Biology:Schistosoma bovis

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Short description: Species of fluke

Schistosoma bovis
Scientific classification edit
Domain: Eukaryota
Kingdom: Animalia
Phylum: Platyhelminthes
Class: Trematoda
Order: Diplostomida
Family: Schistosomatidae
Genus: Schistosoma
Species:
S. bovis
Binomial name
Schistosoma bovis
Sonsino, 1876

Schistosoma bovis is a two-host blood fluke, that causes intestinal schistosomiasis in ruminants in North Africa, Mediterranean Europe and the Middle East. S. bovis is mostly transmitted by Bulinus freshwater snail species. It is one of nine haematobium group species and exists in the same geographical areas as Schistosoma haematobium, with which it can hybridise. S. bovis-haematobium hybrids can infect humans, and have been reported in Senegal since 2009, and a 2013 outbreak in Corsica.

Taxonomy and identification

Schistosoma bovis is a digenetic, two-host blood fluke. It was discovered by Italian parasitologist Prospero Sonsino at Zagazig meat market in Egypt in 1876 from a bull.[1] It is generally similar to other schistosomes, but Sonsino knew that it was larger and its eggs were different from those of the human species (first and only known schistosome at the time), Schistosoma haematobium, discovered by a German physician Theodor Bilharz in 1852,[2][3] then known as Bilharzia haematobium or Distomum haematobium. Sonsino gave the name Bilharzia bovis[4] following the genus classification introduced by another German physician Heinrich Meckel von Hemsbach in 1856 for the species described by Bilharz.[5][6] The eggs of S. bovis are not only larger than those of other schistosomes, but also have thicker spine with an elongated shape in the form a spindle.[7][8] The eggs are therefore the best and simplest identification key from other species.[9][10]

Sonsino later revised the name as Bilharzia crassa in 1877, and then as Gynaecophorus crassa in 1992. Though the genus name remained confusing, Louis-Joseph Alcide Railliet (in 1893) and Raphaël Blanchard (in 1895) revived and maintained the species name, bovis.[4] The valid genus name Schistosoma was accepted by the International Commission on Zoological Nomenclature (ICZN) in 1954,[11] following the name created by David Friedrich Weinland in 1858.[12] Thus, the original Bilharzia bovis became Schistosoma bovis.[4]

Hybrids between S. bovis and the human schistosome, Schistosoma haematobium were first described in 2009 in Northern Senegalese children, and to a lesser degree hybrids between S. bovis and cattle schistosome S. curassoni found only in cattle.[13] S. bovis-haematobium hybrids were also found during the 2013 outbreak traced to the Cavu river on Corsica.[14] As a hybrid increases the host range of the parent species, they affect transmission, and as is known from other schistosome hybrid pairings, morbidity and drug susceptibility, so they are epidemiologically important.[13]

Life cycle

Schistosoma life cycle

Schistosoma bovis infects two hosts, namely ruminants (cattle, goats, sheep, horses and camels) and freshwater snails (Bulinus sp. and Planorbarius sp.).[15]:392 Experimental infections have been proven in Planorbarius metidjensis snails, which are native to Northwestern Africa and the Iberian peninsula.[citation needed]

In water, its free swimming infective larval cercariae can burrow into the skin of its definite host, the ruminant, upon contact. The cercariae enter the host's blood stream, and travel to the liver to mature into adult flukes. Adult flukes can coat themselves with host antigen thus avoiding detection by the host immune system. After a period of about three weeks the young flukes migrate to the mesenteric veins of the gut to copulate. The female fluke lays eggs, which migrate into the lumen of the gut and leave the host upon defecation. In fresh water, the eggs hatch, forming free swimming miracidia.[16][17][18]

Miracidia penetrate into the intermediate host, the freshwater snails[19] of the Bulinus spp., (e.g. B. globosus, B. forskalii, B. nyassanus and B. truncatus), except in Spain,[15]:20 Portugal and Morocco, where Planorbarius metidjensis can transmit.[20] Inside the snail, the miracidium sheds its epithelium, and develops into a mother sporocyst. After two weeks the mother begins forming daughter sporocysts. One month – or more with cooler ambient temperatures – after a miracidium has penetrated into the snail, hundreds to thousands of cercariae of the same sex begin to be released through special areas of the sporocyst wall.[15]:30 The cercariae cycle from the top of the water to the bottom in search of a host. They can enter the host epithelium within minutes.[21][15]:34

