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PMID: 7025749 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

pH-dependent penicillin tolerance of group B streptococci.

Antimicrobial agents and chemotherapy ·Vol. 20 ·No. 1 ·1981-07-00 ·Pages 128-35

Horne D, Tomasz A

Abstract

Group B streptococci lose viability without apparent lysis during treatment with beta-lactam antibiotics and vancomycin. Rapid loss of viability was observed in early-exponential-phase cultures. Cultures in the mid-exponential growth phase exhibited various degrees of resistance to the bactericidal effect of the antibiotics, whereas their susceptibilities to the growth-inhibitory effect remained unchanged. This growth-phase-dependent tolerance was caused by the gradual increase in acidity of the cultures as the cell concentration increased. Retitration of the pH to neutrality made the formerly tolerant bacteria again fully susceptible to the killing effect of penicillin. Conversely, lowering the pH value of the medium resulted in antibiotic tolerance throughout culture growth. The penicillin-binding proteins of whole bacteria and their labeling pattern were found to be independent of culture pH. It is suggested that the mechanism of Ph-dependent tolerance is indirect and may be mediated by an autolysin. The tolerance of group B streptococci for penicillin could be clinically relevant in view of the relatively low pH values known to prevail in the natural host environments colonized by these bacteria.

MeSH Terms
Adult Culture Media Humans Hydrogen-Ion Concentration Infant Penicillin G/pharmacology Penicillin Resistance Streptococcal Infections/microbiology Streptococcus agalactiae/drug effects,growth & development Vancomycin/pharmacology
Chemicals
Culture Media Vancomycin Penicillin G
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Horne D
Tomasz A
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25 references, click to expand
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
1981-07-00
Pages
128-35
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC181644
Subset
IM
Grants
NIAID NIH HHS · AI 16170 · United States
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