Detection of Viral Hemorrhagic Septicemia virus (VHSV) from the leech Myzobdella lugubris Leidy, 1851
© Faisal and Schulz; licensee BioMed Central Ltd. 2009
Received: 4 September 2009
Accepted: 28 September 2009
Published: 28 September 2009
The leech Myzobdella lugubris is widespread in the Lake Erie Watershed, especially Lake St. Clair. However, its role in pathogen transmission is not fully understood. In this same watershed, several widespread fish mortalities associated with the Viral Hemorrhagic Septicemia virus (VHSV) were recorded. Viral Hemorrhagic Septicemia is an emerging disease in the Great Lakes Basin that is deadly to the fish population, yet little is known about its mode of transmission. To assess the potential role of M. lugubris in VHSV transmission, leeches were collected from Lake St. Clair and Lake Erie and pooled into samples of five. Cell culture and reverse transcriptase polymerase chain reaction (RT-PCR) were used to determine the presence of the virus and its identity. Results showed that 57 of the 91 pooled leech samples were positive by cell culture for VHSV and 66 of the 91 pooled leech samples were positive by RT-PCR for the VHSV. Two representative virus isolates were sequenced for further genetic confirmation and genotype classification. VHSV detected within M. lugubris was homologous to the Great Lakes strain of VHSV genotype IVb. This is the first record of the VHSV being detected from within a leech, specifically M. lugubris, and suggests the potential of M. lugubris being involved in VHSV transmission.
The Viral Hemorrhagic Septicemia Virus (VHSV), genotype IVb, is a recent invader to the Great Lakes Basin (GLB) and has been associated with mortalities in a number of freshwater fish species [1–4]. These recent widespread mortality events in the GLB have raised questions concerning potential routes of virus transmission.
Certain leech species have been incriminated as potential vectors for fish viruses, such as, Piscicola salmositica for Infectious Hematopoietic Necrosis Virus in the sockeye salmon, Oncorhynchus nerka Walbaum  and P. geometra for Spring Viraemia of Carp Virus in the case of the common carp, Cyprinus carpio Linnaeus . In a previous study, the leech population in Lake St. Clair, Michigan was found to be dominated by Myzobdella lugubris Leidy, 1851 (Rhynchobdellida: Piscicolida) [Schulz CA, Thomas MV, Fitzgerald S, Faisal M: Leeches (Annelida: Hirudinea) Parasitizing Fish of Lake St. Clair, Michigan. Submitted]. Myzobdella lugubris is an intermittent, haematophagous feeder, with an extraordinary wide host range [7–9] and therefore it is a good candidate leech to contribute to pathogen spread among susceptible host species. In this study we collected attached M. lugubris from fish collected from two sites in the Lake Erie watershed, where VHSV Type IVb was first isolated, and subsequent fish mortalities have taken place over the last few years .
Detached leeches were tentatively identified as M. lugubris in the field and were stored in one liter bottles containing lake water. Overall, 456 leeches were removed and divided into 91 pools of ~five leeches. Leeches remained alive until returned to the laboratory, where their identity was confirmed as M. lugubris according to the accepted morphological criteria [9, 10]. Each leech was briefly immersed into absolute ethanol for surface disinfection, rinsed several times in sterile water, and then sectioned into ~100 μg pieces. Samples were homogenized using a Biomaster Stomacher (Wolf Laboratories Ltd, Pocklington, York, UK) at the high speed setting for 2 min and then diluted with Earle's salt-based minimal essential medium (MEM, Invitrogen, Carlsbad, CA) to produce a 1:4 dilution (w/v) of original tissues. Homogenized leech contents were removed with a sterile transfer pipette, dispensed into a sterile 15 ml centrifuge tube, and centrifuged at 5500 rcf for 20 min in the IEC Multi RF Centrifuge (Thermo Fisher Scientific, Pittsburgh, PA). Supernatants were immediately used for virus isolation.
Virus isolation was performed according to the standard protocols detailed in the American Fisheries Society Blue Book  and the OIE , using the Epithelioma papulosum cyprinii (EPC) cell line . Inoculated 96-well plates containing EPC cells grown with MEM (5% fetal bovine serum) were incubated at 15°C for 7 days, and were observed for the formation of cytopathic effects (CPE). Second and third blind passages were performed and assessed for the presence of VHSV.
Thirteen of the 91 pooled samples of leech homogenates caused CPE on EPC in the form of focal areas of rounded, refractile cells which progressed to full lysis of the cell monolayer. When a second passage was performed on negative samples, four additional samples exhibited CPE. A third passage raised the number of positive samples to 57 out of 91 pools. It is possible that the virus was present in higher titers in the samples which were positive in the first passage of cell culture.
The RT-PCR products of two representative VHSV-positive samples were purified with the Promega Wizard® SV Gel and PCR Clean-up System and were then submitted to the MSU Research Technology Support Facility. The two sequences were aligned by BL2SEQ  and the aligned contig was used for multiple alignments performed by ClustalW . The phylogenetic analysis of the VHSV leech strain with 19 nucleoprotein encoding genes from other species of rhabdovirus was done by using bootstrap test of phylogeny in MEGA 4 . The Neighbor-Joining algorithm was chosen to create the phylogenetic dendrogram containing 1000 bootstrap samplings.
Sequencing of the two leech isolates produced a 780 base pair sequence (GenBank:1227728) that was identical to the VHSV IVb-MI03 strain, the index strain of the Great Lakes VHSV (GenBank:DQ427105).
