Literature DB >> 2480078

Mechanism of penicillin killing in the absence of bacterial lysis.

T D McDowell1, K E Reed.   

Abstract

Exposure of group A streptococci (a nonlytic-death phenotype) to benzylpenicillin (penicillin G) produced a dose-dependent, rapid, and extensive hydrolysis of total cellular RNA, with the subsequent loss of hydrolysis products from the cell. This loss of RNA correlated well with loss of viability and was not accompanied by solubilization of the cell wall or comparable losses of either protein or DNA. Simultaneous treatment with penicillin G and either chloramphenicol or rifampin resulted in reduced levels of killing and the complete inhibition of RNA loss. These findings define a new mechanism of penicillin G-induced killing in the absence of cell wall disruption and suggest a basis for drug-induced antagonism of penicillin G-mediated nonlytic death.

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Year:  1989        PMID: 2480078      PMCID: PMC172737          DOI: 10.1128/AAC.33.10.1680

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  23 in total

1.  Induction of bacterial lysis by penicillin.

Authors:  L S PRESTIDGE; A B PARDEE
Journal:  J Bacteriol       Date:  1957-07       Impact factor: 3.490

2.  Studies on antibiotic synergism and antagonism; the interference of chloramphenicol with the action of penicillin.

Authors:  E JAWETZ; J B GUNNISON; R S SPECK; V R COLEMAN
Journal:  AMA Arch Intern Med       Date:  1951-03

3.  Growth of several cariogenic strains of oral streptococci in a chemically defined medium.

Authors:  B Terleckyj; N P Willett; G D Shockman
Journal:  Infect Immun       Date:  1975-04       Impact factor: 3.441

Review 4.  The mechanism of the irreversible antimicrobial effects of penicillins: how the beta-lactam antibiotics kill and lyse bacteria.

Authors:  A Tomasz
Journal:  Annu Rev Microbiol       Date:  1979       Impact factor: 15.500

5.  Balanced macromolecular biosynthesis in "protoplasts" of Streptococcus faecalis.

Authors:  G S Roth; G D Shockman; L Daneo-Moore
Journal:  J Bacteriol       Date:  1971-03       Impact factor: 3.490

6.  Talk-back regulation: a regulatory response to the inhibitions of cell surface growth.

Authors:  T D McDowell; W McCurdy; K E Reed
Journal:  Microbios       Date:  1989

7.  Unbalanced growth and macromolecular synthesis in Streptococcus mutans FA-1.

Authors:  S J Mattingly; J R Dipersio; M L Higgins; G D Shockman
Journal:  Infect Immun       Date:  1976-03       Impact factor: 3.441

8.  Conservation of cell wall peptidoglycan by strains of Streptococcus mutans and Streptococcus sanguis.

Authors:  M Mychajlonka; T D McDowell; G D Shockman
Journal:  Infect Immun       Date:  1980-04       Impact factor: 3.441

9.  Penicillin-resistant and penicillin-tolerant mutants of group A Streptococci.

Authors:  L Gutmann; A Tomasz
Journal:  Antimicrob Agents Chemother       Date:  1982-07       Impact factor: 5.191

10.  Escherichia coli mutants tolerant to beta-lactam antibiotics.

Authors:  K Kitano; A Tomasz
Journal:  J Bacteriol       Date:  1979-12       Impact factor: 3.490

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  5 in total

1.  Effects of penicillin, ceftriaxone, and doxycycline on morphology of Borrelia burgdorferi.

Authors:  A Kersten; C Poitschek; S Rauch; E Aberer
Journal:  Antimicrob Agents Chemother       Date:  1995-05       Impact factor: 5.191

Review 2.  The development of beta-lactam antibiotics in response to the evolution of beta-lactamases.

Authors:  S Y Essack
Journal:  Pharm Res       Date:  2001-10       Impact factor: 4.200

3.  Localization of penicillin-binding proteins to the splitting system of Staphylococcus aureus septa by using a mercury-penicillin V derivative.

Authors:  T R Paul; A Venter; L C Blaszczak; T R Parr; H Labischinski; T J Beveridge
Journal:  J Bacteriol       Date:  1995-07       Impact factor: 3.490

4.  Effects of medium composition on penicillin-induced hydrolysis and loss of RNA and culture turbidity in group A streptococci.

Authors:  T D McDowell; K E Reed
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

5.  The ClpX chaperone controls autolytic splitting of Staphylococcus aureus daughter cells, but is bypassed by β-lactam antibiotics or inhibitors of WTA biosynthesis.

Authors:  Camilla Jensen; Kristoffer T Bæk; Clement Gallay; Ida Thalsø-Madsen; Lijuan Xu; Ambre Jousselin; Fernando Ruiz Torrubia; Wilhelm Paulander; Ana R Pereira; Jan-Willem Veening; Mariana G Pinho; Dorte Frees
Journal:  PLoS Pathog       Date:  2019-09-13       Impact factor: 6.823

  5 in total

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