Commensal Streptococcus agalactiae isolated from patients seen at University Hospital of Londrina, Paraná, Brazil: capsular types, genotyping, antimicrobial susceptibility and virulence determinants
详细信息    查看全文
  • 作者:Eliane Saori Otaguiri (1)
    Ana Elisa Belotto Morguette (1)
    Eliandro Reis Tavares (1)
    Pollyanna Myrella Capela dos Santos (1)
    Alexandre Tadachi Morey (1)
    Juscélio Donizete Cardoso (1)
    Márcia Regina Eches Perugini (2)
    Lucy Megumi Yamauchi (1)
    Sueli Fumie Yamada-Ogatta (1)
  • 关键词:Group B Streptococcus ; Capsular antigen ; Erythromycin ; Clindamycin ; MLVA typing ; pilus island ; Virulence traits
  • 刊名:BMC Microbiology
  • 出版年:2013
  • 出版时间:December 2013
  • 年:2013
  • 卷:13
  • 期:1
  • 全文大小:240 KB
  • 参考文献:1. McCord N, Owen P, Powls A, Lunan B: A complete audit cycle of intrapartum group B streptococcus prophylaxis. / Health Bull (Edinb) 2001, 59:263-67.
    2. Krohn MA, Hillier SL, Baker CJ: Maternal peripartum complications associated with vaginal group B streptococci colonization. / J Infect Dis 1999, 179:1410-415. CrossRef
    3. Phares CR, Lynfield R, Farley MM, Mohle-Boetani J, Harrison LH, Petit S, Craig AS, Schaffner W, Zansky SM, Gershman K, / et al.: Epidemiology of invasive group B streptococcal disease in the United States, 1999-005. / JAMA 2008, 299:2056-065. CrossRef
    4. Schuchat A: Group B streptococcal disease in newborns: A global perspective on prevention. / Biomed Pharmacother 1995, 49:19-5. CrossRef
    5. Verani JR, Schrag SJ: Group B streptococcal disease in infants: Progress in prevention and continued challenges. / Clin Perinatol 2010, 37:375-92. CrossRef
    6. Verani JR, McGee L, Schrag SJ: Prevention of perinatal group B streptococcal disease-revised guidelines from CDC, 2010. / MMWR Recomm Rep 2010, 59:1-6.
    7. Edmond KM, Kortsalioudaki C, Scott S, Schrag SJ, Zaidi AK, Cousens S, Heath PT: Group B streptococcal disease in infants aged younger than 3?months: Systematic review and meta-analysis. / Lancet 2012, 379:547-56. CrossRef
    8. Edwards MS, Baker CJ: Group B streptococcal infections in elderly adults. / Clin Infect Dis 2005, 41:839-47. CrossRef
    9. Skoff TH, Farley MM, Petit S, Craig AS, Schaffner W, Gershman K, Harrison LH, Lynfield R, Mohle-Boetani J, Zansky S, / et al.: Increasing burden of invasive group B streptococcal disease in nonpregnant adults, 1990-007. / Clin Infect Dis 2009, 49:85-2. CrossRef
    10. Duarte RS, Bellei BC, Miranda OP, Brito MA, Teixeira LM: Distribution of antimicrobial resistance and virulence-related genes among Brazilian group B streptococci recovered from bovine and human sources. / Antimicrob Agents Chemother 2005, 49:97-03. CrossRef
    11. Palmeiro JK, Dalla-Costa LM, Fracalanzza SE, Botelho AC, da Silva Nogueira K, Scheffer MC, de Almeida Torres RS, de Carvalho NS, Cogo LL, Madeira HM: Phenotypic and genotypic characterization of group B streptococcal isolates in southern Brazil. / J Clin Microbiol 2010, 48:4397-403. CrossRef
    12. Correa AB, Silva LG, Pinto Tde C, Oliveira IC, Fernandes FG, Costa NS, Mattos MC, Fracalanzza SE, Benchetrit LC: The genetic diversity and phenotypic characterisation of Streptococcus agalactiae isolates from Rio de Janeiro, Brazil. / Mem Inst Oswaldo Cruz 2011, 106:1002-006. CrossRef
    13. Nakamura PA, Schuab RBB, Neves FP, Pereira CF, Paula GR, Barros RR: Antimicrobial resistance profiles and genetic characterisation of macrolide resistant isolates of Streptococcus agalactiae . / Mem Inst Oswaldo Cruz 2011, 106:119-22. CrossRef
    14. Nagano N, Nagano Y, Toyama M, Kimura K, Tamura T, Shibayama K, Arakawa Y: Nosocomial spread of multidrug-resistant group B streptococci with reduced penicillin susceptibility belonging to clonal complex 1. / J Antimicrob Chemother 2012, 67:849-56. CrossRef
    15. Capanna F, Emonet SP, Cherkaoui A, Irion OP, Schrenzel J, MartinezdeTejada B: Antibiotic resistance patterns among group B Streptococcus isolates: Implications for antibiotic prophylaxis for early-onset neonatal sepsis. / Swiss Med Wkly 2013, 143:0.
