoki yo'qligini baholashlari mumkin avj olish vaqti-vaqti bilan yoki faqat vaqti-vaqti bilan sodir bo'ladigan; endemik, mintaqada yuzaga keladigan muntazam holatlarning barqaror darajasi bilan; epidemik, mintaqada tezkor va juda ko'p sonli holatlar bilan; yoki pandemiya, bu global epidemiya. Agar yuqumli kasallikning sababi noma'lum bo'lsa, epidemiologiya yordamida yuqtirish manbalarini aniqlashda foydalanish mumkin.

Yuqumli kasallik

Yuqumli kasalliklar ba'zida kasal odam bilan aloqa qilish yoki ularning sekretsiyasi bilan osonlikcha yuqganda (masalan, yuqumli kasalliklar) deyiladi. gripp ). Shunday qilib, yuqumli kasallik bu ayniqsa yuqadigan yoki oson yuqadigan yuqumli kasallikning bir qismidir. Vektorli yuqish yoki jinsiy yo'l bilan yuqtirish kabi ko'proq ixtisoslashgan yuqish yo'llari bilan yuqadigan boshqa yuqumli, yuqadigan yoki yuqadigan kasalliklar odatda "yuqumli" deb hisoblanmaydi va ko'pincha tibbiy izolyatsiyani talab qilmaydi (ba'zida erkin deb nomlanadi) karantin ) qurbonlar. Biroq, "yuqumli" va "yuqumli kasallik" so'zlarining ushbu maxsus kontseptsiyasi (oson yuqadigan) har doim ham mashhur foydalanishda hurmat qilinmaydi. Yuqumli kasalliklar odatda odamdan odamga bevosita aloqada yuqadi. Aloqa turlari odamdan odamga va tomchi tarqalishiga bog'liq. Havodan yuqish, ifloslangan narsalar, oziq-ovqat va ichimlik suvi, hayvonlar bilan aloqa qilish, hayvonlar suv havzalari, hasharotlar chaqishi va atrof-muhit suv havzalari kabi bilvosita aloqa yuqumli kasalliklar yuqishining yana bir usuli hisoblanadi.[18]

Anatomik joylashuvi bo'yicha

Infektsiyalarni anatomik joylashuvi yoki bo'yicha tasniflash mumkin organlar tizimi yuqtirilgan, shu jumladan:

Bundan tashqari, yallig'lanish bu erda infektsiya eng keng tarqalgan sababdir zotiljam, meningit va salpingit.

Belgilari va alomatlari

INFEKTSION belgilari kasallik turiga bog'liq. Yuqtirishning ayrim belgilari butun vujudga ta'sir qiladi, masalan charchoq, ishtahani yo'qotish, vazn yo'qotish, isitma, tunda terlash, titroq, og'riq va og'riq. Boshqalar terining alohida tana qismlariga xosdir toshmalar, yo'tal yoki a tumov.

Ba'zi hollarda yuqumli kasalliklar bo'lishi mumkin asemptomatik ma'lum bir xostda ularning ko'pi yoki hatto barchasi uchun. Ikkinchi holda, kasallik faqat simptomsiz tashuvchi bilan aloqada bo'lganidan keyin kasal bo'lib qolgan xostlarda "kasallik" (ta'rifi bo'yicha kasallikni anglatadi) deb ta'riflanishi mumkin. Infektsiya yuqumli kasallik bilan sinonim emas, chunki ba'zi infektsiyalar xostda kasallik keltirib chiqarmaydi.[17]

Bakterial yoki virusli

Bakterial va virusli infektsiyalar ikkalasi ham bir xil simptomlarni keltirib chiqarishi mumkinligi sababli, aniq infektsiyaning sababi qaysi ekanligini ajratib ko'rsatish qiyin bo'lishi mumkin.[19] Ikkalasini farqlash juda muhimdir, chunki virusli infektsiyalarni davolash mumkin emas antibiotiklar bakterial infektsiyalar mumkin.[20]

Virusli va bakterial infeksiyani taqqoslash
XarakterliVirusli infektsiyaBakterial infeksiya
Odatda alomatlarUmuman olganda, virusli infektsiyalar sistematikdir. Bu shuni anglatadiki, ular bir vaqtning o'zida tananing turli qismlarini yoki bir nechta tana tizimini o'z ichiga oladi; ya'ni burun burungi, sinus tiqilishi, yo'tal, tana og'rig'i va boshqalar. Ular virusli davrda bo'lgani kabi ba'zan ham mahalliy bo'lishi mumkin kon'yunktivit yoki "pushti ko'z" va herpes. Faqat bir nechta virusli infektsiyalar gerpes kabi og'riqli. Virusli infektsiyalarning og'rig'i ko'pincha qichima yoki yonish bilan tavsiflanadi.[19]Bakterial infeksiyaning klassik alomatlari mahalliy qizarish, issiqlik, shishish va og'riqdir. Bakterial infeksiyaning o'ziga xos belgilaridan biri bu mahalliy og'riq, tananing ma'lum bir qismida joylashgan og'riqdir. Masalan, agar kesma paydo bo'lsa va bakteriyalar bilan kasallangan bo'lsa, infektsiya joyida og'riq paydo bo'ladi. Bakterial tomoq og'rig'i ko'pincha tomoqning bir tomonida ko'proq og'riq bilan tavsiflanadi. An quloq infektsiyasi og'riq faqat bitta quloqda paydo bo'lsa, bakterial deb tashxis qo'yish ehtimoli yuqori.[19] Yiring va sut rangidagi suyuqlik hosil qiladigan kesma, ehtimol kasallangan.[tushuntirish kerak ][21]
SababiPatogen viruslarPatogen bakteriyalar

Patofiziologiya

Infektsiyalarga tegishli bo'lgan umumiy hodisalar zanjiri mavjud.[22] Voqealar zanjiri bir necha bosqichlarni o'z ichiga oladi - bu yuqumli kasallik, suv ombori, sezgir xostga kirish, chiqish va yangi xostlarga yuqishni o'z ichiga oladi. INFEKTSION rivojlanishi uchun havolalarning har biri xronologik tartibda bo'lishi kerak. Ushbu bosqichlarni tushunish tibbiyot xodimlariga infektsiyani yo'naltirishga va birinchi navbatda uning paydo bo'lishining oldini olishga yordam beradi.[23]

Mustamlaka

An infektsiyasi oyoq tirnoqlari; yiringli (sariq) va natijada yallig'lanish mavjud (tirnoq atrofida qizarish va shish).

Infektsiya organizm tanaga muvaffaqiyatli kirib, o'sishi va ko'payishi bilan boshlanadi. Bu mustamlaka deb nomlanadi. Aksariyat odamlar osonlikcha yuqtirilmaydi. Immun tizimi buzilgan yoki zaiflashganlarda surunkali yoki doimiy infektsiyalarga moyillik kuchayadi. Bostirilgan shaxslar immunitet tizimi ayniqsa sezgir opportunistik infektsiyalar. Uy egasiga kirish xost-patogen interfeysi, odatda orqali sodir bo'ladi shilliq qavat kabi teshiklarda og'iz bo'shlig'i, burun, ko'zlar, jinsiy a'zolar, anus yoki mikrob ochiq yaralar orqali kirishi mumkin. Kirishning dastlabki joyida bir nechta organizm o'sishi mumkin bo'lsa, ko'pchilik ko'chib ketadi va turli organlarda tizimli infektsiyani keltirib chiqaradi. Ba'zi patogenlar mezbon hujayralar ichida o'sib boradi (hujayra ichi), boshqalari tana suyuqliklarida erkin o'sadi.

Yara kolonizatsiya deganda yara ichidagi takrorlanmaydigan mikroorganizmlar tushuniladi, yuqtirgan yaralarda esa takrorlanadigan organizmlar mavjud bo'lib, to'qima shikastlanadi.[24] Hammasi ko'p hujayrali organizmlar tashqi organizmlar tomonidan ma'lum darajada kolonizatsiya qilinadi va ularning katta qismi ikkalasida ham mavjud mututeristik yoki komensal uy egasi bilan munosabatlar. Birinchisiga misol qilib anaerob bakteriyalar kolonizatsiya qiladigan turlar sutemizuvchi yo'g'on ichak va ikkinchisiga misol qilib turli xil turlari keltirilgan stafilokokk mavjud bo'lgan inson terisi. Ushbu kolonizatsiyalarning ikkalasi ham infektsiya deb hisoblanmaydi. Infektsiya va kolonizatsiya o'rtasidagi farq ko'pincha faqat vaziyatga bog'liq. Patogen bo'lmagan organizmlar o'ziga xos sharoitlarda va hatto eng ko'p hollarda patogen bo'lishi mumkin zararli organizm xavfli infektsiyani keltirib chiqarishi uchun ma'lum holatlarni talab qiladi. Kabi ba'zi bir kolonizatsiya qiluvchi bakteriyalar Korynebakteriyalar sp. va streptokokklar viridansi, patogen bakteriyalarning yopishishi va kolonizatsiyasini oldini oladi va shu bilan uy egasi bilan simbiyotik munosabatda bo'ladi, infektsiyani oldini oladi va tezlikni oshiradi jarohatni davolash.

[25][26][27] Ushbu rasm patogen infektsiya bosqichlarini tasvirlaydi.

Uy egasining patogen tomonidan emlanganligi va uning yakuniy natijasi bilan bog'liq bo'lgan o'zgaruvchilar quyidagilarni o'z ichiga oladi.

