Vaughn, C. C. Ecosystem services provided by freshwater mussels. Hydrobiologia 810, 15–27. https://doi.org/10.1007/s10750-017-3139-x (2018).
Christian, A. D., Smith, B. N., Berg, D. J., Smoot, J. C. & Findlay, R. H. Trophic position and potential food sources of 2 species of unionid bivalves (Mollusca:Unionidae) in 2 small Ohio streams. Freshw. Sci. 23, 101–113 (2004).
Vaughn, C. C. Biodiversity losses and ecosystem function in freshwaters: emerging conclusions and research directions. Bioscience 60, 25–35. https://doi.org/10.1525/bio.2010.60.1.7 (2010).
Howard, J. K. & Cuffey, K. M. The functional role of native freshwater mussels in the fluvial benthic environment. Freshw. Biol. 51, 460–474. https://doi.org/10.1111/j.1365-2427.2005.01507.x (2006).
Izumi, T., Yagita, K., Izumiyama, S., Endo, T. & Itoh, Y. Depletion of Cryptosporidium parvum oocysts from contaminated sewage by using freshwater benthic pearl clams (Hyriopsis schlegeli). Appl. Environ. Microbiol. 78, 7420–7428. https://doi.org/10.1128/AEM.01502-12 (2012).
Ismail, N. S., Müller, C. E., Morgan, R. R. & Luthy, R. G. Uptake of contaminants of emerging concern by the bivalves Anodonta californiensis and Corbicula fluminea. Environ. Sci. Technol. 48, 9211–9219. https://doi.org/10.1021/es5011576 (2014).
Ismail, N. S. et al. Improvement of urban lake water quality by removal of Escherichia coli through the action of the bivalve Anodonta californiensis. Environ. Sci. Technol. 49, 1664–1672. https://doi.org/10.1021/es5033212 (2015).
Williams, J. D. et al. A revised list of the freshwater mussels (Mollusca: Bivalvia: Unionida) of the United States and Canada. Freshw. Mollusk Biol. Conserv. 20, 33. https://doi.org/10.31931/fmbc.v20i2.2017.33-58 (2017).
Lydeard, C. et al. The global decline of nonmarine mollusks. Bioscience 54, 321. https://doi.org/10.1641/0006-3568(2004)054[0321:TGDONM]2.0.CO;2 (2004).
Haag, W. R. North American Freshwater Mussels: Natural History, Ecology, and Conservation (Cambridge University Press, Cambridge, 2012).
Strayer, D. L. Effects of alien species on freshwater mollusks in North America. J. N. Am. Benthol. Soc. 18, 74–98. https://doi.org/10.2307/1468010 (1999).
Haag, W. R. Reassessing enigmatic mussel declines in the United States. Freshw. Mollusk Biol. Conserv. 22, 43–60 (2019).
Goldberg, T. L., Dunn, C. D., Leis, E. & Waller, D. L. A novel picornalike virus in a Wabash Pigtoe (Fusconaia flava) from the Upper Mississippi River, USA. Freshw. Mollusk Biol. Conserv. 22, 81–84 (2019).
Downing, J. A., Van Meter, P. & Woolnough, D. A. Suspects and evidence: a review of the causes of extirpation and decline in freshwater mussels. Anim. Biodivers. Conserv. 33, 151–185 (2010).
Zipper, C. E. et al. Freshwater mussel population status and habitat quality in the Clinch Rver, Virginia and Tennessee, USA: a featured collection. J. Am. Water Resour. Assoc. 50, 807–819 (2014).
Jones, J. et al. Clinch River freshwater mussels upstream of Norris Reservoir, Tennessee and Virginia: a quantitative assessment from 2004 to 2009. J. Am. Water Resour. Assoc. 50, 820–836. https://doi.org/10.1111/jawr.12222 (2014).
Jones, J. W. et al. Collapse of the Pendleton Island mussel fauna in the Clinch River, Virginia: setting baseline conditions to guide recovery and restoration. Freshw. Mollusk Biol. Conserv. 21, 36–56 (2018).
Cope, W. G. & Jones, J. W. Recent precipitous declines of endangered freshwater mussels in the Clinch River: an in situ assessment of water quality stressors related to energy development and other land-use. 244 (U.S. Fish and Wildlife Service, Southwestern Virginia Field Office, 2016).
Richard, J. C. Clinch River mussel die-off. Ellipsaria 20, 1–3 (2018).
