Open Access
Original contribution
Issue
Parasite
Volume 18, Number 1, February 2011
Page(s) 79 - 84
DOI https://doi.org/10.1051/parasite/2011181079
Published online 15 February 2011

© PRINCEPS Editions, Paris, 2011, transferred to Société Française de Parasitologie

Licence Creative Commons
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

The largemouth bass (Micropterus salmoides) is an important species in the food web of inland lakes in the Laurentian Great Lakes basin (Bettoli et al., 1992). Due to its key predator-prey relationship with other aquatic organisms, largemouth bass plays a central role in the trophic cascades in the Great Lakes environment. In the state of Michigan, one-half million anglers predominately fish for largemouth bass, representing about 30% of all state licensed anglers (State of Michigan, 2004). Therefore, there is a need to better understand disease conditions, including parasitism, which can have an impact on this popular recreational fishery.

Leeches are known to feed upon a variety of terrestrial and aquatic animals, including fish (Sawyer, 1986). Leeches can be semi-permanent, attaching to only one host for the greater part of their adult life, or their attachment can be intermittent, attaching to several hosts throughout their lifetime (Sawyer, 1986). Adult leeches generally detach themselves from their fish hosts to deposit egg cocoons, from which juvenile leeches emerge after a few months to find their own fish hosts on which to feed, and grow into adults (Sawyer, 1986). The piscicolid leech Myzobdella lugubris is an intermittent blood-sucking parasite that parasitizes on a number of freshwater and estuarine fish species, including the largemouth bass, channel catfish (Ictalurus punctatus), white catfish (I. catus), mottled sculpin (Cottus bairdi), and burbot (Lota lota) (Daniels & Sawyer, 1975; Sawyer et al., 1975; Amin, 1981; Schramm et al., 1981; Muzzall et al., 1987; Morrison & Fox, 1993; Choudhury et al., 2004; Schulz et al., 2011). Interestingly, the life cycle of M. lugubris can involve a crustacean host on which this piscicolid leech deposits its egg cocoons, such as the blue crab, Callinectes sapidus (Daniels & Sawyer, 1975).

The preferred site of attachment for M. lugubris is primarily on the fin soft rays, causing erosion and epithelial hyperplasia (Dechtiar, 1972; Schulz et al., 2011). However, Noga et al. (1990) reported the presence of both ulcerations and attached M. lugubris in the mouth of four adult largemouth bass from Currituck Sound, North Carolina, though the relationship between the leech presence and the mouth ulcerations was never established. Herein, we report on widespread mouth ulcerations in adult largemouth bass caught from eight inland lakes of Michigan with a significant association with the presence of M. lugubris.

Materials and Methods

Fish and sampling sites

A total of 326 adult largemouth bass, Micropterus salmoides, with a mean total length of 30.2 cm ± 5.1 cm and mean total weight of 399.9 g ± 279.3 g were collected in summer months from eight inland lakes in Michigan’s Lower Peninsula between July 2002 and September 2003. The lakes sampled were Jordan Lake, Randall Lake, Norvell Lake, Devils Lake, Eagle Lake, Lake Orion, Union Lake, and Independence Lake (Fig. 1, Table I). Fish were collected primarily by electro-fishing, hook and line angling, and trap nets by biologists from the Michigan Department of Natural Resources. Fish were transported alive in tanks with aerators to the Aquatic Animal Health Laboratory at Michigan State University, East Lansing, Michigan. The number of fish samples from each lake is given in Table I.

thumbnail Fig 1.

Largemouth bass (Micropterus salmoides) were collected from eight collection sites in the Lower Peninsula of Michigan between July 2002 and September 2003.

Table I.

Prevalence of mouth ulcerations and attached Myzobdella lugubris in largemouth bass (Micropterus salmoides) sampled from eight inland lakes in Michigan.

