Three genes involved in the oxidative burst are closely linked in the genome of the snail, Biomphalaria glabrata

International Journal for Parasitology

Volumn 43, Issue 1, 2013, Pages 51-55

  Blouin, Michael S ^a   Bonner, Kaitlin M ^a   Cooper, Becky ^b   Amarasinghe, Vindhya ^a   O'Donnell, Ryan P ^b   Bayne, Christopher J ^a  

^a OREGON STATE UNIVERSITY   (United States)

^b NONE   (United States)

Author keywords

Catalase; Genetics; Peroxiredoxin; Schistosoma mansoni; Snail; Superoxide dismutase

Indexed keywords

CATALASE; COPPER ZINC SUPEROXIDE DISMUTASE; HYDROGEN PEROXIDE; PEROXIREDOXIN 4;

ALLELE; COPPER; ENDOPARASITE; GENOME; HYDROGEN PEROXIDE; OXIDATION; PATHOGEN; REDUCTION; SNAIL; ZINC;

ARTICLE; BIOMPHALARIA; CAT GENE; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE ORDER; GENE OVEREXPRESSION; GENETIC EPISTASIS; GENETIC VARIABILITY; INFECTION RESISTANCE; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATION REDUCTION REACTION; OXIDATIVE STRESS; PRX4 GENE; RESPIRATORY BURST; SCHISTOSOMA MANSONI; SOD1 GENE;

BIOMPHALARIA GLABRATA; GASTROPODA; SCHISTOSOMA MANSONI; TREMATODA;

EID: 84872379900     PISSN: 00207519     EISSN: 18790135     Source Type: Journal    
DOI: 10.1016/j.ijpara.2012.10.020     Document Type: Article

References (38)

