Murchison, E. P. Clonally transmissible cancers in dogs and Tasmanian devils. Oncogene 27, S19–S30 (2008).
Metzger, M. J. et al. Widespread transmission of independent cancer lineages within multiple bivalve species. Nature 534, 705–709 (2016).
Storfer, A. et al. The devil is in the details: Genomics of transmissible cancers in Tasmanian devils. PLoS Pathog. 14, 1–7 (2018).
Nowinsky, M. A. Zur Frage über die Impfung der krebsigen Geschwülste. Zentralbl Med Wissensch. 14, 790–791 (1876).
Murgia, C., Pritchard, J. K., Kim, S. Y., Fassati, A. & Weiss, R. A. Clonal origin and evolution of a transmissible cancer. Cell 126, 477–487 (2006).
Pearse, A. M. & Swift, K. Allograft theory: transmission of devil facial-tumour disease. Nature 439, 549 (2006).
Siddle, H. V. et al. Transmission of a fatal clonal tumor by biting occurs due to depleted MHC diversity in a threatened carnivorous marsupial. Proc. Natl. Acad. Sci. USA 104, 16221–16226 (2007).
Metzger, M. J. J., Reinisch, C., Sherry, J. & Goff, S. P. P. Horizontal transmission of clonal cancer cells causes leukemia in soft-shell clams. Cell 161, 255–263 (2015).
Riquet, F., Simon, A. & Bierne, N. Weird genotypes? Don’t discard them, transmissible cancer could be an explanation. Evol. Appl. 10, 140–145 (2017).
Yonemitsu, M. A. et al. A single clonal lineage of transmissible cancer identified in two marine mussel species in South America and Europe. Elife 8, 1–21 (2019).
Woods, G. M., Bruce Lyons, A. & Bettiol, S. S. A devil of a transmissible cancer. Trop. Med. Infect. Dis. 5, 1–10 (2020).
Ganguly, B., Das, U. & Das, A. K. Canine transmissible venereal tumour: a review. Vet. Comp. Oncol. 14, 1–12 (2016).
Paynter, A. N., Metzger, M. J., Sessa, J. A. & Siddall, M. E. Evidence of horizontal transmission of the cancer-associated Steamer retrotransposon among ecological cohort bivalve species. Dis. Aquat. Organ. https://doi.org/10.3354/dao03113 (2017).
Barber, B. J. Neoplastic diseases of commercially important marine bivalves. Aquat. Living Resour. 17, 449–466 (2004).
Farley, C. A. Sarcomatoid proliferative disease in a wild population of blue mussels (Mytilus edulis). J. Natl. Cancer Inst. 43, 509–516 (1969).
Sparks, A. K. Synopsis of Invertebrate Pathology Exclusive of Insects (Elsevier, 1985).
Muttray, A. F. & Vassilenko, K. Mollusca: disseminated neoplasia in bivalves and the p53 protein family. Adv. Comp. Immunol. https://doi.org/10.1007/978-3-319-76768-0 (1969).
Bihari, N., Mičić, M., Batel, R. & Zahn, R. K. Flow cytometric detection of DNA cell cycle alterations in hemocytes of mussels (Mytilus galloprovincialis) off the Adriatic coast Croatia. Aquat. Toxicol. 64, 121–129 (2003).
Vassilenko, E. & Baldwin, S. A. Using flow cytometry to detect haemic neoplasia in mussels (Mytilus trossulus) from the Pacific Coast of Southern British Columbia Canada. J. Invertebr. Pathol. 117, 68–72 (2014).
Moore, J. D., Elston, R. A., Drum, A. S. & Wilkinson, M. T. Alternate pathogenesis of systemic neoplasia in the bivalve mollusc Mytilus. J. Invertebr. Pathol. 58, 231–243 (1991).
Benabdelmouna, A., Saunier, A., Ledu, C., Travers, M. A. & Morga, B. Genomic abnormalities affecting mussels (Mytilus edulis-galloprovincialis) in France are related to ongoing neoplastic processes, evidenced by dual flow cytometry and cell monolayer analyses. J. Invertebr. Pathol. 157, 45–52 (2018).
Burioli, E. A. V. et al. Implementation of various approaches to study the prevalence, incidence and progression of disseminated neoplasia in mussel stocks. J. Invertebr. Pathol. 168, 107271 (2019).
