Loss of catabolic function in Streptococcus agalactiae strains and its association with neonatal meningitis

被引:8
作者
Domelier, Anne-Sophie
van der Mee-Marquet, Nathalie
Grandet, Adeline
Mereghetti, Laurent
Rosenau, Agnes
Quentin, Roland
机构
[1] Univ Tours, UFR Med, Inst Federatif Rech Bacteries & Risque Maternofet, Equipe Accueil 3854, F-37032 Tours, France
[2] CHRU Trousseau, Serv Bacteriol Hyg, F-37044 Tours 9, France
关键词
D O I
10.1128/JCM.02550-05
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The abilities of 151 Streptococcus agalactiae strains to oxidize 95 carbon sources were studied using the Biolog system. Two populations were constituted: one with a high risk of causing meningitis (HR group; 63 strains), and the other with a lower risk of causing meningitis (LR group; 46 strains). Strains belonging to the HR group were significantly less able to use four carbon sources, i.e., alpha-D-glucose-1-phosphate, D-ribose, beta-methyl-D-glucoside, and D,L-alpha-glycerol phosphate, than strains from the LR group (P <= 0.004). Moreover, strains in the HR group significantly more frequently possessed one of several mobile genetic elements or genome deletions previously shown to be associated with strains responsible for neonatal meningitis than strains in the LR group (P < 0.001). These findings suggest that genetic disruption might have occurred in virulent clones of S. agalactiae. Fifteen biotypes (B1 to B15) were identified from the results of oxidation of the four carbon sources, of which six (B1 to B6) included 92% of the isolates belonging to the HR group. Strains of biotypes B1 to B6 are thus 13 times more likely to be able to invade the central nervous system of neonates than strains of biotypes B7 to B15. In addition, 86% of strains recently associated with neonatal meningitis (42 strains studied) were identified as being of biotypes B1 to B6. Identification of particular S. agalactiae biotypes may therefore be one of the criteria to assist clinicians in assessing the level of risk of neonatal meningitis when a mother and/or her neonate is colonized with S. agalactiae.
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页码:3245 / 3250
页数:6
相关论文
共 45 条
[1]  
*AG NAT ACR SANT, 2001, ANT PREV RISK EARL N
[2]   Use of deoxyribose by intestinal and extraintestinal pathogenic Escherichia coli strains:: a metabolic adaptation involved in competitiveness [J].
Bernier-Fébreau, C ;
du Merle, L ;
Turlin, E ;
Labas, V ;
Ordonez, J ;
Gilles, AM ;
Le Bouguénec, C .
INFECTION AND IMMUNITY, 2004, 72 (10) :6151-6156
[3]   Molecular characterization of serotype III group B-streptococcus isolates causing neonatal meningitis [J].
Bidet, P ;
Brahimi, N ;
Chalas, C ;
Aujard, Y ;
Bingen, E .
JOURNAL OF INFECTIOUS DISEASES, 2003, 188 (08) :1132-1137
[4]  
Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P1
[5]   The serotype of type Ia and III Group B streptococci is determined by the polymerase gene within the polycistronic capsule operon [J].
Chaffin, DO ;
Beres, SB ;
Yim, HH ;
Rubens, CE .
JOURNAL OF BACTERIOLOGY, 2000, 182 (16) :4466-4477
[6]   Rgg coordinates virulence factor synthesis and metabolism in Streptococcus pyogenes [J].
Chaussee, MS ;
Somerville, GA ;
Reitzer, L ;
Musser, JM .
JOURNAL OF BACTERIOLOGY, 2003, 185 (20) :6016-6024
[7]   The population genetics of ecological specialization in evolving Escherichia coli populations [J].
Cooper, VS ;
Lenski, RE .
NATURE, 2000, 407 (6805) :736-739
[8]   Mechanisms causing rapid and parallel losses of ribose catabolism in evolving populations of Escherichia coli B [J].
Cooper, VS ;
Schneider, D ;
Blot, M ;
Lenski, RE .
JOURNAL OF BACTERIOLOGY, 2001, 183 (09) :2834-2841
[9]   Pathoadaptive mutations that enhance virulence:: Genetic organization of the cadA regions of Shigella spp. [J].
Day, WA ;
Fernández, RE ;
Maurelli, AT .
INFECTION AND IMMUNITY, 2001, 69 (12) :7471-7480
[10]   Molecular pathogenesis of neonatal group B streptococcal infection: no longer in its infancy [J].
Doran, KS ;
Nizet, V .
MOLECULAR MICROBIOLOGY, 2004, 54 (01) :23-31