Miamiensis avidus explained

Miamiensis avidus is a species of unicellular marine eukaryote that is a parasite of many different types of fish. It is one of several organisms known to cause the fish disease scuticociliatosis and is considered an economically significant pathogen of farmed fish.[1] M. avidus is believed to be the cause of a 2017 die-off of fish and sharks in the San Francisco Bay.[2]

Taxonomy

M. avidus is a scuticociliate first described in 1964.[3] [4] It was discovered during a study originally aimed at investigating viruses of marine mammals, and was isolated from the bodies of seahorses collected from waters near Miami, Florida. The name of the genus refers to the University of Miami, where the first studies of the ciliate were performed, and the specific name avidus refers to its "greedy feeding habits".

The name Philasterides dicentrarchi was originally applied to a similar ciliate identified as an infectious parasite in Mediterranean sea bass,[5] but is now recognized as a junior synonym of M. avidus.[6] [7] However, a recent study suggests they may in fact be distinct species.[8] The molecular phylogeny of scuticociliates is an active area of research.[9] [10]

Morphology

M. avidus cells are oval-shaped with a relatively pointed anterior end and a contractile vacuole toward the rounded posterior end of the cell. The cells feature several kineties, or rows of cilia along the major axis of the cell body, and a single caudal cilium. Descriptions vary on the number of kineties per cell, from as few as 10 to as many as 14. Each cell possesses one macronucleus and one micronucleus. The original 1964 description emphasized the significance of the morphology of the buccal apparatus and specialized oral cilia in differentiating among related ciliates. Descriptions of these features differ subtly among one another and may differentiate M. avidus from closely related species. The life cycle of M. avidus has been described and includes at least 3 stages: 1) Microstome, which mainly feeds on bacteria; 2) Macrostome, a voracious stage with a larger oral cavity which feeds on host tissues or other protozoans; and 3) tomite, a non-feeding, starvation-induced, smaller, dispersal stage.[11] The intricate sequence in the morphological microstome to macrostome transformation of M. avidus has been described.[12]

Ecological significance

Scuticociliates are free-living marine microorganisms that can function as opportunistic or facultative parasites. M. avidus infects a broad range of teleost species, as well as other groups of marine organisms such as seahorses, sharks, and crustaceans. It is one of the best characterized of the group of scuticoliciates known to cause the fish disease scuticociliatosis, in which histophagous (tissue-eating) ciliates consume the blood, skin, and eventually internal organs of infected fish. The disease has an especially high mortality rate among flatfish, possibly due to their sedentary lifestyle involving high levels of skin contact between individuals. In one comparative study, M. avidus infections spread further within host fish and had a significantly higher mortality rate than did similar scuticociliates.[13] Infections caused by M. avidus have been described in wild fish populations and in aquaculture, where it is an economically significant pathogen. The species is believed to be responsible for a widely reported 2017 scuticociliatosis outbreak on the coast of Northern California, which saw thousands of dead fish and leopard sharks found in the San Francisco Bay.

It is unclear what triggers free-living M. avidus to initiate infection. Experimental infections under laboratory conditions have produced varying results on the mechanism of infection; results in different conditions and with different host species vary in whether free-living ciliates can infect healthy fish or require an abraded or damaged skin surface. Protease enzymes are commonly expressed by infectious parasites that damage host tissue, and are believed to play a role in M. avidus infections.[14] Transformation in M. avidus has been shown to be induced by a prey derived soluble factor, although its exact identity is unknown.[15]

