EDP Sciences logo
Search
Menu
All issues Volume 40 / No 6 (November-December 2009) Vet. Res., 40 6 (2009) 56 References
Free Access
Issue
Vet. Res.
Volume 40, Number 6, November-December 2009
Number of page(s) 11
DOI https://doi.org/10.1051/vetres/2009039
Published online 07 July 2009
How to cite this article Vet. Res. (2009) 40:56
References of  Vet. Res. (2009) 40:56
  1. Aguiar-Alves F., Medeiros F., Fernandes O., Gudziki Pereira R.M., Perdreau-Remington F., Riley L.W., New Staphylococcus aureus genotyping method based on exotoxin (set) genes, J. Clin. Microbiol. (2006) 44:2728–2732 [CrossRef] [PubMed].
  2. Amorena B., García de Jalón J.A., Baselga R., Ducha J., Latre M.V., Ferrer L.M., et al., Infection of rabbit mammary glands with ovine mastitis bacterial strains, J. Comp. Pathol. (1991) 104:289–302 [CrossRef] [PubMed].
  3. Bergonier D., de Cremoux R., Rupp R., Lagriffoul G., Berthelot X., Mastitis of dairy small ruminants, Vet. Res. (2003) 34:689–716 [CrossRef] [PubMed] [EDP Sciences].
  4. Bor A., Winkler M., Gootwine E., Non-clinical intramammary infection in lactating ewes and its association with clinical mastitis, Br. Vet. J. (1989) 145:178–184 [PubMed].
  5. Brussow H., Hendrix R.W., Phage genomics: small is beautiful, Cell (2002) 108:13–16 [CrossRef] [PubMed].
  6. Callon C., Gilbert F.B., De Cremoux R., Montel M.C., Application of variable number of tandem repeat analysis to determine the origin of S. aureus contamination from milk to cheese in goat cheese farms, Food Control (2008) 19:143–150 [CrossRef].
  7. De Haas C.J., Veldkamp K.E., Peschel A., Weerkamp F., Van Wamel W.J., Heezius E.C., et al., Chemotaxis inhibitory protein of Staphylococcus aureus, a bacterial anti-inflammatory agent, J. Exp. Med. (2004) 199:687–695 [CrossRef] [PubMed].
  8. Edgeworth J.D.,Yadegarfar G., Pathak S., Batra R., Cockfield J., Wyncoll D., et al., An outbreak of methicillin-resistant Staphylococcus aureus (MRSA)-ST 239 associated with a high rate of bacteremia, Clin. Infect. Dis. (2007) 44:493–501 [CrossRef] [PubMed].
  9. Endo Y., Yamada T., Matsunaga K., Hayakawa Y., Kaidoh T., Takeuchi S., Phage conversion of exfoliative toxin A in Staphylococcus aureus isolated from cows with mastitis, Vet. Microbiol. (2003) 96:81–90 [CrossRef] [PubMed].
  10. Gilbert F.B., FromageauA., Gelineau L., Poutrel B., Differentiation of bovine Staphylococcus aureus isolates by use of polymorphic tandem repeat typing, Vet. Microbiol. (2006) 117:297–303 [CrossRef] [PubMed].
  11. Goerke C., Papenberg S., Dasbach S., Dietz K., Ziebach R., Kahl B.C., Wolz C., Increased frequency of genomic alterations in Staphylococcus aureus during chronic infection is in part due to phage mobilization, J. Infect. Dis. (2004) 189:724–734 [CrossRef] [PubMed].
  12. Goerke C., Wolz C., Regulatory and genomic plasticity of Staphylococcus aureus during persistent colonization and infection, Int. J. Med. Microbiol. (2004) 294:195–202 [CrossRef] [PubMed].
  13. Haveri M., Taponen S., Vuopio-Varkila J., Salmenlinna S., Pyörälä S., Bacterial genotype affects the manifestation and percistence of bovine Staphylococcus aureus intrammmary infection, J. Clin. Microbiol. (2005) 43:959–961 [CrossRef] [PubMed].
  14. Herron-Olson L., Fitzgerald J.R., Musser J.M., Kapur V., Molecular correlates of host specialization in Staphylococcus aureus, PLoS ONE (2007) 2:e1120.
  15. Iandolo J.J., Worrell V., Groicher K.H., Qian Y., Tian R., Kenton S., et al., Comparative analysis of the genomes of the temperate bacteriophages phi 11 phi 12 and phi 13 of Staphylococcus aureus 8325, Gene (2002) 289:109–118 [CrossRef] [PubMed].
  16. Kuhn G., Francioli P., Blanc D.S., Evidence for clonal evolution among highly polymorphic genes in methicillin-resistant Staphylococcus aureus, J. Bacteriol. (2006) 188:169–178 [CrossRef] [PubMed].
  17. Lina G., Bohach G.A., Nair S.P., Hiramatsu K., Jouvin-Marche E., Mariuzza R., Standard nomenclature for the superantigens expressed by Staphylococcus, J. Infect. Dis. (2004) 189:2334–2336 [CrossRef] [PubMed].
  18. Lindsay J.A., Moore C.E., Day N.P., Peacock S.J., Witney A.A., Stabler R.A., et al., Microarrays reveal that each of the ten dominant lineages of Staphylococcus aureus has a unique combination of surface-associated and regulatory genes, J. Bacteriol. (2006) 188:669–676 [CrossRef] [PubMed].
  19. Lindsay J.A., S. aureus evolution: lineages and mobile genetic elements (MGE), in: Lindsay J.A. (Ed.), Staphylococcus: Molecular genetics, Caister Academic Press, Norfolk UK, 2008, pp. 45–69.
