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{{short description|Opportunistic intestinal infection}}
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'''Microsporidiosis''' is an opportunistic intestinal infection that causes [[diarrhea]] and wasting in [[immunocompromised]] individuals ([[HIV]], for example). It results from different species of [[microsporidia]], a group of microbial (unicellular) fungi.<ref name="urlMicrosporidiosis: Parasitic Infections: Merck Manual Home Health Handbook">{{cite web |url=http://www.merckmanuals.com/home/infections/parasitic_infections/microsporidiosis.html |title=Microsporidiosis: Parasitic Infections: Merck Manual Home Health Handbook |website= |accessdate=}}</ref>
'''Microsporidiosis''' is an opportunistic intestinal infection that causes [[diarrhea]] and [[wasting]] in [[immunocompromised]] individuals ([[HIV]], for example). It results from different species of [[microsporidia]], a group of microbial (unicellular) fungi.<ref name="urlMicrosporidiosis: Parasitic Infections: Merck Manual Home Health Handbook">{{cite web |url=http://www.merckmanuals.com/home/infections/parasitic_infections/microsporidiosis.html |title=Microsporidiosis: Parasitic Infections: Merck Manual Home Health Handbook }}</ref>


In [[HIV]] infected individuals, microsporidiosis generally occurs when [[CD4]]+ [[T cell]] counts fall below 150.
In [[HIV]]-infected individuals, microsporidiosis generally occurs when [[CD4]]+ [[T cell]] counts fall below 150.


''Microsporidia'' have emerged with significant mortality risk in [[Immunodeficiency|immunocompromised]] individuals. These are small, single-celled, obligately [[intracellular parasite]]s linked to water sources as well as wild, and domestic animals.<ref name=Didier05/> They were once considered [[protozoa]]ns or [[protist]]s, but are now known to be [[fungi]],<ref>{{cite journal | last1 = Hibbett | first1 = D.S. | display-authors = etal | year = 2007 | title = A higher level phylogenetic classification of the Fungi | url = http://www.umich.edu/~mycology/resources/Publications/Hibbett-et-al.-2007.pdf | journal = Mycological Research | volume = 111 | issue = 5| pages = 509–47 | doi = 10.1016/j.mycres.2007.03.004 | pmid = 17572334 | s2cid = 4686378 }}</ref> or a sister group to fungi.<ref name=Silar2016>{{Cite book|last1=Silar|first1=Philippe |title=Protistes Eucaryotes : Origine, Evolution et Biologie des Microbes Eucaryotes |publisher=HAL |year=2016 |page=462 |isbn=978-2-9555841-0-1 | url=https://hal.archives-ouvertes.fr/hal-01263138/document}}</ref> The most common causes of microsporidiosis is ''Enterocytozoon bieneusi'' and ''Encephalitozoon intestinalis.''
⚫
==Classification==
⚫
Although it is classified as a [[protozoal disease]] in [[ICD-10]], their phylogenetic placement has been resolved to be within the [[Fungi]], and some sources classify microsporidiosis as a [[mycosis]],<ref>{{MeshName|Microsporidiosis}}</ref> however, they are highly divergent and rapidly evolving.<ref name="pmid15777637">{{cite journal |author=Didier ES |title=Microsporidiosis: an emerging and opportunistic infection in humans and animals |journal=Acta Trop. |volume=94 |issue=1 |pages=61–76 |date=April 2005 |pmid=15777637 |doi=10.1016/j.actatropica.2005.01.010 }}</ref><ref name="pmid10666703">{{cite journal |vauthors=Keeling PJ, Luker MA, Palmer JD |title=Evidence from beta-tubulin phylogeny that microsporidia evolved from within the fungi |journal=Mol. Biol. Evol. |volume=17 |issue=1 |pages=23–31 |date=January 2000 |pmid=10666703 |doi= 10.1093/oxfordjournals.molbev.a026235|url=http://mbe.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=10666703|doi-access=free }}</ref><ref name="PMC2742732">{{cite journal |author=Keeling PJ |last2=Madhani |first2=Hiten D. |title=Five Questions about Microsporidia |journal=PLOS Pathogens |volume=5 |issue=9 |pages=e1000489 |date=September 2009 |pmid=19779558 |pmc=2742732 |doi=10.1371/journal.ppat.1000489 |editor1-last=Madhani |editor1-first=Hiten D.}}</ref>


