Microsporidiosis

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Microsporidiosis
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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. [1]

Contents

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

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

Life cycle of the various organisms that cause microsporidiosis. Microsporidiosis 01.png
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

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

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

Fumagillin has been used in the treatment. [6] [13] Another agent used is albendazole. [14]

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. [15]

Related Research Articles

<i>Giardia duodenalis</i> Parasitic microorganism that causes giardiasis

Giardia duodenalis, also known as Giardia intestinalis and Giardia lamblia, is a flagellated parasitic microorganism of the genus Giardia that colonizes the small intestine, causing a diarrheal condition known as giardiasis. The parasite attaches to the epithelium by a ventral adhesive disc or sucker, and reproduces via binary fission. Giardiasis does not spread via the bloodstream, nor does it spread to other parts of the gastrointestinal tract, but remains confined to the lumen of the small intestine. Giardia has an outer membrane that makes it possible to retain life, even when outside of the host body, and which can make it tolerant to chlorine disinfection. Giardia trophozoites absorb their nutrients from the lumen, and are anaerobes. If the organism is split and stained, its characteristic pattern resembles the familiar "smiley face" symbol.

<span class="mw-page-title-main">Coccidia</span> A subclass of protists

Coccidia (Coccidiasina) are a subclass of microscopic, spore-forming, single-celled obligate intracellular parasites belonging to the apicomplexan class Conoidasida. As obligate intracellular parasites, they must live and reproduce within an animal cell. Coccidian parasites infect the intestinal tracts of animals, and are the largest group of apicomplexan protozoa.

<span class="mw-page-title-main">Microsporidia</span> Phylum of fungi

Microsporidia are a group of spore-forming unicellular parasites. These spores contain an extrusion apparatus that has a coiled polar tube ending in an anchoring disc at the apical part of the spore. They were once considered protozoans or protists, but are now known to be fungi, or a sister group to fungi. These fungal microbes are obligate eukaryotic parasites that use a unique mechanism to infect host cells. They have recently been discovered in a 2017 Cornell study to infect Coleoptera on a large scale. So far, about 1500 of the probably more than one million species are named. Microsporidia are restricted to animal hosts, and all major groups of animals host microsporidia. Most infect insects, but they are also responsible for common diseases of crustaceans and fish. The named species of microsporidia usually infect one host species or a group of closely related taxa. Approximately 10 percent of the species are parasites of vertebrates —several species, most of which are opportunistic, can infect humans, in whom they can cause microsporidiosis.

<span class="mw-page-title-main">Fumagillin</span> Chemical compound

Fumagillin is a complex biomolecule and used as an antimicrobial agent. It was isolated in 1949 from the microbial organism Aspergillus fumigatus.

<span class="mw-page-title-main">Opportunistic infection</span> Infection caused by pathogens that take advantage of an opportunity not normally available

An opportunistic infection is an infection caused by pathogens that take advantage of an opportunity not normally available. These opportunities can stem from a variety of sources, such as a weakened immune system, an altered microbiome, or breached integumentary barriers. Many of these pathogens do not necessarily 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. Opportunistic infections can also be attributed to pathogens which cause mild illness in healthy individuals but lead to more serious illness when given the opportunity to take advantage of an immunocompromised host.

<span class="mw-page-title-main">Cutaneous larva migrans</span> Medical condition

Cutaneous larva migrans is a skin disease in humans, caused by the larvae of various nematode parasites of the hookworm family (Ancylostomatidae). The parasites live in the intestines of dogs, cats, and wild animals; they should not be confused with other members of the hookworm family for which humans are definitive hosts, namely Ancylostoma duodenale and Necator americanus.

<i>Retortamonas</i> Unicellular organism

Retortamonas is a genus of flagellated excavates. It is one of only two genera belonging to the family Retortamonadidae along with the genus Chilomastix. The genus parasitizes a large range of hosts including humans. Species within this genus are considered harmless commensals which reside in the intestine of their host. The wide host diversity is a useful factor given that species are distinguished based on their host rather than morphology. This is because all species share similar morphology, which would present challenges when trying to make classifications based on structural anatomy. Although Retortamonas currently includes over 25 known species, it is possible that some defined species are synonymous, given that such overlapping species have been discovered in the past. Further efforts into learning about this genus must be done such as cross-transmission testing as well as biochemical and genetic studies. One of the most well-known species within this genus is Retortamonas intestinalis, a human parasite that lives in the large intestine of humans.

<span class="mw-page-title-main">Xenoma</span> Growth caused by various species of protists and fungi

A xenoma is a growth caused by various protists and fungi, most notably microsporidia. It can occur on numerous organisms; however is predominantly found on fish.