  • kirish yo'li patogen va u qo'lga kiritadigan mezbon mintaqalarga kirish
  • ichki zaharlanish ma'lum bir organizmning
  • dastlabki emlovning miqdori yoki yuki
  • The immunitetga ega xostning mustamlaka holati

Masalan, bir nechta stafilokokk turlari terida zararsiz bo'lib qoladi, ammo odatda mavjud bo'lganda steril bo'shliq, masalan, a ning kapsulasida qo'shma yoki qorin parda, qarshiliksiz ko'paytiring va zarar etkazing.

Bu qiziqarli fakt gaz xromatografiyasi - mass-spektrometriya, 16S ribosomal RNK tahlil, omika So'nggi o'n yilliklarda odamlarga boshqa ilg'or texnologiyalar aniqroq ayon bo'ldiki, mikrobial kolonizatsiya, hatto odamlar deyarli deb o'ylaydigan muhitda ham juda keng tarqalgan. steril. Bakterial kolonizatsiyani qabul qilish odatiy holdir, qaysi surunkali yaralarni yuqtirgan deb tasniflash mumkinligini va rivojlanish xavfi qancha ekanligini bilish qiyin. Klinik amaliyotda ko'rilgan ko'plab yaralarga qaramay, baholangan alomatlar va belgilar uchun sifatli ma'lumotlar cheklangan. Amerika tibbiyot assotsiatsiyasining "Ratsional klinik tekshiruvlar seriyasi" jurnalidagi surunkali yaralarni ko'rib chiqish og'riqni kuchayishi infektsiya ko'rsatkichi sifatida muhimligini aniqladi.[28] Tadqiqot shuni ko'rsatdiki, eng foydali topilma og'riq darajasining oshishi [ehtimollik darajasi (LR) oralig'i, 11-20] infektsiyani yuqtirishga imkon beradi, ammo og'riqning yo'qligi (ehtimollik darajasi salbiy, 0.64-0.88) infektsiyani istisno qilmang (xulosa LR 0.64-0.88).

Kasallik

Kasallik uy egasining himoya immunitet mexanizmlari buzilgan va organizm mezbonga zarar etkazadigan bo'lsa paydo bo'lishi mumkin. Mikroorganizmlar turli toksinlar yoki halokatli fermentlarni chiqarib, to'qimalarga zarar etkazishi mumkin. Masalan, Tetani Clostridium mushaklarni falaj qiladigan toksinni chiqaradi va stafilokokk zarba va sepsis hosil qiluvchi toksinlarni chiqaradi. Hamma yuqumli kasalliklar barcha xostlarda kasallik keltirib chiqarmaydi. Masalan, yuqtirganlarning 5 foizdan kamrog'i poliomiyelit kasallikni rivojlantirish.[29] Boshqa tomondan, ba'zi yuqumli moddalar yuqori darajada zararli hisoblanadi. The prion sabab bo'ladi telba sigir kasalligi va Kreuzfeldt-Yakob kasalligi har doim yuqtirgan barcha hayvonlarni va odamlarni o'ldiradi.

Doimiy infektsiyalar tanani dastlabki infektsiyadan keyin organizmni tozalashga qodir emasligi sababli yuzaga keladi. Doimiy infektsiyalar, yuqumli organizmning doimiy mavjudligi bilan tavsiflanadi, ko'pincha yashirin infektsiya, vaqti-vaqti bilan faol infektsiyaning qaytalanadigan relapslari bilan. Tananing turli hujayralarini yuqtirish orqali doimiy infektsiyani saqlab turadigan ba'zi viruslar mavjud. Bir vaqtlar qo'lga kiritilgan ba'zi viruslar tanadan hech qachon chiqib ketmaydi. Oddiy misol, gerpes virusi bo'lib, u asabda yashirinishga moyil bo'lib, muayyan holatlar yuzaga kelganda faollashadi.

Doimiy infektsiyalar har yili dunyo miqyosida millionlab o'limlarga sabab bo'ladi.[30] Parazitlar tomonidan surunkali yuqtirish ko'plab rivojlanmagan mamlakatlarda yuqori kasallanish va o'limni keltirib chiqaradi.

Yuqish

Janubiy uy chivinlari (Culex quinquefasciatus ) a vektor sabab bo'lgan patogenlarni yuqtiradi G'arbiy Nil isitmasi va parranda bezgagi Boshqalar orasida.

Yuqumli organizmlarning omon qolishi va boshqa xujayralarda infektsiya tsiklini takrorlashi uchun ular (yoki ularning avlodlari) mavjud bo'lgan suv omboridan chiqib, boshqa joyga yuqtirishlari kerak. Infektsiyani yuqtirish ko'plab potentsial yo'nalishlar orqali amalga oshirilishi mumkin:

  • Tomchi bilan aloqa qilish, deb ham tanilgan nafas olish yo'liva natijada paydo bo'lgan infektsiya deb atash mumkin havo yo'li bilan yuqadigan kasallik. Agar yuqtirgan odam boshqa odamga yo'talsa yoki hapşırsa, iliq va nam tomchilarda to'xtatilgan mikroorganizmlar tanaga burun, og'iz yoki ko'z sirtlari orqali kirishi mumkin.
  • Najas-og'iz orqali yuborish, unda oziq-ovqat mahsulotlari yoki suv ifloslanadi (odamlar ovqat tayyorlashdan oldin qo'llarini yuvmaganliklari yoki tozalanmagan kanalizatsiya ichimlik suvi ta'minotiga chiqarilishi) va ularni iste'mol qiladigan va ichadigan odamlar yuqtirishadi. Odatda fekal-og'iz orqali yuboriladigan patogenlar kiradi Vibrio vabo, Giardiya turlari, rotaviruslar, Entameba histolytica, Escherichia coli va lenta qurtlari.[31] Ushbu patogenlarning aksariyati sabab bo'ladi gastroenterit.
  • Jinsiy yo'l bilan yuqish, natijada kasallik chaqirilishi bilan jinsiy yo'l bilan yuqadigan kasallik
  • Og'iz orqali yuborish, Asosan og'iz orqali yuqadigan kasalliklar, masalan, to'g'ridan-to'g'ri og'zaki aloqa orqali yuqishi mumkin o'pish yoki bilvosita aloqada, masalan, ichimlik stakanini yoki sigaretani birgalikda ishlatish orqali.
  • To'g'ridan-to'g'ri aloqa orqali uzatish, To'g'ridan-to'g'ri aloqa orqali yuqadigan ba'zi kasalliklar kiradi sportchining oyog'i, impetigo va siğil
  • Avtotransport vositasi, jonsiz suv ombori (oziq-ovqat, suv, tuproq) orqali yuqishi.[32]
  • Vertikal uzatish, to'g'ridan-to'g'ri onadan an embrion, homila yoki paytida bola homiladorlik yoki tug'ish. Bu natijasida sodir bo'lishi mumkin oldindan mavjud bo'lgan infektsiya yoki homiladorlik paytida sotib olingan.
  • Yatrogen yuqishkabi tibbiy protseduralar tufayli in'ektsiya yoki transplantatsiya yuqtirilgan material.
  • Vektorli uzatish, a tomonidan uzatiladi vektor, bu an organizm bu sabab bo'lmaydi kasallik o'zi lekin infektsiyani yuqtirish orqali yuqtiradi patogenlar bittadan mezbon boshqasiga.[33]

O'rtasidagi munosabatlar yuqumli kasallik va o'tkazuvchanlik murakkab; agar kasallik tezda o'limga olib keladigan bo'lsa, mikrob boshqa xostga o'tguncha xost o'lishi mumkin.

Tashxis

Yuqumli kasallik diagnostikasi ba'zida bevosita yoki bilvosita yuqumli kasallikni aniqlashni o'z ichiga oladi.[34] Amalda aksariyat mayda yuqumli kasalliklar siğil, teri xo'ppozlar, nafas olish tizimi infektsiyalar va diareya kasalliklari ularning klinik ko'rinishi bilan tashxis qo'yiladi va maxsus qo'zg'atuvchini bilmasdan davolanadi. Kasallikning sababi haqidagi xulosalar bemorning ma'lum bir agent bilan aloqa qilish ehtimoli, jamoada mikrob mavjudligi va boshqa epidemiologik fikrlarga asoslanadi. Etarli kuch sarflanib, ma'lum bo'lgan barcha yuqumli kasalliklarni aniq aniqlash mumkin. Shunga qaramay, identifikatsiyalashning afzalliklari ko'pincha narxdan ustun turadi, chunki ko'pincha muayyan davolanish yo'q, sababi aniq yoki infektsiyaning natijasi benign.

Yuqumli kasallik diagnostikasi deyarli har doim boshlangan kasallik tarixi va fizik tekshiruv. Batafsil identifikatsiyalash usullari bemordan ajratilgan yuqumli kasalliklar madaniyatini o'z ichiga oladi. Madaniyat yuqumli organizmlarni ularning mikroskopik xususiyatlarini o'rganish, patogenlar tomonidan ishlab chiqariladigan moddalar mavjudligini aniqlash va organizmni genotipi bo'yicha to'g'ridan-to'g'ri aniqlash orqali aniqlashga imkon beradi. Boshqa texnikalar (masalan X-nurlari, Mushuklarni skanerlash, PET skanerlashi yoki NMR ) yuqumli razvedkaning o'sishidan kelib chiqadigan ichki anormalliklarning tasvirlarini yaratish uchun ishlatiladi. Rasmlar, masalan, suyakni aniqlashda foydalidir xo'ppoz yoki a gubkali ensefalopatiya tomonidan ishlab chiqarilgan prion.

