Strongyloides stercoralis

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Threadworm
Strongyloides stercoralis larva.jpg
First stage larva (L1) of S. stercoralis
Scientific classification
Kingdom:Animalia
Phylum:Nematoda
Class:Secernentea
Order:Rhabditida
Family:Strongyloididae
Genus:Strongyloides
Species:S. stercoralis
Binomial name
Strongyloides stercoralis
Bavay, 1876
 
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Threadworm
Strongyloides stercoralis larva.jpg
First stage larva (L1) of S. stercoralis
Scientific classification
Kingdom:Animalia
Phylum:Nematoda
Class:Secernentea
Order:Rhabditida
Family:Strongyloididae
Genus:Strongyloides
Species:S. stercoralis
Binomial name
Strongyloides stercoralis
Bavay, 1876

Strongyloides stercoralis is the scientific name of a human parasitic roundworm causing the disease strongyloidiasis. Its common name is threadworm. In the UK and Australia, however, the term threadworm can also refer to nematodes of the genus Enterobius, otherwise known as pinworms.[1]

The Strongyloides stercoralis nematode can parasitize humans. The adult parasitic stage lives in tunnels in the mucosa of the small intestine. The genus Strongyloides contains 53 species,[2][3] and S. stercoralis is the type species. S. stercoralis has been reported in other mammals, including cats and dogs. However, it seems that the species in dogs is typically not S. stercoralis, but the related species S. canis. Non-human primates are more commonly infected with S. fuelleborni and S. cebus, although S. stercoralis has been reported in captive primates. Other species of Strongyloides, naturally parasitic in humans, but with restricted distributions, are S. fuelleborni in central Africa and S. kellyi in Papua New Guinea.

Geographic distribution[edit]

S. stercoralis has a very low prevalence in societies where fecal contamination of soil or water is rare. Hence, it is a very rare infection in developed economies. In developing countries, it is less prevalent in urban areas than in rural areas (where sanitation standards are poor). S. stercoralis can be found in areas with tropical and subtropical climates.[4]

Strongyloidiasis was first described in the 19th century in French soldiers returning home from expeditions in Indochina. Today, the countries of the old Indochina (Vietnam, Cambodia, and Laos) still have endemic strongyloidiasis, with the typical prevalences being 10% or less. Regions of Japan used to have endemic strongyloidiasis, but control programs have eliminated the disease. Strongyloidiasis appears to have a high prevalence in some areas of Brazil and Central America. It is endemic in Africa, but the prevalence is typically low (1% or less). Pockets have been reported from rural Italy, but current status is unknown. In the Pacific islands, strongyloidiasis is rare, although some cases have been reported from Fiji. In tropical Australia, some rural and remote Australian Aboriginal communities have very high prevalences of strongyloidiasis.[5]

In some African countries (e.g., Zaire), S. fuelleborni was more common than S. stercoralis in parasite surveys from the 1970s, but current status is unknown. In Papua New Guinea, S. stercoralis is endemic, but prevalence is low. However, in some areas, another species, S. kellyi,[6] is a very common parasite of children in the New Guinea Highlands and Western Province.[6]

Knowledge of the geographic distribution of strongyloidiasis is of significance to travelers who may acquire the parasite during their stays in endemic areas.

Because strongyloidiasis is transmittable by textiles, such as bedclothes and clothing, care must be taken never to use hotel bed sheets in endemic areas. Personal sleeping bags and using plastic slippers when showering are very important when travelling in tropical regions.

Life cycle[edit]

Strongyloides LifeCycle.gif

The strongyloid's life cycle is heterogonic—it is more complex than that of most nematodes, with its alternation between free-living and parasitic cycles, and its potential for autoinfection and multiplication within the host. The parasitic cycle is homogenic, while the free-living cycle is heterogonic. The heterogonic life cycle is advantageous to the parasite because it allows reproduction for one or more generations in the absence of a host.