==Cause==
==Causative agents==
At least 15 microsporidian species have been recognized<ref>{{Cite web|url=https://www.cdc.gov/dpdx/microsporidiosis/index.html|title=CDC - DPDx - Microsporidiosis|date=2017-12-29|website=www.cdc.gov|language=en-us|access-date=2018-01-04}}</ref> as human [[pathogen]]s, spread across nine genera:
At least 15 microsporidian species have been recognized<ref>{{Cite web|url=https://www.cdc.gov/dpdx/microsporidiosis/index.html|title=CDC - DPDx - Microsporidiosis|date=2017-12-29|website=www.cdc.gov|language=en-us|access-date=2018-01-04}}</ref> as human [[pathogen]]s, spread across nine genera:
* ''[[Anncaliia]]''
* ''[[Anncaliia]]''
Line 46: Line 46:
* ''[[Vittaforma]]''
* ''[[Vittaforma]]''
** ''V. corneae.''
** ''V. corneae.''
* ''Tubulinosema''
* ''Tubulinosema''
** ''T. acridophagus''
** ''T. acridophagus''


The primary causes are ''[[Enterocytozoon bieneusi]]'' and ''[[Encephalitozoon intestinalis]]''.<ref name="pmid18803616">{{cite journal |vauthors=Lanternier F, Boutboul D, Menotti J, etal |title=Microsporidiosis in solid organ transplant recipients: two Enterocytozoon bieneusi cases and review |journal=Transpl Infect Dis |volume=11 |issue=1 |pages=83–8 |date=February 2009 |pmid=18803616 |doi=10.1111/j.1399-3062.2008.00347.x}}</ref>
The primary causes are ''[[Enterocytozoon bieneusi]]'' and ''[[Encephalitozoon intestinalis]]''.<ref name="pmid18803616">{{cite journal |vauthors=Lanternier F, Boutboul D, Menotti J, etal |title=Microsporidiosis in solid organ transplant recipients: two ''Enterocytozoon bieneusi'' cases and review |journal=Transpl Infect Dis |volume=11 |issue=1 |pages=83–8 |date=February 2009 |pmid=18803616 |doi=10.1111/j.1399-3062.2008.00347.x|s2cid=205423324 }}</ref>


==Life cycle==
==Life cycle==
Line 64: Line 64:


==Diagnosis==
==Diagnosis==
#The best option for diagnosis is using PCR.
The best option for diagnosis is using PCR.{{citation needed|date=August 2020}}

Diagnosis with Microsporidia can be done through [[Gram stain|gram]]-[[Gram stain|positive]], [[Acid-fastness|acid-fast]] spores in stool and biopsy material with morphologic demonstration of the organism. Initial detection through light microscopic examination of tissue sections, stools, duodenal aspirates, nasal discharges, [[bronchoalveolar lavage]] fluids, and conjunctival smears.<ref name=Weber94>{{cite journal |vauthors=Weber R, Bryan RT, Schwartz DA, Owen RL |title=Human microsporidial infections |journal=Clin Microbiol Rev |volume=7 |issue=4 |pages=426–61 |date=October 1994 |pmid=7834600 |pmc=358336 |doi=10.1128/CMR.7.4.426 }}</ref> Definitive diagnosis can also be achieved through fluorescein-tagged antibody [[immunofluorescence]] or electron microscopy,<ref name=Weber94/> and species identification can be done through [[Polymerase chain reaction|PCR]].<ref>{{cite journal |vauthors=Kock NP, Petersen H, Fenner T, Sobottka I, Schmetz C, Deplazes P, Pieniazek NJ, Albrecht H, Schottelius J |title=Species-specific identification of microsporidia in stool and intestinal biopsy specimens by the polymerase chain reaction |journal=Eur J Clin Microbiol Infect Dis |volume=16 |issue=5 |pages=369–76 |date=May 1997 |pmid=9228477 |doi=10.1007/BF01726365 }}</ref>