Semptomatik diagnostika

Tashxisga yuqumli kasallikka chalingan har qanday odamda namoyon bo'ladigan alomatlar yordam beradi, ammo shubhani tasdiqlash uchun odatda qo'shimcha diagnostika usullari kerak. Ba'zi belgilar kasallikning o'ziga xos xususiyati va ko'rsatkichidir va ular chaqiriladi patognomonik belgilar; ammo bu juda kam. Barcha infektsiyalar simptomatik emas.[35]

Bolalarda borligi siyanoz, tez nafas olish, yomon periferik perfuziya yoki a petekial toshma jiddiy infektsiya xavfini 5 barobardan ko'proq oshiradi.[36] Boshqa muhim ko'rsatkichlar orasida ota-onalarning tashvishi, klinik instinkt va 40 ° C dan yuqori harorat mavjud.[36]

Mikrobial madaniyat

To'rt ozuqaviy agar oddiy koloniyalar o'sadigan plitalar Gram salbiy bakteriyalar.

Mikrobiologik madaniyat yuqumli kasallikni aniqlashda ishlatiladigan asosiy vositadir. Mikrobial madaniyatda, a o'sish muhiti ma'lum bir agent uchun taqdim etiladi. Keyinchalik kasal bo'lishi mumkin bo'lgan to'qima yoki suyuqlikdan olingan namuna shu muhitda o'sishi mumkin bo'lgan yuqumli razvedka borligi uchun sinovdan o'tkaziladi. Ko'pgina patogen bakteriyalar ozuqa moddalarida osongina o'stiriladi agar, a o'sishi uchun zarur bo'lgan uglevodlar va oqsillarni etkazib beradigan qattiq muhit shakli bakteriya, mo'l-ko'l suv bilan birga. Bitta bakteriya plastinka yuzasida a deb nomlangan ko'rinadigan höyüğe aylanadi koloniya, bu boshqa koloniyalardan ajratilishi yoki birlashtirilib "maysazor" ga aylanishi mumkin. Koloniyaning kattaligi, rangi, shakli va shakli bakteriyalar turiga, o'ziga xos genetik tarkibiga xosdir zo'riqish ) va uning o'sishini qo'llab-quvvatlovchi muhit. Idishga identifikatsiyalashga yordam berish uchun plastinkaga boshqa ingredientlar qo'shiladi. Plitalar tarkibida ba'zi bir bakteriyalarni ko'payishiga imkon beradigan, boshqalarga emas yoki ba'zi bir bakteriyalarga javoban rangini o'zgartiradigan moddalar bo'lishi mumkin. Bu kabi bakteriologik plitalar odatda yuqumli bakteriyalarni klinik identifikatsiyalashda qo'llaniladi. Mikrobial madaniyatni aniqlashda ham foydalanish mumkin viruslar: vosita, bu holda madaniyatga etishtirilgan hujayralar bo'lib, virus yuqishi, so'ngra o'zgarishi yoki o'ldirilishi mumkin. Virusli identifikatsiyalash holatida o'lik hujayralar mintaqasi virus o'sishidan kelib chiqadi va "plakka" deb nomlanadi. Eukaryotik parazitlar shuningdek, ma'lum bir agentni aniqlash vositasi sifatida madaniyatda etishtirilishi mumkin.

Tegishli plastinka madaniyati texnikasi bo'lmagan taqdirda, ba'zi mikroblar tirik hayvonlar ichida etishtirishni talab qiladi. Kabi bakteriyalar Mycobacterium leprae va Treponema pallidum hayvonlarda o'stirilishi mumkin, garchi serologik va mikroskopik usullar tirik hayvonlardan foydalanishni keraksiz holga keltirsa. Viruslar odatda madaniyat yoki hayvonlarning o'sishiga alternativalar yordamida aniqlanadi. Ba'zi viruslar etishtirilishi mumkin embrionlangan tuxum. Yana bir foydali identifikatsiya qilish usuli - bu Xenodiagnosis yoki yuqumli kasallikning o'sishini qo'llab-quvvatlash uchun vektordan foydalanish. Chagas kasalligi bu eng muhim misol, chunki qo'zg'atuvchining borligini bevosita namoyish etish qiyin, Trypanosoma cruzi bemorda, shuning uchun aniq tashxis qo'yishni qiyinlashtiradi. Bunday holda, xenodiagnosis diagnostikasidan foydalanishni o'z ichiga oladi vektor Chagas agenti T. kruzi, yuqtirilmagan triatomin bug, bu yuqtirganlikda gumon qilingan kishidan qon ovqatini oladi. Xato keyinchalik o'sishi uchun tekshiriladi T. kruzi uning ichaklarida.

Mikroskopiya

Yuqumli kasalliklarni aniqlashda yana bir asosiy vosita hisoblanadi mikroskopiya. Yuqorida muhokama qilingan madaniyatning deyarli barcha usullari, bir muncha vaqt, yuqumli vositani aniq aniqlash uchun mikroskopik tekshiruvga tayanadi. Mikroskopiya oddiy vositalar bilan, masalan birikma bilan amalga oshirilishi mumkin yorug'lik mikroskopi, yoki an kabi murakkab asboblar bilan elektron mikroskop. Bemorlardan olingan namunalar to'g'ridan-to'g'ri yorug'lik mikroskopida ko'rish mumkin va ko'pincha tezda identifikatsiyaga olib kelishi mumkin. Mikroskopiya ko'pincha bilan birgalikda ishlatiladi biokimyoviy binoni texnikasi va birgalikda ishlatilganda juda aniq bo'lishi mumkin antikor asoslangan texnikalar. Masalan, dan foydalanish antikorlar sun'iy ravishda qilingan lyuminestsent (lyuminestsent yorliqli antikorlar) o'ziga xoslikni bog'lash va aniqlashga yo'naltirilishi mumkin antijenler patogen mavjud. A lyuminestsentsiya mikroskopi keyinchalik klinik namunalar yoki o'stirilgan hujayralar ichida ichki antigenlarga bog'langan lyuminestsent etiketli antikorlarni aniqlash uchun ishlatiladi. Ushbu usul ayniqsa yorug'lik mikroskopi to'g'ridan-to'g'ri virusni aniqlashga qodir bo'lmagan virusli kasalliklarni aniqlashda foydalidir.

Yuqumli kasalliklarni aniqlashda boshqa mikroskopik protseduralar ham yordam berishi mumkin. Deyarli barcha hujayralar bir qator asosiy moddalar bilan osonlikcha bo'yalgan bo'yoqlar tufayli elektrostatik salbiy zaryadlangan uyali molekulalar va bo'yoqdagi musbat zaryadlar orasidagi tortishish. Hujayra odatda mikroskop ostida shaffof bo'lib, dog 'yordamida hujayra kontrastini uning fonida oshiradi. Kabi bo'yoq bilan hujayralarni bo'yash Giemsa dog 'yoki billur binafsha mikroskopistga uning kattaligi, shakli, ichki va tashqi komponentlarini va boshqa hujayralar bilan birikmalarini tavsiflashga imkon beradi. Bakteriyalarning turli xil bo'yash protseduralariga reaktsiyasi taksonomik tasnif mikroblarning Ikkita usul Gramli dog ' va kislotaga chidamli dog ', bu bakteriyalarni tasniflash va kasallik diagnostikasi uchun ishlatiladigan standart yondashuvlardir. Gram-dog'da bakteriyalar guruhlari aniqlanadi Firmicutes va Aktinobakteriyalar, ikkalasida ham ko'plab muhim inson patogenlari mavjud. Kislota tez bo'yash protsedurasi Actinobacterial avlodini aniqlaydi Mikobakteriya va Nokardiya.

Biokimyoviy sinovlar

Yuqumli kasalliklarni aniqlashda ishlatiladigan biokimyoviy testlar aniqlashni o'z ichiga oladi metabolik yoki fermentativ ma'lum bir yuqumli kasallikka xos bo'lgan mahsulotlar. Bakteriyalar fermentlanganligi sababli uglevodlar ularga xos naqshlarda tur va turlari, aniqlash fermentatsiya mahsulotlar odatda bakterial identifikatsiyalashda ishlatiladi. Kislotalar, spirtli ichimliklar va gazlar odatda ushbu testlarda bakteriyalar etishtirilganda aniqlanadi tanlangan suyuq yoki qattiq muhit.

Ning izolyatsiyasi fermentlar yuqtirilgan to'qimalardan yuqumli kasallikning biokimyoviy diagnostikasi uchun ham asos bo'lishi mumkin. Masalan, odamlar buni qila olmaydi RNK nusxalari na teskari transkriptaz va bu fermentlarning mavjudligi virusli infektsiyalarning o'ziga xos turlariga xosdir. Virusli oqsilning qobiliyati gemagglutinin bog'lash qizil qon hujayralari birgalikda aniqlanadigan matritsaga virusli infektsiya uchun biokimyoviy test sifatida ham tavsiflanishi mumkin, ammo qat'iyan aytganda gemaglutinin bu ferment va metabolik funktsiyaga ega emas.

