Literature DB >> 9695909

Starvation recovery of Staphylococcus aureus 8325-4.

Mark O Clements, Simon J Foster.   

Abstract

Nutrient limitation of Staphylococcus aureus induces a starvation-survival state which enables it to survive until sufficient nutrients become available to support growth. The response of starved S. aureus cells to nutritional upshift was analysed to characterize the recovery mechanism which results in the resumption of rapid growth. S. aureus 8325-4 starved for 7 d in a chemically defined medium limited for glucose was able to resume growth upon the addition of complex medium (brain heart infusion broth) or a mixture of amino acids and glucose. The addition of either glucose or amino acids alone did not lead to recovery of cells. Prior to the first cell division event, a lag period of about 120-150 min was observed, the duration of which was independent of the length of starvation survival. During this lag period, RNA synthesis increased immediately upon the addition of nutrients whilst protein synthesis was delayed by approximately 5 min. Cells rapidly enlarged within 30 min of recovery, and initiation of chromosome replication could be detected after 90 min. Changes in the profile of proteins expressed during the recovery period revealed that several starvation-specific proteins were down-regulated within 30 min, whilst other proteins were common to both starvation and recovery. Two proteins were identified which were only transiently expressed during the first 60 min of recovery. Protein synthesis could be detected during recovery even if the cells had been treated with the RNA synthesis inhibitor rifampicin for 30 min prior to the addition of recovery nutrients, demonstrating that several proteins are translated from long-lived mRNA transcripts present in starved cells.

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Year:  1998        PMID: 9695909     DOI: 10.1099/00221287-144-7-1755

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  9 in total

1.  Characterization of the major superoxide dismutase of Staphylococcus aureus and its role in starvation survival, stress resistance, and pathogenicity.

Authors:  M O Clements; S P Watson; S J Foster
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Quantification of expression of Staphylococcus epidermidis housekeeping genes with Taqman quantitative PCR during in vitro growth and under different conditions.

Authors:  S J Vandecasteele; W E Peetermans; R Merckx; J Van Eldere
Journal:  J Bacteriol       Date:  2001-12       Impact factor: 3.490

3.  Catalase (KatA) and alkyl hydroperoxide reductase (AhpC) have compensatory roles in peroxide stress resistance and are required for survival, persistence, and nasal colonization in Staphylococcus aureus.

Authors:  Kate Cosgrove; Graham Coutts; Ing-Marie Jonsson; Andrej Tarkowski; John F Kokai-Kun; James J Mond; Simon J Foster
Journal:  J Bacteriol       Date:  2006-11-17       Impact factor: 3.490

4.  CtaA of Staphylococcus aureus is required for starvation survival, recovery, and cytochrome biosynthesis.

Authors:  M O Clements; S P Watson; R K Poole; S J Foster
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

5.  Fluorescent methods to study DNA, RNA, proteins and cytoplasmic membrane polarization in the pentachlorophenol-mineralizing bacterium Sphingomonas sp. UG30 during nutrient starvation in water.

Authors:  T J Denich; L A Beaudette; H Lee; J T Trevors
Journal:  J Fluoresc       Date:  2005-03       Impact factor: 2.217

Review 6.  Staphylococcus aureus pathogenesis in diverse host environments.

Authors:  Divya Balasubramanian; Lamia Harper; Bo Shopsin; Victor J Torres
Journal:  Pathog Dis       Date:  2017-01-01       Impact factor: 3.166

7.  The Staphylococcus aureus alternative sigma factor sigmaB controls the environmental stress response but not starvation survival or pathogenicity in a mouse abscess model.

Authors:  P F Chan; S J Foster; E Ingham; M O Clements
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

8.  Metabolic activity of Staphylococcus epidermidis is high during initial and low during late experimental foreign-body infection.

Authors:  Stefaan Johan Vandecasteele; Willy Eduard Peetermans; An Carbonez; Johan Van Eldere
Journal:  J Bacteriol       Date:  2004-04       Impact factor: 3.490

Review 9.  Current Perspectives on Viable but Non-culturable State in Foodborne Pathogens.

Authors:  Xihong Zhao; Junliang Zhong; Caijiao Wei; Chii-Wann Lin; Tian Ding
Journal:  Front Microbiol       Date:  2017-04-04       Impact factor: 5.640

  9 in total

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