Laboratory and sample processing

Fish were anesthetized with 250 mg/liter Tricaine Methanesulfonate (MS-222, Argent Chemicals, Redmond, WA) and their buccal cavity thoroughly examined for the presence of ulcers and leeches. Leeches, when present, were collected, their numbers/fish recorded, and kept separately in vials containing saline (0.6% NaCl solution). Leeches were allowed to relax using menthol crystals (5-methyl-2-[1-methylethyl] cyclohexanol, Sigma-Aldrich Chemical Co., St. Louis, MO) added to a Petri dish of water and were then compressed gently with a glass slide (Pritchard and Kruse 1982). They were then fixed in an alcoholformalin- acetic acid (AFA) fixative for 24 hours and stored in 70% ethanol at room temperature until stained. Fixed leeches passed through descending strengths of ethanol (70%, 50%, and 35%), a single stage of distilled water, and were then stained with Mayer’s hematoxylin stain (Sigma), each immersion lasting 15-30 min, depending on the size of the leech. Once the leech was stained, it was dehydrated through ascending stages of ethanol immersion (85%, 95%, and 100%), lasting 15-30 min, and lastly, cleared by xylene (J.T. Baker, Phillipsburg, NJ). Mounted preparations from representative leeches were made and used for species identification (Pritchard & Kruse, 1982). Taxonomic identification of leeches followed the schemes of Sawyer et al. (1975), Khan & Meyer (1976), Barta (1991), Apakupakul et al. (1999), and Hoffman (1999).

Statistical analyses

A one-way analysis of variance (ANOVA) was conducted to determine the significance of mouth ulcerations and leech prevalence. Additionally, Tukeyadjusted multiple comparisons were used to compare the prevalences of mouth ulcerations and leeches among lakes. A P-value less than 0.05 was considered significant. Calculations were performed using the SAS version 9.2 software (SAS Institute, Inc., Cary, North Carolina).

Results

Examining the buccal cavity of largemouth bass revealed the presence of leeches crawling freely, attached to buccal mucosa, or buried in furrows within the mucosa. The overall prevalence of leeches in largemouth bass’ buccal cavity in the eight lakes combined was relatively high (20%, 64 out of 326 fish examined). Most fish harbored more than three leeches, but as many as six or seven leeches were common in fish from Lake Orion and Devils Lake. There were significant differences in leech prevalence among lakes with Lake Orion and Devils Lake being the highest at 34% and 29%, respectively (Table I). On the contrary, no leeches were attached to the buccal mucosa in fish from Union Lake.

All leeches attached to the buccal mucosa of largemouth bass shared the same morphological criteria. Leech bodies were grayish to dark red, often contained scattered pigment cells, and measured 24-36 mm in length when relaxed (Fig. 2). All leeches exhibited the cylindrical body morphology; divided at the 13th segment into a narrow anterior and a wider posterior region; had one pair of eyes; and a concave caudal sucker.

thumbnail Fig 2.

A specimen of Myzobdella lugubris compressed and stained with Mayer’s hematoxylin.

Clinical examination revealed the presence of widespread ulcerations of the buccal mucosa at the roof of the mouth as well as on the tongue mucosa. The prevalence of buccal ulcerations was relatively high since it was found in 105 out of 326 largemouth bass examined (32%). In several fish, leeches were found embedded in the buccal mucosa, particularly at the roof of the mouth (Fig. 3A). Even though leeches were within the mucosa, they were in continuous movement, a matter that caused detachment of the mucosal layer. Most of the ulcers exhibited deeper hemorrhagic centers with inflamed irregular edges (Fig. 3B). The size of ulcers varied from minute to relatively large. In advanced cases, ulceration covered a considerable portion of the buccal mucosa, often with yellowish-white material (Fig. 3C). In some instances, ulcers were found on the tongue with larger hemorrhagic areas surrounding the leech attachment sites (Fig. 3D).

thumbnail Fig 3.

Myzobdella lugubris. (A) burrowing into the buccal mucosa of a largemouth bass (arrow) from Orion Lake; (B) ulcerations and leeches (arrows) in the roof of the mouth of a largemouth bass from Orion Lake; (C) severe ulceration associated with a leech infestation in the roof of the mouth of a largemouth bass from Devils Lake with suppurative inflammation and subsequent pus formation (arrow); and (D) M. lugubris (arrow) attached to the tongue of a largemouth bass from Devils Lake.

