Opportunistic infection: Difference between revisions
m Task 18 (cosmetic): eval 10 templates: del empty params (6×); hyphenate params (1×); del |url-status= (1×); |
Immcarle140 (talk | contribs) The introduction was made more robust, and sources were added. The “types of infections” section was reworked: broken into sections by pathogen types, and short descriptions and sources added to each pathogen listed. Pathogens previously listed but lacking a strong foundation in existing review literature were removed. A brief definition was added to the beginning of the causes section. A section was added on the role of opportunistic infection in AIDS. |
||
Line 23: | Line 23: | ||
| deaths = |
| deaths = |
||
}} |
}} |
||
An '''opportunistic infection''' is an [[infection]] caused by [[pathogen]]s ([[bacteria]], [[fungus|fungi]], [[Parasitism|parasites]] or [[virus]]es) that take advantage of an opportunity not normally available. These opportunities can stem from a variety of sources, such as a [[weakened immune system]] (as can occur in [[AIDS|acquired immunodeficiency syndrome]] or when being treated with [[Immunosuppressive drug|immunosuppressive drugs]], as in [[Treatment of cancer|cancer treatment]]),<ref name=":1">{{Citation|last=Justiz Vaillant|first=Angel A.|title=Immunodeficiency|date=2021|url=http://www.ncbi.nlm.nih.gov/books/NBK500027/|work=StatPearls|place=Treasure Island (FL)|publisher=StatPearls Publishing|pmid=29763203|access-date=2021-03-09|last2=Qurie|first2=Ahmad}}</ref> an altered [[microbiome]] (such as a disruption in [[Gut flora|gut microbiota]]), or breached [[Integumentary system|integumentary]] barriers (as in [[penetrating trauma]]). Many of these pathogens do not cause disease in a healthy host that has a non-compromised immune system, and can, in some cases, act as [[Commensalism|commensals]] until the balance of the immune system is disrupted.<ref name=":2">{{Cite journal|last=Schroeder|first=Max R.|last2=Stephens|first2=David S.|date=2016-09-21|title=Macrolide Resistance in Streptococcus pneumoniae|url=http://journal.frontiersin.org/Article/10.3389/fcimb.2016.00098/abstract|journal=Frontiers in Cellular and Infection Microbiology|volume=6|doi=10.3389/fcimb.2016.00098|issn=2235-2988|pmc=PMC5030221|pmid=27709102}}</ref><ref>{{Cite journal|last=Achermann|first=Y.|last2=Goldstein|first2=E. J. C.|last3=Coenye|first3=T.|last4=Shirtliff|first4=M. E.|date=2014-07-01|title=Propionibacterium acnes: from Commensal to Opportunistic Biofilm-Associated Implant Pathogen|url=https://cmr.asm.org/content/27/3/419|journal=Clinical Microbiology Reviews|language=en|volume=27|issue=3|pages=419–440|doi=10.1128/CMR.00092-13|issn=0893-8512|pmc=PMC4135900|pmid=24982315}}</ref> Opportunistic infections can also be attributed to pathogens that cause mild illness in healthy individuals but lead to more serious illness when given the opportunity to take advantage of an immunocompromised host.<ref>{{Cite journal|last=Caballero|first=Mauricio T.|last2=Polack|first2=Fernando P.|date=2018-02-20|title=Respiratory syncytial virus is an “opportunistic” killer|url=http://doi.wiley.com/10.1002/ppul.23963|journal=Pediatric Pulmonology|language=en|volume=53|issue=5|pages=664–667|doi=10.1002/ppul.23963|pmc=PMC5947624|pmid=29461021}}</ref> |
|||
An '''opportunistic infection''' is an [[infection]] caused by [[pathogen]]s ([[bacteria]], [[virus]]es, [[fungus|fungi]], or [[protozoa]]) that take advantage of an opportunity not normally available, such as a host with a [[immunodeficiency|weakened immune system]], an altered [[microbiota]] (such as a disrupted [[gut flora|gut microbiota]]), or breached [[integumentary system|integumentary]] barriers. Many of these pathogens do not cause disease in a healthy host that has a normal immune system. However, a compromised immune system, which is seriously debilitated and has lowered resistance to infection, a [[penetrating trauma|penetrating injury]], or a lack of competition from normal [[commensalism|commensals]] presents an opportunity for the pathogen to infect. |
|||
== Types of infections== |
== Types of opportunistic infections== |
||
{{Further|Immunodeficiency}} |
{{Further|Immunodeficiency}} |
||
A wide variety of pathogens are involved in opportunistic infection and can cause a similarly wide range in pathologies. A partial list of opportunistic pathogens and their associated presentations includes: |
|||
A partial listing of opportunistic organisms includes: |
|||
=== Bacteria === |
|||
* ''[[Aspergillus]]'' sp. |
|||
* ''[[Candida albicans]]'' |
|||
* ''[[Clostridioides difficile]]'' (formerly known as ''Clostridium difficile'') is a species of bacteria that is known to cause gastrointestinal infection and is typically associated with the [[Hospital-acquired infection|hospital setting]]. <ref>{{Cite journal|last=Czepiel|first=Jacek|last2=Dróżdż|first2=Mirosław|last3=Pituch|first3=Hanna|last4=Kuijper|first4=Ed J.|last5=Perucki|first5=William|last6=Mielimonka|first6=Aleksandra|last7=Goldman|first7=Sarah|last8=Wultańska|first8=Dorota|last9=Garlicki|first9=Aleksander|last10=Biesiada|first10=Grażyna|date=2019-04-03|title=Clostridium difficile infection: review|url=http://link.springer.com/10.1007/s10096-019-03539-6|journal=European Journal of Clinical Microbiology & Infectious Diseases|language=en|volume=38|issue=7|pages=1211–1221|doi=10.1007/s10096-019-03539-6|issn=0934-9723|pmc=PMC6570665|pmid=30945014}}</ref><ref>{{Cite journal|last=Guh|first=Alice Y.|last2=Kutty|first2=Preeta K.|date=2018-10-02|title=Clostridioides difficile Infection|url=http://annals.org/article.aspx?doi=10.7326/AITC201810020|journal=Annals of Internal Medicine|language=en|volume=169|issue=7|pages=ITC49|doi=10.7326/AITC201810020|issn=0003-4819|pmc=PMC6524133|pmid=30285209}}</ref> |
|||
* ''[[Clostridium difficile (bacteria)|Clostridium difficile]]'' |
|||
* ''[[Legionella pneumophila]]'' is a bacterium that causes [[Legionnaires' disease|Legionnaire’s disease]], a [[Respiratory tract infection|respiratory infection]].<ref>{{Cite journal|last=Chahin|first=Abdullah|last2=Opal|first2=Steven M.|date=March 2017|title=Severe Pneumonia Caused by Legionella pneumophila|url=https://linkinghub.elsevier.com/retrieve/pii/S0891552016300952|journal=Infectious Disease Clinics of North America|language=en|volume=31|issue=1|pages=111–121|doi=10.1016/j.idc.2016.10.009|pmc=PMC7135102|pmid=28159171}}</ref><ref>{{Cite journal|last=Berjeaud|first=Jean-Marc|last2=Chevalier|first2=Sylvie|last3=Schlusselhuber|first3=Margot|last4=Portier|first4=Emilie|last5=Loiseau|first5=Clémence|last6=Aucher|first6=Willy|last7=Lesouhaitier|first7=Olivier|last8=Verdon|first8=Julien|date=2016-04-08|title=Legionella pneumophila: The Paradox of a Highly Sensitive Opportunistic Waterborne Pathogen Able to Persist in the Environment|url=http://journal.frontiersin.org/Article/10.3389/fmicb.2016.00486/abstract|journal=Frontiers in Microbiology|volume=7|doi=10.3389/fmicb.2016.00486|issn=1664-302X|pmc=PMC4824771|pmid=27092135}}</ref> |
|||
* ''[[Coccidioides immitis]]'' |
|||