Serologik usullar mikroorganizmlarni aniqlash uchun ishlatiladigan juda sezgir, o'ziga xos va ko'pincha o'ta tezkor sinovlardir. Ushbu testlar antitelning antigen bilan maxsus bog'lanish qobiliyatiga asoslangan. Antigen, odatda yuqumli razvedka tomonidan ishlab chiqarilgan oqsil yoki uglevod, antikor bilan bog'lanadi. Keyinchalik, ushbu majburiylik testga bog'liq bo'lgan turli xil ko'rinadigan ko'rinadigan hodisalar zanjirini o'rnatadi. Masalan, "Strep tomoq "tez-tez bir necha daqiqada tashxis qo'yiladi va qo'zg'atuvchisi tomonidan antigen paydo bo'lishiga asoslanadi, S. pyogenes, bu bemorning tomog'idan paxta sumkasi bilan olinadi. Serologik testlar, agar mavjud bo'lsa, odatda tanib olishning afzal usuli hisoblanadi, ammo testlarni ishlab chiqish qimmatga tushadi va testda ishlatiladigan reagentlar ko'pincha talab qiladi sovutish. Ba'zi serologik usullar juda qimmatga tushadi, ammo odatda "strep testi" dan foydalanilganda ular arzon bo'lishi mumkin.[17]

Murakkab serologik texnikalar ishlab chiqilgan bo'lib, ular ma'lum bo'lgan narsalarga aylandi Immunoassaylar. Immunoassaylar ba'zi anjomlar yordamida aniqlanishi mumkin bo'lgan elektromagnit yoki zarracha nurlanish signalini ishlab chiqarish uchun asosiy antitel - antigen bilan bog'lanishni asosi sifatida ishlatishi mumkin. Noma'lum signallarni maqsad antigenini miqdorini aniqlashga imkon beradigan standartlar bilan taqqoslash mumkin. Yuqumli kasalliklarni tashxislashda yordam berish uchun immunoassaylar antigenlarni yuqumli moddalar yoki chet el agentiga javoban yuqtirilgan organizm tomonidan hosil bo'lgan oqsillardan aniqlashi yoki o'lchashi mumkin. Masalan, A immunoassay virus zarrachasidan sirt oqsili mavjudligini aniqlashi mumkin. Immunoassay B boshqa tomondan, organizmning immun tizimi tomonidan ishlab chiqarilgan, virusni zararsizlantirish va yo'q qilishga imkon beradigan antikorlarni aniqlashi yoki o'lchashi mumkin.

Asbob yordamida antikor - antigenni bog'lash bilan bog'liq bo'lgan ikkinchi darajali reaktsiyalar natijasida hosil bo'lgan juda kichik signallarni o'qish uchun foydalanish mumkin. Yuqumli kasallik diagnostikasi uchun iqtisodiy jihatdan samarali avtomatlashtirilgan jarayonni amalga oshirish uchun asboblar namuna olishni, reagentlardan foydalanishni, reaktsiya vaqtlarini, signallarni aniqlashni, natijalarni hisoblashni va ma'lumotlarni boshqarishni boshqarishi mumkin.

PCR asosidagi diagnostika

Ga asoslangan texnologiyalar polimeraza zanjiri reaktsiyasi (PCR) usuli bir necha sabablarga ko'ra yaqin kelajakda diagnostikaning deyarli barcha oltin standartlariga aylanadi. Birinchidan, yuqumli kasalliklar agentlari katalogi shu darajaga yetdiki, deyarli inson populyatsiyasining barcha muhim yuqumli kasalliklari aniqlandi. Ikkinchidan, yuqumli kasallik odam organizmida kasallikka olib kelishi uchun o'sishi kerak; kasallikka olib kelishi uchun asosan o'z nuklein kislotalarini ko'paytirishi kerak. Yuqtirilgan to'qimalarda nuklein kislota kuchayishi PCR yordamida yuqumli kasallikni aniqlash imkoniyatini beradi. Uchinchidan, PCRni boshqarish uchun zarur vositalar, astarlar, dan olingan genomlar yuqumli agentlar va vaqt o'tishi bilan bu genomlar ma'lum bo'ladi, agar ular hali bo'lmasa.

Shunday qilib, har qanday yuqumli kasallikni tez va aniq aniqlashning texnologik qobiliyati hozirda mavjud. PCR-ni diagnostika qilishning standart vositasi sifatida ishlatishning qolgan yagona to'siqlari uning narxi va qo'llanilishida bo'lib, ularning ikkalasini ham engib bo'lmaydi. Bir nechta kasalliklarning tashxisi PCR usullarini ishlab chiqishda foyda keltirmaydi, masalan, ba'zilari klostridial kasalliklar (qoqshol va botulizm ). Ushbu kasalliklar juda kuchli bo'lgan yuqumli bakteriyalarning nisbatan oz sonli qismi tomonidan biologik zaharlanishdir neyrotoksinlar. Yuqumli razvedkaning sezilarli ko'payishi sodir bo'lmaydi, bu PCR ning har qanday bakteriyalar mavjudligini aniqlash qobiliyatini cheklaydi.

Metagenomik ketma-ketlik

Zaiflashtiradigan va hayotga xavf soladigan kasalliklarni keltirib chiqaradigan bakteriyalar, viruslar va boshqa patogenlarning keng assortimentini hisobga olgan holda, yuqtirish sababini tezda aniqlash qobiliyati juda muhimdir, ammo ko'pincha qiyin. Masalan, holatlarning yarmidan ko'pi ensefalit, zamonaviy klinik laboratoriya usullaridan foydalangan holda keng ko'lamli sinovlarga qaramay, miyaga ta'sir qiladigan og'ir kasallik aniqlanmagan bo'lib qolmoqda. Metagenomika Hozirgi kunda klinik foydalanish uchun izlanishlar olib borilmoqda va bitta hamma narsani qamrab olgan test yordamida infektsiyani aniqlashning sezgir va tezkor usuli sifatida umid baxsh etadi. Ushbu test hozirgi PCR sinovlariga o'xshaydi; ammo, genetik materialni kuchaytirish, ishlatishdan ko'ra xolisdir astarlar ma'lum bir yuqumli vosita uchun. Ushbu kuchaytirish bosqichidan keyin keyingi avlod ketma-ketligi va tekislashni taqqoslash minglab organizm va virus genomlarining katta ma'lumotlar bazalaridan foydalanish.

Metagenomik sekvensiya, ayniqsa, bemor bo'lganida tashxis qo'yish uchun foydalidir immunitet tanqisligi. Infektsion vositalarning tobora kengayib borishi immunosupressiyaga chalingan shaxslarga jiddiy zarar etkazishi mumkin, shuning uchun klinik skrining ko'pincha kengroq bo'lishi kerak. Bundan tashqari, simptomlarni ifodalash ko'pincha atipik bo'lib, prezentatsiya asosida klinik tashxis qo'yish qiyinlashadi. Uchinchidan, antikorlarni aniqlashga asoslangan diagnostika usullari muvaffaqiyatsizlikka uchraydi. Antikorlarni emas, balki yuqumli moddalarning mavjudligini aniqlaydigan patogenlar uchun keng, sezgir sinov juda kerakli.

Sinovlar ko'rsatkichi

Odatda bor ko'rsatma yuqumli razvedkaning o'ziga xos identifikatsiyasi uchun faqatgina bunday identifikatsiya kasallikni davolashda yoki oldini olishda yordam berishi yoki samarali terapevtik yoki profilaktika choralari ishlab chiqilishidan oldin kasallikning borishi to'g'risida bilimlarni oshirishi mumkin. Masalan, 1980 yillarning boshlarida, paydo bo'lishidan oldin AZT davolash uchun OITS, kasallikning davomiyligi bemorning qon namunalari tarkibini kuzatib borish bilan yaqindan kuzatib borildi, garchi natijasi bemorga boshqa davolash usullarini taklif qilmasa ham. Qisman, tashqi ko'rinishdagi ushbu tadqiqotlar OIV ma'lum jamoalarda ilgarilashga ruxsat berilgan gipotezalar virusni yuqtirish yo'liga kelsak. Kasallik qanday yuqganini tushunib, yangi yuqumli kasalliklar sonini kamaytirishga qaratilgan kampaniyalarda resurslar eng katta xavf ostida bo'lgan jamoalarga yo'naltirilishi mumkin. O'ziga xos serologik diagnostik identifikatsiya qilish va keyinchalik genotipik yoki OIVning molekulyar identifikatsiyasi, shuningdek, gipotezalarni ishlab chiqishga imkon berdi vaqtinchalik va geografik virusning kelib chiqishi, shuningdek boshqa ko'plab farazlar.[17] Molekulyar diagnostika vositalarining rivojlanishi shifokorlar va tadqiqotchilarga davolash samaradorligini nazorat qilish imkoniyatini berdi retrovirusga qarshi dorilar. Molecular diagnostics are now commonly used to identify HIV in healthy people long before the onset of illness and have been used to demonstrate the existence of people who are genetically resistant to HIV infection. Thus, while there still is no cure for AIDS, there is great therapeutic and predictive benefit to identifying the virus and monitoring the virus levels within the blood of infected individuals, both for the patient and for the community at large.

Oldini olish

Washing one's hands, a form of gigiena, is an effective way to prevent the spread of infectious disease.[37]

Techniques like hand washing, wearing gowns, and wearing face masks can help prevent infections from being passed from one person to another. Aseptik texnika was introduced in medicine and surgery in the late 19th century and greatly reduced the incidence of infections caused by surgery. Tez-tez qo'lni yuvish remains the most important defense against the spread of unwanted organisms.[38] There are other forms of prevention such as avoiding the use of illicit drugs, using a prezervativ, wearing gloves, and having a healthy lifestyle with a balanced diet and regular exercise. Cooking foods well and avoiding foods that have been left outside for a long time is also important.

Antimicrobial substances used to prevent transmission of infections include:

  • antiseptiklar, which are applied to living to'qima /teri
  • dezinfektsiyalovchi vositalar, tirik bo'lmagan narsalarda topilgan mikroorganizmlarni yo'q qiladigan.
  • antibiotiklar, deb nomlangan profilaktik when given as prevention rather as treatment of infection. However, long term use of antibiotics leads to resistance of bacteria. While humans do not become immune to antibiotics, the bacteria does. Thus, avoiding using antibiotics longer than necessary helps preventing bacteria from forming mutations that aide in antibiotic resistance.