Moore, C. A., Beckmann, N. & Patricia Morse, M. Cytoskeletal structure of diseased and normal hemocytes of Mya arenaria. J. Invertebr. Pathol. 60, 141–147 (1992).
Carballal, M. J., Barber, B. J., Iglesias, D. & Villalba, A. Neoplastic diseases of marine bivalves. J. Invertebr. Pathol. https://doi.org/10.1016/j.jip.2015.06.004 (2015).
Odintsova, N. A. Leukemia-like cancer in bivalves. Russ. J. Mar. Biol. 46, 59–67 (2020).
Smolarz, K., Renault, T. & Wołowicz, M. Ultrastructural study of neoplastic cells in Macoma balthica (Bivalvia) from the Gulf of Gdansk (Poland). J. Invertebr. Pathol. 92, 79–84 (2006).
Carella, F. et al. Nuclear morphometry and ploidy of normal and neoplastic haemocytes in mussels. PLoS ONE 12, e0173219 (2017).
Smolowitz, R. M. & Reinisch, C. L. Indirect peroxidase staining using monoclonal antibodies specific for Mya arenaria neoplastic cells. J. Invertebr. Pathol. 48, 139–145 (1986).
Carella, F., Figueras, A., Novoa, B. & De Vico, G. Cytomorphology and PCNA expression pattern in bivalves Mytilus galloprovincialis and Cerastoderma edule with haemic neoplasia. Dis. Aquat. Organ. 105, 81–87 (2013).
McDonald, J. H., Seed, R. & Koehn, R. K. Allozymes and morphometric characters of three species of Mytilus in the Northern and Southern Hemispheres. Mar. Biol. 111, 323–333 (1991).
Larraín, M. A., Zbawicka, M., Araneda, C., Gardner, J. P. A. & Wenne, R. Native and invasive taxa on the Pacific coast of South America: impacts on aquaculture, traceability and biodiversity of blue mussels (Mytilus spp.). Evol. Appl. 11, 298–311 (2018).
Pye, R. J. et al. A second transmissible cancer in Tasmanian devils. Proc. Natl. Acad. Sci. USA 113, 374–379 (2016).
Strakova, A. et al. Mitochondrial genetic diversity, selection and recombination in a canine transmissible cancer. Elife 5, 1–25 (2016).
Rawson, P. D. & Harper, F. M. Colonization of the northwest Atlantic by the blue mussel, Mytilus trossulus postdates the last glacial maximum. Mar. Biol. 156, 1857–1868 (2009).
Wenne, R., Bach, L., Zbawicka, M., Strand, J. & McDonald, J. H. A first report on coexistence and hybridization of Mytilus trossulus and M. edulis mussels in Greenland. Polar Biol. 39, 343–355 (2016).
Laakkonen, H. M., Hardman, M., Strelkov, P. & Väinölä, R. Cycles of trans-Arctic dispersal and vicariance, and diversification of the amphi-boreal marine fauna. J. Evol. Biol. https://doi.org/10.1111/jeb.13674 (2020).
Zbawicka, M., Wenne, R. & Burzyński, A. Mitogenomics of recombinant mitochondrial genomes of Baltic Sea Mytilus mussels. Mol. Genet. Genom. 289, 1275–1287 (2014).
Śmietanka, B. & Burzyński, A. Disruption of doubly uniparental inheritance of mitochondrial DNA associated with hybridization area of European Mytilus edulis and Mytilus trossulus in Norway. Mar. Biol. https://doi.org/10.1007/s00227-017-3235-5 (2017).
Sunila, I. Histopathology of mussels (Mytilus edulis L.) from the Tvarminne area, the Gulf of Finland (Baltic Sea). Ann. Zool. Fennici 24, 55–69 (1987).
Usheva, L. N. & Frolova, L. T. Neoplasia in the connective tissue tumor in the mussel Mytilus trossulus from a polluted region of Nakhodka Bay, the Sea of Japan. Ontogenez 31, 63–70 (2000).
Maiorova, M. A. & Odintsova, N. A. β integrin-like protein-mediated adhesion and its disturbances during cell cultivation of the mussel Mytilus trossulus. Cell Tissue Res. 361, 581–592 (2015).
Marigomez, I., Lekube, X. & Cancio, I. Immunochemical localisation of proliferating cells in mussel digestive gland tissue. Histochem. J. 31, 781–788 (1999).