* [[Mycobacterium avium complex|''Mycobacterium avium complex'']] (MAC) is a group of two bacteria, ''M. avium'' and ''M. intracellulare'', that typically co-infect, leading to a lung infection called [[mycobacterium avium-intracellulare infection]]. <ref>{{Cite journal|last=O. Falkinham|first=Joseph|last2=Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia 24061, USA|date=2018|title=Mycobacterium avium complex: Adherence as a way of life|url=http://www.aimspress.com/article/10.3934/microbiol.2018.3.428|journal=AIMS Microbiology|language=en|volume=4|issue=3|pages=428–438|doi=10.3934/microbiol.2018.3.428|issn=2471-1888|pmc=PMC6604937|pmid=31294225}}</ref><ref>{{Cite journal|last=Pan|first=Sheng-Wei|last2=Shu|first2=Chin-Chung|last3=Feng|first3=Jia-Yih|last4=Su|first4=Wei-Juin|date=June 2020|title=Treatment for Mycobacterium avium complex lung disease|url=https://linkinghub.elsevier.com/retrieve/pii/S0929664620301790|journal=Journal of the Formosan Medical Association|language=en|volume=119|pages=S67–S75|doi=10.1016/j.jfma.2020.05.006}}</ref> |
|||
* ''[[Cryptococcus neoformans]]'' |
|||
* ''[[Mycobacterium tuberculosis]]'' is a species of bacteria that causes [[tuberculosis]], a respiratory infection.<ref>{{Cite journal|last=Gordon|first=Stephen V.|last2=Parish|first2=Tanya|date=2018-04-01|title=Microbe Profile: Mycobacterium tuberculosis: Humanity's deadly microbial foe|url=https://www.microbiologyresearch.org/content/journal/micro/10.1099/mic.0.000601|journal=Microbiology|language=en|volume=164|issue=4|pages=437–439|doi=10.1099/mic.0.000601|issn=1350-0872}}</ref> |
|||
* ''[[Cryptosporidium]]'' |
|||
* ''[[Pseudomonas aeruginosa]]'' is a bacterium that can cause respiratory infections. It is frequently associated with [[cystic fibrosis]] and hospital-acquired infections.<ref>{{Cite journal|last=Pang|first=Zheng|last2=Raudonis|first2=Renee|last3=Glick|first3=Bernard R.|last4=Lin|first4=Tong-Jun|last5=Cheng|first5=Zhenyu|date=January-February 2019|title=Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies|url=https://linkinghub.elsevier.com/retrieve/pii/S0734975018301976|journal=Biotechnology Advances|language=en|volume=37|issue=1|pages=177–192|doi=10.1016/j.biotechadv.2018.11.013}}</ref> |
|||
* ''[[Cytomegalovirus]]'' |
|||
* ''[[Salmonella]]'' is a [[genus]] of bacteria, known to cause gastrointestinal infections.<ref>{{Cite journal|last=Lamas|first=Alexandre|last2=Miranda|first2=José Manuel|last3=Regal|first3=Patricia|last4=Vázquez|first4=Beatriz|last5=Franco|first5=Carlos Manuel|last6=Cepeda|first6=Alberto|date=January 2018|title=A comprehensive review of non-enterica subspecies of Salmonella enterica|url=https://linkinghub.elsevier.com/retrieve/pii/S0944501317304159|journal=Microbiological Research|language=en|volume=206|pages=60–73|doi=10.1016/j.micres.2017.09.010}}</ref> |
|||
* ''[[Geomyces destructans]]'' (bats) |
|||
* ''[[Staphylococcus aureus]]'' is a bacterium known to cause skin infections and [[sepsis]], among other pathologies. Notably, ''S. aureus'' has evolved several [[Drug resistance|drug-resistant]] strains, including [[Methicillin-resistant Staphylococcus aureus|MRSA]].<ref>{{Cite journal|last=Jenul|first=Christian|last2=Horswill|first2=Alexander R.|date=2019-03-22|title=Regulation of Staphylococcus aureus Virulence|url=http://www.asmscience.org/content/journal/microbiolspec/10.1128/microbiolspec.GPP3-0031-2018|journal=Microbiology Spectrum|language=en|volume=7|issue=2|doi=10.1128/microbiolspec.GPP3-0031-2018|issn=2165-0497|pmc=PMC6452892|pmid=30953424}}</ref><ref>{{Cite journal|last=Kong|first=Cin|last2=Neoh|first2=Hui-min|last3=Nathan|first3=Sheila|date=2016-03-15|title=Targeting Staphylococcus aureus Toxins: A Potential form of Anti-Virulence Therapy|url=http://www.mdpi.com/2072-6651/8/3/72|journal=Toxins|language=en|volume=8|issue=3|pages=72|doi=10.3390/toxins8030072|issn=2072-6651|pmc=PMC4810217|pmid=26999200}}</ref> |
|||
* ''[[Histoplasma capsulatum]]'' |
|||
* ''[[Streptococcus pneumoniae]]'' is a bacterium that causes respiratory infections. <ref name=":2" /> |
|||
* ''[[Isospora belli]]'' |
|||
* ''[[Streptococcus pyogenes]]'' (also known as group A ''Streptococcus'') is a bacterium that can cause a variety of pathologies, including [[impetigo]] and [[Streptococcal pharyngitis|strep throat]], as well as other, more serious, illnesses.<ref>{{Cite journal|last=Jespersen|first=Magnus G.|last2=Lacey|first2=Jake A.|last3=Tong|first3=Steven Y.C.|last4=Davies|first4=Mark R.|date=December 2020|title=Global genomic epidemiology of Streptococcus pyogenes|url=https://linkinghub.elsevier.com/retrieve/pii/S1567134820304408|journal=Infection, Genetics and Evolution|language=en|volume=86|pages=104609|doi=10.1016/j.meegid.2020.104609}}</ref><ref>{{Cite journal|last=Brouwer|first=Stephan|last2=Barnett|first2=Timothy C.|last3=Rivera-Hernandez|first3=Tania|last4=Rohde|first4=Manfred|last5=Walker|first5=Mark J.|date=2016-06-17|title=Streptococcus pyogenes adhesion and colonization|url=http://doi.wiley.com/10.1002/1873-3468.12254|journal=FEBS Letters|language=en|volume=590|issue=21|pages=3739–3757|doi=10.1002/1873-3468.12254}}</ref> |
|||
* ''[[JC virus|Polyomavirus JC polyomavirus]]'', the virus that causes [[Progressive multifocal leukoencephalopathy]]. |
|||
* ''[[Kaposi's Sarcoma]] caused by [[Human herpesvirus 8]] (HHV8)'', also called Kaposi's sarcoma-associated herpesvirus (KSHV) |
|||
=== Fungi === |
|||
* ''[[Legionellosis|Legionnaires' Disease (Legionella pneumophila)]]'' |
|||
* ''[[Microsporidium]]'' |
|||
* ''[[Aspergillus]]'' is a fungus, commonly associated with respiratory infection.<ref>{{Cite journal|last=Latgé|first=Jean-Paul|last2=Chamilos|first2=Georgios|date=2019-11-13|title=Aspergillus fumigatus and Aspergillosis in 2019|url=https://cmr.asm.org/content/33/1/e00140-18|journal=Clinical Microbiology Reviews|language=en|volume=33|issue=1|pages=e00140–18, /cmr/33/1/CMR.00140–18.atom|doi=10.1128/CMR.00140-18|issn=0893-8512|pmc=PMC6860006|pmid=31722890}}</ref> <ref name=":3">{{Cite journal|last=José|first=Ricardo J.|last2=Periselneris|first2=Jimstan N.|last3=Brown|first3=Jeremy S.|date=June 2020|title=Opportunistic bacterial, viral and fungal infections of the lung|url=https://linkinghub.elsevier.com/retrieve/pii/S1357303920300530|journal=Medicine|language=en|volume=48|issue=6|pages=366–372|doi=10.1016/j.mpmed.2020.03.006|pmc=PMC7206443|pmid=32390758}}</ref> |
|||
* ''[[Mycobacterium avium complex]] (MAC) (Nontuberculosis Mycobacterium)'' |
|||
* ''[[Candida albicans]]'' is a species of fungus that is associated with [[Oral candidiasis|oral thrush]] and gastrointestinal infection. <ref>{{Cite journal|last=Akpan|first=A|date=2002-08-01|title=Oral candidiasis|url=https://pmj.bmj.com/lookup/doi/10.1136/pmj.78.922.455|journal=Postgraduate Medical Journal|volume=78|issue=922|pages=455–459|doi=10.1136/pmj.78.922.455|pmc=PMC1742467|pmid=12185216}}</ref><ref>{{Cite journal|last=Erdogan|first=Askin|last2=Rao|first2=Satish S. C.|date=2015-03-19|title=Small Intestinal Fungal Overgrowth|url=http://link.springer.com/10.1007/s11894-015-0436-2|journal=Current Gastroenterology Reports|language=en|volume=17|issue=4|pages=16|doi=10.1007/s11894-015-0436-2|issn=1522-8037}}</ref> |
|||
* ''[[Mycobacterium tuberculosis]]'' |
|||
* ''[[Coccidioides immitis]]'' is a fungus known for causing [[Coccidioidomycosis]], more commonly known as Valley Fever. <ref>{{Cite journal|last=Mu|first=Anandit|last2=Shein|first2=Thwe Thwe|last3=Jayachandran|first3=Priya|last4=Paul|first4=Simon|date=2017-09-14|title=Immune Reconstitution Inflammatory Syndrome in Patients with AIDS and Disseminated Coccidioidomycosis: A Case Series and Review of the Literature|url=http://journals.sagepub.com/doi/10.1177/2325957417729751|journal=Journal of the International Association of Providers of AIDS Care (JIAPAC)|language=en|volume=16|issue=6|pages=540–545|doi=10.1177/2325957417729751|issn=2325-9582}}</ref> |