⚫
===Classification===
⚫
Although it is classified as a [[protozoal disease]] in [[ICD-10]], their phylogenetic placement has been resolved to be within the [[Fungi]], and some sources classify microsporidiosis as a [[mycosis]],<ref>{{MeshName|Microsporidiosis}}</ref> however, they are highly divergent and rapidly evolving.<ref name="pmid15777637">{{cite journal |author=Didier ES |title=Microsporidiosis: an emerging and opportunistic infection in humans and animals |journal=Acta Trop. |volume=94 |issue=1 |pages=61–76 |date=April 2005 |pmid=15777637 |doi=10.1016/j.actatropica.2005.01.010 }}</ref><ref name="pmid10666703">{{cite journal |vauthors=Keeling PJ, Luker MA, Palmer JD |title=Evidence from beta-tubulin phylogeny that microsporidia evolved from within the fungi |journal=Mol. Biol. Evol. |volume=17 |issue=1 |pages=23–31 |date=January 2000 |pmid=10666703 |doi= 10.1093/oxfordjournals.molbev.a026235|doi-access=free }}</ref><ref name="PMC2742732">{{cite journal |author=Keeling PJ |last2=Madhani |first2=Hiten D. |title=Five Questions about Microsporidia |journal=PLOS Pathogens |volume=5 |issue=9 |pages=e1000489 |date=September 2009 |pmid=19779558 |pmc=2742732 |doi=10.1371/journal.ppat.1000489 |editor1-last=Madhani |editor1-first=Hiten D. |doi-access=free }}</ref>


==Treatment==
==Treatment==
[[Fumagillin]] has been used in the treatment.<ref name="pmid18803616"/><ref name="pmid12075057">{{cite journal |vauthors=Molina JM, Tourneur M, Sarfati C, etal |title=Fumagillin treatment of intestinal microsporidiosis |journal=N. Engl. J. Med. |volume=346 |issue=25 |pages=1963–9 |date=June 2002 |pmid=12075057 |doi=10.1056/NEJMoa012924 }}</ref>
[[Fumagillin]] has been used in the treatment.<ref name="pmid18803616"/><ref name="pmid12075057">{{cite journal |vauthors=Molina JM, Tourneur M, Sarfati C, etal |title=Fumagillin treatment of intestinal microsporidiosis |journal=N. Engl. J. Med. |volume=346 |issue=25 |pages=1963–9 |date=June 2002 |pmid=12075057 |doi=10.1056/NEJMoa012924 |doi-access=free }}</ref> Another agent used is [[albendazole]].<ref name=Didier05>{{cite journal |vauthors=Didier ES, Maddry JA, Brindley PJ, Stovall ME, Didier PJ |title=Therapeutic strategies for human microsporidia infections |journal=Expert Rev Anti Infect Ther |volume=3 |issue=3 |pages=419–34 |date=June 2005 |pmid=15954858 |doi=10.1586/14787210.3.3.419 |s2cid=42354627 }}</ref>


Another agent used is [[albendazole]].<ref name="pmid15954858">{{cite journal |vauthors=Didier ES, Maddry JA, Brindley PJ, Stovall ME, Didier PJ |title=Therapeutic strategies for human microsporidia infections |journal=Expert Rev Anti Infect Ther |volume=3 |issue=3 |pages=419–34 |date=June 2005 |pmid=15954858 |doi=10.1586/14787210.3.3.419 }}</ref>
Because of its severe mortality risk in immunocompromised individuals, two main agents are used: [[Albendazole]], which inhibits [[tubulin]], and [[Fumagillin]], which inhibits methionine aminopeptidase type two.<ref>{{cite journal |vauthors=Han B, Weiss LM |title=Therapeutic targets for the treatment of microsporidiosis in humans |journal=Expert Opin Ther Targets |volume=22 |issue=11 |pages=903–915 |date=November 2018 |pmid=30336698 |pmc=6300147 |doi=10.1080/14728222.2018.1538360 }}</ref>


