1887

Abstract

, commonly known as group B streptococcus (GBS), is a cause of infectious disease in numerous animal species. This study examined the genetic relatedness of piscine, dolphin and human GBS isolates and bovine GBS reference strains from different geographical regions using serological and molecular serotyping and multilocus sequence typing (MLST) techniques. Piscine isolates originating from Kuwait, Brazil, Israel and the USA were capsular serotype Ia, a serotype previously unreported in GBS isolated from fish. Sequence typing of piscine isolates produced six sequence types (ST-7, ST-257, ST-258, ST-259, ST-260 and ST-261), the latter five representing allelic designations and allelic combinations not previously reported in the MLST database. Genomic diversity existed between dolphin and piscine GBS isolates from Kuwait and other geographical areas. Piscine GBS isolates from Brazil, Israel, Honduras and the USA appeared to represent a distinct genetic population of strains that were largely unrelated to human and bovine GBS. The Kuwait dolphin and piscine lineage (ST-7, Ia) was also associated with human neonatal infections in Japan. Comparative genomics of piscine, human and bovine GBS could help clarify those genes important for host tropism, the emergence of unique pathogenic clones and whether these hosts act as reservoirs of one another's pathogenic lineages.

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2008-11-01
2019-11-22
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References

  1. Baya, A. M., Lupiani, B., Hetrick, F. M., Roberson, B. S., Lukacovic, R., May, E. & Poukish, C. ( 1990; ). Association of Streptococcus sp. with fish mortalities in the Chesapeake Bay and its tributaries. J Fish Dis 13, 251–253.[CrossRef]
    [Google Scholar]
  2. Bisharat, N., Crook, D. W., Leigh, J., Harding, R. M., Ward, P. N., Coffey, T. J., Maiden, M. C., Peto, T. & Jones, N. ( 2004; ). Hyperinvasive neonatal group B streptococcus has arisen from a bovine ancestor. J Clin Microbiol 42, 2161–2167.[CrossRef]
    [Google Scholar]
  3. Bisharat, N., Jones, N., Marchaim, D., Block, C., Harding, R. M., Yagupsky, P., Peto, T. & Crook, D. W. ( 2005; ). Population structure of group B streptococcus from a low-incidence region for invasive neonatal disease. Microbiology 151, 1875–1881.[CrossRef]
    [Google Scholar]
  4. Bohnsack, J. F., Whiting, A. A., Martinez, G., Jones, N., Adderson, E. E., Detrick, S., Blashchke-Bonkowsky, A. J., Bisharat, N. & Gottschalk, M. ( 2004; ). Serotype III Streptococcus agalactiae from bovine milk and human neonatal infections. Emerg Infect Dis 10, 1412–1419.[CrossRef]
    [Google Scholar]
  5. Bohnsack, J. F., Whiting, A. A., Gottschalk, M., Dunn, D. M., Weiss, R., Azimi, P. H., Phillips, J. B., Weisman, L. E., Rhoads, G. G. & Lin, F.-Y. C. ( 2008; ). Population structure of invasive and colonizing strains of Streptococcus agalactiae from neonates of six US academic centers from 1995–1999. J Clin Microbiol 46, 1285–1291.[CrossRef]
    [Google Scholar]
  6. Brochet, M., Couvé, E., Zouine, M., Vallaeys, T., Rusniok, C., Lamy, M.-C., Buchrieser, C., Trieu-Cuot, P., Kunst, F. & other authors ( 2006; ). Genomic diversity and evolution within the species Streptococcus agalactiae. Microbes Infect 8, 1227–1243.[CrossRef]
    [Google Scholar]
  7. Brown, J. H. ( 1939; ). Double-zone β-hemolytic streptococci: their cultural characteristics, serological grouping, occurrence and pathogenic significance. J Bacteriol 37, 133–144.