    16. Leclercq R: Mechanisms of resistance to macrolides and lincosamides: Nature of the resistance elements and their clinical implications. / Clin Infect Dis 2002, 34:482-92. CrossRef
    17. Clancy J, Petitpas J, Dib-Hajj F, Yuan W, Cronan M, Kamath AV, Bergeron J, Retsema JA: Molecular cloning and functional analysis of a novel macrolide-resistance determinant, mefA , from Streptococcus pyogenes . / Mol Microbiol 1996, 22:867-79. CrossRef
    18. Cieslewicz MJ, Chaffin D, Glusman G, Kasper D, Madan A, Rodrigues S, Fahey J, Wessels MR, Rubens CE: Structural and genetic diversity of group B streptococcus capsular polysaccharides. / Infect Immun 2005, 73:3096-103. CrossRef
    19. Slotved HC, Kong F, Lambertsen L, Sauer S, Gilbert GL: Serotype IX, a Proposed New Streptococcus agalactiae Serotype. / J Clin Microbiol 2007, 45:2929-936. CrossRef
    20. Murayama SY, Seki C, Sakata H, Sunaoshi K, Nakayama E, Iwata S, Sunakawa K, Ubukata K: Capsular type and antibiotic resistance in Streptococcus agalactiae isolates from patients, ranging from newborns to the elderly, with invasive infections. / Antimicrob Agents Chemother 2009, 53:2650-653. CrossRef
    21. Madzivhandila M, Adrian PV, Cutland CL, Kuwanda L, Madhi SA: Distribution of pilus islands of group B streptococcus associated with maternal colonization and invasive disease in South Africa. / J Med Microbiol 2013, 62:249-53. CrossRef
    22. Marques MB, Kasper DL, Pangburn MK, Wessels MR: Prevention of C3 deposition by capsular polysaccharide is a virulence mechanism of type III group B streptococci. / Infect Immun 1992, 60:3986-993.