|||
* [[Pneumocystis pneumonia|''Pneumocystis jirovecii'']], previously known as [[Pneumocystis carinii|''Pneumocystis carinii'' f. ''hominis'']] |
|||
* ''[[Cryptococcus neoformans]]'' is a fungus that causes [[cryptococcosis]], which can lead to pulmonary infection as well as nervous system infections, like [[meningitis]].<ref>{{Cite journal|last=Kwon-Chung|first=K. J.|last2=Fraser|first2=J. A.|last3=Doering|first3=T. L.|last4=Wang|first4=Z. A.|last5=Janbon|first5=G.|last6=Idnurm|first6=A.|last7=Bahn|first7=Y.-S.|date=2014-07-01|title=Cryptococcus neoformans and Cryptococcus gattii, the Etiologic Agents of Cryptococcosis|url=http://perspectivesinmedicine.cshlp.org/lookup/doi/10.1101/cshperspect.a019760|journal=Cold Spring Harbor Perspectives in Medicine|language=en|volume=4|issue=7|pages=a019760–a019760|doi=10.1101/cshperspect.a019760|issn=2157-1422|pmc=PMC4066639|pmid=24985132}}</ref> <ref>{{Cite journal|last=Maziarz|first=Eileen K.|last2=Perfect|first2=John R.|date=March 2016|title=Cryptococcosis|url=https://linkinghub.elsevier.com/retrieve/pii/S0891552015000951|journal=Infectious Disease Clinics of North America|language=en|volume=30|issue=1|pages=179–206|doi=10.1016/j.idc.2015.10.006|pmc=PMC5808417|pmid=26897067}}</ref> |
|||
* ''[[Pseudomonas aeruginosa]]'' |
|||
* ''[[Histoplasma capsulatum]]'' is a species of fungus known to cause [[histoplasmosis]], which can present with an array of symptoms, but often involves respiratory infection.<ref>{{Cite journal|last=Horwath|first=Michael C|last2=Fecher|first2=Roger A|last3=Deepe|first3=George S|date=2015-06-10|title=Histoplasma capsulatum , lung infection and immunity|url=https://www.futuremedicine.com/doi/10.2217/fmb.15.25|journal=Future Microbiology|language=en|volume=10|issue=6|pages=967–975|doi=10.2217/fmb.15.25|issn=1746-0913|pmc=PMC4478585|pmid=26059620}}</ref><ref>{{Citation|last=Mittal|first=Jamie|title=Histoplasma Capsulatum: Mechanisms for Pathogenesis|date=2018|url=http://link.springer.com/10.1007/82_2018_114|work=Fungal Physiology and Immunopathogenesis|volume=422|pages=157–191|editor-last=Rodrigues|editor-first=Marcio L.|place=Cham|publisher=Springer International Publishing|language=en|doi=10.1007/82_2018_114|isbn=978-3-030-30236-8|pmc=PMC7212190|pmid=30043340|access-date=2021-03-09|last2=Ponce|first2=Maria G.|last3=Gendlina|first3=Inessa|last4=Nosanchuk|first4=Joshua D.}}</ref> |
|||
* ''[[Salmonella]]'' |
|||
* ''[[Pseudogymnoascus destructans]]'' (formerly known as ''Geomyces destructans'') is a fungus that causes [[white-nose syndrome]] in [[Bat|bats]].<ref>{{Cite journal|last=Seyedmousavi|first=Seyedmojtaba|last2=Bosco|first2=Sandra de M G|last3=de Hoog|first3=Sybren|last4=Ebel|first4=Frank|last5=Elad|first5=Daniel|last6=Gomes|first6=Renata R|last7=Jacobsen|first7=Ilse D|last8=Jensen|first8=Henrik E|last9=Martel|first9=An|last10=Mignon|first10=Bernard|last11=Pasmans|first11=Frank|date=2018-04-01|title=Fungal infections in animals: a patchwork of different situations|url=https://academic.oup.com/mmy/article/56/suppl_1/S165/4925968|journal=Medical Mycology|language=en|volume=56|issue=suppl_1|pages=S165–S187|doi=10.1093/mmy/myx104|issn=1369-3786|pmc=PMC6251577|pmid=29538732}}</ref> |
|||
* ''[[Staphylococcus aureus]]'' |
|||
* ''[[Microsporidia]]'' is a group of fungi that infect species across the [[Animal|animal kingdom]], one species of which can cause [[microsporidiosis]] in immunocompromised human hosts.<ref>{{Cite journal|last=Stentiford|first=G.D.|last2=Becnel|first2=-->J.J.|last3=Weiss|first3=L.M.|last4=Keeling|first4=P.J.|last5=Didier|first5=E.S.|last6=Williams|first6=B-->.A.P.|last7=Bjornson|first7=S.|last8=Kent|first8=M-->.L.|last9=Freeman|first9=M.A.|last10=Brown|first10=M.J.F.|last11=Troemel|first11=E-->.R.|date=April 2016|title=Microsporidia – Emergent Pathogens in the Global Food Chain|url=https://linkinghub.elsevier.com/retrieve/pii/S1471492215002652|journal=Trends in Parasitology|language=en|volume=32|issue=4|pages=336–348|doi=10.1016/j.pt.2015.12.004|pmc=PMC4818719|pmid=26796229}}</ref> |
|||
* ''[[Streptococcus pneumoniae]]'' |
|||
* ''[[Pneumocystis jirovecii]]'' (formerly known as ''Pneumocystis carinii'') is a fungus that causes [[pneumocystis pneumonia]], a respiratory infection.<ref>{{Cite journal|last=Sokulska|first=Magdalena|last2=Kicia|first2=Marta|last3=Wesołowska|first3=Maria|last4=Hendrich|first4=Andrzej B.|date=2015-08-19|title=Pneumocystis jirovecii—from a commensal to pathogen: clinical and diagnostic review|url=http://link.springer.com/10.1007/s00436-015-4678-6|journal=Parasitology Research|language=en|volume=114|issue=10|pages=3577–3585|doi=10.1007/s00436-015-4678-6|issn=0932-0113|pmc=PMC4562001|pmid=26281787}}</ref> |
|||
* ''[[Streptococcus pyogenes]]'' |
|||
* ''[[Toxoplasma gondii]]'' |
|||
=== Parasites === |
|||
* ''[[Cryptosporidium]]'' is a [[Protozoa|protozoan]] that infects the [[gastrointestinal tract]].<ref>{{Cite journal|last=Gerace|first=Elisabetta|last2=Presti|first2=Vincenzo Di Marco Lo|last3=Biondo|first3=Carmelo|date=2019-12-01|title=Cryptosporidium infection: epidemiology, pathogenesis, and differential diagnosis|url=https://akjournals.com/doi/10.1556/1886.2019.00019|journal=European Journal of Microbiology and Immunology|language=en|volume=9|issue=4|pages=119–123|doi=10.1556/1886.2019.00019|issn=2062-8633|pmc=PMC6945992|pmid=31934363}}</ref> |
|||
* ''[[Toxoplasma gondii]]'' is a protozoan, known for causing [[toxoplasmosis]].<ref>{{Cite journal|last=Mendez|first=Oscar A.|last2=Koshy|first2=Anita A.|date=2017-07-20|editor-last=Gubbels|editor-first=Marc-Jan|title=Toxoplasma gondii: Entry, association, and physiological influence on the central nervous system|url=https://dx.plos.org/10.1371/journal.ppat.1006351|journal=PLOS Pathogens|language=en|volume=13|issue=7|pages=e1006351|doi=10.1371/journal.ppat.1006351|issn=1553-7374|pmc=PMC5519211|pmid=28727854}}</ref><ref>{{Cite journal|last=Hunter|first=Christopher A.|last2=Sibley|first2=L. David|date=2012-10-16|title=Modulation of innate immunity by Toxoplasma gondii virulence effectors|url=http://www.nature.com/articles/nrmicro2858|journal=Nature Reviews Microbiology|language=en|volume=10|issue=11|pages=766–778|doi=10.1038/nrmicro2858|issn=1740-1526|pmc=PMC3689224|pmid=23070557}}</ref> |
|||
=== Viruses === |
|||
* ''[[Cytomegalovirus]]'' is a family of opportunistic viruses, most frequently associated with respiratory infection.<ref name=":3" /><ref>{{Cite journal|last=Fonseca Brito|first=Luís|last2=Brune|first2=Wolfram|last3=Stahl|first3=Felix R.|date=2019-08-08|title=Cytomegalovirus (CMV) Pneumonitis: Cell Tropism, Inflammation, and Immunity|url=https://www.mdpi.com/1422-0067/20/16/3865|journal=International Journal of Molecular Sciences|language=en|volume=20|issue=16|pages=3865|doi=10.3390/ijms20163865|issn=1422-0067|pmc=PMC6719013|pmid=31398860}}</ref> |
|||
