The htrA ( degP ) Gene of Listeria monocytogenes 10403S Is Essential for Optimal Growth under Stress Conditions
Open Access
- 1 April 2004
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 70 (4) , 1935-1943
- https://doi.org/10.1128/aem.70.4.1935-1943.2004
Abstract
This report describes a mutant of Listeria monocytogenes strain 10403S (serotype 1/2a) with a defective response to conditions of high osmolarity, an environment that L. monocytogenes encounters in some ready-to-eat foods. A library of L. monocytogenes clones mutagenized with Tn 917 was generated and scored for sensitivity to 4% NaCl in order to identify genes responsible for growth or survival in elevated-NaCl environments. One of the L. monocytogenes Tn 917 mutants, designated strain OSM1, was selected, and the gene interrupted by the transposon was sequenced. A BLAST search with the putative translated amino acid sequence indicated that the interrupted gene product was a homolog of htrA ( degP ), a gene coding for a serine protease identified as a stress response protein in several gram-positive and gram-negative bacteria. An htrA deletion strain, strain LDW1, was constructed, and the salt-sensitive phenotype of this strain was complemented by introduction of a plasmid carrying the wild-type htrA gene, demonstrating that htrA is necessary for optimal growth under conditions of osmotic stress. Additionally, strain LDW1 was tested for its response to temperature and H 2 O 2 stresses. The results of these growth assays indicated that strain LDW1 grew at a lower rate than the wild-type strain at 44°C but at a rate similar to that of the wild-type strain when incubated at 4°C. In addition, strain LDW1 was significantly more sensitive to a 52°C heat shock than the wild-type strain. Strain LDW1 was also defective in its response to H 2 O 2 challenge at 37°C, since 100 or 150 μg of H 2 O 2 was more inhibitory for the growth of strain LDW1 than for that of the parent strain. The stress response phenotype observed for strain LDW1 is similar to that observed for other HtrA − organisms, which suggests that L. monocytogenes HtrA may play a role in degrading misfolded proteins that accumulate under stress conditions.Keywords
This publication has 40 references indexed in Scilit:
- Identification and disruption ofbtlA, a locus involved in bile tolerance and general stress resistance inListeria monocytogenesFEMS Microbiology Letters, 2003
- PDZ Domains Facilitate Binding of High Temperature Requirement Protease A (HtrA) and Tail-specific Protease (Tsp) to Heterologous Substrates through Recognition of the Small Stable RNA A (ssrA)-encoded PeptideJournal of Biological Chemistry, 2002
- Role of the htrA Gene in Klebsiella pneumoniae VirulenceInfection and Immunity, 2002
- Identification of Proteins Involved in the Heat Stress Response of Bacillus cereus ATCC 14579Applied and Environmental Microbiology, 2002
- Starvation and osmotic stress induced multiresistancesInternational Journal of Food Microbiology, 2000
- Selective degradation of unfolded proteins by the self-compartmentalizing HtrA protease, a periplasmic heat shock protein in Escherichia coliJournal of Molecular Biology, 1999
- Food-Related Illness and Death in the United StatesEmerging Infectious Diseases, 1999
- Effects of pH or aw stress on growth of Listeria monocytogenesInternational Journal of Food Microbiology, 1998
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- Physiological studies on the growth and utilization of sugars by Listeria speciesCanadian Journal of Microbiology, 1989