Similar to leech prevalence, buccal ulceration prevalence was highest in Lake Orion (53%) and Devils Lake (68%) and did not exist in the leech-free Union Lake. Moreover, ulcer prevalence varied significantly among lakes. For example, the prevalence of ulcers in fish from Devils Lake was significantly higher than Eagle, Independence, Randall, and Union lakes (P < 0.01). The difference in ulceration prevalence between Randall Lake and Jordan and Norvell lakes was statistically significant (P < 0.05). Additionally, the prevalence of ulcers in fish from Lake Orion was greater than the prevalence of ulcers in fish from Randall, Union, Eagle, and Independence lakes, and was statistically significant (P < 0.05). When the individual fish data of the eight lakes was combined, statistical analysis revealed that the interaction between the prevalence of ulcers and the prevalence of leeches was statistically significant (P < 0.05).

Discussion

Morphological criteria indicated that the leeches collected in this study were all Myzobdella lugubris Leidy 1851 (Sawyer et al., 1975; Khan & Meyer, 1976; Barta, 1991; Hoffman, 1999). It was surprising that M. lugubris was noticed only in the buccal cavity, since it is known also to attach to skin (Miller & Olson, 1973; Muzzall et al., 1987; Morrison & Fox, 1993; Choudhury et al., 2004), fins (Daniels & Sawyer, 1975; Schramm et al., 1981; Muzzall et al., 1987; Morrison & Fox, 1993), and isthmus (Schramm et al., 1981; Morrison & Fox, 1993). Moreover, statistical analyses revealed that M. lugubris prevalence is significantly related to the buccal ulceration, suggesting that the leech feeding habits and ability to burrow into the mucosa are most likely the cause of these ulcers. Indeed, most of the recent ulcers observed took the size and shape of the M. lugubris contour. The ulceration is probably exacerbated by the intermittent nature of M. lugubris parasitism, which is associated with continuous attachment, detachment, and movement into other parts of the mucosa. This study and that of Noga et al. (1990) in the largemouth bass are the only reports of M. lugubris having a tendency toward buccal mucosa.

Myzobdella lugubris produces two types of secretions that lyse host epithelium and aid in the attachment to host surfaces (Michel & Devillez, 1978; Appy & Cone, 1982). The tissue damage caused by this leech compromises the integrity of bass buccal mucosa and allows for potential invasion by pathogenic bacteria and viruses. In this context, recent studies from the authors’ laboratory have demonstrated that M. lugubris carries the Viral Hemorrhagic Septicemia Virus (Faisal & Schulz, 2009), a disease that has devastated important fish stocks in the Laurentian Great Lakes; and Flavobacterium psychrophilum, the causative agent of both Bacterial Coldwater Disease and Rainbow Trout Fry Syndrome, which can cause high mortalities in salmonids (Schulz & Faisal, 2010). Other species of leeches are well known for functioning as vehicles for transmission of infectious agents in fish (Dombrowski, 1952; Ahne, 1985; Cusack & Cone, 1986; Kruse et al., 1989; Jones & Woo, 1992; Zintl et al., 2000; Kikuchi et al., 2002; Hemmingsen et al., 2005; Kikuchi & Fukatsu, 2005). Whether or not M. lugubris transmits pathogens to the largemouth bass is currently unknown and deserves further investigation.

Prevalence of M. lugubris varied greatly from one lake to the other. Many biological, chemical, and physical components of each waterbody determine the presence and infection parameters of a certain parasite in a locale, including the presence and density of susceptible hosts, the prevailing temperature, the composition of the fish community, and the presence of other parasite species (Kennedy, 2009). Unfortunately, the information available on the hydrobiology of each of the lakes is not enough to allow identification of the factors that led to high leech prevalence in lakes Orion and Devils or its total absence in Union Lake. The presented data represents the most comprehensive account of M. lugubris prevalence in largemouth bass in Michigan’s inland lakes. The inland lakes from which largemouth bass samples were collected were never examined previously for leeches of largemouth bass. Therefore, the findings from this study are considered to be new geographical range extensions for M. lugubris.

Declaration of New Geographic Range for Myzobdella Lugubris Leidy 1851

  • . Prevalence: varied from 0-34 (average 20%).

  • . Site of infection: buccal cavity.

  • . Type host: largemouth bass.