* ''[[Human polyomavirus 2|Human Polyomavirus 2]]'' (also known as JC virus) is known to cause [[progressive multifocal leukoencephalopathy]] (PML). <ref>{{Cite journal|last=Bohra|first=Chandrashekar|last2=Sokol|first2=Lubomir|last3=Dalia|first3=Samir|date=2017-11-01|title=Progressive Multifocal Leukoencephalopathy and Monoclonal Antibodies: A Review|url=http://journals.sagepub.com/doi/10.1177/1073274817729901|journal=Cancer Control|language=en|volume=24|issue=4|pages=107327481772990|doi=10.1177/1073274817729901|issn=1073-2748|pmc=PMC5937251|pmid=28975841}}</ref><ref>{{Cite journal|last=Kartau|first=Marge|last2=Sipilä|first2=Jussi OT|last3=Auvinen|first3=Eeva|last4=Palomäki|first4=Maarit|last5=Verkkoniemi-Ahola|first5=Auli|date=2019-12-02|title=Progressive Multifocal Leukoencephalopathy: Current Insights|url=https://www.dovepress.com/progressive-multifocal-leukoencephalopathy-current-insights-peer-reviewed-article-DNND|journal=Degenerative Neurological and Neuromuscular Disease|language=en|volume=Volume 9|pages=109–121|doi=10.2147/DNND.S203405|issn=1179-9900|pmc=PMC6896915|pmid=31819703}}</ref> |
|||
* ''[[Kaposi's sarcoma-associated herpesvirus|Human herpesvirus 8]]'' (also known as Kaposi sarcoma-associated herpesvirus) is a virus associated with [[Kaposi's sarcoma|Kaposi sarcoma]], a type of cancer.<ref>{{Cite journal|last=Radu|first=Oana|last2=Pantanowitz|first2=Liron|date=2013-02-01|title=Kaposi Sarcoma|url=http://meridian.allenpress.com/aplm/article/137/2/289/65260/Kaposi-Sarcoma|journal=Archives of Pathology & Laboratory Medicine|language=en|volume=137|issue=2|pages=289–294|doi=10.5858/arpa.2012-0101-RS|issn=1543-2165}}</ref><ref>{{Cite journal|last=Cesarman|first=Ethel|last2=Damania|first2=Blossom|last3=Krown|first3=Susan E.|last4=Martin|first4=Jeffrey|last5=Bower|first5=Mark|last6=Whitby|first6=Denise|date=2019-01-31|title=Kaposi sarcoma|url=http://www.nature.com/articles/s41572-019-0060-9|journal=Nature Reviews Disease Primers|language=en|volume=5|issue=1|pages=9|doi=10.1038/s41572-019-0060-9|issn=2056-676X|pmc=PMC6685213|pmid=30705286}}</ref> |
|||
== Causes == |
== Causes == |
||
[[Immunodeficiency]] or [[immunosuppression]] can be caused by: |
[[Immunodeficiency]] or [[immunosuppression]] are characterized by the absence of or disruption in components of the immune system, leading to lower-than-normal levels of immune function and immunity against pathogens.<ref name=":1" /> They can be caused by a variety of factors, including: |
||
* [[Malnutrition]] |
* [[Malnutrition]] |
||
* [[Fatigue (medical)|Fatigue]] |
* [[Fatigue (medical)|Fatigue]] |
||
Line 71: | Line 82: | ||
The lack of or the disruption of [[List of microbiota species of the lower reproductive tract of women|normal vaginal microbiota]] allows the proliferation of [[List of bacterial vaginosis microbiota|opportunistic microorganisms]] and will cause the opportunistic infection - [[bacterial vaginosis]].<ref name="AfricaNel2014">{{cite journal|last1=Africa|first1=Charlene|last2=Nel|first2=Janske|last3=Stemmet|first3=Megan|title=Anaerobes and Bacterial Vaginosis in Pregnancy: Virulence Factors Contributing to Vaginal Colonisation|journal=International Journal of Environmental Research and Public Health|volume=11|issue=7|year=2014|pages=6979–7000|issn=1660-4601|doi=10.3390/ijerph110706979|pmid=25014248|pmc=4113856}}</ref><ref name=Mastro2013>{{cite journal|last1=Mastromarino|first1=Paola|last2=Vitali|first2=Beatrice|last3=Mosca|first3=Luciana|title=Bacterial vaginosis: a review on clinical trials with probiotics|url=http://www.newmicrobiologica.org/PUB/allegati_pdf/2013/3/229.pdf|journal=New Microbiologica|date=2013|volume=36|issue=3|pages=229–238|pmid=23912864}}</ref><ref>{{cite journal|last1=Mastromarino|first1=Paola|last2=Vitali|first2=Beatrice|last3=Mosca|first3=Luciana|title=Bacterial vaginosis: a review on clinical trials with probiotics|url=http://www.newmicrobiologica.org/PUB/allegati_pdf/2013/3/229.pdf|journal=New Microbiologica|date=2013|volume=36|issue=3|pages=229–238|pmid=23912864}}</ref><ref>{{cite journal|last1=Knoester|first1=M.|last2=Lashley|first2=L. E. E. L. O.|last3=Wessels|first3=E.|last4=Oepkes|first4=D.|last5=Kuijper|first5=E. J.|title=First Report of Atopobium vaginae Bacteremia with Fetal Loss after Chorionic Villus Sampling|journal=Journal of Clinical Microbiology|volume=49|issue=4|year=2011|pages=1684–1686|issn=0095-1137|doi=10.1128/JCM.01655-10|pmid=21289141|pmc=3122803}}</ref> |
The lack of or the disruption of [[List of microbiota species of the lower reproductive tract of women|normal vaginal microbiota]] allows the proliferation of [[List of bacterial vaginosis microbiota|opportunistic microorganisms]] and will cause the opportunistic infection - [[bacterial vaginosis]].<ref name="AfricaNel2014">{{cite journal|last1=Africa|first1=Charlene|last2=Nel|first2=Janske|last3=Stemmet|first3=Megan|title=Anaerobes and Bacterial Vaginosis in Pregnancy: Virulence Factors Contributing to Vaginal Colonisation|journal=International Journal of Environmental Research and Public Health|volume=11|issue=7|year=2014|pages=6979–7000|issn=1660-4601|doi=10.3390/ijerph110706979|pmid=25014248|pmc=4113856}}</ref><ref name=Mastro2013>{{cite journal|last1=Mastromarino|first1=Paola|last2=Vitali|first2=Beatrice|last3=Mosca|first3=Luciana|title=Bacterial vaginosis: a review on clinical trials with probiotics|url=http://www.newmicrobiologica.org/PUB/allegati_pdf/2013/3/229.pdf|journal=New Microbiologica|date=2013|volume=36|issue=3|pages=229–238|pmid=23912864}}</ref><ref>{{cite journal|last1=Mastromarino|first1=Paola|last2=Vitali|first2=Beatrice|last3=Mosca|first3=Luciana|title=Bacterial vaginosis: a review on clinical trials with probiotics|url=http://www.newmicrobiologica.org/PUB/allegati_pdf/2013/3/229.pdf|journal=New Microbiologica|date=2013|volume=36|issue=3|pages=229–238|pmid=23912864}}</ref><ref>{{cite journal|last1=Knoester|first1=M.|last2=Lashley|first2=L. E. E. L. O.|last3=Wessels|first3=E.|last4=Oepkes|first4=D.|last5=Kuijper|first5=E. J.|title=First Report of Atopobium vaginae Bacteremia with Fetal Loss after Chorionic Villus Sampling|journal=Journal of Clinical Microbiology|volume=49|issue=4|year=2011|pages=1684–1686|issn=0095-1137|doi=10.1128/JCM.01655-10|pmid=21289141|pmc=3122803}}</ref> |
||
== Opportunistic Infection and HIV/AIDS == |
|||
HIV is a virus that targets [[T cell|T cells]] of the [[immune system]] and, as a result, HIV infection can lead to progressively worsening immunodeficiency, a condition ideal for the development of opportunistic infection.<ref>{{Cite journal|last=Doitsh|first=Gilad|last2=Greene|first2=Warner C.|date=2016-03-09|title=Dissecting How CD4 T Cells Are Lost During HIV Infection|url=https://linkinghub.elsevier.com/retrieve/pii/S1931312816300531|journal=Cell Host & Microbe|language=en|volume=19|issue=3|pages=280–291|doi=10.1016/j.chom.2016.02.012|pmc=PMC4835240|pmid=26962940}}</ref><ref>{{Cite journal|last=Fenwick|first=Craig|last2=Joo|first2=Victor|last3=Jacquier|first3=Patricia|last4=Noto|first4=Alessandra|last5=Banga|first5=Riddhima|last6=Perreau|first6=Matthieu|last7=Pantaleo|first7=Giuseppe|date=2019-12-27|title=T‐cell exhaustion in HIV infection|url=https://onlinelibrary.wiley.com/doi/abs/10.1111/imr.12823|journal=Immunological Reviews|language=en|volume=292|issue=1|pages=149–163|doi=10.1111/imr.12823|issn=0105-2896|pmc=PMC7003858|pmid=31883174}}</ref> Because of this, respiratory and central nervous system opportunistic infections, including tuberculosis and meningitis, respectively, are associated with later-stage HIV infection, as are numerous other infectious pathologies.