Maiorova, M. A. & Odintsova, N. A. Proliferative potential of larval cells of the mussel Mytilus trossulus and their capacity to differentiate into myogenic cells in culture. Russ. J. Mar. Biol. 42, 281–285 (2016).
Voronezhskaya, E. E., Nezlin, L. P., Odintsova, N. A., Plummer, J. T. & Croll, R. P. Neuronal development in larval mussel Mytilus trossulus (Mollusca: Bivalvia). Zoomorphology 127, 97–110 (2008).
Presa, P., Pérez, M., Diz, A. P., Perez, M. & Diz, A. P. Polymorphic microsatellite markers for blue mussels (Mytilus spp.). Conserv. Genet. 3, 441–443 (2002).
Zouros, E. Biparental inheritance through uniparental transmission: the doubly uniparental inheritance (DUI) of mitochondrial DNA. Evol. Biol. 40, 1–31 (2013).
Kumar, S., Stecher, G., Li, M., Knyaz, C. & Tamura, K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol. Biol. Evol. 35, 1547–1549 (2018).
Paabo, S., Irwin, M. & Wilson, C. DNA damage promotes jumping between templates during enzymatic amplification. J. Biol. Chem. 265, 4718–4721 (1990).
Bradley, R. D. & Hillis, D. A. Recombinant DNA sequences generated by PCR amplification. Mol. Biol. Evol. 14, 592–593 (1997).
Letunic, I. & Bork, P. Interactive Tree of Life (iTOL) v4: recent updates and new developments. Nucl. Acids Res. 47, 256–259 (2019).
Martin, D. P., Murrell, B., Golden, M., Khoosal, A. & Muhire, B. RDP4: detection and analysis of recombination patterns in virus genomes. Virus Evol. 1, 1–5 (2015).
Breton, S., Burger, G., Stewart, D. T. & Blier, P. U. Comparative analysis of gender-associated complete mitochondrial genomes in marine mussels (Mytilus spp.). Genetics 172, 1107–1119 (2006).
Marko, P. B. et al. The ‘Expansion-contraction’ model of Pleistocene biogeography: rocky shores suffer a sea change?. Mol. Ecol. 19, 146–169 (2010).
Crego-Prieto, V., Juanes, F. & Garcia-Vazquez, E. Aquaculture and the spread of introduced mussel genes in British Columbia. Biol. Invasions https://doi.org/10.1007/s10530-015-0853-z (2015).
Chung, J. M. et al. Molecular phylogenetic study of bivalvia from four countries (China, Japan, Russia and Myanmar) using 3 types of primers. Korean J. Malacol. 35, 137–148 (2019).
Layton, K. K. S., Martel, A. L., Hebert, P. D. N. & Layton, K. K. S. Patterns of DNA barcode variation in Canadian Marine molluscs. PLoS ONE 9, 1–9 (2014).
deWaard, J. R. et al. A reference library for Canadian invertebrates with 1.5 million barcodes, voucher specimens, and DNA samples. Sci. Data 6, 1–12 (2019).
Clement, M., Snell, Q., Walker, P., Posada, D. & Crandall, K. TCS: Estimating Gene Genealogies. Parallel Distrib. Process. Symp. Int. 2, 184 (2002).
Leigh, J. W. & Bryant, D. POPART: full-feature software for haplotype network construction. Methods Ecol. Evol. 6, 1110–1116 (2015).
Kartavtsev, Y. P., Masalkova, N. A. & Katolikova, M. V. Genetic and morphometric variability in settlements of two mussel species (Mytilus ex. Gr. Edulis), Mytilus trossulus and Mytilus galloprovincialis, in the Northwestern Sea of Japan. J. Shellfish Res. 37, 103–119 (2018).
Larraín, M. A., González, P., Pérez, C. & Araneda, C. Comparison between single and multi-locus approaches for specimen identification in Mytilus mussels. Sci. Rep. 9, 1–13 (2019).
Inoue, K., Waite, J. H., Matsuoka, M., Odo, S. & Harayama, S. Interspecific variations in adhesive protein sequences of Mytilus edulis, M. galloprovincialis, and M. trossulus. Biol. Bull. 189, 370–375 (1995).