  • . Other reported hosts: Acipenser brevirostrum, Acrocheilus alutaceus, Ambloplites rupestris, Ancylopsetta quadrocellata, Aplodinotus grunniens, Awaous guamensis, Callinectes sapidus, Carpiodes cyprinus, Catostomus macrocheilus, C. columbianus, Cottus bairdi, Eleotris sandwicensis, Esox lucius, Fundulus grandus, F. heteroclitus, F. majalis, F. similes, Ictalurus catus, I. melas, I. natalis, I. nebulosus, I. punctatus, Lepomis cyanellus, L. macrochirus, Lota lota, Micropterus dolomieu, M. salmoides, M. saxatilis, Moxostoma macrolepidotum, Mugil cephalus, Notemigonus crysoleucas, Notropis atherinoides, Palaemontetes pugio, Paralichthys lethostigma, Penaeus setiferus, Perca flavescens, Percina caprodes, Pomoxis annularis, P. nibromaculatus, Pterois volitans, Ptychocheilus oregonensis, Sander vitreus, and Sicyopterus stimpsoni.

  • . New location(s) based on the present study: the following inland lakes in Michigan’s Lower Peninsula: Lakes Devil, Eagle, Independence, Jordan, Norvell, Orion, Randall, and Union.

  • . Other reported localities in North America: The U.S. states of Alabama, Arizona, California, Connecticut, Florida, Georgia, Hawaii, Kentucky, Louisiana, New Jersey, Maryland, Massachusetts, Michigan, Mississippi, North Carolina, South Carolina, Texas, Virginia, Washington, and West Virginia. It was also reported from the Canadian provinces of New Brunswick and Ontario.

  • . Representative publications: Appy & Dadswell, 1981; Becker & Dauble, 1979; Choudhury et al., 2004; Font & Tate, 1994; Klemm, 1972; Klemm, 1982; Klemm, 1991; Miller & Olson, 1973; Sawyer, 1972; and Sawyer et al., 1975.

  • . Specimen deposited: AMNH, in submittal process.

Acknowledgments

The authors would like to thank the Michigan Department of Natural Resources for providing the samples from the various lakes and the funding to support this research, and the current and previous staff members of the Aquatic Animal Health Laboratory at Michigan State University for their help in this study.