Neves, R. J. Proceedings of the Workshop on Die-offs of Freshwater Mussels in the United States (U.S. Fish and Wildlife Service, Upper Mississippi River Conservation Committee, 1986).
Starliper, C. E., Powell, J., Garner, J. T. & Schill, W. B. Predominant bacteria isolated from moribund Fusconaia ebena ebonyshells experiencing die-offs in Pickwick Reservoir, Tennessee River, Alabama. J. Shellfish Res. 30, 359–366. https://doi.org/10.2983/035.030.0223 (2011).
Grizzle, J. M. & Brunner, C. J. Infectious diseases of freshwater mussels and other freshwater bivalve mollusks. Rev. Fish. Sci. 17, 425–467 (2009).
Leis, E. et al. Building a response network to investigate potential pathogens associated with unionid mortality events. Ellipsaria 20, 44–45 (2018).
Henley, W. F., Beaty, B. B. & Jones, J. W. Evaluations of organ tissues from Actinonaias pectorosa collected during a mussel die-off in 2016 at Kyles Ford, Clinch River, Tennessee. J. Shellfish Res. 38, 681. https://doi.org/10.2983/035.038.0320 (2019).
Leis, E., Erickson, S., Waller, D., Richard, J. & Goldberg, T. A comparison of bacteria cultured from unionid mussel hemolymph between stable populations in the Upper Mississippi River basin and populations affected by a mortality event in the Clinch River. Freshw. Mollusk Biol. Conserv. 22, 70–80 (2019).
Garcia, C. et al. Ostreid herpesvirus 1 detection and relationship with Crassostrea gigas spat mortality in France between 1998 and 2006. Vet. Res. 42, 73. https://doi.org/10.1186/1297-9716-42-73 (2011).
Arzul, I., Corbeil, S., Morga, B. & Renault, T. Viruses infecting marine molluscs. J. Invertebr. Pathol. 147, 118–135. https://doi.org/10.1016/j.jip.2017.01.009 (2017).
Zhang, Z., Sufang, D., Yimin, X. & Jie, W. Studies on the mussel Hyriopsis cumingii plague. I. a new viral infectious disease. Acta Hydrobiol. Sin. 26, 308–312 (1986).
Zhong, L., Xiao, T.-Y., Huang, J., Dai, L.-Y. & Liu, X.-Y. Histopathological examination of bivalve mussel Hyriopsis cumingii lea artificially infected by virus. Acta Hydrobiol. Sin. 35, 666–671 (2011).
Shi, M. et al. Redefining the invertebrate RNA virosphere. Nature 540, 539–543. https://doi.org/10.1038/nature20167 (2016).
Zhang, Y. Z., Shi, M. & Holmes, E. C. Using metagenomics to characterize an expanding vrosphere. Cell 172, 1168–1172. https://doi.org/10.1016/j.cell.2018.02.043 (2018).
Bergoin, M. & Tijssen, P. Molecular biology of Densovirinae. Contrib. Microbiol. 4, 12–32. https://doi.org/10.1159/000060329 (2000).
Mietzsch, M., Penzes, J. J. & Agbandje-McKenna, M. Twenty-five years of structural parvovirology. Viruses https://doi.org/10.3390/v11040362 (2019).
Cotmore, S. F. et al. ICTV virus taxonomy profile: Parvoviridae. J. Gen. Virol. 100, 367–368. https://doi.org/10.1099/jgv.0.001212 (2019).
Ganesh, B., Masachessi, G. & Mladenova, Z. Animal picobirnavirus. Virus Dis. 25, 223–238. https://doi.org/10.1007/s13337-014-0207-y (2014).
Gustafson, L. L. et al. Evaluation of a nonlethal technique for hemolymph collection in Elliptio complanata, a freshwater bivalve (Mollusca: Unionidae). Dis. Aquat. Organ. 65, 159–165. https://doi.org/10.3354/dao065159 (2005).
Lees, D. Viruses and bivalve shellfish. Int. J. Food Microbiol. 59, 81–116. https://doi.org/10.1016/S0168-1605(00)00248-8 (2000).
Faust, C., Stallknecht, D., Swayne, D. & Brown, J. Filter-feeding bivalves can remove avian influenza viruses from water and reduce infectivity. Proc. R. Soc. B 276, 3727–3735. https://doi.org/10.1098/rspb.2009.0572 (2009).