<ref>{{Cite journal|last=Bruchfeld|first=Judith|last2=Correia-Neves|first2=Margarida|last3=Källenius|first3=Gunilla|date=2015-02-26|title=Tuberculosis and HIV Coinfection: Table 1.|url=http://perspectivesinmedicine.cshlp.org/lookup/doi/10.1101/cshperspect.a017871|journal=Cold Spring Harbor Perspectives in Medicine|language=en|volume=5|issue=7|pages=a017871|doi=10.1101/cshperspect.a017871|issn=2157-1422|pmc=PMC4484961|pmid=25722472}}</ref><ref>{{Cite journal|last=Tenforde|first=Mark W|last2=Shapiro|first2=Adrienne E|last3=Rouse|first3=Benjamin|last4=Jarvis|first4=Joseph N|last5=Li|first5=Tianjing|last6=Eshun-Wilson|first6=Ingrid|last7=Ford|first7=Nathan|date=2018-07-25|editor-last=Cochrane Infectious Diseases Group|title=Treatment for HIV-associated cryptococcal meningitis|url=http://doi.wiley.com/10.1002/14651858.CD005647.pub3|journal=Cochrane Database of Systematic Reviews|language=en|doi=10.1002/14651858.CD005647.pub3|pmc=PMC6513250|pmid=30045416}}</ref> Kaposi’s sarcoma, a virally-associated cancer, has higher incidence rates in HIV-positive patients than in the general population. <ref>{{Cite journal|last=Rees|first=Chris A.|last2=Keating|first2=Elizabeth M.|last3=Lukolyo|first3=Heather|last4=Danysh|first4=Heather E.|last5=Scheurer|first5=Michael E.|last6=Mehta|first6=Parth S.|last7=Lubega|first7=Joseph|last8=Slone|first8=Jeremy S.|last9=The Baylor Pediatric HIV-Related Malignancy Consortium|date=2016-04-15|title=Mapping the Epidemiology of Kaposi Sarcoma and Non-Hodgkin Lymphoma Among Children in Sub-Saharan Africa: A Review: Pediatric HIV-Related Malignancies in Africa|url=http://doi.wiley.com/10.1002/pbc.26021|journal=Pediatric Blood & Cancer|language=en|volume=63|issue=8|pages=1325–1331|doi=10.1002/pbc.26021|pmc=PMC7340190|pmid=27082516}}</ref> As immune function declines and HIV-infection progresses to AIDS, individuals are at an increased risk of opportunistic infections that their immune systems are no longer capable of responding properly to. Because of this, opportunistic infections are a leading cause of HIV/AIDS-related deaths.<ref>{{Citation|last=Sadiq|first=Usama|title=Prevention Of Opportunistic Infections In HIV|date=2021|url=http://www.ncbi.nlm.nih.gov/books/NBK513345/|work=StatPearls|place=Treasure Island (FL)|publisher=StatPearls Publishing|pmid=30020717|access-date=2021-03-09|last2=Shrestha|first2=Utsav|last3=Guzman|first3=Nilmarie}}</ref> |
|||
== Prevention == |
== Prevention == |
Revision as of 02:28, 9 March 2021
Opportunistic infection | |
---|---|
Chest X-ray of a patient who first had influenza and then developed Haemophilus influenzae pneumonia, presumably opportunistic | |
Specialty | Infectious diseases |
An opportunistic infection is an infection caused by pathogens (bacteria, fungi, parasites or viruses) that take advantage of an opportunity not normally available. These opportunities can stem from a variety of sources, such as a weakened immune system (as can occur in acquired immunodeficiency syndrome or when being treated with immunosuppressive drugs, as in cancer treatment),[1] an altered microbiome (such as a disruption in gut microbiota), or breached integumentary barriers (as in penetrating trauma). Many of these pathogens do not cause disease in a healthy host that has a non-compromised immune system, and can, in some cases, act as commensals until the balance of the immune system is disrupted.[2][3] Opportunistic infections can also be attributed to pathogens that cause mild illness in healthy individuals but lead to more serious illness when given the opportunity to take advantage of an immunocompromised host.[4]
Types of opportunistic infections
A wide variety of pathogens are involved in opportunistic infection and can cause a similarly wide range in pathologies. A partial list of opportunistic pathogens and their associated presentations includes:
Bacteria
- Clostridioides difficile (formerly known as Clostridium difficile) is a species of bacteria that is known to cause gastrointestinal infection and is typically associated with the hospital setting. [5][6]
- Legionella pneumophila is a bacterium that causes Legionnaire’s disease, a respiratory infection.[7][8]
- Mycobacterium avium complex (MAC) is a group of two bacteria, M. avium and M. intracellulare, that typically co-infect, leading to a lung infection called mycobacterium avium-intracellulare infection. [9][10]
- Mycobacterium tuberculosis is a species of bacteria that causes tuberculosis, a respiratory infection.[11]
- Pseudomonas aeruginosa is a bacterium that can cause respiratory infections. It is frequently associated with cystic fibrosis and hospital-acquired infections.[12]
- Salmonella is a genus of bacteria, known to cause gastrointestinal infections.[13]
- Staphylococcus aureus is a bacterium known to cause skin infections and sepsis, among other pathologies. Notably, S. aureus has evolved several drug-resistant strains, including MRSA.[14][15]
- Streptococcus pneumoniae is a bacterium that causes respiratory infections. [2]
- Streptococcus pyogenes (also known as group A Streptococcus) is a bacterium that can cause a variety of pathologies, including impetigo and strep throat, as well as other, more serious, illnesses.[16][17]
Fungi
- Aspergillus is a fungus, commonly associated with respiratory infection.[18] [19]
- Candida albicans is a species of fungus that is associated with oral thrush and gastrointestinal infection. [20][21]
- Coccidioides immitis is a fungus known for causing Coccidioidomycosis, more commonly known as Valley Fever. [22]
- Cryptococcus neoformans is a fungus that causes cryptococcosis, which can lead to pulmonary infection as well as nervous system infections, like meningitis.[23] [24]
- Histoplasma capsulatum is a species of fungus known to cause histoplasmosis, which can present with an array of symptoms, but often involves respiratory infection.[25][26]
- Pseudogymnoascus destructans (formerly known as Geomyces destructans) is a fungus that causes white-nose syndrome in bats.[27]
- Microsporidia is a group of fungi that infect species across the animal kingdom, one species of which can cause microsporidiosis in immunocompromised human hosts.[28]
- Pneumocystis jirovecii (formerly known as Pneumocystis carinii) is a fungus that causes pneumocystis pneumonia, a respiratory infection.[29]
Parasites
- Cryptosporidium is a protozoan that infects the gastrointestinal tract.[30]
- Toxoplasma gondii is a protozoan, known for causing toxoplasmosis.[31][32]
Viruses
- Cytomegalovirus is a family of opportunistic viruses, most frequently associated with respiratory infection.[19][33]
- Human Polyomavirus 2 (also known as JC virus) is known to cause progressive multifocal leukoencephalopathy (PML). [34][35]
- Human herpesvirus 8 (also known as Kaposi sarcoma-associated herpesvirus) is a virus associated with Kaposi sarcoma, a type of cancer.[36][37]
Causes
Immunodeficiency or immunosuppression are characterized by the absence of or disruption in components of the immune system, leading to lower-than-normal levels of immune function and immunity against pathogens.[1] They can be caused by a variety of factors, including:
- Malnutrition
- Fatigue
- Recurrent infections
- Immunosuppressing agents for organ transplant recipients
- Advanced HIV infection
- Chemotherapy for cancer
- Genetic predisposition
- Skin damage
- Antibiotic treatment leading to disruption of the physiological microbiome, thus allowing some microorganisms to outcompete others and become pathogenic (e.g. disruption of intestinal microbiota may lead to Clostridium difficile infection)
- Medical procedures
- Pregnancy
- Aging
- Leukopenia (i.e. neutropenia and lymphocytopenia)
- Burns
The lack of or the disruption of normal vaginal microbiota allows the proliferation of opportunistic microorganisms and will cause the opportunistic infection - bacterial vaginosis.[38][39][40][41]
Opportunistic Infection and HIV/AIDS
HIV is a virus that targets T cells of the immune system and, as a result, HIV infection can lead to progressively worsening immunodeficiency, a condition ideal for the development of opportunistic infection.[42][43] Because of this, respiratory and central nervous system opportunistic infections, including tuberculosis and meningitis, respectively, are associated with later-stage HIV infection, as are numerous other infectious pathologies.[44][45] Kaposi’s sarcoma, a virally-associated cancer, has higher incidence rates in HIV-positive patients than in the general population. [46] As immune function declines and HIV-infection progresses to AIDS, individuals are at an increased risk of opportunistic infections that their immune systems are no longer capable of responding properly to. Because of this, opportunistic infections are a leading cause of HIV/AIDS-related deaths.[47]
Prevention
Since opportunistic infections can cause severe disease, much emphasis is placed on measures to prevent infection. Such a strategy usually includes restoration of the immune system as soon as possible, avoiding exposures to infectious agents, and using antimicrobial medications ("prophylactic medications") directed against specific infections.[48]
Restoration of immune system
- In patients with HIV, starting antiretroviral therapy is especially important for restoration of the immune system and reducing the incidence rate of opportunistic infections[49][50]
- In patients undergoing chemotherapy, completion of and recovery from treatment is the primary method for immune system restoration. In a select subset of high risk patients, granulocyte colony stimulating factors (G-CSF) can be used to aid immune system recovery.[51][52]
Avoidance of infectious exposure
The following may be avoided as a preventative measure to reduce risk of infection:
- Eating undercooked meat or eggs, unpasteurized dairy products or juices
- Potential sources of tuberculosis (high risk healthcare facilities, regions with high rates of tuberculosis, patients with known tuberculosis)
- Any oral exposure to feces.[53]
- Contact with farm animals, especially those with diarrhea: source of Toxoplasma gondii, Cryptosporidium parvum
- Cat feces (e.g. cat litter): source of Toxoplasma gondii, Bartonella spp.
- Soil/dust in areas where there is known histoplasmosis, coccidiomycosis
- Reptiles, chicks, and ducklings that are a common source of Salmonella.
- Unprotected sexual intercourse with individuals with known sexually transmitted infections.
Prophylactic medications
Individuals at higher risk are often prescribed prophylactic medication to prevent an infection from occurring. A patient's risk level for developing an opportunistic infection is approximated using the patient's CD4 T-cell count and sometimes other markers of susceptibility. Common prophylaxis treatments include the following:[53]
Infection | When to Give Prophylaxis | Agent |
---|---|---|
Pneumocystis jirovecii | CD4 < 200 cells/mm3 or oropharyngeal candidasis (thrush) | TMP-SMX |
Toxoplasma gondii | CD4 < 100 cells/mm3 and positive Toxoplasma gondii IgG immunoassay | TMP-SMX |
Mycobacterium avium complex | CD4 < 50 | Azithromycin |
Treatment
Treatment depends on the type of opportunistic infection, but usually involves different antibiotics.
Veterinary treatment
Opportunistic infections caused by feline leukemia virus and feline immunodeficiency virus retroviral infections can be treated with lymphocyte T-cell immunomodulator.
References
- ^ a b Justiz Vaillant, Angel A.; Qurie, Ahmad (2021), "Immunodeficiency", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 29763203, retrieved 2021-03-09
- ^ a b Schroeder, Max R.; Stephens, David S. (2016-09-21). "Macrolide Resistance in Streptococcus pneumoniae". Frontiers in Cellular and Infection Microbiology. 6. doi:10.3389/fcimb.2016.00098. ISSN 2235-2988. PMC 5030221. PMID 27709102.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Achermann, Y.; Goldstein, E. J. C.; Coenye, T.; Shirtliff, M. E. (2014-07-01). "Propionibacterium acnes: from Commensal to Opportunistic Biofilm-Associated Implant Pathogen". Clinical Microbiology Reviews. 27 (3): 419–440. doi:10.1128/CMR.00092-13. ISSN 0893-8512. PMC 4135900. PMID 24982315.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Caballero, Mauricio T.; Polack, Fernando P. (2018-02-20). "Respiratory syncytial virus is an "opportunistic" killer". Pediatric Pulmonology. 53 (5): 664–667. doi:10.1002/ppul.23963. PMC 5947624. PMID 29461021.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Czepiel, Jacek; Dróżdż, Mirosław; Pituch, Hanna; Kuijper, Ed J.; Perucki, William; Mielimonka, Aleksandra; Goldman, Sarah; Wultańska, Dorota; Garlicki, Aleksander; Biesiada, Grażyna (2019-04-03). "Clostridium difficile infection: review". European Journal of Clinical Microbiology & Infectious Diseases. 38 (7): 1211–1221. doi:10.1007/s10096-019-03539-6. ISSN 0934-9723. PMC 6570665. PMID 30945014.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Guh, Alice Y.; Kutty, Preeta K. (2018-10-02). "Clostridioides difficile Infection". Annals of Internal Medicine. 169 (7): ITC49. doi:10.7326/AITC201810020. ISSN 0003-4819. PMC 6524133. PMID 30285209.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Chahin, Abdullah; Opal, Steven M. (March 2017). "Severe Pneumonia Caused by Legionella pneumophila". Infectious Disease Clinics of North America. 31 (1): 111–121. doi:10.1016/j.idc.2016.10.009. PMC 7135102. PMID 28159171.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Berjeaud, Jean-Marc; Chevalier, Sylvie; Schlusselhuber, Margot; Portier, Emilie; Loiseau, Clémence; Aucher, Willy; Lesouhaitier, Olivier; Verdon, Julien (2016-04-08). "Legionella pneumophila: The Paradox of a Highly Sensitive Opportunistic Waterborne Pathogen Able to Persist in the Environment". Frontiers in Microbiology. 7. doi:10.3389/fmicb.2016.00486. ISSN 1664-302X. PMC 4824771. PMID 27092135.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ O. Falkinham, Joseph; Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia 24061, USA (2018). "Mycobacterium avium complex: Adherence as a way of life". AIMS Microbiology. 4 (3): 428–438. doi:10.3934/microbiol.2018.3.428. ISSN 2471-1888. PMC 6604937. PMID 31294225.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link) - ^ Pan, Sheng-Wei; Shu, Chin-Chung; Feng, Jia-Yih; Su, Wei-Juin (June 2020). "Treatment for Mycobacterium avium complex lung disease". Journal of the Formosan Medical Association. 119: S67 – S75. doi:10.1016/j.jfma.2020.05.006.
