Coffey Tracey J, Daniels Margaret, Enright Mark C, Spratt Brian G
Wellcome Trust Centre for the Epidemiology of Infectious Disease, Department of Zoology, University of Oxford, Oxford OX1 3FY, UK.
Molecular Microbiology Group, School of Biological Sciences, University of Sussex, Brighton BN1 9QG, UK.
Microbiology (Reading). 1999 Aug;145 ( Pt 8):2023-2031. doi: 10.1099/13500872-145-8-2023.
The high prevalence of penicillin resistance among Streptococcus pneumoniae isolates from Uruguay has been associated with the emergence of a penicillin-resistant clone of serotype 14. Isolates of this clone were identical by multilocus sequence typing to members of the Spanish penicillin-resistant serotype 9V clone and possessed indistinguishable forms of the penicillin-binding protein 2b and 2x genes. Their pbp1a genes were also identical, except at the 3' end. The serotype 14 isolates were shown to be a variant of the Spanish serotype 9V clone which arose by a 22.2 kb recombinational replacement that introduced the capsular biosynthetic locus, and part of the neighbouring pbp1a gene, from a serotype 14 isolate. One end of the recombinational replacement was within the first gene of the capsular polysaccharide operon, cpsA, as the sequence of the upstream dexB gene, through most of cpsA, was identical in the penicillin-resistant serotype 9V and 14 isolates, but the sequences differed in the rest of cpsA and in cpsB. The other recombinational junction was at the end of the divergently transcribed pbp1a gene, which is approximately 11.6 kb downstream of the capsular biosynthetic locus. Isolates of this serotype variant were also detected in Spain and Denmark. Penicillin-resistant serotype 14 isolates from Poland were also closely related to the penicillin-resistant serotype 9V clone, but have emerged independently, as one end of the recombinational replacement was upstream of dexB and the other was within pbp1a, but at a different position from that in the serotype 14 variants from Uruguay, Spain and Denmark. Serotype 14 variants of the Spanish serotype 9V clone have therefore arisen on more than one occasion by large recombinational replacements that extend from the start of the cps region into the pbp1a gene.
乌拉圭肺炎链球菌分离株中青霉素耐药性的高流行率与血清型14的青霉素耐药克隆的出现有关。通过多位点序列分型,该克隆的分离株与西班牙青霉素耐药血清型9V克隆的成员相同,并具有难以区分的青霉素结合蛋白2b和2x基因形式。它们的pbp1a基因除了3'端外也相同。血清型14分离株被证明是西班牙血清型9V克隆的一个变体,它是通过22.2 kb的重组替换产生的,该替换从血清型14分离株引入了荚膜生物合成位点以及相邻pbp1a基因的一部分。重组替换的一端位于荚膜多糖操纵子的第一个基因cpsA内,因为在青霉素耐药血清型9V和14分离株中,上游dexB基因的序列,直至cpsA的大部分,都是相同的,但cpsA的其余部分和cpsB的序列不同。另一个重组连接点位于反向转录的pbp1a基因的末端,该基因位于荚膜生物合成位点下游约11.6 kb处。在西班牙和丹麦也检测到了这种血清型变体的分离株。来自波兰的青霉素耐药血清型14分离株也与青霉素耐药血清型9V克隆密切相关,但它们是独立出现的,因为重组替换的一端位于dexB上游,另一端位于pbp1a内,但位置与来自乌拉圭、西班牙和丹麦的血清型14变体不同。因此,西班牙血清型9V克隆的血清型14变体是通过从cps区域开始延伸到pbp1a基因的大型重组替换多次出现的。