Heath, D. D., Rawson, P. D. & Hilbish, T. J. PCR-based nuclear markers identify alien blue mussel Mytilus spp. genotypes on the west coast of Canada. Can. J. Fish. Aquat. Sci. 52, 2621–2627 (1995).
Rawson, P. D., Secor, C. L. & Hilbish, T. J. The effects of natural hybridization on the regulation of doubly uniparental mtDNA inheritance in blue mussels (Mytilus spp.). Genetics 144, 241–248 (1996).
Rawson, P. D. & Hilbish, T. J. Distribution of male and female mtDNA lineages in populations of blue mussels, Mytilus trossulus and M. galloprovincialis, along the Pacific coast of North America. Mar. Biol. 124, 245–250 (1995).
Cremonte, F., Vázquez, N. & Silva, M. R. Gonad atrophy caused by disseminated neoplasia in Mytilus chilensis cultured in the Beagle channel, Tierra Del Fuego Province Argentina. J. Shellfish Res. 30, 845–849 (2011).
Ciocan, C. & Sunila, I. Disseminated neoplasia in blue mussels, Mytilus galloprovincialis, from the Black Sea Romania. Mar. Pollut. Bull. 50, 1335–1339 (2005).
Gombač, M., Sitar, R., Pogačnik, M., Arzul, I. & Jenčič, V. Haemocytic neoplasia in Mediterranean mussels (Mytilus galloprovincialis). Mar. Freshw. Behav. Physiol. 46, 135–143 (2013).
Villalba, A., Mourelle, S. G., Carballal, M. J. & López, C. Symbionts and diseases of farmed mussels Mytilus galloprovincialis throughout the culture process in the Rias of Galicia (NW Spain). Dis. Aquat. Organ. 31, 127–139 (1997).
Cremonte, F., Puebla, C., Tillería, J. & Videla, V. Estudio histopatológico del chorito Mytilus chilensis (Mytilidae) y del culengue Gari solida (Psammobiidae) en el sur de Chile. Lat. Am. J. Aquat. Res. 43, 248–254 (2015).
Vassilenko, E. I., Muttray, A. F., Schulte, P. M. & Baldwin, S. A. Variations in p53-like cDNA sequence are correlated with mussel haemic neoplasia: a potential molecular-level tool for biomonitoring. Mutat. Res. Genet. Toxicol. Environ. Mutagen. https://doi.org/10.1016/j.mrgentox.2010.06.001 (2010).
Caza, F., Bernet, E., Veyrier, F. J., Betoulle, S. & St-Pierre, Y. Hemocytes released in seawater act as Trojan horses for spreading of bacterial infections in mussels. Sci. Rep. 10, 1–12 (2020).
Rebbeck, C. A., Leroi, A. M. & Burt, A. Mitochondrial capture by a transmissible cancer. Science (80-) 331, 303 (2011).
Rawson, P. D. & Hilbish, T. J. Asymmetric introgression of mitochondrial DNA among European populations of Blue Mussels (Mytilus spp.). Evolution (N. Y.) 52, 100–108 (1998).
Kijewski, A., Zbawicka, M., Väinölä, R. & Wenne, T. K. Introgression and mitochondrial DNA heteroplasmy in the Baltic populations of mussels Mytilus trossulus and M. edulis. Mar. Biol. https://doi.org/10.1007/s00227-006-0316-2 (2006).
Burzyński, A., Zbawicka, M., Skibinski, D. O. F. & Wenne, R. Evidence for recombination of mtDNA in the marine mussel Mytilus trossulus from the Baltic. Mol. Biol. Evol. 20, 388–392 (2003).
Burzynski, A., Zbawicka, M., Skibinski, D. O. F. & Wenne, R. Doubly uniparental inheritance is associated with high polymorphism for rearranged and recombinant control region haplotypes in Baltic Mytilus trossulus. Genetics 174, 1081–1094 (2006).
Stuckas, H., Stoof, K., Quesada, H. & Tiedemann, R. Evolutionary implications of discordant clines across the Baltic Mytilus hybrid zone (Mytilus edulis and Mytilus trossulus). Heredity (Edinb). 103, 146–156 (2009).
Cao, L., Kenchington, E. & Zouros, E. Differential segregation patterns of sperm mitochondria in embryos of the Blue Mussel (Mytilus edulis). Genetics https://doi.org/10.1534/genetics.166.2.883 (2004).
Source: Ecology - nature.com