One of the ways to prevent or slow down the transmission of infectious diseases is to recognize the different characteristics of various diseases.[39] Some critical disease characteristics that should be evaluated include zaharlanish, distance traveled by victims, and level of contagiousness. The human strains of Ebola virus, for example, incapacitate their victims extremely quickly and kill them soon after. As a result, the victims of this disease do not have the opportunity to travel very far from the initial infection zone.[40] Also, this virus must spread through skin lesions or permeable membranes such as the eye. Thus, the initial stage of Ebola is not very contagious since its victims experience only internal hemorrhaging. As a result of the above features, the spread of Ebola is very rapid and usually stays within a relatively confined geographical area. Aksincha, Inson immunitet tanqisligi virusi (OIV ) kills its victims very slowly by attacking their immune system.[17] As a result, many of its victims transmit the virus to other individuals before even realizing that they are carrying the disease. Also, the relatively low virulence allows its victims to travel long distances, increasing the likelihood of an epidemik.

Another effective way to decrease the transmission rate of infectious diseases is to recognize the effects of kichik dunyo tarmoqlari.[39] In epidemics, there are often extensive interactions within hubs or groups of infected individuals and other interactions within discrete hubs of susceptible individuals. Despite the low interaction between discrete hubs, the disease can jump to and spread in a susceptible hub via a single or few interactions with an infected hub. Thus, infection rates in small-world networks can be reduced somewhat if interactions between individuals within infected hubs are eliminated (Figure 1). However, infection rates can be drastically reduced if the main focus is on the prevention of transmission jumps between hubs. The use of needle exchange programs in areas with a high density of drug users with HIV is an example of the successful implementation of this treatment method. [6][to'liq iqtibos kerak ] Another example is the use of ring culling or vaccination of potentially susceptible livestock in adjacent farms to prevent the spread of the og'iz-og'iz virus in 2001.[41]

A general method to prevent transmission of vektor -borne pathogens is zararkunandalarga qarshi kurash.

In cases where infection is merely suspected, individuals may be karantin ostida until the incubation period has passed and the disease manifests itself or the person remains healthy. Groups may undergo quarantine, or in the case of communities, a kordon sanatoriyasi may be imposed to prevent infection from spreading beyond the community, or in the case of protective sequestration, into a community. Public health authorities may implement other forms of ijtimoiy masofani saqlash, such as school closings, to control an epidemic.

Immunitet

Meri Mallon (a.k.a. Typhoid Mary) was an asymptomatic carrier of tifo isitmasi. Over the course of her career as a cook, she infected 53 people, three of whom died.

Infection with most pathogens does not result in death of the host and the offending organism is ultimately cleared after the symptoms of the disease have waned.[16] Bu jarayon talab qiladi immune mechanisms to kill or inactivate the emlash patogenning. Specific acquired immunitet against infectious diseases may be mediated by antikorlar va / yoki T limfotsitlar. Immunity mediated by these two factors may be manifested by:

  • a direct effect upon a pathogen, such as antibody-initiated to'ldiruvchi -dependent bacteriolysis, opsonoization, fagotsitoz and killing, as occurs for some bacteria,
  • neutralization of viruses so that these organisms cannot enter cells,
  • or by T lymphocytes, which will kill a cell parasitized by a microorganism.

The immune system response to a microorganism often causes symptoms such as a high isitma va yallig'lanish, and has the potential to be more devastating than direct damage caused by a microbe.[17]

Resistance to infection (immunitet ) may be acquired following a disease, by asymptomatic carriage of the pathogen, by harboring an organism with a similar structure (crossreacting), or by emlash. Knowledge of the protective antigens and specific acquired host immune factors is more complete for primary pathogens than for opportunistik patogenlar.There is also the phenomenon of podaning immuniteti which offers a measure of protection to those otherwise vulnerable people when a large enough proportion of the population has acquired immunity from certain infections.

Immune resistance to an infectious disease requires a critical level of either antigen-specific antibodies and/or T cells when the host encounters the pathogen. Some individuals develop natural sarum antibodies to the surface polisakkaridlar of some agents although they have had little or no contact with the agent, these natural antibodies confer specific protection to adults and are passively transmitted to newborns.

Uy egasining genetik omillari

The organism that is the target of an infecting action of a specific infectious agent is called the host. The host harbouring an agent that is in a mature or sexually active stage phase is called the definitive host. The intermediate host comes in contact during the larvae stage. A host can be anything living and can attain to asexual and sexual reproduction.[42]The clearance of the pathogens, either treatment-induced or spontaneous, it can be influenced by the genetic variants carried by the individual patients. For instance, for genotype 1 hepatitis C treated with Pegillangan interferon-alfa-2a yoki Pegillangan interferon-alfa-2b (brand names Pegasys or PEG-Intron) combined with ribavirin, it has been shown that genetic polymorphisms near the human IL28B gene, encoding interferon lambda 3, are associated with significant differences in the treatment-induced clearance of the virus. This finding, originally reported in Nature,[43] showed that genotype 1 hepatitis C patients carrying certain genetic variant alleles near the IL28B gene are more possibly to achieve sustained virological response after the treatment than others. Later report from Nature[44] demonstrated that the same genetic variants are also associated with the natural clearance of the genotype 1 hepatitis C virus.

Muolajalar

When infection attacks the body, infektsiyaga qarshi drugs can suppress the infection. Several broad types of anti-infective drugs exist, depending on the type of organism targeted; they include antibacterial (antibiotik; shu jumladan antitubercular ), virusga qarshi, qo'ziqorinlarga qarshi va parazitga qarshi (shu jumladan antiprotozoal va antihelminthic ) agentlar. Depending on the severity and the type of infection, the antibiotic may be given by mouth or by injection, or may be applied lokal ravishda. Severe infections of the miya are usually treated with vena ichiga yuborish antibiotiklar. Sometimes, multiple antibiotics are used in case there is qarshilik to one antibiotic. Antibiotics only work for bacteria and do not affect viruses. Antibiotics work by slowing down the multiplication of bacteria or killing the bacteria. The most common classes of antibiotics used in medicine include penitsillin, sefalosporinlar, aminoglikozidlar, makrolidlar, kinolonlar va tetratsiklinlar.[45][46]

Not all infections require treatment, and for many o'z-o'zini cheklash infections the treatment may cause more side-effects than benefits. Antimikrobiyal boshqarma is the concept that healthcare providers should treat an infection with an antimicrobial that specifically works well for the target pathogen for the shortest amount of time and to only treat when there is a known or highly suspected pathogen that will respond to the medication.[47]

Epidemiologiya

Deaths due to infectious and parasitic diseases per million persons in 2012
  28–81
  82–114
  115–171
  172–212
  213–283
  284–516
  517–1,193
  1,194–2,476
  2,477–3,954
  3,955–6,812
Nogironlik uchun belgilangan hayot yili for infectious and parasitic diseases per 100,000 inhabitants in 2004.[48]
  ma'lumotlar yo'q
  ≤250
  250–500
  500–1000
  1000–2000
  2000–3000
  3000–4000
  4000–5000
  5000–6250
  6250–12,500
  12,500–25,000
  25,000–50,000
  ≥50,000

In 2010, about 10 million people died of infectious diseases.[49]

The Jahon Sog'liqni saqlash tashkiloti collects information on global deaths by International Classification of Disease (ICD) code categories. The following table lists the top infectious disease by number of deaths in 2002. 1993 data is included for comparison.

Worldwide mortality due to infectious diseases[50][51]
RankO'lim sababiDeaths 2002
(millionda)
Foiz
all deaths
Deaths 1993
(millionda)
1993 Rank
Yo'qAll infectious diseases14.725.9%16.432.2%
1Pastki nafas yo'llarining infektsiyalari[52]3.96.9%4.11
2OIV /OITS2.84.9%0.77
3Diareya kasalliklari[53]1.83.2%3.02
4Sil kasalligi (Sil kasalligi)1.62.7%2.73
5Bezgak1.32.2%2.04
6Qizamiq0.61.1%1.15
7Ko'k yo'tal0.290.5%0.367
8Tetanoz0.210.4%0.1512
9Menenjit0.170.3%0.258
10Sifilis0.160.3%0.1911
11Gepatit B0.100.2%0.936
12–17Tropik kasalliklar (6)[54]0.130.2%0.539, 10, 16–18
Note: Other causes of death include maternal and perinatal conditions (5.2%), nutritional deficiencies (0.9%),
noncommunicable conditions (58.8%), and injuries (9.1%).

The top three single agent/disease killers are OIV /OITS, Sil kasalligi va bezgak. While the number of deaths due to nearly every disease have decreased, deaths due to HIV/AIDS have increased fourfold. Childhood diseases include ko'kyo'tal, poliomiyelit, difteriya, qizamiq va qoqshol. Children also make up a large percentage of lower respiratory and diarrheal deaths. In 2012, approximately 3.1 million people have died due to lower respiratory infections, making it the number 4 leading cause of death in the world.[55]

Historic pandemics

Marselning katta o'lati in 1720 killed 100,000 people in the city and the surrounding provinces

With their potential for unpredictable and explosive impacts, infectious diseases have been major actors in human tarix.[56] A pandemiya (or global epidemik ) is a disease that affects people over an extensive geographical area. Masalan:

  • Yustinian vabosi, from 541 to 542, killed between 50% and 60% of Europe's population.[57]
  • The Qora o'lim of 1347 to 1352 killed 25 million in Europe over 5 years. The plague reduced the old world population from an estimated 450 million to between 350 and 375 million in the 14th century.
  • Kirish chechak, measles, and tifus to the areas of Central and South America by European explorers during the 15th and 16th centuries caused pandemics among the native inhabitants. Between 1518 and 1568 disease pandemics are said to have caused the population of Meksika to fall from 20 million to 3 million.[58]
  • Birinchi Evropa gripp epidemic occurred between 1556 and 1560, with an estimated mortality rate of 20%.[58]
  • Chechak killed an estimated 60 million Europeans during the 18th century[59] (approximately 400,000 per year).[60] Up to 30% of those infected, including 80% of the children under 5 years of age, died from the disease, and one-third of the survivors went blind.[61]
  • 19-asrda, sil kasalligi killed an estimated one-quarter of the adult population of Europe;[62] by 1918 one in six deaths in France were still caused by TB.
  • The Influenza Pandemic of 1918 (or the Ispan grippi ) killed 25–50 million people (about 2% of world population of 1.7 billion).[63] Bugun Gripp kills about 250,000 to 500,000 worldwide each year.