Our findings shed light on the potential role leeches may play in VHSV transmission. While this study does not confirm that Myzobdella lugubris does indeed transmit the virus to susceptible hosts, this is the first time that VHSV (of any genotype) has been isolated from leeches, or other invertebrates. Myzobdella lugubris is an intermittent, generalist species; therefore the detection of VHSV within M. lugubris may pose a threat to VHSV-susceptible host species, not only in the Great Lakes basin, but also in other watersheds to which infected M. lugubris may be transferred.
The authors thank Mike Thomas and the crew of the Michigan Department of Natural Resources Lake St. Clair Mt. Clemens Fisheries Research Station and David Blair Commercial Fisheries for their assistance with sample collection. In order to conduct the study, we are indebted to the generous funding provided by the Great Lakes Fishery Trust (''Viral Hemorrhagic Septicemia Virus in the Great Lakes'' Project #08WRGR0006) and the United States Department of Agriculture (''Critical Issues: Plant and Animal Pests and Diseases'' Project #2007-37610-18383).
- Elsayed E, Faisal M, Thomas M, Whelan G, Batts W, Winton J: Isolation of viral haemorrhagic septicaemia virus from muskellunge, Esox masquinongy (Mitchill), in Lake St. Clair, Michigan, USA reveals a new sublineage of the North American genotype. J Fish Dis. 2006, 29: 611-619. 10.1111/j.1365-2761.2006.00755.x.View ArticlePubMedGoogle Scholar
- Gagné N, MacKinnon AM, Boston L, Souter B, Cook-Versloot M, Griffiths S, Olivier G: Isolation of viral hemorrhagic septicemia virus from mummichog, stickleback, striped bass and brown trout in eastern Canada. J Fish Dis. 2007, 30: 213-223. 10.1111/j.1365-2761.2007.00802.x.View ArticlePubMedGoogle Scholar
- Groocock GH, Getchell RG, Wooster GA, Britt KL, Batts WN, Winton JR, Casey RN, Casey JW, Bowser PR: Detection of viral hemorrhagic septicemia in round gobies in New York State (USA) waters of Lake Ontario and the St. Lawrence River. Dis Aquat Org. 2007, 76 (3): 187-192. 10.3354/dao076187.View ArticlePubMedGoogle Scholar
- Lumsden JS, Morrison B, Yason C, Russell S, Young K, Yazdanpanah A, Huber P, Al-Hussinee L, Stone D, Way K: Mortality event in freshwater drum Aplodinotus grunniens from Lake Ontario, Canada, associated with viral haemorrhagic septicemia virus, Type IV. Dis Aquat Org. 2007, 76 (2): 99-111. 10.3354/dao076099.View ArticlePubMedGoogle Scholar
- Mulcahy D, Klaybor D, Batts WN: Isolation of infectious hematopoietic necrosis virus from a leech (Piscicola salmositica) and a copepod (Salmincola sp.), ectoparasites of sockeye salmon Oncorhynchus nerka. Dis Aquat Org. 1990, 8: 29-34. 10.3354/dao008029.View ArticleGoogle Scholar
- Ahne W: Argulus foliaceus L. and Piscicola geometra L. as mechanical vectors of spring viremia of carp virus (SVCV). J Fish Dis. 1985, 8: 241-242. 10.1111/j.1365-2761.1985.tb01220.x.View ArticleGoogle Scholar
- Davies RW: The geographic distribution of freshwater Hirudinoidea in Canada. Can J Zool. 1973, 51: 531-545. 10.1139/z73-078.View ArticleGoogle Scholar
- Klemm DJ: Leeches (Annelida: Hirudinea) of North America. 1982, Cincinnati, Ohio: U.S. Environmental Protection Agency, Environmental and Monitoring Support Laboratory. EPA-600/3-82-025Google Scholar
- Hoffman G: Parasites of North American Freshwater Fishes. 1999, Ithaca, NY: Cornell University PressGoogle Scholar
- Peckarsky BL, Fraissinet PR, Penton MA, Conklin DJ: Freshwater Macroinvertebrates of Northeastern North America. 1990, Cornell University Publishing, Ithaca, New YorkGoogle Scholar
- American Fisheries Society-Fish Health Section: Suggested procedures for the detection and identification of certain finfish and shellfish pathogens. 2007, American Fisheries Society: Bethesda, MDGoogle Scholar
- Office International des Epizooties (OIE): Chapter 2.1.5 Viral Hemorrhagic Septicemia. Manual of Diagnostic Tests for Aquatic Animals. 2006, World Animal Health Organization, Paris, 4Google Scholar
- Fijan N, Sulimanović Đ, Bearzotti M, Mužinić D, Zwillenberg LO, Chilmonczyk S, Vautherot JF, de Kinkelin P: Some properties of the epithelioma papulosum cyprini (EPC) cell line from carp Cyprinus carpio. Ann Inst Pasteur Virol. 1983, 134E: 207-220. 10.1016/S0769-2617(83)80060-4.View ArticleGoogle Scholar
- Tatusova TA, Madden TL: Blast 2 sequences - a new tool for comparing protein and nucleotide sequences. Microbiol Lett. 1999, 174 (2): 247-250. 10.1111/j.1574-6968.1999.tb13575.x.View ArticleGoogle Scholar
- Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignments through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22: 4673-4680. 10.1093/nar/22.22.4673.PubMed CentralView ArticlePubMedGoogle Scholar
- Tamura K, Dudley J, Nei M, Kumar S: MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24: 1596-1599. 10.1093/molbev/msm092.View ArticlePubMedGoogle Scholar
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