    [Google Scholar]
  8. Davies, H. D., Jones, N., Whittam, T. S., Elsayed, S., Bisharat, N. & Baker, C. J. ( 2004; ). Multilocus sequence typing of serotype III group B streptococcus and correlation with pathogenic potential. J Infect Dis 189, 1097–1102.[CrossRef]
    [Google Scholar]
  9. Duremdez, R., Al-Marzouk, A., Qasem, J. A., Al-Harbi, A. & Gharabally, H. ( 2004; ). Isolation of Streptococcus agalactiae from cultured silver pomfret, Pampus argenteus (Euphrasen), in Kuwait. J Fish Dis 27, 307–310.[CrossRef]
    [Google Scholar]
  10. Eldar, A., Bejerano, Y. & Bercovier, H. ( 1994; ). Streptococcus shiloi and Streptococcus difficile: two new streptococcal species causing a meningoencephalitis in fish. Curr Microbiol 28, 139–143.[CrossRef]
    [Google Scholar]
  11. Elliott, J. A., Facklam, R. R. & Richter, C. B. ( 1990; ). Whole-cell protein patterns of nonhemolytic group B, type 1b, streptococci isolated from humans, mice, cattle, frogs, and fish. J Clin Microbiol 28, 628–630.
    [Google Scholar]
  12. Evans, J. J., Klesius, P. H., Glibert, P. M., Shoemaker, C. A., Al Sarawi, M. A., Landsberg, J., Duremdez, R., Al Marzouk, A. & Al Zenki, S. ( 2002; ). Characterization of β-haemolytic Group B Streptococcus agalactiae in cultured seabream, Sparus auratus (L.), and wild mullet, Liza klunzingeri (Day), in Kuwait. J Fish Dis 25, 505–513.[CrossRef]
    [Google Scholar]
  13. Evans, J. J., Pasnik, D. J., Klesius, P. H. & Al-Ablani, S. ( 2006; ). First report of Streptococcus agalactiae and Lactococcus garvieae from a wild bottlenose dolphin (Tursiops truncatus). J Wildl Dis 42, 561–569.[CrossRef]
    [Google Scholar]
  14. Facklam, R. R., Padula, J. F., Thacker, L. G., Wortham, E. C. & Sconyers, B. J. ( 1974; ). Presumptive identification of group A, B, and D streptococci. Appl Microbiol 27, 107–113.
    [Google Scholar]
  15. Feil, E. J., Li, B. C., Aanensen, D. M., Hanage, W. P. & Spratt, B. G. ( 2004; ). eBurst: inferring patterns of evolutionary descent among clusters of related bacterial genotypes from multilocus sequence typing data. J Bacteriol 186, 1518–1530.[CrossRef]
    [Google Scholar]
  16. Finch, L. A. & Martin, D. R. ( 1984; ). Human and bovine group B streptococci: two distinct populations. J Appl Bacteriol 57, 273–278.[CrossRef]
    [Google Scholar]
  17. Gherardi, G., Imperi, M., Baldassarri, L., Pataracchia, M., Alfarone, G., Recchia, S., Orefici, G., Dicuonzo, G. & Creti, R. ( 2007; ). Molecular epidemiology and distribution of serotypes, surface proteins, and antibiotic resistance among group B streptococci in Italy. J Clin Microbiol 45, 2909–2916.[CrossRef]
    [Google Scholar]
  18. Jones, N., Bohnsack, J. F., Takahashi, S., Oliver, K. A., Chan, M.-S., Kunst, F., Glaser, P., Rusniok, C., Crook, D. W. M. & other authors ( 2003; ). Multilocus sequence typing system for group B streptococcus. J Clin Microbiol 41, 2530–2536.[CrossRef]
    [Google Scholar]
  19. Jones, N., Oliver, K. A., Barry, J., Harding, R. M., Bisharat, N., Spratt, B. G., Peto, T., Crook, D. W. & , the Oxford Group B Streptococcus Consortium ( 2006; ). Enhanced invasiveness of bovine-derived neonatal sequence type 17 group B streptococcus is independent of capsular serotype. Clin Infect Dis 42, 915–924.[CrossRef]
    [Google Scholar]
  20. Kawata, K., Anzai, T., Senna, K., Kikuchi, N., Ezawa, A. & Takahashi, T. ( 2004; ). Simple and rapid PCR method for identification of streptococcal species relevant to animal infections based on 23S rDNA sequence. FEMS Microbiol Lett 237, 57–64.[CrossRef]
    [Google Scholar]
  21. Kumar, S., Tamura, K. & Nei, M. ( 2004; ). mega3: integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Brief Bioinform 5, 150–163.[CrossRef]
    [Google Scholar]