==References==
==References==
{{Reflist}}
{{Reflist}}
#http://www.ivami.com/es/microbiologia-veterinaria-molecular/2219-i-enterocytozoon-bieneusi-i-diagnostico-molecular-pcr


== External links ==
== External links ==
⚫
* CDC's [https://web.archive.org/web/20131020105150/http://www.dpd.cdc.gov/dpdx/HTML/Microsporidiosis.htm microsporidiosis] info page.
{{Medical resources
{{Medical resources
| DiseasesDB = 31870
| DiseasesDB = 31870
| ICD10 = {{ICD10|B|60|8|b|50}}
| ICD10 = {{ICD10|B|60|8|b|50}}
| ICD9 = {{ICD9|136.8}}
| ICD9 = {{ICD9|136.8}}
| ICDO =
| ICDO =
| OMIM =
| OMIM =
| MedlinePlus =
| MedlinePlus =
| eMedicineSubj = med
| eMedicineSubj = med
| eMedicineTopic = 1469
| eMedicineTopic = 1469
| MeshID = D016881
| MeshID = D016881
}}
}}
⚫
* CDC's [https://web.archive.org/web/20131020105150/http://www.dpd.cdc.gov/dpdx/HTML/Microsporidiosis.htm microsporidiosis] info page.


{{Mycoses}}
{{Mycoses}}

Latest revision as of 05:02, 29 June 2024

Microsporidiosis
SpecialtyInfectious diseases Edit this on Wikidata

Microsporidiosis is an opportunistic intestinal infection that causes diarrhea and wasting in immunocompromised individuals (HIV, for example). It results from different species of microsporidia, a group of microbial (unicellular) fungi.[1]

In HIV-infected individuals, microsporidiosis generally occurs when CD4+ T cell counts fall below 150.

Microsporidia have emerged with significant mortality risk in immunocompromised individuals. These are small, single-celled, obligately intracellular parasites linked to water sources as well as wild, and domestic animals.[2] They were once considered protozoans or protists, but are now known to be fungi,[3] or a sister group to fungi.[4] The most common causes of microsporidiosis is Enterocytozoon bieneusi and Encephalitozoon intestinalis.

Cause

[edit]

At least 15 microsporidian species have been recognized[5] as human pathogens, spread across nine genera:

The primary causes are Enterocytozoon bieneusi and Encephalitozoon intestinalis.[6]

Life cycle

[edit]
Life cycle of the various organisms that cause microsporidiosis.

(Coded to image at right).

  1. The infective form of microsporidia is the resistant spore and it can survive for an extended period of time in the environment.
  2. The spore extrudes its polar tubule and infects the host cell.
  3. The spore injects the infective sporoplasm into the eukaryotic host cell through the polar tubule.
  4. Inside the cell, the sporoplasm undergoes extensive multiplication either by merogony (binary fission) or schizogony (multiple fission).
  5. This development can occur either in direct contact with the host cell cytoplasm (E. bieneusi) or inside a vacuole called a parasitophorous vacuole (E. intestinalis). Either free in the cytoplasm or inside a parasitophorous vacuole, microsporidia develop by sporogony to mature spores.
  6. During sporogony, a thick wall is formed around the spore, which provides resistance to adverse environmental conditions. When the spores increase in number and completely fill the host cell cytoplasm, the cell membrane is disrupted and releases the spores to the surroundings.
  7. These free mature spores can infect new cells thus continuing the cycle.