Emerging diseases

In most cases, microorganisms live in harmony with their hosts via o'zaro yoki komensal o'zaro ta'sirlar. Diseases can emerge when existing parasites become pathogenic or when new pathogenic parasites enter a new host.

  1. Koevolyutsiya o'rtasida parazit va mezbon can lead to hosts becoming chidamli to the parasites or the parasites may evolve greater zaharlanish, olib boradi immunopathological disease.
  2. Human activity is involved with many paydo bo'lgan yuqumli kasalliklar, kabi atrof-muhit o'zgarishi enabling a parasite to occupy new nişler. When that happens, a patogen that had been confined to a remote habitat has a wider distribution and possibly a new mezbon organizm. Parasites jumping from nonhuman to human hosts are known as zoonozlar. Under disease invasion, when a parasite invades a new host species, it may become pathogenic in the new host.[64]

Several human activities have led to the emergence of zoonoz human pathogens, including viruses, bacteria, protozoa, and rickettsia,[65] va tarqalishi vektorli kasalliklar,[64] Shuningdek qarang globalization and disease va yovvoyi tabiat kasalligi:

  • Encroachment on wildlife yashash joylari. The construction of new villages and housing developments in rural areas force animals to live in dense populations, creating opportunities for microbes to mutate and emerge.[66]
  • O'zgarishlar qishloq xo'jaligi. The introduction of new crops attracts new crop pests and the microbes they carry to farming communities, exposing people to unfamiliar diseases.
  • Yo'q qilish yomg'ir o'rmonlari. As countries make use of their rain forests, by building roads through forests and clearing areas for settlement or commercial ventures, people encounter insects and other animals harboring previously unknown microorganisms.
  • Nazorat qilinmaydi urbanizatsiya. The rapid growth of cities in many developing countries tends to concentrate large numbers of people into crowded areas with poor sanitation. These conditions foster transmission of contagious diseases.
  • Zamonaviy transport. Ships and other cargo carriers often harbor unintended "passengers", that can spread diseases to faraway destinations. While with international jet-airplane travel, people infected with a disease can carry it to distant lands, or home to their families, before their first symptoms appear.

Kasallikning mikrob nazariyasi

Sharqiy nemis pochta markalari depicting four antique mikroskoplar. Advancements in microscopy were essential to the early study of infectious diseases.

Yilda Antik davr, Yunoncha tarixchi Fukidid (c. 460 – c. 400 BCE) was the first person to write, in his account of the Afina vabosi, that diseases could spread from an infected person to others.[67][68] Uning ichida On the Different Types of Fever (c. AD 175), the Greco-Roman physician Galen speculated that plagues were spread by "certain seeds of plague", which were present in the air.[69] In Sushruta Samhita, the ancient Indian physician Sushruta theorized: "Leprosy, fever, consumption, diseases of the eye, and other infectious diseases spread from one person to another by sexual union, physical contact, eating together, sleeping together, sitting together, and the use of same clothes, garlands and pastes."[70][71] This book has been dated to about the sixth century BC.[72]

A basic form of contagion theory was proposed by Fors tili shifokor Ibn Sino (known as Avicenna in Europe) in Tibbiyot kanoni (1025), which later became the most authoritative medical textbook in Europe up until the 16th century. In Book IV of the Canon, Ibn Sina discussed epidemiyalar, outlining the classical miazma nazariyasi and attempting to blend it with his own early contagion theory. He mentioned that people can transmit disease to others by breath, noted contagion with sil kasalligi, and discussed the transmission of disease through water and dirt.[73] The concept of invisible contagion was later discussed by several Islom ulamolari ichida Ayyubid Sultonligi who referred to them as najasat ("impure substances"). The fiqh olim Ibn al-Haj al-Abdari (c. 1250–1336), while discussing Islamic diet va gigiena, gave warnings about how contagion can contaminate water, food, and garments, and could spread through the water supply, and may have implied contagion to be unseen particles.[74]

Qachon Qora o'lim Bubonik vabo yetdi Al-Andalus in the 14th century, the Arab physicians Ibn Khatima (c. 1369) and Ibn al-Xatib (1313–1374) hypothesised that infectious diseases were caused by "minute bodies" and described how they can be transmitted through garments, vessels and earrings.[75] Ideas of contagion became more popular in Europe during the Uyg'onish davri, particularly through the writing of the Italian physician Girolamo Frakastoro.[76] Anton van Leyvenxuk (1632–1723) advanced the science of mikroskopiya by being the first to observe microorganisms, allowing for easy visualization of bacteria.

19-asrning o'rtalarida Jon Snow va Uilyam Budd did important work demonstrating the contagiousness of typhoid and cholera through contaminated water. Both are credited with decreasing epidemics of cholera in their towns by implementing measures to prevent contamination of water.[77] Lui Paster proved beyond doubt that certain diseases are caused by infectious agents, and developed a vaccine for quturish. Robert Koch, provided the study of infectious diseases with a scientific basis known as Koch postulatlari. Edvard Jenner, Jonas Salk va Albert Sabin developed effective vaccines for chechak va poliomiyelit, which would later result in the yo'q qilish and near-eradication of these diseases, respectively. Aleksandr Fleming discovered the world's first antibiotik, Penitsillin, which Florey and Chain then developed. Gerxard Domagk ishlab chiqilgan sulfanamidlar, the first broad spectrum sintetik antibacterial drugs.

Tibbiy mutaxassislar

The tibbiy davolanish of infectious diseases falls into the tibbiyot sohasi ning Yuqumli kasallik and in some cases the study of propagation pertains to the field of Epidemiologiya. Generally, infections are initially diagnosed by birlamchi tibbiy yordam physicians or ichki kasalliklar mutaxassislar. For example, an "uncomplicated" zotiljam will generally be treated by the internist yoki pulmonolog (lung physician). The work of the infectious diseases specialist therefore entails working with both patients and general practitioners, as well as laboratory scientists, immunologlar, bakteriologlar va boshqa mutaxassislar.

An infectious disease team may be alerted when:

Jamiyat va madaniyat

A number of studies have reported associations between pathogen load in an area and human behavior. Higher pathogen load is associated with decreased size of ethnic and religious groups in an area. This may be due high pathogen load favoring avoidance of other groups, which may reduce pathogen transmission, or a high pathogen load preventing the creation of large settlements and armies that enforce a common culture. Higher pathogen load is also associated with more restricted sexual behavior, which may reduce pathogen transmission. It also associated with higher preferences for health and attractiveness in mates. Yuqori tug'ilish darajasi and shorter or less parental care per child is another association that may be a compensation for the higher mortality rate. There is also an association with ko'pburchak which may be due to higher pathogen load, making selecting males with a high genetic resistance increasingly important. Higher pathogen load is also associated with more collectivism and less individualism, which may limit contacts with outside groups and infections. There are alternative explanations for at least some of the associations although some of these explanations may in turn ultimately be due to pathogen load. Thus, polygyny may also be due to a lower male:female ratio in these areas but this may ultimately be due to male infants having increased mortality from infectious diseases. Another example is that poor socioeconomic factors may ultimately in part be due to high pathogen load preventing economic development.[78]

Qadimgi toshlar

Uzoq jag'lari va tishlari bo'lgan dinozavrning bosh suyagi.
Herrerasaurus bosh suyagi.

Evidence of infection in fossil remains is a subject of interest for paleopatologlar, scientists who study occurrences of injuries and illness in extinct life forms. Signs of infection have been discovered in the bones of carnivorous dinosaurs. When present, however, these infections seem to tend to be confined to only small regions of the body. A skull attributed to the early carnivorous dinosaur Herrerasaurus ischigualastensis exhibits pit-like wounds surrounded by swollen and porous bone. The unusual texture of the bone around the wounds suggests they were afflicted by a short-lived, non-lethal infection. Scientists who studied the skull speculated that the bite marks were received in a fight with another Herrerasaurus. Other carnivorous dinosaurs with documented evidence of infection include Akrokantozaurus, Allosaurus, Tiranozavr and a tyrannosaur from the Kirtland shakllanishi. The infections from both tyrannosaurs were received by being bitten during a fight, like the Herrerasaurus namuna.[79]

Kosmik fazo

2006 yilda o'tkazilgan "Space Shuttle" tajribasi shuni aniqladi Salmonella typhimurium, sabab bo'lishi mumkin bo'lgan bakteriya ovqatdan zaharlanish, kosmosda o'stirilganda ko'proq zararli bo'ldi.[80] 2013 yil 29 aprelda Rensselaer politexnika instituti olimlari tomonidan moliyalashtirildi NASA, davomida xabar bergan kosmik parvoz ustida Xalqaro kosmik stantsiya, mikroblar ga moslashganga o'xshaydi kosmik muhit "Yerda kuzatilmagan" usullar bilan va "o'sish o'sishiga olib kelishi mumkin bo'lgan va zaharlanish ".[81] Yaqinda, 2017 yilda, bakteriyalar ga nisbatan ancha chidamli ekanligi aniqlandi antibiotiklar va kosmosning deyarli vaznsizligida rivojlanish.[82] Mikroorganizmlar dan omon qolish kuzatilgan vakuum tashqi makon.[83][84]