  22. Lin, F. Y., Whiting, A., Adderson, E., Takahashi, S., Dunn, D. M., Weiss, R., Azimi, P. H., Philips, J. B., III, Weisman, L. E. & other authors ( 2006; ). Phylogenetic lineages of invasive and colonizing strains of serotype III group B streptococci from neonates: a multicenter prospective study. J Clin Microbiol 44, 1257–1261.[CrossRef]
    [Google Scholar]
  23. Luan, S. L., Granlund, M., Sellin, M., Lagergard, T., Spratt, B. G. & Norgren, M. ( 2005; ). Multilocus sequence typing of Swedish invasive group B streptococcus isolates indicates a neonatally associated genetic lineage and capsule switching. J Clin Microbiol 43, 3727–3733.[CrossRef]
    [Google Scholar]
  24. MacFaddin, J. F. ( 2000; ). Biochemical Tests for Identification of Medical Bacteria, 3rd edn. Philadelphia, PA: Lippincott Williams & Wilkins.
  25. Martinez, G., Harel, J., Higgins, R., LaCouture, S., Daignault, D. & Gottschalk, M. ( 2000; ). Characterization of Streptococcus agalactiae isolates of bovine and human origin by randomly amplified polymorphic DNA analysis. J Clin Microbiol 38, 71–78.
    [Google Scholar]
  26. Martins, E. R., Pessanha, M. A., Ramirez, M. & Melo-Cristino, J. ( 2007; ). Analysis of group B streptococcal isolates from infants and pregnant women in Portugal revealing two lineages with enhanced invasiveness. J Clin Microbiol 45, 3224–3229.[CrossRef]
    [Google Scholar]
  27. Nagano, Y., Nagano, N., Takahashi, S., Murono, K., Fujita, K., Taguchi, F. & Okuwaki, Y. ( 1991; ). Restriction endonuclease digest patterns of chromosomal DNA from group B β-haemolytic streptococci. J Med Microbiol 35, 297–303.[CrossRef]
    [Google Scholar]
  28. Nagano, N., Nagano, Y. & Taguchi, F. ( 2002; ). High expression of a C protein β antigen gene among invasive strains from certain clonally related groups of type Ia and Ib group B streptococci. Infect Immun 70, 4643–4649.[CrossRef]
    [Google Scholar]
  29. Oliveira, I. C., de Mattos, M. C., Pinto, T. A., Ferreira-Carvalho, B. T., Benchetrit, L. C., Whiting, A. A., Bohnsack, J. F. & Figueiredo, A. M. ( 2006; ). Genetic relatedness between group B streptococci originating from bovine mastitis and a human group B streptococcus type V cluster displaying an identical pulsed-field gel electrophoresis pattern. Clin Microbiol Infect 12, 887–893.[CrossRef]
    [Google Scholar]
  30. Pattison, I. H., Matthews, P. R. J. & Howell, D. G. ( 1955; ). The type classification of group B streptococci, with special reference to bovine strains apparently lacking in type polysaccharide. J Pathol Bacteriol 69, 51–60.[CrossRef]
    [Google Scholar]
  31. Plumb, J. A., Schachte, J. H., Gaines, J. L., Peltier, W. & Carroll, B. ( 1974; ). Streptococcus sp. from marine fishes along the Alabama and Northwest Florida coast of the Gulf of Mexico. Trans Am Fish Soc 103, 358–361.[CrossRef]
    [Google Scholar]
  32. Poyart, C., Tazi, A., Réglier-Poupet, H., Billoët, A., Tavares, N., Raymond, J. & Trieu-Cuot, P. ( 2007; ). Multiplex PCR assay for rapid and accurate capsular typing of group B streptococci. J Clin Microbiol 45, 1985–1988.[CrossRef]
    [Google Scholar]
  33. Ramaswamy, S. V., Ferrieri, P., Flores, A. E. & Paoletti, L. C. ( 2006; ). Molecular characterization of nontypable group B streptococcus. J Clin Microbiol 44, 2398–2403.[CrossRef]
    [Google Scholar]
  34. Robinson, J. A. & Meyer, F. P. ( 1966; ). Streptococcal fish pathogen. J Bacteriol 92, 512
    [Google Scholar]
  35. Salvador, R., Muller, E. E., de Freitas, J. C., Leonhadt, J. H., Pretto-Giordano, L. G. & Dias, J. A. ( 2005; ). Isolation and characterization of Streptococcus spp. group B in Nile tilapias (Oreochromis niloticus) reared in hapas nets and earth nurseries in the northern region of Parana State, Brazil. Ciência Rural Santa Maria 35, 1374–1378.[CrossRef]
    [Google Scholar]