In the free-living cycle, the rhabditiform larvae passed in the stool can either molt twice and become infective filariform larvae (direct development) or molt four times and become free-living adult males and females that mate and produce eggs from which rhabditiform larvae hatch. In the direct development, first-stage larvae (L1) transform into infective larvae (IL) via three molts. The indirect route results first in the development of free-living adults that mate; the female lays eggs, which hatch and then develop into IL. The direct route gives IL faster (three days) versus the indirect route (seven to 10 days). However, the indirect route results in an increase in the number of IL produced. Speed of development of IL is traded for increased numbers. The free-living males and females of S. stercoralis die after one generation; they do not persist in the soil. The latter, in turn, can either develop into a new generation of free-living adults or develop into infective filariform larvae. The filariform larvae penetrate the human host skin to initiate the parasitic cycle.

The infectious larvae penetrate the skin when it contacts soil. While S. stercoralis is attracted to chemicals such as carbon dioxide or sodium chloride, these chemicals are not specific. Larvae have been thought to locate their hosts via chemicals in the skin, the predominant one being urocanic acid, a histidine metabolite on the uppermost layer of skin that is removed by sweat or the daily skin-shedding cycle.[7] Urocanic acid concentrations can be up to five times greater in the foot than any other part of the human body. Some of them enter the superficial veins and ride the blood flow to the lungs, where they enter the alveoli. They are then coughed up and swallowed into the gut, where they parasitise the intestinal mucosa (duodenum and jejunum). In the small intestine, they molt twice and become adult female worms. The females live threaded in the epithelium of the small intestine and, by parthenogenesis, produce eggs, which yield rhabditiform larvae. Only females will reach reproductive adulthood in the intestine. Female strongyloids reproduce through parthenogenesis. The eggs hatch in the intestine and young larvae are then excreted in the feces. It takes about two weeks to reach egg development from the initial skin penetration. By this process, S. stercoralis can cause both respiratory and gastrointestinal symptoms. The worms also participate in autoinfection, in which the rhabditiform larvae become infective filariform larvae, which can penetrate either the intestinal mucosa (internal autoinfection) or the skin of the perianal area (external autoinfection); in either case, the filariform larvae may follow the previously described route, being carried successively to the lungs, the bronchial tree, the pharynx, and the small intestine, where they mature into adults; or they may disseminate widely in the body. To date, occurrence of autoinfection in humans with helminthic infections is recognized only in Strongyloides stercoralis and Capillaria philippinensis infections. In the case of Strongyloides, autoinfection may explain the possibility of persistent infections for many years in persons not having been in an endemic area and of hyperinfections in immunodepressed individuals.

Morphology[edit]

Whereas males grow to only about 0.9 mm (0.04 in) in length, females can grow from 2.0 to 2.5 mm (0.08 to 0.10 in). Both genders also possess a tiny buccal capsule and cylindrical esophagus without a posterior bulb.[8] In the free-living stage, the esophagi of both sexes are rhabditiform. Males can be distinguished from females by two structures: the spicules and gubernaculum.

Autoinfection[edit]

An unusual feature of S. stercoralis is autoinfection. Only one other species in the Strongyloides genus, S. felis, has this trait. Autoinfection is the development of L1 into small infective larvae in the gut of the host. These autoinfective larvae penetrate the wall of the lower ileum or colon or the skin of the perianal region, enter the circulation again, travel to the lungs, and then to the small intestine, thus repeating the cycle. Autoinfection makes strongyloidiasis due to S. stercoralis an infection with several unusual features.

Persistence of infection is the first of these important features. Because of autoinfection, humans have been known to still be infected up to 65 years after they were first exposed to the parasite (e.g., World War II or Vietnam War veterans). Once a host is infected with S. stercoralis, infection is lifelong unless effective treatment eliminates all adult parasites and migrating autoinfective larvae.