Enterocytozoon bieneusi is a species of the order Chytridiopsida which infects the intestinal epithelial cells. It is an obligate intracellular parasite.

Antiparasitics are a class of medications which are indicated for the treatment of parasitic diseases, such as those caused by helminths, amoeba, ectoparasites, parasitic fungi, and protozoa, among others. Antiparasitics target the parasitic agents of the infections by destroying them or inhibiting their growth; they are usually effective against a limited number of parasites within a particular class. Antiparasitics are one of the antimicrobial drugs which include antibiotics that target bacteria, and antifungals that target fungi. They may be administered orally, intravenously or topically. Overuse or misuse of antiparasitics can lead to the development of antimicrobial resistance.

Encephalitozoon intestinalis is a parasite. It can cause microsporidiosis.

Karyolysus is a genus of coccidia. With the exception of K. sonomae whose vertebrate host is the yellow-legged frog, species in this genus only infect lizards of the genus Lacerta.

<i>Encephalitozoon cuniculi</i> Microsporidial pathogen

Encephalitozoon cuniculi is a microsporidial pathogen of mammals with world-wide distribution. An important cause of neurologic and renal disease in rabbits, E. cuniculi can also cause disease in immunocompromised people.

Acroeimeria is a genus of parasites that contains those species which initially develop immediately beneath the brush-border of the intestinal epithelium, but the meronts and gamonts of which are early on extruded to form a layer on the surface of the gut mucosa. Morphologically they are similar to the Eimeria to which they are closely related. The genus was described in 1989 by Paperna and Landsberg.

<i>Cystoisospora belli</i> Species of single-celled organism

Cystoisospora belli, previously known as Isospora belli, is a parasite that causes an intestinal disease known as cystoisosporiasis. This protozoan parasite is opportunistic in immune suppressed human hosts. It primarily exists in the epithelial cells of the small intestine, and develops in the cell cytoplasm. The distribution of this coccidian parasite is cosmopolitan, but is mainly found in tropical and subtropical areas of the world such as the Caribbean, Central and S. America, India, Africa, and S.E. Asia. In the U.S., it is usually associated with HIV infection and institutional living.

<span class="mw-page-title-main">Parasitophorous vacuole</span>

The parasitophorous vacuole (PV) is a structure produced by apicomplexan parasites in the cells of its host. The PV allows the parasite to develop while protected from the phagolysosomes of the host cell.

<i>Ordospora colligata</i> Intracellular parasite

Ordospora colligata is an intracellular parasite belonging to the Microsporidia. It is an obligatory gut parasite with the crustacean Daphnia magna as its only host. So far it has been reported from Europe and Asia.

Nematocida parisii is a parasitic species of Microsporidia fungi found in wild isolates of the common nematode, Caenorhabditis elegans. The fungus forms spores and replicates in the intestines before leaving the host.

Mycotypha microspora, also known as Microtypha microspora, is a filamentous fungus in the division Zygomycota. It was discovered in a Citrus aurantium peel in 1932 by E. Aline Fenner, who proposed a new genus Mycotypha to accommodate it. Mycotypha africana, which is another species in the genus Mycotypha, is closely related to M. microspora. The fungus has subsequently been isolated from both outdoor and indoor settings around the world, and is typically found in soil and dung. The species rarely causes infections in humans, but has recently been involved in the clinical manifestation of the life-threatening disease mucormycosis.

<i>Enterospora nucleophila</i> Species of parasitic protist

Enterospora nucleophila is a microsporidian infecting the gilt-head bream. It develops primarily within the nuclei of rodlet cells and enterocytes, at the intestinal epithelium. It can also be found in cytoplasmic position within other cell types, including phagocytes, at subepithelial layers. It is the causative agent of emaciative microsporidiosis of gilthead sea bream, a chronic condition manifested as a severe growth arrestment, normally accompanied by trickling mortality.

References

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  7. 1 2 Weber R, Bryan RT, Schwartz DA, Owen RL. Human microsporidial infections. Clin Microbiol Rev. 1994 Oct;7(4):426-61. doi: 10.1128/cmr.7.4.426. PMID: 7834600; PMCID: PMC358336.
  8. Kock NP, Petersen H, Fenner T, Sobottka I, Schmetz C, Deplazes P, Pieniazek NJ, Albrecht H, Schottelius J. Species-specific identification of microsporidia in stool and intestinal biopsy specimens by the polymerase chain reaction. Eur J Clin Microbiol Infect Dis. 1997 May;16(5):369-76. doi: 10.1007/BF01726365. PMID: 9228477.
  9. Microsporidiosis at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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  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.
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  14. 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.
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