1. Abreu I.A., Cabelli D.E. Superoxide dismutases - a review of the metal-associated mechanistic variations. BBA Proteins Proteom. 2010, 1804:263-274.
2. Backström N., Forstmeier W., Schielzeth H., Mellenius H., Nam K., Bolund E., Webster M.T., öst T., Schneider M., Kempenaers B., Ellegren H. The recombination landscape of the zebra finch Taeniopygia guttata genome. Genome Res. 2010, 20:485-495.
3. Bayne C.J. Successful parasitism of vector snail Biomphalaria glabrata by the human blood fluke (trematode) Schistosoma mansoni: a 2009 assessment. Mol. Biochem. Parasitol. 2009, 165:8-18.
4. Beckman K.B., Ames B.N. The free radical theory of aging matures. Physiol. Rev. 1998, 78:547-581.
5. 2 than susceptible snails. J. Parasitol. 2005, 91:275-279.
6. Bender R.C., Goodall C.P., Blouin M.S., Bayne C.J. Variation in expression of Biomphalaria glabrata SOD1: a potential controlling factor in susceptibility/resistance to Schistosoma mansoni. Dev. Comp. Immunol. 2007, 31:874-878.
7. Bonner K.M., Bayne C.J., Larson M.K., Blouin M.S. Effects of Cu/Zn superoxide dismutase (sod1) genotype and genetic background on growth, reproduction and defense in Biomphalaria glabrata. PLoS Negl. Trop. Dis. 2012, 6:e1701.
8. Dobzhansky T. Genetics of the Evolutionary Process 1970, Columbia University Press, Columbia, NY.
9. Dowling D.K., Simmons L.W. Reactive oxygen species as universal constraints in life-history evolution. Proc. Biol. Sci. 2009, 276:1737-1745.
10. Fink R.C., Scandalios J.G. Molecular evolution and structure-function relationships of the superoxide dismutase gene families in angiosperms and their relationship to other eukaryotic and prokaryotic superoxide dismutases. Arch. Biochem. Biophys. 2002, 399:19-36.
11. Fiston-Lavier A.S., Singh N.D., Lipatov M., Petrov D.A. Drosophila melanogaster recombination rate calculator. Gene 2010, 463:18-20.
12. Ford E.B. Ecological Genetics 1975, Chapman and Hall, London. fourth ed.
13. Goodall C.P., Bender R.C., Broderick E.J., Bayne C.J. Constitutive differences in Cu/Zn superoxide dismutase mRNA levels and activity in hernocytes of Biomphalaria glabrata (Mollusca) that are either susceptible or resistant to Schistosoma mansoni (Trematoda). Mol. Biochem. Parasitol. 2004, 137:321-328.
14. Goodall C.P., Bender R.C., Brooks J.K., Bayne C.J. Biomphalaria glabrata cytosolic copper/zinc superoxide dismutase (SOD1) gene: association of SOD1 alleles with resistance/susceptibility to Schistosoma mansoni. Mol. Biochem. Parasitol. 2006, 147:207-210.
15. Green T.J., Dixon T.J., Devic E., Adlard R.D., Barnes A.C. Differential expression of genes encoding anti-oxidant enzymes in Sydney rock oysters, Saccostrea glomerata (Gould) selected for disease resistance. Fish Shellfish Immunol. 2009, 26:799-810.
16. Hahn U.K., Bender R.C., Bayne C.J. Killing of Schistosoma mansoni sporocysts by hemocytes from resistant Biomphalaria glabrata: role of reactive oxygen species. J. Parasitol. 2001, 87:292-299.
17. Hillier L.W., Miller R.D., Baird S.E., Chinwalla A., Fulton L.A., Koboldt D.C., Waterston R.H. Comparison of C. elegans and C. briggsae genome sequences reveals extensive conservation of chromosome organization and synteny. PLoS Biol. 2007, 5:e167.
18. Hohenlohe P.A., Bassham S., Currey M., Cresko W.A. Extensive linkage disequilibrium and parallel adaptive divergence across threespine stickleback genomes. Philos. Trans. R. Soc. Lond. B Biol. Sci. 2012, 367:395-408.
19. Jones C.S., Lockyer A.E., Rollinson D., Piertney S.B., Noble L.R. Isolation and characterization of microsatellite loci in the freshwater gastropod, Biomphalaria glabrata, an intermediate host for Schistosoma mansoni. Mol. Ecol. 1999, 8:2149-2151.
20. Knight M., Raghavan N., Goodall C., Cousin C., Ittiprasert W., Sayed A., Miller A., Williams D.L., Bayne C.J. Biomphalaria glabrata peroxiredoxin: effect of Schistosoma mansoni infection on differential gene regulation. Mol. Biochem. Parasitol. 2009, 167:20-31.
21. Loker E.S. Gastropod immunobiology. Adv. Exp. Med. Biol. 2010, 708:17-43.
22. Mavarez J., Amarista M., Pointier J.P., Jarne P. Microsatellite variation in the freshwater schistosome-transmitting snail Biomphalaria glabrata. Mol. Ecol. 2000, 9:1009-1011.
23. Monaghan P., Metcalfe N.B., Torres R. Oxidative stress as a mediator of life history trade-offs: mechanisms, measurements and interpretation. Ecol. Lett. 2009, 12:75-92.
24. Mone Y., Ribou A.C., Cosseau C., Duval D., Theron A., Mitta G., Gourbal B. An example of molecular co-evolution: reactive oxygen species (ROS) and ROS scavenger levels in Schistosoma mansoni/Biomphalaria glabrata interactions. Int. J. Parasitol. 2011, 41:721-730.
25. Mourao Mde M., Dinguirard N., Franco G.R., Yoshino T.P. Role of the endogenous antioxidant system in the protection of Schistosoma mansoni primary sporocysts against exogenous oxidative stress. PLoS Negl. Trop. Dis. 2009, 3:e550.
26. Nappi A.J., Ottaviani E. Cytotoxicity and cytotoxic molecules in invertebrates. BioEssays 2000, 22:469-480.
27. Phillips P.C. Epistasis - the essential role of gene interactions in the structure and evolution of genetic systems. Nat. Rev. Genet. 2008, 9:855-867.
28. Ramasarma T. Many faces of superoxide dismutase, originally known as erythrocuprein. Curr. Sci. 2007, 92:184-191.
29. Richards C.S., Shade P.C. The genetic variation of compatibility in Biomphalaria glabrata and Schistosoma mansoni. J. Parasitol. 1987, 73:1146-1151.
30. Riehle M.M., Markianos K., Niaré O., Xu J., Li J., Touré A.M., Podiougou B., Oduol F., Diawara S., Diallo M., Coulibaly B., Ouatara A., Kruglyak L., Traoré S.F., Vernick K.D. Natural malaria infection in Anopheles gambiae is regulated by a single genomic control region. Science 2006, 312:577-579.
31. Shoukry N., El-Assal F.M., Soliman G.N., Mansour N.S. Susceptibility of three successive snail generations from positive and negative laboratory bred Biomphalaria alexandrina from different localities in Egypt to infection with Schistosoma mansoni from Giza. J. Egypt. Soc. Parasitol. 1997, 27:317-329.
32. Sinervo B., Svensson E. Correlational selection and the evolution of genomic architecture. Heredity 2002, 89:329-338.
33. Stevison L., Noor M. Genetic and evolutionary correlates of fine-scale recombination rate variation in Drosophila persimilis. J. Mol. Evol. 2010, 71:332-345.
34. Theron A., Coustau C., Rognon A., Gourbiere S., Blouin M.S. Effects of laboratory culture on compatibility between snails and schistosomes. Parasitology 2008, 135:1179-1188.
35. Vianey-Liaud M., Dussart G. Aspects of pairing and reproduction in the hermaphrodite freshwater snail Biomphalaria glabrata (Gastropoda: Pulmonata). J. Mollus. Stud. 2002, 68:243-248.
36. Webster J.P., Gower C.M., Blair L. Do hosts and parasites coevolve? Empirical support from the Schistosoma system. Am. Nat. 2004, 164(Suppl. 5):S33-S51.
37. Webster J.P., Woolhouse M.E.J. Selection and strain specificity of compatibility between snail intermediate hosts and their parasitic schistosomes. Evolution 1998, 52:1627-1634.
38. Weir B.S. Inferences about linkage disequilibrium. Biometrics 1979, 35:235-254.