Symptoms[edit]

Main article: Strongyloidiasis

Many people infected are usually asymptomatic at first. Symptoms include dermatitis: swelling, itching, larva currens, and mild hemorrhage at the site where the skin has been penetrated. If the parasite reaches the lungs, the chest may feel as if it is burning, and wheezing and coughing may result, along with pneumonia-like symptoms (Löffler's syndrome). The intestines could eventually be invaded, leading to burning pain, tissue damage, sepsis, and ulcers. Chronic diarrhea can be a symptom.[9] In severe cases, edema may result in obstruction of the intestinal tract, as well as loss of peristaltic contractions.[10]

Strongyloidiasis in immunocompetent individuals is usually an indolent disease. However, in immunocompromised individuals, it can cause a hyperinfective syndrome (also called disseminated strongyloidiasis) due to the reproductive capacity of the parasite inside the host. This hyperinfective syndrome can have a mortality rate close to 90% if disseminated.[11][12][13]

Immunosuppressive drugs, such as those used for tissue transplantation (especially corticosteroids) can increase the rate of autoinfection to the point where an overwhelming number of larvae migrate through the lungs, which in many cases can prove fatal. In addition, diseases such as human T-lymphotropic virus 1, which enhance the Th1 arm of the immune system and lessen the Th2 arm, increase the disease state.[12] Another consequence of autoinfection is the autoinfective larvae can carry gut bacteria back into the body. About 50% of people with hyperinfection present with bacterial disease due to enteric bacteria. Also, a unique effect of autoinfective larvae is larva currens due to the rapid migration of the larvae through the skin. Larva currens appears as a red line that moves rapidly (more than 5 cm or 2 in per day), and then quickly disappears. It is pathognomonic for autoinfective larvae and can be used as a diagnostic criterion for strongyloidiasis due to S. stercoralis.

Diagnosis[edit]

Locating juvenile larvae, either rhabditiform or filariform, in recent stool samples will confirm the presence of this parasite.[14] Other techniques used include direct fecal smears, culturing fecal samples on agar plates, serodiagnosis through ELISA, and duodenal fumigation. Still, diagnosis can be difficult because of the varying juvenile parasite load on a daily basis.

Treatment[edit]

Ideally, prevention, by improved sanitation (proper disposal of feces), practicing good hygiene (washing of hands), etc., is used before any drug regimen is administered.

Ivermectin is the drug of first choice for treatment because of higher tolerance in patients.[5] Thiabendazole was used previously, but, owing to its high prevalence of side effects (dizziness, vomiting, nausea, malaise) and lower efficacy, it has been superseded by ivermectin and as second-line albendazole. However, these drugs have little effect on the majority of these autoinfective larvae during their migration through the body. Hence, repeated treatments with ivermectin must be administered to kill adult parasites that develop from the autoinfective larvae.

In the UK, mebendazole and piperazine are currently (2007) preferred.[15] Mebendazole has a much higher failure rate in clinical practice than albendazole, thiabendazole, or ivermectin.[16]

Chemoattractant[edit]

This parasite depends on chemical cues to find a potential host. It uses sensor neurons of class AFD to identify cues excreted by the host.[17]S. stercoralis is attracted to nonspecific attractants of warmth, carbon dioxide, and sodium chloride. Urocanic acid, a component of skin secretions in mammals, is a major chemoattractant. Larvae of S. stercoralis are strongly attracted to this compound.[7] This compound can be suppressed by metal ions, suggesting a possible strategy for preventing infection.

See also[edit]

References[edit]