Shuningdek qarang

Adabiyotlar

  1. ^ Definition of "infection" from several medical dictionaries – Retrieved on 2012-04-03
  2. ^ "Utilizing antibiotics agents effectively will preserve present day medication". Yangiliklar Gana. 2015 yil 21-noyabr. Olingan 21 noyabr 2015.
  3. ^ "Types of Fungal Diseases". www.cdc.gov. 2019-06-27. Olingan 2019-12-09.
  4. ^ Mada, Pradeep Kumar; Jamil, Radia T.; Alam, Mohammed U. (2019), "Cryptococcus (Cryptococcosis)", StatPearls, StatPearls nashriyoti, PMID  28613714, olingan 2019-12-09
  5. ^ "About Parasites". www.cdc.gov. 2019-02-25. Olingan 2019-12-09.
  6. ^ Brown, Peter J. (1987). "Microparasites and Macroparasites". Madaniy antropologiya. 2 (1): 155–71. doi:10.1525/can.1987.2.1.02a00120. JSTOR  656401.
  7. ^ Alberto Signore (2013). "About inflammation and infection" (PDF). EJNMMI tadqiqotlari. 8 (3).
  8. ^ GBD 2013 o'limi va o'lim sabablari, hamkasblar (2014 yil 17-dekabr). "Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990–2013: a systematic analysis for the Global Burden of Disease Study". Lanset. 385 (9963): 117–71. doi:10.1016 / S0140-6736 (14) 61682-2. PMC  4340604. PMID  25530442.
  9. ^ "Infectious Disease, Internal Medicine". Association of American Medical Colleges. Arxivlandi asl nusxasi 2015-02-06 da. Olingan 2015-08-20. Infectious disease is the subspecialty of internal medicine dealing with the diagnosis and treatment of communicable diseases of all types, in all organs, and in all ages of patients.
  10. ^ Kayser, Fritz H; Kurt A Bienz; Johannes Eckert; Rolf M Zinkernagel (2005). Tibbiy mikrobiologiya. Shtutgart: Georg Thieme Verlag. p. 398. ISBN  978-3-13-131991-3.
  11. ^ Grinde, Bjørn (2013-10-25). "Herpesviruses: latency and reactivation – viral strategies and host response". Og'iz mikrobiologiyasi jurnali. 5: 22766. doi:10.3402/jom.v5i0.22766. ISSN  0901-8328. PMC  3809354. PMID  24167660.
  12. ^ Elsevier, Dorlandning tibbiyotga oid illyustratsion lug'ati, Elsevier.
  13. ^ "Acute infections (MPKB)". mpkb.org. Olingan 2019-12-09.
  14. ^ Boldog, Istvan; Albrecht, Thomas; Porter, David D. (1996), Baron, Samuel (ed.), "Persistent Viral Infections", Tibbiy mikrobiologiya (4th ed.), Galveston shahridagi Texas tibbiyot filiali, ISBN  978-0-9631172-1-2, PMID  21413348, olingan 2020-01-23
  15. ^ a b Foster, John (2018). Mikrobiologiya. Nyu-York: Norton. p. 39. ISBN  978-0-393-60257-9.
  16. ^ a b This section incorporates jamoat mulki materials included in the text: Tibbiy mikrobiologiya Fourth Edition: 8-bob (1996). Baron, Samuel MD. Galveston shahridagi Texas tibbiyot universiteti. Tibbiy mikrobiologiya. Galveston shahridagi Texas tibbiyot filiali. 1996 yil. ISBN  9780963117212. Asl nusxasidan arxivlandi 2009 yil 29 iyun. Olingan 2013-11-27.CS1 maint: BOT: original-url holati noma'lum (havola)
  17. ^ a b v d e f Rayan KJ, Rey CG, nashr. (2004). Sherris tibbiyot mikrobiologiyasi (4-nashr). McGraw tepaligi. ISBN  978-0-8385-8529-0.
  18. ^ Higurea & Pietrangelo 2016[sahifa kerak ]
  19. ^ a b v "Bacterial vs. Viral Infections – Do You Know the Difference?" National Information Program on Antibiotics
  20. ^ Robert N. Golden; Fred Peterson (2009). The Truth About Illness and Disease. Infobase nashriyoti. p. 181. ISBN  978-1438126371.
  21. ^ "Yuqtirish". Rencare. Arxivlandi asl nusxasi 2012 yil 5 martda. Olingan 4 iyul 2013.
  22. ^ Yuqtirish tsikli – Retrieved on 2010-01-21 Arxivlandi 2014 yil 17-may, soat Orqaga qaytish mashinasi
  23. ^ Understanding Infectious Diseases Arxivlandi 2009-09-24 da Orqaga qaytish mashinasi Science.Education.Nih.Gov article – Retrieved on 2010-01-21
  24. ^ Negut, Irina; Grumezescu, Valentina; Grumezescu, Alexandru Mihai (2018-09-18). "Treatment Strategies for Infected Wounds". Molekulalar. 23 (9): 2392. doi:10.3390/molecules23092392. ISSN  1420-3049. PMC  6225154. PMID  30231567.
  25. ^ Duerkop, Breck A; Hooper, Lora V (2013-07-01). "Resident viruses and their interactions with the immune system". Tabiat immunologiyasi. 14 (7): 654–59. doi:10.1038/ni.2614. PMC  3760236. PMID  23778792.
  26. ^ "Bacterial Pathogenesis at Washington University". StudyBlue. Sent-Luis. Olingan 2016-12-02.
  27. ^ "Print Friendly". www.lifeextension.com. Arxivlandi asl nusxasi 2016-12-02 kunlari. Olingan 2016-12-02.
  28. ^ Reddy M, Gill SS, Wu W, et al. (Fevral 2012). "Ushbu bemorda surunkali yara infektsiyasi bormi?". JAMA. 307 (6): 605–11. doi:10.1001 / jama.2012.98. PMID  22318282.
  29. ^ http://www.immunize.org/catg.d/p4215.pdf
  30. ^ Chronic Infection Information Retrieved on 2010-01-14 Arxivlandi 2015 yil 22-iyul, soat Orqaga qaytish mashinasi
  31. ^ Ichak parazitlari va infektsiyasi Arxivlandi 2010-10-28 da Orqaga qaytish mashinasi fungusfocus.com - 2010-01-21 da olingan
  32. ^ "Clinical Infectious Disease – Introduction". www.microbiologybook.org. Olingan 2017-04-19.
  33. ^ Pathogens and vectors. MetaPathogen.com.
  34. ^ Seventer JM, Hochberg NS (October 2016). "Principles of Infectious Diseases: Transmission, Diagnosis, Prevention, and Control". Xalq salomatligi xalqaro ensiklopediyasi: 22–39. doi:10.1016/B978-0-12-803678-5.00516-6. ISBN  9780128037089. PMC  7150340.
  35. ^ Lyubin-Sternak, Suncanika; Mestrovich, Tomislav (2014). "Sharh: Chlamydia trachonmatis va genital mikoplazmiyalar: insonning reproduktiv salomatligiga ta'siri bo'lgan patogenlar". Patogenlar jurnali. 2014 (183167): 3. doi:10.1155/2014/183167. PMC  4295611. PMID  25614838.
  36. ^ a b Van den Bruel A, Haj-Hassan T, Thompson M, Buntinx F, Mant D (March 2010). "Diagnostic value of clinical features at presentation to identify serious infection in children in developed countries: a systematic review". Lanset. 375 (9717): 834–45. doi:10.1016/S0140-6736(09)62000-6. PMID  20132979. S2CID  28014329.
  37. ^ Bloomfield SF, Aiello AE, Cookson B, O'Boyle C, Larson EL (2007). "The effectiveness of hand hygiene procedures including hand-washing and alcohol-based hand sanitizers in reducing the risks of infections in home and community settings". Amerika yuqumli kasalliklarni nazorat qilish jurnali. 35 (10): S27–S64. doi:10.1016/j.ajic.2007.07.001. PMC  7115270.
  38. ^ ""Generalized Infectious Cycle" Diagram Illustration". science.education.nih.gov. Arxivlandi asl nusxasi 2009-09-24. Olingan 2010-01-21.
  39. ^ a b Watts, Duncan (2003). Six degrees: the science of a connected age. London: Uilyam Xayneman. ISBN  978-0-393-04142-2.
  40. ^ Preston, Richard (1995). The hot zone. Garden City, N.Y.: Anchor Books. ISBN  978-0-385-49522-6.
  41. ^ Ferguson NM, Donnelly CA, Anderson RM (May 2001). "The foot-and-mouth epidemic in Great Britain: pattern of spread and impact of interventions". Ilm-fan. 292 (5519): 1155–60. Bibcode:2001 yil ... 292.1155F. doi:10.1126 / science.1061020. PMID  11303090. S2CID  16914744.
  42. ^ Barreto ML, Teixeira MG, Carmo EH (2006). "Infectious diseases epidemiology". Epidemiologiya va jamiyat salomatligi jurnali. 60 (3): 192–95. doi:10.1136/jech.2003.011593. PMC  2465549. PMID  16476746.
  43. ^ Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sulkowski M, McHutchison JG, Goldstein DB (2009). "IL28B-ning genetik o'zgarishi gepatit C davolashga bog'liq virusni tozalashni bashorat qilmoqda". Tabiat. 461 (7262): 399–401. Bibcode:2009 yil natur.461..399G. doi:10.1038 / nature08309. PMID  19684573. S2CID  1707096.