    23. Lauer P, Rinaudo CD, Soriani M, Margarit I, Maione D, Rosini R, Taddei AR, Mora M, Rappuoli R, Grandi G, Telford JL: Genome analysis reveals pili in Group B Streptococcus . / Science 2005, 309:105. CrossRef
    24. Sharma P, Lata H, Arya DK, Kashyap AK, Kumar H, Dua M, Ali A, Johri AK: Role of pilus proteins in adherence and invasion of Streptococcus agalactiae to the lung and cervical epithelial cells. / J Biol Chem 2013, 288:4023-034. CrossRef
    25. Rinaudo CD, Rosini R, Galeotti CL, Berti F, Necchi F, Reguzzi V, Ghezzo C, Telford JL, Grandi G, Maione D: Specific involvement of pilus type 2a in biofilm formation in group B Streptococcus . / PLoS One 2010, 5:e9216. CrossRef
    26. Maisey HC, Quach D, Hensler ME, Liu GY, Gallo RL, Nizet V, Doran KS: A group B streptococcal pilus protein promotes phagocyte resistance and systemic virulence. / FASEB J 2008, 22:1715-724. CrossRef
    27. Pritzlaff CA, Chang JC, Kuo SP, Tamura GS, Rubens CE, Nizet V: Genetic basis for the beta-haemolytic/cytolytic activity of group B Streptococcus . / Mol Microbiol 2001, 39:236-47. CrossRef
    28. Doran KS, Chang JC, Benoit VM, Eckmann L, Nizet V: Group B streptococcal beta-hemolysin/cytolysin promotes invasion of human lung epithelial cells and the release of interleukin-8. / J Infect Dis 2002, 185:196-03. CrossRef
    29. Liu GY, Doran KS, Lawrence T, Turkson N, Puliti M, Tissi L, Nizet V: Sword and shield: linked group B streptococcal beta-hemolysin/cytolysin and carotenoid pigment function to subvert host phagocyte defense. / Proc Natl Acad Sci U S A 2004, 101:14491-4496. CrossRef
    30. Baker JR, Pritchard DG: Action pattern and substrate specificity of the hyaluronan lyase from group B streptococci. / Biochem J 2000,348(Pt 2):465-71. CrossRef
    31. Benchetrit LC, Fracalanzza SE, Peregrino H, Camelo AA, Sanches LA: Carriage of Streptococcus agalactiae in women and neonates and distribution of serological types: a study in Brazil. / J Clin Microbiol 1982, 15:787-90.
    32. Haguenoer E, Baty G, Pourcel C, Lartigue MF, Domelier AS, Rosenau A, Quentin R, Mereghetti L, Lanotte P: A multi locus variable number of tandem repeat analysis (MLVA) scheme for Streptococcus agalactiae genotyping. / BMC Microbiol 2011, 11:171. CrossRef
    33. Radtke A, Lindstedt BA, Afset JE, Bergh K: Rapid multiple- locus variant-repeat assay (MLVA) for genotyping of Streptococcus agalactiae . / J Clin Microbiol 2010, 48:2502-508. CrossRef
    34. Uh Y, Kim HY, Jang IH, Hwang GY, Yoon KJ: Correlation of serotypes and genotypes of macrolide-resistant Streptococcus agalactiae . / Yonsei Med J 2005, 46:480-83. CrossRef
    35. Rosini R, Rinaudo CD, Soriani M, Lauer P, Mora M, Maione D, Taddei A, Santi I, Ghezzo C, Brettoni C, / et al.: Identification of novel genomic islands coding for antigenic pilus -like structures in Streptococcus agalactiae . / Mol Microbiol 2006, 61:126-41. CrossRef
    36. Martins ER, Andreu A, Melo-Cristino J, Ramirez M: Distribution of Pilus islands in streptococcus agalactiae that cause human infections: Insights into evolution and implication for vaccine development. / Clin Vaccine Immunol 2013, 20:313-16. CrossRef
    37. Forquin MP, Tazi A, Rosa-Fraile M, Poyart C, Trieu-Cuot P, Dramsi S: The putative glycosyltransferase-encoding gene cylJ and the group B Streptococcus (GBS)-specific gene cylK modulate hemolysin production and virulence of GBS. / Infect Immun 2007, 75:2063-066. CrossRef
    38. Merritt K, Jacobs NJ: Characterization and incidence of pigment production by human clinical group B streptococci. / J Clin Microbiol 1978, 8:105-07.
    39. Milligan TW, Baker CJ, Straus DC, Mattingly SJ: Association of elevated levels of extracellular neuraminidase with clinical isolates of type III group B streptococci. / Infect Immun 1978, 21:738-46.
    40. Granlund M, Oberg L, Sellin M, Norgren M: Identification of a novel insertion element, IS1548, in group B streptococci, predominantly in strains causing endocarditis. / J Infect Dis 1998, 177:967-76. CrossRef
    41. Horan TC, Andrus M, Dudeck MA: CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting. / Am J Infect Control 2008, 36:309-32. CrossRef
    42. de Paris F, Machado AB, Gheno TC, Ascoli BM, Oliveira KR, Barth AL: Group B Streptococcus detection: comparison of PCR assay and culture as a screening method for pregnant women. / Braz J Infect Dis 2011, 15:323-27.
