[Morphological changes in penicillin-resistant Streptococcus pneumoniae and beta-lactamase-nonproducing, ampicillin-resistant Haemophilus influenzae after exposure to oral antibacterial agents].

The Japanese journal of antibiotics Pub Date : 2012-10-01
Naoko Chiba, Miyuki Morozumi, Kimiko Ubukata
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Abstract

Morphological changes in penicillin-resistant Streptococcus pneumoniae (PRSP) and beta-lactamase-nonproducing, ampicillin-resistant Haemophilus influenzae (BLNAR) after exposure to oral antibacterial agents could be observed over time under a phase-contrast microscope. Morphological changes in BLNAR were also observed using a scanning electron microscope. The organisms used in this study were ME19F strain identified as genotypic(g) gPRSP (serotype: 19F) and JPH002 strain identified as gBLNAR (serotype: b). The antibacterial agents used were amoxicillin (AMPC), cefditoren (CDTR), tebipenem (TBPM), and tosufloxacin (TFLX). The concentration of each antibacterial agent to which the bacteria were exposed was set at the blood level one hour after Cmax when administered to children at the usual dose. Bacteriolysis of gPRSP cells started after exposure of only 20minutes to TBPM, and 90% of the cells were lysed within 2 hours. A high bactericidal action of TBPM on gPRSP was supported by these findings. When gBLNAR was exposed to AMPC and TBPM, lysis from spheroplasts and cells with vacuoles were sometimes observed. In contrast, after gBLNAR was exposed to CDTR, lysis occurred after marked filamentation in the cells, but after exposure to TFLX, cells deduced to be killed after mild filamentation without lysis. Time-dependent morphological changes that reflect the differences in bactericidal activity and PBP affinity among beta-lactams provide beneficial information to select antibacterial agents.

[接触口服抗菌剂后耐青霉素肺炎链球菌和不产生β -内酰胺酶、耐氨苄西林流感嗜血杆菌的形态学变化]。
在相对比显微镜下,可以观察到暴露于口服抗菌药物后,耐青霉素肺炎链球菌(PRSP)和不产生β -内酰胺酶的耐氨苄西林流感嗜血杆菌(BLNAR)的形态学变化。扫描电镜下观察BLNAR的形态学变化。本研究使用的微生物为基因型(g)的ME19F菌株gPRSP(血清型:19F)和基因型为gBLNAR的JPH002菌株(血清型:b)。使用的抗菌药物为阿莫西林(AMPC)、头孢地托伦(CDTR)、替比培南(TBPM)和托苏沙星(TFLX)。这些细菌接触到的每一种抗菌剂的浓度被设定为Cmax后一小时的血液水平,以常规剂量给孩子服用。gPRSP细胞仅在TBPM作用20分钟后开始细菌溶解,90%的细胞在2小时内被溶解。这些发现支持了TBPM对gPRSP的高杀菌作用。当gBLNAR暴露于AMPC和TBPM时,有时会观察到球质体和液泡细胞的裂解。相比之下,gBLNAR暴露于CDTR后,细胞在明显的丝化后发生裂解,但暴露于TFLX后,细胞在轻度丝化后未发生裂解而被杀死。随时间变化的形态变化反映了β -内酰胺之间的杀菌活性和PBP亲和力的差异,为选择抗菌剂提供了有益的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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