  44. ^ Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O'Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M (2009). "IL28B genetik o'zgarishi va gepatit C virusini o'z-o'zidan tozalash". Tabiat. 461 (7265): 798–801. Bibcode:2009 yil natur.461..798T. doi:10.1038 / nature08463. PMC  3172006. PMID  19759533.
  45. ^ Fair RJ, Tor Y (2014). "Antibiotics and Bacterial Resistance in the 21st Century". Tibbiy kimyo istiqbollari. 6: 25–64. doi:10.4137/PMC.S14459. PMC  4159373. PMID  25232278. Olingan 13 may 2020.
  46. ^ "Antibiotics: List of Common Antibiotics & Types". Drugs.com. Olingan 2020-11-10.
  47. ^ O'Brien, Deirdre J.; Gould, Ian M. (August 2013). "Maximizing the impact of antimicrobial stewardship". Yuqumli kasalliklar bo'yicha hozirgi fikr. 26 (4): 352–58. doi:10.1097/QCO.0b013e3283631046. PMID  23806898. S2CID  5487584.
  48. ^ Jahon Sog'liqni saqlash tashkiloti (2009 yil fevral). "Age-standardized DALYs per 100,000 by cause, and Member State, 2004".
  49. ^ "Could Ebola rank among the deadliest communicable diseases?". CBC News. 20 oktyabr 2014 yil.
  50. ^ "The World Health Report (Annex Table 2)" (PDF). 2004.
  51. ^ "Table 5" (PDF). 1995.
  52. ^ Lower respiratory infections include various pnevmoniya, gripplar va o'tkir bronxit.
  53. ^ Diarrheal diseases are caused by many different organisms, including vabo, botulizm va E. coli bir nechtasini nomlash. See also: Intestinal infectious diseases
  54. ^ Tropical diseases include Chagas kasalligi, dang isitmasi, limfatik filariaz, leyshmanioz, onhocerciasis, shistozomiya va tripanozomiya.
  55. ^ "WHO | The top 10 causes of death". JSSV. Olingan 2015-09-24.
  56. ^ Fauci AS, Morens DM (2012). "The perpetual challenge of infectious diseases". Nyu-England tibbiyot jurnali. 366 (5): 454–61. doi:10.1056/NEJMra1108296. PMID  22296079.
  57. ^ "Infectious and Epidemic Disease in History" Arxivlandi 2012 yil 12-iyul, soat Arxiv.bugun
  58. ^ a b Dobson AP, Carter ER (1996). "Infectious Diseases and Human Population History" (PDF). BioScience. 46 (2): 115–26. doi:10.2307/1312814. JSTOR  1312814.
  59. ^ "Chechak". North Carolina Digital History.
  60. ^ Kichkintoy va Vaksiniya. Milliy Biotexnologiya Axborot Markazi. Arxivlandi 2009 yil 1 iyun, soat Orqaga qaytish mashinasi
  61. ^ Barquet, Nicolau (15 October 1997). "Smallpox: The Triumph over the Most Terrible of the Ministers of Death". Ichki tibbiyot yilnomalari. 127 (8_Part_1): 635–42. doi:10.7326/0003-4819-127-8_Part_1-199710150-00010. PMID  9341063. S2CID  20357515.
  62. ^ Multidrug-Resistant "Tuberculosis". Kasalliklarni nazorat qilish va oldini olish markazlari. Arxivlandi 2010 yil 9 mart, soat Orqaga qaytish mashinasi
  63. ^ "Influenza of 1918 (Spanish Flu) and the US Navy". 20 Fevral 2006. Arxivlangan asl nusxasi 2006 yil 20 fevralda.
  64. ^ a b Krauss H; Weber A; Appel M (2003). Zoonoses: Infectious Diseases Transmissible from Animals to Humans (3-nashr). Vashington, Kolumbiya: ASM Press. ISBN  978-1-55581-236-2.
  65. ^ Potter P (July 2013). "Summer buzz". Rivojlanayotgan yuqumli kasalliklar. 19 (3): 1184. doi:10.3201/eid1907.AC1907. PMC  3903457.
  66. ^ Peter Daszak; Endryu A. Kanningem; Alex D. Hyatt (27 January 2000). "Emerging Infectious Diseases of Wildlife – Threats to Biodiversity and Human Health". Ilm-fan. 287 (5452): 443–49. Bibcode:2000Sci...287..443D. doi:10.1126/science.287.5452.443. PMID  10642539.
  67. ^ Singer, Charles and Dorothea (1917) "The scientific position of Girolamo Fracastoro [1478?–1553] with especial reference to the source, character and influence of his theory of infection," Tibbiyot tarixi yilnomalari, 1 : 1–34; Qarang: p. 14.
  68. ^ Thucydides with Richard Crawley, trans., Peloponnes urushining tarixi (London: J.M. Dent & Sons, Ltd., 1910), Book III, § 51, 131-32 betlar.
  69. ^ Nutton, Vivian (1983) "The seeds of disease: an explanation of contagion and infection from the Greeks to the Renaissance," Tibbiyot tarixi, 27 (1) : 1–34; Qarang: p. 10. Available at: AQSh Milliy tibbiyot kutubxonasi, Milliy sog'liqni saqlash institutlari
  70. ^ Rastogi, Nalin; Rastogi, R (1985-01-01). "Leprosy in ancient India". International Journal of Leprosy and Other Mycobacterial Diseases. 52 (4): 541–43. PMID  6399073.
  71. ^ Susruta; Bhishagratna, Kunja Lal (1907–1916). An English translation of the Sushruta samhita, based on original Sanskrit text. Kaviraj Kunja Lal Bhishagratna tomonidan tahrir qilingan va nashr etilgan. With a full and comprehensive introd., translation of different readings, notes, comparative views, index, glossary and plates. Gerstein – University of Toronto. Kalkutta.
  72. ^ Hoernle, A. F. Rudolf (August Friedrich Rudolf) (1907). Studies in the medicine of ancient India. Gerstein – University of Toronto. Oxford : At the Clarendon Press.
  73. ^ Birn, Jozef Patrik (2012). Qora o'lim ensiklopediyasi. ABC-CLIO. p. 29. ISBN  978-1598842531.
  74. ^ Reid, Megan H. (2013). Law and Piety in Medieval Islam. Kembrij universiteti matbuoti. pp. 106, 114, 189–90. ISBN  978-1107067110.
  75. ^ Majeed, Azeem (22 December 2005). "Islom tibbiyotni qanday o'zgartirdi". BMJ. 331 (7531): 1486–87. doi:10.1136 / bmj.331.7531.1486. ISSN  0959-8138. PMC  1322233. PMID  16373721.
  76. ^ Beretta M (2003). "Uyg'onish davrida Lucretian atomizmi va yuqumli kasalliklarning tiklanishi". Medicina Nei Secoli. 15 (2): 129–54. PMID  15309812.
  77. ^ Moorhead Robert (2002 yil noyabr). "Uilyam Budd va tifo bezgagi". J R Soc Med. 95 (11): 561–64. doi:10.1258 / jrsm.95.11.561. PMC  1279260. PMID  12411628.
  78. ^ Nettle D (2009). "Odamlarning xulq-atvorining xilma-xilligiga ekologik ta'sir: so'nggi topilmalarni ko'rib chiqish". Ekol tendentsiyalari. Evol. 24 (11): 618–24. doi:10.1016 / j.tree.2009.05.013. PMID  19683831.
  79. ^ Molnar, R. E., 2001, "Tereopod paleopatologiyasi: adabiyot tadqiqotlari": In: Mezozoy umurtqali hayoti, Tanke, D. H. va Carpenter tomonidan tahrirlangan, K., Indiana University Press, 337-63 betlar.
  80. ^ Kaspermeyer, Djo (2007 yil 23 sentyabr). "Bakteriyalarning kasallik keltirib chiqaradigan qobiliyatini o'zgartiradigan kosmik parvoz ko'rsatilgan". Arizona shtati universiteti. Olingan 14 sentyabr 2017.
  81. ^ Kim V va boshq. (2013 yil 29 aprel). "Kosmik parvoz Pseudomonas aeruginosa tomonidan biofilm hosil bo'lishiga yordam beradi". PLOS ONE. 8 (4): e6237. Bibcode:2013PLoSO ... 862437K. doi:10.1371 / journal.pone.0062437. PMC  3639165. PMID  23658630.
  82. ^ Dvorskiy, Jorj (2017 yil 13 sentyabr). "Dahshatli tadqiqotlar nima uchun ba'zi bakteriyalar kosmosdagi giyohvand moddalarga chidamli ekanligini ko'rsatadi". Gizmodo. Olingan 14 sentyabr 2017.
  83. ^ Doz, K .; Biger-Doz, A .; Dillmann, R .; Gill, M.; Kerz, O .; Klayn, A .; Meinert, H.; Navrot, T .; Risi, S .; Stridde, C. (1995). "ERA-eksperiment" kosmik biokimyo"" (PDF). Kosmik tadqiqotlardagi yutuqlar. 16 (8): 119–29. Bibcode:1995 yil AdSpR..16..119D. doi:10.1016 / 0273-1177 (95) 00280-R. PMID  11542696.[doimiy o'lik havola ]
  84. ^ Xornek G.; Eschayler, U .; Reyts, G.; Wehner, J .; Willimek, R .; Strauch, K. (1995). "Kosmosga biologik ta'sirlar: EURECA I bo'yicha ERA" Eksobiologik birlik "tajribasi natijalari". Adv. Space Res. 16 (8): 105–18. Bibcode:1995 yil AdSpR..16..105H. doi:10.1016 / 0273-1177 (95) 00279-N. PMID  11542695.

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