Geographical distribution

S. bovis infects snails in Africa north of the equator, Europe (Sardinia, Corsica, Spain) and the Middle East as far as Iraq.[15]:20 S. bovis-haematobium hybrids have been reported first in Senegal in the early 1990s,[22] and then an outbreak in 2013 in Corsica.[23]

Diagnosis

Laboratory

The diagnosis of schistosomiasis can be made by microscopically examining the feces for the egg. The S. bovis egg is terminally spiked, spindle shaped, and the largest in size compared to other Schistosoma eggs at 202 μm length and 72μm width.[15]:396 In chronic infections, or if eggs are difficult to find, an intradermal injection of Schistosome antigen to form a wheal can determine infection. Alternatively diagnosis can be made by complement fixation tests.[19]

(As of 2012) commercial serological tests have included ELISA and an indirect immunofluorescence test, hampered by a low sensitivity ranging from 21% to 71%.[24] Exposure to any Schistosoma eggs or cercariae can cause false positive serological test results for individual Schistosoma species, unless highly specific antigens are used.[15]:402

Various polymerase chain reaction (PCR) assays to differentiate S. bovis from other schistosomes in urine and naturally infected snails for surveillance purposes have been described since 2010.[25]

Pathology

The ova are initially deposited in the muscularis propria of the gut which leads to ulceration of the overlaying tissue. Infections are characterized by pronounced acute inflammation, blood and reactive epithelial changes. Granulomas and multinucleated giant cells may be seen.[citation needed]

Immunopathology

The immune system responds to eggs in the liver causing hypersensitivity; an immune response is necessary to prevent damage to hepatocytes. The hosts' antibodies bind to the tegument of the schistosome but not for long since the tegument is shed every few hours. The schistosome can also take on host proteins. Schistomiasis can be divided into three phases; Within the haematobium group S. bovis and S. curassoni appear to be closely related: (1) the migratory phase lasting from penetration to maturity, (2) the acute phase which occurs when the schistosomes begin producing eggs, and (3) the chronic phase which occurs mainly in endemic areas.[19]

Gene expression

S. bovis is one of the few non-bacterial species with a known moonlighting protein. Glyceraldehyde-3-phosphate dehydrogenase (GAPD) is also a common MP in bacteria.[26]

Treatment

Historically, antimonials and trichlorphon were tested against visceral schistosome infection in cattle.[27]:245–248, 265–273 Antimony affects phosphofructokinase activity in Schistosoma, hycanthone intercalates Schistosoma DNA and the organophosphorus metabolite dichlorvos inhibits acetylcholinesterase, "but progressively less so in S. bovis".[15]:44

Since the 1980s the drug of choice is praziquantel, a quinolone derivative which disrupts membranes, leading to calcium influx. It clears eggs from stool, and affects adult but not immature worms.[15]:44–45 Damaged and dying flukes can be trapped in the liver and cause fatal portal vein thrombosis.[27]

Disease prevention

The main cause of schistosomiasis is the dumping of human and animal waste into water supplies. Hygienic disposal of waste would be sufficient to eliminate the disease.[19]