- ^ Gordon, Stephen V.; Parish, Tanya (2018-04-01). "Microbe Profile: Mycobacterium tuberculosis: Humanity's deadly microbial foe". Microbiology. 164 (4): 437–439. doi:10.1099/mic.0.000601. ISSN 1350-0872.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ Pang, Zheng; Raudonis, Renee; Glick, Bernard R.; Lin, Tong-Jun; Cheng, Zhenyu (January–February 2019). "Antibiotic resistance in Pseudomonas aeruginosa: mechanisms and alternative therapeutic strategies". Biotechnology Advances. 37 (1): 177–192. doi:10.1016/j.biotechadv.2018.11.013.
{{cite journal}}
: CS1 maint: date format (link) - ^ Lamas, Alexandre; Miranda, José Manuel; Regal, Patricia; Vázquez, Beatriz; Franco, Carlos Manuel; Cepeda, Alberto (January 2018). "A comprehensive review of non-enterica subspecies of Salmonella enterica". Microbiological Research. 206: 60–73. doi:10.1016/j.micres.2017.09.010.
- ^ Jenul, Christian; Horswill, Alexander R. (2019-03-22). "Regulation of Staphylococcus aureus Virulence". Microbiology Spectrum. 7 (2). doi:10.1128/microbiolspec.GPP3-0031-2018. ISSN 2165-0497. PMC 6452892. PMID 30953424.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Kong, Cin; Neoh, Hui-min; Nathan, Sheila (2016-03-15). "Targeting Staphylococcus aureus Toxins: A Potential form of Anti-Virulence Therapy". Toxins. 8 (3): 72. doi:10.3390/toxins8030072. ISSN 2072-6651. PMC 4810217. PMID 26999200.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Jespersen, Magnus G.; Lacey, Jake A.; Tong, Steven Y.C.; Davies, Mark R. (December 2020). "Global genomic epidemiology of Streptococcus pyogenes". Infection, Genetics and Evolution. 86: 104609. doi:10.1016/j.meegid.2020.104609.
- ^ Brouwer, Stephan; Barnett, Timothy C.; Rivera-Hernandez, Tania; Rohde, Manfred; Walker, Mark J. (2016-06-17). "Streptococcus pyogenes adhesion and colonization". FEBS Letters. 590 (21): 3739–3757. doi:10.1002/1873-3468.12254.
- ^ Latgé, Jean-Paul; Chamilos, Georgios (2019-11-13). "Aspergillus fumigatus and Aspergillosis in 2019". Clinical Microbiology Reviews. 33 (1): e00140–18, /cmr/33/1/CMR.00140–18.atom. doi:10.1128/CMR.00140-18. ISSN 0893-8512. PMC 6860006. PMID 31722890.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ a b José, Ricardo J.; Periselneris, Jimstan N.; Brown, Jeremy S. (June 2020). "Opportunistic bacterial, viral and fungal infections of the lung". Medicine. 48 (6): 366–372. doi:10.1016/j.mpmed.2020.03.006. PMC 7206443. PMID 32390758.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Akpan, A (2002-08-01). "Oral candidiasis". Postgraduate Medical Journal. 78 (922): 455–459. doi:10.1136/pmj.78.922.455. PMC 1742467. PMID 12185216.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Erdogan, Askin; Rao, Satish S. C. (2015-03-19). "Small Intestinal Fungal Overgrowth". Current Gastroenterology Reports. 17 (4): 16. doi:10.1007/s11894-015-0436-2. ISSN 1522-8037.
- ^ Mu, Anandit; Shein, Thwe Thwe; Jayachandran, Priya; Paul, Simon (2017-09-14). "Immune Reconstitution Inflammatory Syndrome in Patients with AIDS and Disseminated Coccidioidomycosis: A Case Series and Review of the Literature". Journal of the International Association of Providers of AIDS Care (JIAPAC). 16 (6): 540–545. doi:10.1177/2325957417729751. ISSN 2325-9582.
- ^ Kwon-Chung, K. J.; Fraser, J. A.; Doering, T. L.; Wang, Z. A.; Janbon, G.; Idnurm, A.; Bahn, Y.-S. (2014-07-01). "Cryptococcus neoformans and Cryptococcus gattii, the Etiologic Agents of Cryptococcosis". Cold Spring Harbor Perspectives in Medicine. 4 (7): a019760 – a019760. doi:10.1101/cshperspect.a019760. ISSN 2157-1422. PMC 4066639. PMID 24985132.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Maziarz, Eileen K.; Perfect, John R. (March 2016). "Cryptococcosis". Infectious Disease Clinics of North America. 30 (1): 179–206. doi:10.1016/j.idc.2015.10.006. PMC 5808417. PMID 26897067.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Horwath, Michael C; Fecher, Roger A; Deepe, George S (2015-06-10). "Histoplasma capsulatum , lung infection and immunity". Future Microbiology. 10 (6): 967–975. doi:10.2217/fmb.15.25. ISSN 1746-0913. PMC 4478585. PMID 26059620.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Mittal, Jamie; Ponce, Maria G.; Gendlina, Inessa; Nosanchuk, Joshua D. (2018), Rodrigues, Marcio L. (ed.), "Histoplasma Capsulatum: Mechanisms for Pathogenesis", Fungal Physiology and Immunopathogenesis, vol. 422, Cham: Springer International Publishing, pp. 157–191, doi:10.1007/82_2018_114, ISBN 978-3-030-30236-8, PMC 7212190, PMID 30043340, retrieved 2021-03-09
{{citation}}
: CS1 maint: PMC format (link) - ^ Seyedmousavi, Seyedmojtaba; Bosco, Sandra de M G; de Hoog, Sybren; Ebel, Frank; Elad, Daniel; Gomes, Renata R; Jacobsen, Ilse D; Jensen, Henrik E; Martel, An; Mignon, Bernard; Pasmans, Frank (2018-04-01). "Fungal infections in animals: a patchwork of different situations". Medical Mycology. 56 (suppl_1): S165 – S187. doi:10.1093/mmy/myx104. ISSN 1369-3786. PMC 6251577. PMID 29538732.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Stentiford, G.D.; Becnel, -->J.J.; Weiss, L.M.; Keeling, P.J.; Didier, E.S.; Williams, B-->.A.P.; Bjornson, S.; Kent, M-->.L.; Freeman, M.A.; Brown, M.J.F.; Troemel, E-->.R. (April 2016). "Microsporidia – Emergent Pathogens in the Global Food Chain". Trends in Parasitology. 32 (4): 336–348. doi:10.1016/j.pt.2015.12.004. PMC 4818719. PMID 26796229.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Sokulska, Magdalena; Kicia, Marta; Wesołowska, Maria; Hendrich, Andrzej B. (2015-08-19). "Pneumocystis jirovecii—from a commensal to pathogen: clinical and diagnostic review". Parasitology Research. 114 (10): 3577–3585. doi:10.1007/s00436-015-4678-6. ISSN 0932-0113. PMC 4562001. PMID 26281787.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Gerace, Elisabetta; Presti, Vincenzo Di Marco Lo; Biondo, Carmelo (2019-12-01). "Cryptosporidium infection: epidemiology, pathogenesis, and differential diagnosis". European Journal of Microbiology and Immunology. 9 (4): 119–123. doi:10.1556/1886.2019.00019. ISSN 2062-8633. PMC 6945992. PMID 31934363.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Mendez, Oscar A.; Koshy, Anita A. (2017-07-20). Gubbels, Marc-Jan (ed.). "Toxoplasma gondii: Entry, association, and physiological influence on the central nervous system". PLOS Pathogens. 13 (7): e1006351. doi:10.1371/journal.ppat.1006351. ISSN 1553-7374. PMC 5519211. PMID 28727854.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Hunter, Christopher A.; Sibley, L. David (2012-10-16). "Modulation of innate immunity by Toxoplasma gondii virulence effectors". Nature Reviews Microbiology. 10 (11): 766–778. doi:10.1038/nrmicro2858. ISSN 1740-1526. PMC 3689224. PMID 23070557.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Fonseca Brito, Luís; Brune, Wolfram; Stahl, Felix R. (2019-08-08). "Cytomegalovirus (CMV) Pneumonitis: Cell Tropism, Inflammation, and Immunity". International Journal of Molecular Sciences. 20 (16): 3865. doi:10.3390/ijms20163865. ISSN 1422-0067. PMC 6719013. PMID 31398860.