    43. Imperi M, Pataracchia M, Alfarone G, Baldassarri L, Orefici G, Creti R: A multiplex PCR assay for the direct identification of the capsular type (Ia to IX) of Streptococcus agalactiae . / J Microbiol Methods 2010, 80:212-14. CrossRef
    44. Hunter PR, Gaston MA: Numerical index of the discriminatory variability of typing systems: An application of Simpson’s index of diversity. / J Clin Microbiol 1988, 26:2465-466.
    45. CLSI: / Performance standards for antimicrobial susceptibility testing. Twenty-second informational supplement (M100-S22). Wayne, PA: Clinical and Laboratory Standards Institute; 2012.
    46. Seppala H, Nissinen A, Yu Q, Huovinen P: Three different phenotypes of erythromycin-resistant Streptococcus pyogenes in Finland. / J Antimicrob Chemother 1993, 32:885-91. CrossRef
  • 作者单位:Eliane Saori Otaguiri (1)
    Ana Elisa Belotto Morguette (1)
    Eliandro Reis Tavares (1)
    Pollyanna Myrella Capela dos Santos (1)
    Alexandre Tadachi Morey (1)
    Juscélio Donizete Cardoso (1)
    Márcia Regina Eches Perugini (2)
    Lucy Megumi Yamauchi (1)
    Sueli Fumie Yamada-Ogatta (1)

    1. Laboratório de Biologia Molecular de Microrganismos, Departamento de Microbiologia, Centro de Ciências Biológicas, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, PR 445, km 380, Londrina, Paraná, CEP 86057-970, Brazil
    2. Laboratório de Microbiologia Clínica, Departamento de Patologia, Análises Clínicas e Toxicológicas, Centro de Ciências da Saúde, Universidade Estadual de Londrina, Londrina, Paraná, Brazil
  • ISSN:1471-2180
文摘
Background Streptococcus agalactiae or Group B Streptococci (GBS) have the ability to access various host sites, which reflects its adaptability to different environments during the course of infection. This adaptation is due to the expression of virulence factors that are involved with survival, invasion and bacterial persistence in the host. This study aimed to characterize GBS isolates from women of reproductive age seen at University Hospital of Londrina, according to capsular typing, genetic relatedness, antimicrobial susceptibility profile and occurrence of virulence determinants. Results A total of 83 GBS isolates were enrolled in this study. Capsular types Ia (42.2%), II (10.8%), III (14.5%) and V (30.1%) were identified in most GBS. One isolate each was classified as type IX and non-typeable. A total of 15 multiple locus variable number of tandem repeat analysis (MLVA) types were identified among the isolates, seven were singletons and eight were represented by more than four isolates. All isolates were susceptible to penicillin, ampicillin, cefepime, cefotaxime, chloramphenicol, levofloxacin and vancomycin. Resistance to erythromycin and clindamycin was observed in 19.3 and 13.3% of isolates, respectively. All isolates resistant to clindamycin were simultaneously resistant to erythromycin and were distributed in the capsular types III and V. One isolate showed the constitutive macrolide-lincosamide-streptogramin B (cMLSB) phenotype and ten showed the inducible MLSB (iMLSB) phenotype. The mechanism of resistance to erythromycin and clindamycin more prevalent among these isolates was mediated by the gene ermA, alone or in combination with the gene ermB. The isolates displaying resistance only to erythromycin belonged to capsular type Ia, and showed the M phenotype, which was mediated by the mefA/E gene. All isolates harbored the gene hylB and at least one pilus variant, PI-1, PI-2a or PI-2b. Although cylE was observed in all GBS, four isolates were classified as gamma-hemolytic and carotenoid pigment non-producers. Conclusions Our results indicate the potential virulence of commensal GBS isolates, reinforcing the need for continued screening for this bacterium to prevent infections. The distribution of capsular and pili antigens, and MLVA profiles was also identified, which may contribute to the development of new strategies for the prevention and treatment of GBS infection.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700