References

  1. Amin O.M. Leeches (Hirudinea) from Wisconsin, and the description of the spermatophore of Placobdella ornate. Transactions of the American Microscopical Society, 1981, 100, 42–51. [CrossRef] [Google Scholar]
  2. Ahne W. Argulus foliaceus L. and Piscicola geometra L. as mechanical vectors of spring viremia of carp virus (SVCV). Journal of Fish Diseases, 1985, 8, 241–242. [CrossRef] [Google Scholar]
  3. Apakupakul K., Siddall M.E. & Burreson E.M. Higher level relationships of leeches (Annelida: Clitellata: Euhirudinea) based on morphology and gene sequences. Molecular Phylogenetic Evolution, 1999, 12, 350–359. [CrossRef] [PubMed] [Google Scholar]
  4. Appy R.G. & Cone D.K. Attachment of Myzobdella lugubris (Hirudinea: Piscicolidae) to logperch, Percina caprodes, and brown bullhead, Ictalurus nebulosis. Transactions of the American Microscopical Society, 1982, 101, 135–141. [CrossRef] [Google Scholar]
  5. Appy R.G. & Dadswell M.J. Marine and estuarine piscicolid leeches (Hirudinea) of the Bay of Fundy and adjacent waters with a key to species. Canadian Journal of Zoology, 1981, 59, 183–192. [CrossRef] [Google Scholar]
  6. Barta J.R. The Dactylosomatidae. Advanced Parasitology, 1991, 30, 1–37. [CrossRef] [Google Scholar]
  7. Becker C.D. & Dauble D.D. Records of piscivorus leeches (Hirudinea) from the central Columbia River, Washington state. Fishery Bulletin, 1979, 76, 4, 926–931. [Google Scholar]
  8. Bettoli P.W., Maceina M.J., Noble R.L. & Betsill R.K. Piscivory in largemouth bass as a function of aquatic vegetation abundance. North American Journal of Fisheries Management, 1992, 12, 509–516. [CrossRef] [Google Scholar]
  9. Choudhury A., Hoffnagle T.L. & Cole R.A. Parasites of native and nonnative fishes of the Little Colorado River, Grand Canyon, Arizona. Journal of Parasitology, 2004, 90,5, 1042–1053. [CrossRef] [Google Scholar]
  10. Cusack R. & Cone D.K. A review of parasites as vectors of viral and bacterial diseases of fish. Journal of Fish Diseases, 1986, 9, 169–171. [CrossRef] [Google Scholar]
  11. Daniels B.A. & Sawyer R.T. The biology of the leech Myzobdella lugubris infesting blue crabs and catfish. Biological Bulletin, 1975, 148, 193–198. [CrossRef] [Google Scholar]
  12. Dechtiar A.O. Parasites of fish from Lake of the Woods, Ontario. Journal of the Fishery Research Board of Canada, 1972, 29, 275–283. [CrossRef] [Google Scholar]
  13. Dombrowski H. Die Karpfenlause, Argulus foliaceus. Fischblatter, 1952, 2, 145–146. [Google Scholar]
  14. Faisal M. & Schulz C.A. Detection of Viral Hemorrhagic Septicemia virus (VHSV) from the leech Myzobdella lugubris Leidy, 1851. Parasites and Vectors, 2009, 2, 45–48. [CrossRef] [Google Scholar]
  15. Font W.F. & Tate D.C. Helminth parasites of native Hawaiian freshwater fishes: an example of extreme ecological isolation. Journal of Parasitology, 1994, 80, 5, 682–688. [CrossRef] [Google Scholar]
  16. Hemmingsen W., Jansen P.A. & Mackenzie K. Crabs, leeches, and trypanosomes: an unholy trinity? Marine Pollution Bulletin, 2005, 50, 336–339. [CrossRef] [PubMed] [Google Scholar]
  17. Hoffman G. Parasite of North American Freshwater Fishes. Comstock Publishing Associates, Ithaca, 1999, 539. [Google Scholar]
  18. Jones S.R. & Woo P.T. Vector specificity of Trypanosoma catostomi and its infectivity to freshwater fishes. Journal of Parasitology, 1992, 78, 87–92. [CrossRef] [Google Scholar]
  19. Khan R.A. & Meyer M.C. Taxonomy and biology of some Newfoundland marine leeches (Rhynchobdellae: Piscicolidae). Journal of the Fishery Research Board of Canada, 1976, 33, 1699–1714. [CrossRef] [Google Scholar]
  20. Kennedy C.R. The ecology of parasites of freshwater fishes: the search for patterns. Parasitology, 2009, 136, 12, 1653–1662. [CrossRef] [PubMed] [Google Scholar]
  21. Kikuchi Y. & Fukatsu T. Rickettsia infection in natural leech populations. Microbial Ecology, 2005, 49, 265–271. [CrossRef] [PubMed] [Google Scholar]
  22. Kikuchi Y., Sameshima S., Kitade O., Kojima J. & Fukatsu T. Novel clade of Rickettsia spp. from leeches. Applied Environmental Microbiology, 2002, 68, 999–1004. [CrossRef] [Google Scholar]
  23. Klemm D.J. The leeches (Annelida: Hirudinea) of Michigan. The Michigan Academician, 1972, 4, 4, 405–444. [Google Scholar]
  24. Klemm D.J. Leeches (Annelida: Hirudinea) of North America. U.S. Environmental Protection Agency, 1982, EPA-600/3-82-025. [Google Scholar]