Diagnosis

[edit]

The best option for diagnosis is using PCR.[citation needed]

Diagnosis with Microsporidia can be done through gram-positive, acid-fast spores in stool and biopsy material with morphologic demonstration of the organism. Initial detection through light microscopic examination of tissue sections, stools, duodenal aspirates, nasal discharges, bronchoalveolar lavage fluids, and conjunctival smears.[7] Definitive diagnosis can also be achieved through fluorescein-tagged antibody immunofluorescence or electron microscopy,[7] and species identification can be done through PCR.[8]

Classification

[edit]

Although it is classified as a protozoal disease in ICD-10, their phylogenetic placement has been resolved to be within the Fungi, and some sources classify microsporidiosis as a mycosis,[9] however, they are highly divergent and rapidly evolving.[10][11][12]

Treatment

[edit]

Fumagillin has been used in the treatment.[6][13] Another agent used is albendazole.[2]

Because of its severe mortality risk in immunocompromised individuals, two main agents are used: Albendazole, which inhibits tubulin, and Fumagillin, which inhibits methionine aminopeptidase type two.[14]

References

[edit]
  1. ^ "Microsporidiosis: Parasitic Infections: Merck Manual Home Health Handbook".
  2. ^ a b Didier ES, Maddry JA, Brindley PJ, Stovall ME, Didier PJ (June 2005). "Therapeutic strategies for human microsporidia infections". Expert Rev Anti Infect Ther. 3 (3): 419–34. doi:10.1586/14787210.3.3.419. PMID 15954858. S2CID 42354627.
  3. ^ Hibbett, D.S.; et al. (2007). "A higher level phylogenetic classification of the Fungi" (PDF). Mycological Research. 111 (5): 509–47. doi:10.1016/j.mycres.2007.03.004. PMID 17572334. S2CID 4686378.
  4. ^ Silar, Philippe (2016). Protistes Eucaryotes : Origine, Evolution et Biologie des Microbes Eucaryotes. HAL. p. 462. ISBN 978-2-9555841-0-1.
  5. ^ "CDC - DPDx - Microsporidiosis". www.cdc.gov. 2017-12-29. Retrieved 2018-01-04.
  6. ^ a b Lanternier F, Boutboul D, Menotti J, et al. (February 2009). "Microsporidiosis in solid organ transplant recipients: two Enterocytozoon bieneusi cases and review". Transpl Infect Dis. 11 (1): 83–8. doi:10.1111/j.1399-3062.2008.00347.x. PMID 18803616. S2CID 205423324.
  7. ^ a b Weber R, Bryan RT, Schwartz DA, Owen RL (October 1994). "Human microsporidial infections". Clin Microbiol Rev. 7 (4): 426–61. doi:10.1128/CMR.7.4.426. PMC 358336. PMID 7834600.
  8. ^ Kock NP, Petersen H, Fenner T, Sobottka I, Schmetz C, Deplazes P, Pieniazek NJ, Albrecht H, Schottelius J (May 1997). "Species-specific identification of microsporidia in stool and intestinal biopsy specimens by the polymerase chain reaction". Eur J Clin Microbiol Infect Dis. 16 (5): 369–76. doi:10.1007/BF01726365. PMID 9228477.
  9. ^ Microsporidiosis at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  10. ^ Didier ES (April 2005). "Microsporidiosis: an emerging and opportunistic infection in humans and animals". Acta Trop. 94 (1): 61–76. doi:10.1016/j.actatropica.2005.01.010. PMID 15777637.
  11. ^ Keeling PJ, Luker MA, Palmer JD (January 2000). "Evidence from beta-tubulin phylogeny that microsporidia evolved from within the fungi". Mol. Biol. Evol. 17 (1): 23–31. doi:10.1093/oxfordjournals.molbev.a026235. PMID 10666703.
  12. ^ Keeling PJ; Madhani, Hiten D. (September 2009). Madhani, Hiten D. (ed.). "Five Questions about Microsporidia". PLOS Pathogens. 5 (9): e1000489. doi:10.1371/journal.ppat.1000489. PMC 2742732. PMID 19779558.
  13. ^ Molina JM, Tourneur M, Sarfati C, et al. (June 2002). "Fumagillin treatment of intestinal microsporidiosis". N. Engl. J. Med. 346 (25): 1963–9. doi:10.1056/NEJMoa012924. PMID 12075057.
  14. ^ Han B, Weiss LM (November 2018). "Therapeutic targets for the treatment of microsporidiosis in humans". Expert Opin Ther Targets. 22 (11): 903–915. doi:10.1080/14728222.2018.1538360. PMC 6300147. PMID 30336698.
[edit]
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