  20. Meulemans L., Hermans K., Duchateau L., Haesebrouck F., High and low virulence Staphylococcus aureus strains in a rabbit skin infection model, Vet. Microbiol. (2007) 125:333–340 [CrossRef] [PubMed].
  21. Moore P.C.L., Lindsay J.A., Genetic variation among hospital isolates of methicillin-sensitive Staphylococcus aureus: evidence for horizontal transfer of virulence genes, J. Clin. Microbiol. (2001) 39:2760–2767 [CrossRef] [PubMed].
  22. O'Neill E., Pozzi C., Houston P., Humphreys H., Robinson D.A., Loughman A., et al., A novel Staphylococcus aureus biofilm phenotype mediated by the fibronectin-binding proteins, FnBPA and FnBPB, J. Bacteriol. (2008) 190:3835–3850 [CrossRef] [PubMed].
  23. Pantucek R., Doskar J., RuzickovaV., Kasparek P., Oracova E., Kvardova V., Rosypal S., Identification of bacteriophage types and their carriage in Staphylococcus aureus, Arch. Virol. (2004) 149:1689–1703 [CrossRef] [PubMed].
  24. Pichon C., Felden B., Small RNA genes expressed from Staphylococcus aureus genomic and pathogenicity islands with specific expression among pathogenic strains, Proc. Natl. Acad. Sci. USA (2005) 102:14249–14254 [CrossRef] [PubMed].
  25. Popowicz G.M., Dubin G., Stec-Niemczyk J., Czarny A., Dubin A., Potempa J., Holak T.A., Functional and structural characterization of Spl proteases from Staphylococcus aureus, J. Mol. Biol. (2006) 358:270–279 [CrossRef] [PubMed].
  26. Robinson D.A., Enright M.C., Evolutionary models of emergence of methicillin-resistant Staphylococcus aureus, Antimicrob. Agents Chemother. (2003) 47:3926–3934 [CrossRef] [PubMed].
  27. Rodriguez-Calleja J.M., Garcia-Lopez I., Santos J.A., Otero A., Garcia-Lopez M., Molecular and phenotypic typing of Staphylococcus aureus isolates from rabbit meat, Res. Microbiol. (2006) 157:496–502 [CrossRef] [PubMed].
  28. Rooijakkers S.H., Ruyken M., Roos A., Daha M.R., Presanis J.S., Sim R.B., Immun invasion by a staphylococcal complement inhibitor that acts on C3 convertases, Nat. Immunol. (2005) 920–927.
  29. Rozen S., Skaletsky H., Primer3 on the WWW for general users and for biologist programmers, Methods Mol. Biol. (2000) 132:365–386 [PubMed].
  30. Sabat A., Melles D.C., Martirosian G., Grundmann H., van Belkum A., Hryniewicz W., Distribution of the serine-aspartate repeat protein-encoding sdr genes among nasal-carriage and invasive Staphylococcus aureus strains, J. Clin. Microbiol. (2006) 44:1135–1138 [CrossRef] [PubMed].
  31. Straub J.A., Hertel C., Hammes W.P., A 23S rDNA-targeted polymerase chain reaction-based system for detection of Staphylococcus aureus in meat starter cultures and dairy products, J. Food Prot. (1999) 62:1150–1156 [PubMed].
  32. Sung J.M., Lloyd D.H., Lindsay J.A., Staphylococcus aureus host specificity: comparative genomics of human versus animal isolates by multi-strain microarray, Microbiology (2008) 154:1949–1959 [CrossRef] [PubMed].
  33. Tenover F.C., McDougal L.K., Goering R.V., Killgore G., Projan S.J., Patel J.B., Dunman P.M., Characterization of a strain of community-associated methicillin-resistant Staphylococcus aureus widely disseminated in the United States, J. Clin. Microbiol. (2006) 44:108–118 [CrossRef] [PubMed].
  34. Vancraeynest D., Hermans K., Haesebrouck F., Genotypic and phenotypic screening of high and low virulence Staphylococcus aureus isolates from rabbits for biofilm formation and MSCRAMMs, Vet. Microbiol. (2004) 103:241–247 [CrossRef] [PubMed].
  35. Vautor E., Abadie G., Guibert J.M., Huard C., Pepin M., Genotyping of Staphylococcus aureus isolated from various sites on farms with dairy sheep using pulsed-field gel electrophoresis, Vet. Microbiol. (2003) 96:69–79 [CrossRef] [PubMed].
  36. Vautor E., Abadie G., Guibert J.M., Chevalier N., Pepin M., Nasal carriage of Staphylococcus aureus in dairy sheep, Vet. Microbiol. (2005) 106:235–239 [CrossRef] [PubMed].
  37. Vautor E., Magnone V., Rios G., Le Brigand K., Bergonier D., Lina G., et al., Genetic differences among Staphylococcus aureus isolates from dairy ruminant species: a single-dye DNA microaaray approach, Vet. Microbiol. (2008) 133:105–114 [CrossRef] [PubMed].
  38. Wagner P.L., Waldor M.K., Bacteriophage control of bacterial virulence, Infect. Immun. (2002) 70:3985–3993 [CrossRef] [PubMed].
  39. Winter A., Mastitis in ewes, In Pract. (2001) 23:160–163.
  40. Witney A.A., Marsden G.L., Holden M.T., Stabler R.A., Husain S.E., Vass J.K., et al., Design validation, and application of a seven-strain Staphylococcus aureus PCR product microarray for comparative genomics, Appl. Environ. Microbiol. (2005) 71:7504–7514 [CrossRef] [PubMed].