Fédière, G. in Parvoviruses. From Molecular Biology to Pathology and Therapeutic Uses. Contributions to Microbiology. Vol. 4 (eds S. Faisst & J. Rommelaere) 1–11 (Karger, 2000).
Kalagayan, H. et al. IHHN virus as an etiological factor in runt-deformity syndrome (RDS) of juvenile Penaeus vannamei cultured in Hawaii. J. World Aquacult. Soc. 22, 235–243. https://doi.org/10.1111/j.1749-7345.1991.tb00740.x (1991).
Ito, K., Kidokoro, K., Shimura, S., Katsuma, S. & Kadono-Okuda, K. Detailed investigation of the sequential pathological changes in silkworm larvae infected with Bombyx densovirus type 1. J. Invertebr. Pathol. 112, 213–218. https://doi.org/10.1016/j.jip.2012.12.005 (2013).
Jiang, H. et al. Genetic engineering of Periplaneta fuliginosa densovirus as an improved biopesticide. Arch. Virol. 152, 383–394. https://doi.org/10.1007/s00705-006-0844-6 (2007).
Ledermann, J. P., Suchman, E. L., Black, W. C. & Carlson, J. O. Infection and pathogenicity of the mosquito densoviruses AeDNV, HeDNV, and APeDNV in Aedes aegypti mosquitoes (Diptera: Culicidae). J. Econ. Entomol. 97, 1828–1835. https://doi.org/10.1093/jee/97.6.1828 (2004).
Szelei, J. et al. Susceptibility of North-American and European crickets to Acheta domesticus densovirus (AdDNV) and associated epizootics. J. Invertebr. Pathol. 106, 394–399. https://doi.org/10.1016/j.jip.2010.12.009 (2011).
Kouassi, N. et al. Pathogenicity of diatraea saccharalis densovirus to host insets and characterization of its viral genome. Virol. Sin. 22, 53–60. https://doi.org/10.1007/s12250-007-0062-8 (2007).
Bowater, R. et al. A parvo-like virus in cultured redclaw crayfish Cherax quadricarinatus from Queensland, Australia. Dis. Aquat. Organ. 50, 79–86. https://doi.org/10.3354/dao050079 (2002).
Johnson, R. M. & Rasgon, J. L. Densonucleosis viruses (‘densoviruses’) for mosquito and pathogen control. Curr. Opin. Insect. Sci. 28, 90–97. https://doi.org/10.1016/j.cois.2018.05.009 (2018).
Hewson, I. et al. Densovirus associated with sea-star wasting disease and mass mortality. Proc. Natl. Acad. Sci. USA 111, 17278–17283. https://doi.org/10.1073/pnas.1416625111 (2014).
Fritts, A. K., Peterson, J. T., Hazelton, P. D. & Bringolf, R. B. Evaluation of methods for assessing physiological biomarkers of stress in freshwater mussels. Can. J. Fish. Aquat. Sci. 72, 1450–1459. https://doi.org/10.1139/cjfas-2014-0564 (2015).
Cunningham, A. A., Daszak, P. & Wood, J. L. N. One health, emerging infectious diseases and wildlife: two decades of progress?. Philos. Trans. R. Soc. Lond. B https://doi.org/10.1098/rstb.2016.0167 (2017).
Patterson, M. A. et al. Freshwater Mussel Propagation for Restoration (Cambridge University Press, Cambridge, 2018).
Toohey-Kurth, K., Sibley, S. D. & Goldberg, T. L. Metagenomic assessment of adventitious viruses in commercial bovine sera. Biologicals 47, 64–68. https://doi.org/10.1016/j.biologicals.2016.10.009 (2017).
Löytynoja, A. Phylogeny-aware alignment with PRANK. Methods Mol. Biol. 1079, 155–170. https://doi.org/10.1007/978-1-62703-646-7_10 (2014).
Talavera, G. & Castresana, J. Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst. Biol. 56, 564–577. https://doi.org/10.1080/10635150701472164 (2007).
Abascal, F., Zardoya, R. & Telford, M. TranslatorX: multiple alignment of nucleotide sequences guided by amino acid translations. Nucleic Acids Res. 38, W7-13. https://doi.org/10.1093/nar/gkq291 (2010).
Guindon, S. et al. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst. Biol. 59, 307–321. https://doi.org/10.1093/sysbio/syq010 (2010).
R Core Team. R: A language and environment for statistical computing, version 3.6.3. https://www.R-project.org (R Foundation for Statistical Computing, Vienna, 2019).
Source: Ecology - nature.com