Notes and References

  1. Book: Jung. Sung-Ju. Woo. Patrick T.K.. Woo. Patrick T.K.. Buchmann. Kurt. Fish parasites: pathobiology and protection. limited. 2012. CABI. Wallingford, Oxfordshire. 9781845938062. 73-91. Chapter 5: Miamiensis avidus and related species.
  2. News: Shaban. Bigad. Witte. Rachel. Horn. Michael. Thousands of Sharks, Other Sea Life Mysteriously Die in San Francisco Bay. 25 November 2017. NBC Bay Area.
  3. THOMPSON. JESSE C.. MOEWUS. LISELOTTE. Miamiensis avidus n. g., n. sp., a Marine Facultative Parasite in the Ciliate Order Hymenostomatida. The Journal of Protozoology. August 1964. 11. 3. 378–381. 10.1111/j.1550-7408.1964.tb01766.x.
  4. Warren, A. . 2009 . Miamiensis avidus Thompson & Moewus, 1964 . 427063 . 24 November 2017 . World Ciliophora Database.
  5. Dragesco. Armelle. Dragesco. Jean. Coste. Françoise. Gasc. Charles. Romestand. Bernard. Raymond. Jean-Christophe. Bouix. Georges. Philasterides dicentrarchi, n. sp., (ciliophora, scuticociliatida), a histophagous opportunistic parasite of Dicentrarchus labrax (Linnaeus, 1758), a reared marine fish. European Journal of Protistology. August 1995. 31. 3. 327–340. 10.1016/S0932-4739(11)80097-0.
  6. Web site: Miamiensis avidus (Ciliate) (Philasterides dicentrarchi). UniProt Taxonomy. 25 November 2017.
  7. Jung. SJ. Kitamura. SI. Song. JY. Oh. MJ. Miamiensis avidus (Ciliophora: Scuticociliatida) causes systemic infection of olive flounder Paralichthys olivaceus and is a senior synonym of Philasterides dicentrarchi. Diseases of Aquatic Organisms. 18 January 2007. 73. 3 . 227–234. 10.3354/dao073227. free. 17330742 .
  8. DE FELIPE. ANA-PAULA. LAMAS. JESÚS. SUEIRO. ROSA-ANA. FOLGUEIRA. IRIA. LEIRO. JOSÉ-MANUEL. New data on flatfish scuticociliatosis reveal that Miamiensis avidus and Philasterides dicentrarchi are different species. Parasitology. 29 May 2017. 144. 10. 1394–1411. 10.1017/S0031182017000749. 28552088 . 10261/177213. free.
  9. Miao. Miao. Wang. Yangang. Li. Liqiong. Al-Rasheid. Khaled A. S.. Song. Weibo. Molecular phylogeny of the scuticociliate, Philaster (Protozoa, Ciliophora), with a description of a new species, P. apodigitiformis sp. nov.. Systematics and Biodiversity. December 2009. 7. 4. 381–388. 10.1017/S1477200009990193. 2009SyBio...7..381M .
  10. Gao. Feng. Katz. Laura A.. Song. Weibo. Insights into the phylogenetic and taxonomy of philasterid ciliates (Protozoa, Ciliophora, Scuticociliatia) based on analyses of multiple molecular markers. Molecular Phylogenetics and Evolution. August 2012. 64. 2. 308–317. 10.1016/j.ympev.2012.04.008. 22525941. 2012MolPE..64..308G .
  11. GÓMEZ-SALADÍN . EDUARDO . SMALL . EUGENE B. . Starvation Induces Tomitogenesis in Strain Ma/2 . Journal of Eukaryotic Microbiology . November 1993 . 40 . 6 . 727–730 . 10.1111/j.1550-7408.1993.tb04466.x.
  12. GÓMEZ-SALADIN . EDUARDO . SMALL . EUGENE B. . Oral Morphogenesis of the Microstome to Macrostome Transformation in Miamiensis avidus Strain Ma/2 . The Journal of Eukaryotic Microbiology . May 1993 . 40 . 3 . 363–370 . 10.1111/j.1550-7408.1993.tb04929.x.
  13. Song. JY. Kitamura. SI. Oh. MJ. Kang. HS. Lee. JH. Tanaka. SJ. Jung. SJ. Pathogenicity of Miamiensis avidus (syn. Philasterides dicentrarchi), Pseudocohnilembus persalinus, Pseudocohnilembus hargisi and Uronema marinum (Ciliophora, Scuticociliatida). Diseases of Aquatic Organisms. 12 February 2009. 83. 133–143. 10.3354/dao02017. free. 19326794 .
  14. Seo. Jung Soo. Jeon. Eun Ji. Jung. Sung Hee. Park. Myoung Ae. Kim. Jin Woo. Kim. Ki Hong. Woo. Sung Ho. Lee. Eun Hye. Molecular cloning and expression analysis of peptidase genes in the fish-pathogenic scuticociliate Miamiensis avidus. BMC Veterinary Research. 2013. 9. 1. 10. 10.1186/1746-6148-9-10. 3599101. 23311870 . free .
  15. GOMEZ-SALADÍN . EDUARDO . SMALL . EUGENE B. . Prey-induced Transformation of Miamiensis avidus Strain Ma/2 by a Soluble Factor . The Journal of Eukaryotic Microbiology . September 1993 . 40 . 5 . 550–556 . 10.1111/j.1550-7408.1993.tb06106.x.