Nagano Noriyuki, Nagano Yukiko, Kimura Kouji, Tamai Kiyoko, Yanagisawa Hideji, Arakawa Yoshichika
Department of Bacterial Pathogenesis and Infection Control, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan.
Antimicrob Agents Chemother. 2008 Dec;52(12):4258-67. doi: 10.1128/AAC.00596-08. Epub 2008 Sep 22.
The recent emergence of group B streptococcal isolates exhibiting increased penicillin MICs at the Funabashi Municipal Medical Center and other hospitals in Japan prompted a comparative analysis of the penicillin-binding proteins (PBPs) from those strains with the PBPs from penicillin-susceptible strains comprising four neonatal invasive strains isolated from 1976 to 1988 and two recent isolates. The PBP sequences of the penicillin-susceptible strains were highly conserved, irrespective of their isolation date. Of six strains with reduced susceptibility to penicillin (penicillin MICs, 0.25 to 0.5 mug/ml), strains R1, R2, R5, and R6 shared a unique set of five amino acid substitutions, including V405A adjacent to the (402)SSN(404) motif in PBP 2X and one in PBP 2B. The remaining two strains, R3 and R4, shared several substitutions, including Q557E adjacent to the (552)KSG(554) motif in PBP 2X, in addition to the substitutions in PBP 2B, which are commonly found among penicillin-insusceptible strains. Strains R7 and R8, which had a penicillin MIC of 1 mug/ml, shared a unique set of eight amino acid substitutions (two in PBP 2X; two in PBP 2B, including G613R adjacent to the (614)KTG(616) motif; three in PBP 1A; and one in PBP 2A), and the Q557E substitution in PBP 2X was common to R3 and R4. The binding of Bocillin FL was reduced or not detected in some PBPs, including PBP 2X of penicillin-insusceptible strains, but no significant reduction in the level of pbp2x transcription was found in such strains. The results of phylogenetic comparative analyses imply the absence of epidemic penicillin-insusceptible strains, and several genetic lineages of penicillin-insusceptible strains have been independently emerging through the accumulation of mutations in their pbp genes, especially in pbp2x.
日本船桥市立医疗中心及其他医院近期出现了对青霉素最低抑菌浓度(MIC)升高的B族链球菌分离株,这促使人们对这些菌株的青霉素结合蛋白(PBP)与青霉素敏感菌株的PBP进行比较分析,青霉素敏感菌株包括1976年至1988年分离出的4株新生儿侵袭性菌株以及2株近期分离株。青霉素敏感菌株的PBP序列高度保守,与分离日期无关。在6株对青霉素敏感性降低的菌株(青霉素MIC为0.25至0.5μg/ml)中,R1、R2、R5和R6菌株共有一组独特的5个氨基酸替换,包括PBP 2X中与(402)SSN(404)基序相邻的V405A以及PBP 2B中的一个替换。其余两株菌株R3和R4共有几个替换,包括PBP 2X中与(552)KSG(554)基序相邻的Q557E,此外还有PBP 2B中的替换,这些替换在青霉素不敏感菌株中很常见。青霉素MIC为1μg/ml的R7和R8菌株共有一组独特的8个氨基酸替换(PBP 2X中有2个;PBP 2B中有2个,包括与(614)KTG(616)基序相邻的G613R;PBP 1A中有3个;PBP 2A中有1个),PBP 2X中的Q557E替换在R3和R4中也有。在一些PBP中,包括青霉素不敏感菌株的PBP 2X,Bocillin FL的结合减少或未检测到,但在这些菌株中未发现pbp2x转录水平有显著降低。系统发育比较分析结果表明不存在流行的青霉素不敏感菌株,并且几种青霉素不敏感菌株的遗传谱系是通过其pbp基因,特别是pbp2x中突变的积累而独立出现的。