Molecular epidemiology of group B streptococci in Ireland: associations between serotype, invasive status and presence of genes encoding putative virulence factors

被引:18
作者
Dore, N
Bennett, D
Kaliszer, M
Cafferkey, M
Smyth, CJ
机构
[1] Childrens Univ Hosp, Irish Meningococcal & Meningitis Reference Lab, Dublin 1, Ireland
[2] Rotunda Hosp, Dublin 1, Ireland
[3] Univ Dublin Trinity Coll, Adelaide & Meath Hosp, Dept Community Hlth, Dublin 24, Ireland
[4] Royal Coll Surgeons Ireland, Dept Clin Microbiol, Dublin 2, Ireland
[5] Univ Dublin Trinity Coll, Moyne Inst Prevent Med, Dept Microbiol, Dublin 2, Ireland
关键词
D O I
10.1017/S0950268803008847
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Group B streptococcal isolates (n=159) from the three Dublin maternity hospitals, were serotyped and analysed for the bac, bca, hylB, pepB, and rib genes. The serotype distribution of the isolates was la, 19.5%; Ib, 18.9%; 11, 10.7%; 111, 29.5%; IV, 1.9%; V, 15.1%; non-typeable, 4.4%. There was a statistically significant association between the serotype and invasive status (carriage or infection) of isolates (P<0.005), but no significant association between serotype and degree of invasiveness was demonstrated. The presence or absence of each analysed gene was not associated with the invasive status of isolates. Statistically significant associations were revealed between bca and hylB (IS1548) (P=0.0004) and between bac and bca (P=0.014). The bac, bca, hylB (IS1548) and rib genes and the numbers of tandem repeats in the bca gene showed significant associations with serotype. Almost 50% of serotype III isolates possessed at least one of the bac and bca genes and 55-65% of strains of serotypes la, Ib and 11 possessed the rib gene. Most serotype III isolates had IS1548 in their hylB genes. Serotype Ib was the only serotype in which more than half of the strains contained more tandem repeats in the bca gene than the overall mean for the GBS population studied of 7.4 repeats. These findings indicate that some previously reported associations between putative virulence factors and GBS disease require further study and clarification.
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页码:823 / 833
页数:11
相关论文
共 52 条
[31]   bca, beta gene, and gene product divergency in reference and prototype strains of Streptococcus agalactiae [J].
Maeland, JA ;
Bevanger, L ;
Iversen, G ;
Lyng, RV .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1999, 6 (06) :986-988
[32]   GROUP-B STREPTOCOCCI - NEW CHALLENGE IN NEONATAL INFECTIONS [J].
MCCRACKEN, GH .
JOURNAL OF PEDIATRICS, 1973, 82 (04) :703-706
[33]   CLONED ALPHA AND BETA C-PROTEIN ANTIGENS OF GROUP-B STREPTOCOCCI ELICIT PROTECTIVE IMMUNITY [J].
MICHEL, JL ;
MADOFF, LC ;
KLING, DE ;
KASPER, DL ;
AUSUBEL, FM .
INFECTION AND IMMUNITY, 1991, 59 (06) :2023-2028
[34]   ASSOCIATION OF ELEVATED LEVELS OF EXTRACELLULAR NEURAMINIDASE WITH CLINICAL ISOLATES OF TYPE-III GROUP-B STREPTOCOCCI [J].
MILLIGAN, TW ;
BAKER, CJ ;
STRAUS, DC ;
MATTINGLY, SJ .
INFECTION AND IMMUNITY, 1978, 21 (03) :738-746
[35]  
Moyo S. R., 2000, Central African Journal of Medicine, V46, P115
[36]   IDENTIFICATION OF A HIGH-VIRULENCE CLONE OF TYPE-III STREPTOCOCCUS-AGALACTIAE (GROUP-B STREPTOCOCCUS) CAUSING INVASIVE NEONATAL DISEASE [J].
MUSSER, JM ;
MATTINGLY, SJ ;
QUENTIN, R ;
GOUDEAU, A ;
SELANDER, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4731-4735
[37]   A serotype VIII strain among colonizing group B streptococcal isolates in Boston, Massachusetts [J].
Paoletti, LJ ;
Bradford, J ;
Paoletti, LC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3759-3760
[38]   GROUP-B STREPTOCOCCAL NEURAMINIDASE IS ACTUALLY A HYALURONIDASE [J].
PRITCHARD, DG ;
LIN, B .
INFECTION AND IMMUNITY, 1993, 61 (08) :3234-3239
[39]   CHARACTERIZATION OF THE GROUP-B STREPTOCOCCAL HYALURONATE LYASE [J].
PRITCHARD, DG ;
LIN, B ;
WILLINGHAM, TR ;
BAKER, JR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 315 (02) :431-437
[40]   CHARACTERIZATION OF STREPTOCOCCUS-AGALACTIAE STRAINS BY MULTILOCUS ENZYME GENOTYPE AND SEROTYPE - IDENTIFICATION OF MULTIPLE VIRULENT CLONE FAMILIES THAT CAUSE INVASIVE NEONATAL DISEASE [J].
QUENTIN, R ;
HUET, H ;
WANG, FS ;
GESLIN, P ;
GOUDEAU, A ;
SELANDER, RK .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (10) :2576-2581