Survival of Vibrio cholerae in nutrient-poor environments is associated with a novel "persister" phenotype

In response to antibiotic and/or environmental stress, some species of bacteria shift to a "persister" phenotype. Although toxigenic Vibrio cholerae, responsible for the disease cholera, can be found in nutrient-poor aquatic environments in endemic areas, the underlying mechanism(s) by whi...

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Veröffentlicht in:PloS one 2012-09, Vol.7 (9), p.e45187
Hauptverfasser: Jubair, Mohamma, Morris, Jr, J Glenn, Ali, Afsar
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Ali, Afsar
description In response to antibiotic and/or environmental stress, some species of bacteria shift to a "persister" phenotype. Although toxigenic Vibrio cholerae, responsible for the disease cholera, can be found in nutrient-poor aquatic environments in endemic areas, the underlying mechanism(s) by which culturable cells persist in these environmental reservoirs is largely unknown. Here we report that introduction of V. cholerae into a nutrient-poor filter sterilized lake water (FSLW) microcosm promoted a shift to what we have defined as a "persister" phenotype (PP) which was culturable for >700 days. Direct transfer of PP of V. cholerae from original microcosms to freshly prepared FSLW resulted in the same pattern of persistence seen in the original microcosms. Scanning electron microscopy of cells persisting for over 700 days demonstrated cell morphologies that were very small in size, with a high degree of aggregation associated with flagella emanating from all aspects of the cell. V. cholerae PP cells reverted to a typical V. cholerae morphology when transferred to nutrient-rich L- broth. Cell-free supernatants obtained from microcosms at 24 hours, 180 days, and 700 days all showed >2-fold increase in CAI-1 signaling molecules, consistent with quorum sensing activity, as has been described for Pseudomonas aeruginosa persister cells. Chitin and phosphate promoted cell growth. Our data suggest that nutrient stress can select a V. cholerae persister phenotype in environmental reservoirs, with these strains then seeding subsequent cholera epidemics in response to chitin and phosphate availability.
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Although toxigenic Vibrio cholerae, responsible for the disease cholera, can be found in nutrient-poor aquatic environments in endemic areas, the underlying mechanism(s) by which culturable cells persist in these environmental reservoirs is largely unknown. Here we report that introduction of V. cholerae into a nutrient-poor filter sterilized lake water (FSLW) microcosm promoted a shift to what we have defined as a "persister" phenotype (PP) which was culturable for &gt;700 days. Direct transfer of PP of V. cholerae from original microcosms to freshly prepared FSLW resulted in the same pattern of persistence seen in the original microcosms. Scanning electron microscopy of cells persisting for over 700 days demonstrated cell morphologies that were very small in size, with a high degree of aggregation associated with flagella emanating from all aspects of the cell. V. cholerae PP cells reverted to a typical V. cholerae morphology when transferred to nutrient-rich L- broth. Cell-free supernatants obtained from microcosms at 24 hours, 180 days, and 700 days all showed &gt;2-fold increase in CAI-1 signaling molecules, consistent with quorum sensing activity, as has been described for Pseudomonas aeruginosa persister cells. Chitin and phosphate promoted cell growth. 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Although toxigenic Vibrio cholerae, responsible for the disease cholera, can be found in nutrient-poor aquatic environments in endemic areas, the underlying mechanism(s) by which culturable cells persist in these environmental reservoirs is largely unknown. Here we report that introduction of V. cholerae into a nutrient-poor filter sterilized lake water (FSLW) microcosm promoted a shift to what we have defined as a "persister" phenotype (PP) which was culturable for &gt;700 days. Direct transfer of PP of V. cholerae from original microcosms to freshly prepared FSLW resulted in the same pattern of persistence seen in the original microcosms. Scanning electron microscopy of cells persisting for over 700 days demonstrated cell morphologies that were very small in size, with a high degree of aggregation associated with flagella emanating from all aspects of the cell. V. cholerae PP cells reverted to a typical V. cholerae morphology when transferred to nutrient-rich L- broth. Cell-free supernatants obtained from microcosms at 24 hours, 180 days, and 700 days all showed &gt;2-fold increase in CAI-1 signaling molecules, consistent with quorum sensing activity, as has been described for Pseudomonas aeruginosa persister cells. Chitin and phosphate promoted cell growth. Our data suggest that nutrient stress can select a V. cholerae persister phenotype in environmental reservoirs, with these strains then seeding subsequent cholera epidemics in response to chitin and phosphate availability.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23028836</pmid><doi>10.1371/journal.pone.0045187</doi><tpages>e45187</tpages><oa>free_for_read</oa></addata></record>
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subjects Adaptation, Physiological
Antibiotics
Aquatic ecosystems
Aquatic environment
Bacteria
Biofilms
Biology
Chitin
Chitin - pharmacology
Cholera
Culture Media
Cytology
Disease Reservoirs - microbiology
Electron microscopy
Environmental aspects
Environmental stress
Epidemics
Flagella
Fresh Water - microbiology
Genotype & phenotype
Infections
Influence
Medicine
Microbial Viability - drug effects
Microcosms
Microscopy, Electron, Scanning
Morphology
Nutrients
Pathogens
Phenotype
Phosphates
Phosphates - pharmacology
Physiological aspects
Pseudomonas aeruginosa
Public health
Quorum Sensing - drug effects
Quorum Sensing - physiology
Reservoirs
Scanning electron microscopy
Seeding
Signaling
Stress, Physiological
Survival
Vibrio cholerae
Vibrio cholerae - drug effects
Vibrio cholerae - physiology
Vibrio cholerae - ultrastructure
Water purification
Water-borne diseases
Waterborne diseases
title Survival of Vibrio cholerae in nutrient-poor environments is associated with a novel "persister" phenotype
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