  25. Klemm D.J. Taxonomy and pollution ecology of the Great Lakes region leeches (Annelida: Hirudinea). The Michigan Academician, 1991, 24, 37–103. [Google Scholar]
  26. Kruse P., Steinhagen D. & Korting W. Development of Trypanoplasma borreli (Mastigophora: Kinetoplastida) in the leech vector Piscicola geometra and its infectivity for the common carp, Cyprinus carpio. Journal of Parasitology, 1989, 75, 527–530. [CrossRef] [Google Scholar]
  27. Michel C. & Devillez E.J. Digestion, in: Physiology of Annelids. Mill P.J. (ed.), Academic Press, London, 1978, 509–554. [Google Scholar]
  28. Miller R.L. & Olson Jr., A.C. Fish parasites occurring in thirteen southern California reservoirs. California Fish and Game, 1973, 59, 3, 196–206. [Google Scholar]
  29. Morrison J.R. & Fox S.R. Control of an infestation of a fish leech (Myzobdella lugubris) on catfishes in tanks and earthen ponds. Journal of Aquatic Animal Health, 1993, 5, 110–114. [CrossRef] [Google Scholar]
  30. Muzzall P.M., Whelan G.E. & Peebles C.R. Parasites of burbot, Lota lota (family Gadidae), from the Ford River in the Upper Peninsula of Michigan. Canadian Journal of Zoology, 1987, 65, 2825–2827. [CrossRef] [Google Scholar]
  31. Noga E.J., Bullis R.A. & Miller G.C. Epidemic oral ulceration in largemouth bass (Micropterus salmoides) associated with the leech Myzobdella lugubris. Journal of Wildlife Diseases, 1990, 26, 132–134. [PubMed] [Google Scholar]
  32. Pritchard M.H. & Kruse G.O.W. The Collection and Preservation of Animal Parasites. University of Nebraska Press, Lincoln, Nebraska, 1982. [Google Scholar]
  33. Sawyer R.T. North American freshwater leeches, exclusive of the Piscicolidae: with a key to all species. Illinois Biological Monographs, 1972, 46, 1–154. [Google Scholar]
  34. Sawyer R.T., Lawler A.R. & Overstreet R.M. Marine leeches of the eastern United States and the Gulf of Mexico, with a key to the species. Natural History, 1975, 9, 633–667. [CrossRef] [Google Scholar]
  35. Schramm J.C., Hardman C.H. & Tarter D.C. The occurrence of Myzobdella lugubris and Piscicolaria reducta (Hirudinea: Piscicolidae) on fishes from West Virginia. Transactions of the American Microscopical Society, 1981, 100, 4, 427–428. [CrossRef] [Google Scholar]
  36. Schulz C.A. & Faisal M. The bacterial community associated with the leech Myzobdella lugubris Leidy (Annelida: Hirudinea) from Lake Erie, Michigan, USA. Parasite, 2010, 17, 2, 113–121. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]
  37. Schulz C.A., Thomas M.V., Fitzgerald S. & Faisal M. Leeches (Annelida: Hirudinida) parasitizing fish of Lake St. Clair, Michigan, USA. Comparative Parasitology, 2011, in press. [Google Scholar]
  38. State of Michigan. Smallmouth and Largemouth Bass Regulations Committee (SALBRC): black bass fishing seasons in Michigan: background, research review, and recommendations. By Mary Bremigan, Gary Towns, James Breck, Neal Godby, Scott Hanshue, Robert Moody, Thomas Rozich, and Michael Thomas. April 2004. http://www.michigandnr.com/PUBLICATIONS/PDFS/Fishing/BassRegulations.pdf. [Google Scholar]
  39. Zintl A., Voorheis H.P. & Holland C.V. Experimental infections of farmed eels with different Trypanosoma granulosum life-cycle stages and investigation of pleomorphism. Journal of Parasitology, 2000, 86, 56–59. [Google Scholar]

All Tables

Table I.

Prevalence of mouth ulcerations and attached Myzobdella lugubris in largemouth bass (Micropterus salmoides) sampled from eight inland lakes in Michigan.

All Figures

thumbnail Fig 1.

Largemouth bass (Micropterus salmoides) were collected from eight collection sites in the Lower Peninsula of Michigan between July 2002 and September 2003.

In the text
thumbnail Fig 2.

A specimen of Myzobdella lugubris compressed and stained with Mayer’s hematoxylin.

In the text
thumbnail Fig 3.

Myzobdella lugubris. (A) burrowing into the buccal mucosa of a largemouth bass (arrow) from Orion Lake; (B) ulcerations and leeches (arrows) in the roof of the mouth of a largemouth bass from Orion Lake; (C) severe ulceration associated with a leech infestation in the roof of the mouth of a largemouth bass from Devils Lake with suppurative inflammation and subsequent pus formation (arrow); and (D) M. lugubris (arrow) attached to the tongue of a largemouth bass from Devils Lake.

In the text

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