References

  1. Pitchford, R. J. (1965). "Differences in the egg morphology and certain biological characteristics of some African and Middle Eastern schistosomes, genus Schistosoma, with terminal-spined eggs". Bulletin of the World Health Organization 32 (1): 105–120. PMID 14292062. 
  2. Southgate, V.R.; Knowles, R.J. (1975). "Observations on Schistosoma bovis Sonsino, 1876" (in en). Journal of Natural History 9 (3): 273–314. doi:10.1080/00222937500770201. ISSN 0022-2933. Bibcode1975JNatH...9..273S. http://www.tandfonline.com/doi/abs/10.1080/00222937500770201. 
  3. Khalil, M. (1924). "On the Morphology of Schistosoma bovis" (in en). Journal of Helminthology 2 (2): 81–86. doi:10.1017/S0022149X00003059. ISSN 1475-2697. https://www.cambridge.org/core/journals/journal-of-helminthology/article/abs/on-the-morphology-of-schistosoma-bovis/05E11753D7E569EE3E6FBBA9129B1892. 
  4. 4.0 4.1 4.2 Styles, Ch. Wardell (1896). "The inspection of meats for animal parasites" (in en). Bulletin of the U.S. Department of Agriculture. 10. U.S. Government Printing Office. pp. 60. https://books.google.com/books?id=9IwmAQAAMAAJ. 
  5. Meckel von Hemsbach, Heinrich (2018). Mikrogeologie: Ueber die Concremente im thierischen Organismus (Reprint 2018 ed.). Berlin: De Gruyter. pp. 114. ISBN 978-3-11-171606-0. OCLC 1029825577. https://www.worldcat.org/oclc/1029825577. 
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  7. Schwetz, J. (1956). "Some new Comparative Investigations on Three Physopsis Borne Schistosomes: Schistosoma Haematobium, S. Bovis and S. Intercalatum 1" (in en). The American Journal of Tropical Medicine and Hygiene 5 (6): 1071–1085. doi:10.4269/ajtmh.1956.5.1071. ISSN 0002-9637. PMID 13381883. https://ajtmh.org/doi/10.4269/ajtmh.1956.5.1071. 
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  9. Alves, William (1949). "The Eggs of Schistosoma bovis , S. mattheei and S. haematobium" (in en). Journal of Helminthology 23 (3–4): 127–134. doi:10.1017/S0022149X00032466. PMID 15402061. https://www.cambridge.org/core/product/identifier/S0022149X00032466/type/journal_article. 
  10. Soentjens, Patrick; Cnops, Lieselotte; Huyse, Tine; Yansouni, Cedric; De Vos, Daniel; Bottieau, Emmanuel; Clerinx, Jan; Van Esbroeck, Marjan (2016). "Diagnosis and Clinical Management of Schistosoma haematobium – Schistosoma bovis Hybrid Infection in a Cluster of Travelers Returning From Mali" (in en). Clinical Infectious Diseases 63 (12): 1626–1629. doi:10.1093/cid/ciw493. ISSN 1058-4838. PMID 27941144. 
  11. Hemming, Francis (1954). Opinions and Declarations Rendered by the International Commission on Zoological Nomenclature (Volume 4 Part 16). 4. London: International Trust for Zoological Nomenclature. pp. 177–200. https://www.biodiversitylibrary.org/item/107760#page/7/mode/1up. 
  12. Weinland, David Friedrich (1858) (in en). Human Cestoides: An Essay on the Tapeworms of Man. Cambridge (UK): Metcalf and Company. pp. 87. https://books.google.com/books?id=biotAAAAYAAJ. 
  13. 13.0 13.1 Huyse, Tine; Webster, Bonnie L.; Geldof, Sarah; Stothard, J. Russell; Diaw, Oumar T.; Polman, Katja; Rollinson, David (2009). "Bidirectional introgressive hybridization between a cattle and human schistosome species". PLOS Pathogens 5 (9): e1000571. doi:10.1371/journal.ppat.1000571. PMID 19730700. 
  14. Jérôme Boissier et al. (2016). "Outbreak of urogenital schistosomiasis in Corsica (France): an epidemiological case study". The Lancet Infectious Diseases 16 (8): 971–979. doi:10.1016/S1473-3099(16)00175-4. PMID 27197551. https://hal.archives-ouvertes.fr/hal-01364002/file/Boissier-2016-LancetID-Outbreak-MANUSCRIT.pdf. 