{{cite journal}}
: CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Bohra, Chandrashekar; Sokol, Lubomir; Dalia, Samir (2017-11-01). "Progressive Multifocal Leukoencephalopathy and Monoclonal Antibodies: A Review". Cancer Control. 24 (4): 107327481772990. doi:10.1177/1073274817729901. ISSN 1073-2748. PMC 5937251. PMID 28975841.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Kartau, Marge; Sipilä, Jussi OT; Auvinen, Eeva; Palomäki, Maarit; Verkkoniemi-Ahola, Auli (2019-12-02). "Progressive Multifocal Leukoencephalopathy: Current Insights". Degenerative Neurological and Neuromuscular Disease. Volume 9: 109–121. doi:10.2147/DNND.S203405. ISSN 1179-9900. PMC 6896915. PMID 31819703.
{{cite journal}}
:|volume=
has extra text (help)CS1 maint: PMC format (link) CS1 maint: unflagged free DOI (link) - ^ Radu, Oana; Pantanowitz, Liron (2013-02-01). "Kaposi Sarcoma". Archives of Pathology & Laboratory Medicine. 137 (2): 289–294. doi:10.5858/arpa.2012-0101-RS. ISSN 1543-2165.
- ^ Cesarman, Ethel; Damania, Blossom; Krown, Susan E.; Martin, Jeffrey; Bower, Mark; Whitby, Denise (2019-01-31). "Kaposi sarcoma". Nature Reviews Disease Primers. 5 (1): 9. doi:10.1038/s41572-019-0060-9. ISSN 2056-676X. PMC 6685213. PMID 30705286.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Africa, Charlene; Nel, Janske; Stemmet, Megan (2014). "Anaerobes and Bacterial Vaginosis in Pregnancy: Virulence Factors Contributing to Vaginal Colonisation". International Journal of Environmental Research and Public Health. 11 (7): 6979–7000. doi:10.3390/ijerph110706979. ISSN 1660-4601. PMC 4113856. PMID 25014248.
{{cite journal}}
: CS1 maint: unflagged free DOI (link) - ^ Mastromarino, Paola; Vitali, Beatrice; Mosca, Luciana (2013). "Bacterial vaginosis: a review on clinical trials with probiotics" (PDF). New Microbiologica. 36 (3): 229–238. PMID 23912864.
- ^ Mastromarino, Paola; Vitali, Beatrice; Mosca, Luciana (2013). "Bacterial vaginosis: a review on clinical trials with probiotics" (PDF). New Microbiologica. 36 (3): 229–238. PMID 23912864.
- ^ Knoester, M.; Lashley, L. E. E. L. O.; Wessels, E.; Oepkes, D.; Kuijper, E. J. (2011). "First Report of Atopobium vaginae Bacteremia with Fetal Loss after Chorionic Villus Sampling". Journal of Clinical Microbiology. 49 (4): 1684–1686. doi:10.1128/JCM.01655-10. ISSN 0095-1137. PMC 3122803. PMID 21289141.
- ^ Doitsh, Gilad; Greene, Warner C. (2016-03-09). "Dissecting How CD4 T Cells Are Lost During HIV Infection". Cell Host & Microbe. 19 (3): 280–291. doi:10.1016/j.chom.2016.02.012. PMC 4835240. PMID 26962940.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Fenwick, Craig; Joo, Victor; Jacquier, Patricia; Noto, Alessandra; Banga, Riddhima; Perreau, Matthieu; Pantaleo, Giuseppe (2019-12-27). "T‐cell exhaustion in HIV infection". Immunological Reviews. 292 (1): 149–163. doi:10.1111/imr.12823. ISSN 0105-2896. PMC 7003858. PMID 31883174.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Bruchfeld, Judith; Correia-Neves, Margarida; Källenius, Gunilla (2015-02-26). "Tuberculosis and HIV Coinfection: Table 1". Cold Spring Harbor Perspectives in Medicine. 5 (7): a017871. doi:10.1101/cshperspect.a017871. ISSN 2157-1422. PMC 4484961. PMID 25722472.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Tenforde, Mark W; Shapiro, Adrienne E; Rouse, Benjamin; Jarvis, Joseph N; Li, Tianjing; Eshun-Wilson, Ingrid; Ford, Nathan (2018-07-25). Cochrane Infectious Diseases Group (ed.). "Treatment for HIV-associated cryptococcal meningitis". Cochrane Database of Systematic Reviews. doi:10.1002/14651858.CD005647.pub3. PMC 6513250. PMID 30045416.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Rees, Chris A.; Keating, Elizabeth M.; Lukolyo, Heather; Danysh, Heather E.; Scheurer, Michael E.; Mehta, Parth S.; Lubega, Joseph; Slone, Jeremy S.; The Baylor Pediatric HIV-Related Malignancy Consortium (2016-04-15). "Mapping the Epidemiology of Kaposi Sarcoma and Non-Hodgkin Lymphoma Among Children in Sub-Saharan Africa: A Review: Pediatric HIV-Related Malignancies in Africa". Pediatric Blood & Cancer. 63 (8): 1325–1331. doi:10.1002/pbc.26021. PMC 7340190. PMID 27082516.
{{cite journal}}
: CS1 maint: PMC format (link) - ^ Sadiq, Usama; Shrestha, Utsav; Guzman, Nilmarie (2021), "Prevention Of Opportunistic Infections In HIV", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30020717, retrieved 2021-03-09
- ^ David Schlossberg (2015-04-23). Clinical Infectious Disease. Cambridge University Press. pp. 688–. ISBN 978-1-107-03891-2.
- ^ Ledergerber, B.; Egger, M.; Erard, V.; Weber, R.; Hirschel, B.; Furrer, H.; Battegay, M.; Vernazza, P.; Bernasconi, E. (Dec 15, 1999). "AIDS-related opportunistic illnesses occurring after initiation of potent antiretroviral therapy: the Swiss HIV Cohort Study". JAMA. 282 (23): 2220–2226. doi:10.1001/jama.282.23.2220. ISSN 0098-7484. PMID 10605973. Retrieved 2015-05-09.
- ^ Brooks, John T.; Kaplan, Jonathan E.; Holmes, King K.; Benson, Constance; Pau, Alice; Masur, Henry (Mar 1, 2009). "HIV-associated opportunistic infections--going, going, but not gone: the continued need for prevention and treatment guidelines". Clinical Infectious Diseases. 48 (5): 609–611. doi:10.1086/596756. ISSN 1537-6591. PMID 19191648. Retrieved 2015-05-09.
- ^ Freifeld, Alison G.; Bow, Eric J.; Sepkowitz, Kent A.; Boeckh, Michael J.; Ito, James I.; Mullen, Craig A.; Raad, Issam I.; Rolston, Kenneth V.; Young, Jo-Anne H. (Feb 15, 2011). "Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the infectious diseases society of america". Clinical Infectious Diseases. 52 (4): e56–93. doi:10.1093/cid/cir073. ISSN 1537-6591. PMID 21258094. Retrieved 2015-05-09.
- ^ Smith, Thomas J.; Khatcheressian, James; Lyman, Gary H.; Ozer, Howard; Armitage, James O.; Balducci, Lodovico; Bennett, Charles L.; Cantor, Scott B.; Crawford, Jeffrey (Jul 1, 2006). "2006 update of recommendations for the use of white blood cell growth factors: an evidence-based clinical practice guideline". Journal of Clinical Oncology. 24 (19): 3187–3205. doi:10.1200/JCO.2006.06.4451. ISSN 1527-7755. PMID 16682719. Retrieved 2015-05-09.
- ^ a b "Guidelines for the prevention and treatment of opportunistic infections in adults and adolescents with HIV: recommendations from the Centers for Disease Control and Prevention, the National Institutes of Health, and the HIV Medicine Association of the Infectious Diseases Society of America" (PDF). 26 May 2020. Retrieved 28 November 2020.