  1. ^ Vanderkooi, M. (2000). Village Medical Manual (5th ed.). Pasadena: William Carey Library. ISBN 0878087788. 
  2. ^ Speare, R. (1989). "Identification of species of Strongyloides". In Grove, D. I. Strongyloidiasis: a major roundworm infection of man. London: Taylor & Francis. pp. 11–83. ISBN 0850667321. 
  3. ^ Skerratt, L. F. (1995). "Strongyloides spearei n. sp. (Nematoda: Strongyloididae) from the common wombat Vombatus ursinus (Marsupialia: Vombatidae)". Systematic Parasitology 32 (2): 81–89. doi:10.1007/BF00009506. 
  4. ^ Segarra-Newnham, M. (2007). "Manifestations, diagnosis, and treatment of Strongyloides stercoralis infection". Ann Pharmacother 41 (12): 1992–2001. doi:10.1345/aph.1K302. PMID 17940124. 
  5. ^ a b Johnston, F. H.; Morris, P. S.; Speare, R.; McCarthy, J.; Currie, B.; Ewald, D.; Page, W.; Dempsey, K. (2005). "Strongyloidiasis: A review of the evidence for Australian practitioners". The Australian Journal of Rural Health 13 (4): 247–54. doi:10.1111/j.1440-1584.2005.00710.x. PMID 16048468. 
  6. ^ a b Dorris, M.; Viney, M. E.; Blaxter, M. L. (2002). "Molecular phylogenetic analysis of the genus Strongyloides and related nematodes". International Journal for Parasitology 32 (12): 1507–17. doi:10.1016/s0020-7519(02)00156-x. PMID 12392916. 
  7. ^ a b Safer, D.; Brenes, M.; Dunipace, S.; Schad, G. (2007). "Urocanic acid is a major chemoattractant for the skin-penetrating parasitic nematode Strongyloides stercoralis". Proceedings of the National Academy of Sciences 104 (5): 1627. doi:10.1073/pnas.0610193104. 
  8. ^ Roberts, J., Jr.; Janovy (2005). Foundations of Parasitology (7th ed.). Boston: McGraw Hill. p. 412. ISBN 0071112715. 
  9. ^ Thamwiwat, Alisa; Mejia, Rojelio; Nutman, Thomas B.; Bates, Jeffrey T. (6 July 2014). "Strongyloidiasis as a Cause of Chronic Diarrhea, Identified Using Next-Generation Strongyloides stercoralis-Specific Immunoassays". Current Tropical Medicine Reports 1 (3): 145–147. doi:10.1007/s40475-014-0026-7. 
  10. ^ Roberts, J., Jr.; Janovy (2005). Foundations of Parasitology (7th ed.). Boston: McGraw Hill. pp. 414–415. ISBN 0071112715. 
  11. ^ Igra-Siegman, Y; Kapila, R; Sen, P; Kaminski, ZC; Louria, DB (1981). "Syndrome of hyperinfection with Strongyloides stercoralis". Reviews of infectious diseases 3 (3): 397–407. doi:10.1093/clinids/3.3.397. PMID 7025145. 
  12. ^ a b Marcos, L. A.; Terashima, A.; Dupont, H. L.; Gotuzzo, E. (2008). "Strongyloides hyperinfection syndrome: An emerging global infectious disease". Transactions of the Royal Society of Tropical Medicine and Hygiene 102 (4): 314–318. doi:10.1016/j.trstmh.2008.01.020. PMID 18321548.  edit
  13. ^ Newberry, AM; Williams, DN; Stauffer, WM; Boulware, DR; Hendel-Paterson, BR; Walker, PF (Nov 2005). "Strongyloides hyperinfection presenting as acute respiratory failure and gram-negative sepsis.". Chest 128 (5): 3681–4. PMID 16304332. 
  14. ^ Roberts, J., Jr.; Janovy (2005). Foundations of Parasitology (7th ed.). Boston: McGraw Hill. p. 415. ISBN 0071112715. 
  15. ^ NHS Direct Health Encyclopedia by: Dr. Dave Cheever
  16. ^ Boulware, DR; Stauffer, WM; Hendel-Paterson, BR; Rocha, JL; Seet, RC; Summer, AP; Nield, LS; Supparatpinyo, K; Chaiwarith, R; Walker, PF (June 2007). "Maltreatment of Strongyloides infection: case series and worldwide physicians-in-training survey.". The American Journal of Medicine 120 (6): 545.e1–8. doi:10.1016/j.amjmed.2006.05.072. PMC 1950578. PMID 17524758. 
  17. ^ Forbes, WM; Ashton, FT; Boston, R; Zhu, X; Schad, GA (2004). "Chemoattraction and chemorepulsion of Strongyloides stercoralis infective larvae on a sodium chloride gradient is mediated by amphidial neuron pairs ASE and ASH, respectively". Veterinary parasitology 120 (3): 189–98. doi:10.1016/j.vetpar.2004.01.005. PMID 15041094. 

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