  15. 15.0 15.1 15.2 15.3 15.4 15.5 15.6 15.7 15.8 Adel A. F. Mahmoud (2001). Schistosomiasis. Imperial College Press. pp. 524. ISBN 978-186094-146-7. https://books.google.com/books?id=G0Aa4J_rjiIC&pg=PA20. Retrieved 31 July 2016. 
  16. Agnew, Alison M.; Murare, H. M.; Lucas, S. B.; Doenhoff, M. J. (1989). "Schistosoma bovis as an immunological analogue of S. haematobium" (in en). Parasite Immunology 11 (4): 329–340. doi:10.1111/j.1365-3024.1989.tb00671.x. ISSN 0141-9838. PMID 2506507. https://onlinelibrary.wiley.com/doi/10.1111/j.1365-3024.1989.tb00671.x. 
  17. Bushara, H. O.; Omer, O. H.; Malik, K. H. E.; Taylor, M. G. (1994). "The effect of multiple transfers of immune serum on maturingSchistosoma bovis infections in calves" (in en). Parasitology Research 80 (3): 198–202. doi:10.1007/BF00932674. ISSN 1432-1955. PMID 8036232. https://doi.org/10.1007/BF00932674. 
  18. de la Torre-Escudero, Eduardo; Pérez-Sánchez, Ricardo; Manzano-Román, Raúl; Oleaga, Ana (2017). "Schistosoma bovis -host interplay: Proteomics for knowing and acting" (in en). Molecular and Biochemical Parasitology 215: 30–39. doi:10.1016/j.molbiopara.2016.07.009. PMID 27485556. https://linkinghub.elsevier.com/retrieve/pii/S0166685116300986. 
  19. 19.0 19.1 19.2 19.3 Black, J. (2005). Microbiology: Principles and Explorations. Wiley, New York. 
  20. "Schistosoma bovis: variability of cercarial production as related to the snail hosts: Bulinus truncatus, B. wright and Planorbarius metidjensis". Int J Parasitol 17 (8): 1431–4. Dec 1987. doi:10.1016/0020-7519(87)90078-6. PMID 3440697. 
  21. Roberts, L.; Janovy, J. (1996). Foundations of Parasitology (5th ed.). Wm. C. Brown Publishers, Dubuque, Iowa. 
  22. Webster, Bonnie L.; Diaw, Oumar T.; Seye, Mohmoudane M.; Webster, Joanne P.; Rollinson, David (2013). "Introgressive hybridization of Schistosoma haematobium group species in Senegal: species barrier break down between ruminant and human schistosomes". PLOS Neglected Tropical Diseases 7 (4): e2110. doi:10.1371/journal.pntd.0002110. ISSN 1935-2735. PMID 23593513. 
  23. Boissier, Jérôme; Grech-Angelini, Sébastien; Webster, Bonnie L.; Allienne, Jean-François; Huyse, Tine; Mas-Coma, Santiago; Toulza, Eve; Barré-Cardi, Hélène et al. (2016). "Outbreak of urogenital schistosomiasis in Corsica (France): an epidemiological case study". The Lancet. Infectious Diseases 16 (8): 971–979. doi:10.1016/S1473-3099(16)00175-4. ISSN 1474-4457. PMID 27197551. 
  24. "Evaluation of eight serological tests for diagnosis of imported schistosomiasis". Clin Vaccine Immunol 19 (6): 948–53. 2012. doi:10.1128/CVI.05680-11. PMID 22441394. 
  25. "Differentiating Schistosoma haematobium from Schistosoma magrebowiei and other closely related schistosomes by polymerase chain reaction amplification of a species specific mitochondrial gene.". Tropical Parasitology 4 (1): 38–42. 2014. doi:10.4103/2229-5070.129163. PMID 24754026. 
  26. Henderson, Brian; Martin, Andrew (2011). "Bacterial Moonlighting Proteins and Bacterial Virulence". Between Pathogenicity and Commensalism. 358. Berlin, Heidelberg: Springer Berlin Heidelberg. 155–213. doi:10.1007/82_2011_188. ISBN 978-3-642-36559-1. 
  27. 27.0 27.1 Reinecke, RK (1983). "Phylum plathelminthes". Veterinary helminthology. Durban, SouthAfrica: Butterworths. 

External links

Wikidata ☰ Q28431216 entry