  36. Schuchat, A. ( 1998; ). Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin Microbiol Rev 11, 497–513.
    [Google Scholar]
  37. Seifert, K. N., Adderson, E. E., Whiting, A., Bohnsack, J. F., Crowley, P. J. & Brady, L. J. ( 2006; ). A unique serine-rich repeat protein (Srr-2) and novel surface antigen (epsilon) associated with a virulent lineage of serotype III Streptococcus agalactiae. Microbiology 152, 1029–1040.[CrossRef]
    [Google Scholar]
  38. Suanyuk, N., Kanghear, H., Khongpradit, R. & Supamattaya, K. ( 2005; ). Streptococcus agalactiae infection in tilapia (Oreochromis niloticus). Songklanakarin J Sci Technol Aquat Sci 27, 307–319.
    [Google Scholar]
  39. Sukhnanand, S., Dogan, B., Ayodele, M. O., Zadoks, R. N., Craver, M. P. J., Dumas, N. B., Schukken, Y. H., Boor, K. J. & Wiedmann, M. ( 2005; ). Molecular subtyping and characterization of bovine and human Streptococcus agalactiae isolates. J Clin Microbiol 43, 1177–1186.[CrossRef]
    [Google Scholar]
  40. Takahashi, S., Detrick, S., Whiting, A. A., Blaschke-Bonkowksy, A. J., Aoyagi, Y., Adderson, E. E. & Bohnsack, J. F. ( 2002; ). Correlation of phylogenetic lineages of group B streptococci, identified by analysis of restriction-digestion patterns of genomic DNA, with infB alleles and mobile genetic elements. J Infect Dis 186, 1034–1038.[CrossRef]
    [Google Scholar]
  41. Tettelin, H., Masignani, V., Cieslewicz, M. J., Donati, C., Medini, D., Ward, N. L., Angiuoli, S. V. & Crabtree, J. ( 2005; ). Genome analysis of multiple pathogenic isolates of Streptococcus agalactiae: implications for the microbial “pan-genome”. Proc Natl Acad Sci U S A 102, 13950–13955.[CrossRef]
    [Google Scholar]
  42. Vandamme, P., Devriese, L. A., Pot, B., Kersters, K. & Melin, P. ( 1997; ). Streptococcus difficile is a nonhemolytic group B, type Ib streptococcus. Int J Syst Bacteriol 47, 81–85.[CrossRef]
    [Google Scholar]
  43. Wilkinson, H. W. ( 1978; ). Analysis of group B streptococcal types associated with disease in human infants and adults. J Clin Microbiol 7, 176–179.
    [Google Scholar]
  44. Wilkinson, H. W., Thacker, L. G. & Facklam, R. R. ( 1973; ). Nonhemolytic group B streptococci of human, bovine, and ichthyic origin. Infect Immun 7, 496–498.
    [Google Scholar]
  45. Zappulli, V., Mazzariol, S., Cavicchiolo, L., Petterino, C., Bargelloni, L. & Castagnaro, M. ( 2005; ). Fatal necrotizing fasciitis and myositis in a captive common bottlenose dolphin (Tursiops truncatus) associated with Streptococcus agalactiae. J Vet Diagn Invest 17, 617–622.[CrossRef]
    [Google Scholar]
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