Literature DB >> 1444406

Physiological studies of chloramine resistance developed by Klebsiella pneumoniae under low-nutrient growth conditions.

M H Stewart1, B H Olson.   

Abstract

This study investigated the physiological mechanisms of resistance to chloramines developed by Klebsiella pneumoniae grown in a nutrient-limited environment. Growth under these conditions resulted in cells that were smaller than cells grown under high-nutrient conditions and extensively aggregated. Cellular aggregates ranged from 10 to more than 10,000 cells per aggregate, with a mean population aggregate size of 90 cells. This aggregation may have been facilitated by the presence of extracellular polymer material. By using glucose as a reference of capsule content, it was determined that growth under low-nutrient conditions produced cells with 8 x 10(-14) to 41 x 10(-14) g of carbohydrate per cell, with a mean +/- standard deviation of 27 x 10(-14) +/- 16 x 10(-14) g of carbohydrate per cell. In comparison, growth under high-nutrient conditions resulted in 2.7 x 10(-14) to 5.9 x 10(-14) g of carbohydrate per cell, with a mean and standard deviation of 4.3 x 10(-14) +/- 1.2 x 10(-14) g of carbohydrate per cell. Cell wall and cell membrane lipids also varied with growth conditions. The ratio of saturated to unsaturated fatty acids in cells grown under low-nutrient conditions was approximately five times greater than that in cells grown under high-nutrient conditions, suggesting possible differences in membrane permeability. An analysis of sulfhydryl (-SH) groups revealed no quantitative difference with respect to growth conditions. However, upon exposure to chloramines, only 33% of the -SH groups of cells grown under low-nutrient conditions were oxidized, compared with 80% oxidization of -SH groups in cells grown under high-nutrient conditions. The reduced effectiveness of chloramine oxidization of -SH groups in cells grown under low-nutrient conditions may be due to restricted penetration of chloramines into the cells, conformational changes of enzymes, or a combination of both factors. The results of this study suggest that chloramine resistance developed under low-nutrient growth conditions may be a function of multiple physiological factors, including cellular aggregation and protection of sulfhydryl groups within the cell.

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Year:  1992        PMID: 1444406      PMCID: PMC183027          DOI: 10.1128/aem.58.9.2918-2927.1992

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  27 in total

1.  Initial phases of starvation and activity of bacteria at surfaces.

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2.  Starvation and nutrient resuscitation of Klebsiella pneumoniae isolated from oil well waters.

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3.  Starvation-induced cross protection against heat or H2O2 challenge in Escherichia coli.

Authors:  D E Jenkins; J E Schultz; A Matin
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

4.  Inactivation of biofilm bacteria.

Authors:  M W LeChevallier; C D Cawthon; R G Lee
Journal:  Appl Environ Microbiol       Date:  1988-10       Impact factor: 4.792

5.  N-(2-Oxoacyl)amino acids and nitriles as final products of dipeptide chlorination mediated by the myeloperoxidase/H2O2/Cl- system.

Authors:  T Stelmaszyńska; J M Zgliczynski
Journal:  Eur J Biochem       Date:  1978-12-01

6.  Influence of unsaturated fatty acid membrane component on sensitivity of an Escherichia coli fatty acid auxotroph to conditions of nutrient depletion.

Authors:  E M Massa; A López Vińals; R N Farías
Journal:  Appl Environ Microbiol       Date:  1988-08       Impact factor: 4.792

7.  Differential regulation by cyclic AMP of starvation protein synthesis in Escherichia coli.

Authors:  J E Schultz; G I Latter; A Matin
Journal:  J Bacteriol       Date:  1988-09       Impact factor: 3.490

8.  Outer membrane of Salmonella typhimurium. Transmembrane diffusion of some hydrophobic substances.

Authors:  H Nikaido
Journal:  Biochim Biophys Acta       Date:  1976-04-16

9.  Membrane fatty acid and virulence changes in the viable but nonculturable state of Vibrio vulnificus.

Authors:  K Linder; J D Oliver
Journal:  Appl Environ Microbiol       Date:  1989-11       Impact factor: 4.792

10.  Impact of growth conditions on resistance of Klebsiella pneumoniae to chloramines.

Authors:  M H Stewart; B H Olson
Journal:  Appl Environ Microbiol       Date:  1992-08       Impact factor: 4.792

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  7 in total

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2.  Starvation-Induced Stress Resistance in Lactococcus lactis subsp. lactis IL1403.

Authors:  A Hartke; S Bouche; X Gansel; P Boutibonnes; Y Auffray
Journal:  Appl Environ Microbiol       Date:  1994-09       Impact factor: 4.792

3.  Chlorine, chloramine, chlorine dioxide, and ozone susceptibility of Mycobacterium avium.

Authors:  R H Taylor; J O Falkinham; C D Norton; M W LeChevallier
Journal:  Appl Environ Microbiol       Date:  2000-04       Impact factor: 4.792

4.  Escherichia coli resistance to chlorine and glutathione synthesis in response to oxygenation and starvation.

Authors:  S Saby; P Leroy; J C Block
Journal:  Appl Environ Microbiol       Date:  1999-12       Impact factor: 4.792

5.  Chlorine disinfection of atypical mycobacteria isolated from a water distribution system.

Authors:  Corinne Le Dantec; Jean-Pierre Duguet; Antoine Montiel; Nadine Dumoutier; Sylvie Dubrou; Véronique Vincent
Journal:  Appl Environ Microbiol       Date:  2002-03       Impact factor: 4.792

6.  Effects of starvation on physiological activity and chlorine disinfection resistance in Escherichia coli O157:H7.

Authors:  J T Lisle; S C Broadaway; A M Prescott; B H Pyle; C Fricker; G A McFeters
Journal:  Appl Environ Microbiol       Date:  1998-12       Impact factor: 4.792

Review 7.  Antiseptics and disinfectants: activity, action, and resistance.

Authors:  G McDonnell; A D Russell
Journal:  Clin Microbiol Rev       Date:  1999-01       Impact factor: 26.132

  7 in total

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