Acid stress management by Cronobacter sakazakii

Typeset version

 

TY  - JOUR
  - Alvarez-Ordonez, A,Cummins, C,Deasy, T,Clifford, T,Begley, M,Hill, C
  - 2014
  - May
  - International Journal of Food Microbiology
  - Acid stress management by Cronobacter sakazakii
  - Validated
  - Altmetric: 1 ()
  - C. sakazakii Acid stress Powdered infant formula Transposon mutagenesis ompR Acid tolerance response POWDERED INFANT FORMULA ENTERICA SEROVAR TYPHIMURIUM RNA WOBBLE POSITIONS ESCHERICHIA-COLI ENTEROBACTER-SAKAZAKII TOLERANCE RESPONSE BIOFILM FORMATION PRETERM INFANTS ORGANIC-ACIDS SPP.
  - 178
  - 21
  - 28
  - Cronobacter sakazakii is a foodborne pathogenic microorganism associated with sporadic cases of neonatal meningitis, necrotising enterocolitis, septicaemia, bloody diarrhoea and brain abscesses acquired through the consumption of contaminated powdered infant formula (PIF). This study aimed to investigate the growth of C sakazakii DPC6529, a particularly stress tolerant clinical isolate, in acidified laboratory media and PIF. The possibility of a stationary-phase acid tolerance response (ATR) was also investigated. C. sakazakii DPC6529 grew in LB broth acidified to pH 4.2 with hydrochloric acid (HCl) and was capable of relatively fast growth in PIF acidified to pH 5.0 with HCI, representing the stomach pH reported for newborns and infants. Moreover, bacterial growth in LB broth supplemented with 1% (w/v) glucose gave rise to a stationary-phase ATR which resulted in enhanced survival against a subsequent acid challenge at pH 3.0.A transposon mutagenesis approach was used to shed light on some of the molecular mechanisms involved in the response C sakazakii DPC6529 to normally lethal acid exposures. The data suggests that repairing damage in proteins and nucleic acids, posttranscriptional modification of tRNA molecules and maintenance of the integrity of the cellular envelope are key processes in the defence against acid stress. Clones carrying transposon insertions in genes encoding the envelope stress response regulators CpxR and OmpR were identified as acid-sensitive mutants. Further analyses of the ompR defective mutant and its complemented counterpart evidenced that OmpR is a key player in the response of C. sakazakii to acid stress, although it was not essential to mount an active stationary-phase ATR, at least under the tested conditions. The ability of C sakazakii DPC6529 to grow in acid environments and to develop an adaptive stationary-phase ATR may allow for its survival or even proliferation within the infant gastrointestinal tract after consumption of contaminated milk formulae. (c) 2014 Elsevier B.V. All rights reserved.
  - 10.1016/j.ijfoodmicro.2014.03.001
DA  - 2014/05
ER  - 
@article{V271356011,
   = {Alvarez-Ordonez,  A and Cummins,  C and Deasy,  T and Clifford,  T and Begley,  M and Hill,  C },
   = {2014},
   = {May},
   = {International Journal of Food Microbiology},
   = {Acid stress management by Cronobacter sakazakii},
   = {Validated},
   = {Altmetric: 1 ()},
   = {C. sakazakii Acid stress Powdered infant formula Transposon mutagenesis ompR Acid tolerance response POWDERED INFANT FORMULA ENTERICA SEROVAR TYPHIMURIUM RNA WOBBLE POSITIONS ESCHERICHIA-COLI ENTEROBACTER-SAKAZAKII TOLERANCE RESPONSE BIOFILM FORMATION PRETERM INFANTS ORGANIC-ACIDS SPP.},
   = {178},
  pages = {21--28},
   = {{Cronobacter sakazakii is a foodborne pathogenic microorganism associated with sporadic cases of neonatal meningitis, necrotising enterocolitis, septicaemia, bloody diarrhoea and brain abscesses acquired through the consumption of contaminated powdered infant formula (PIF). This study aimed to investigate the growth of C sakazakii DPC6529, a particularly stress tolerant clinical isolate, in acidified laboratory media and PIF. The possibility of a stationary-phase acid tolerance response (ATR) was also investigated. C. sakazakii DPC6529 grew in LB broth acidified to pH 4.2 with hydrochloric acid (HCl) and was capable of relatively fast growth in PIF acidified to pH 5.0 with HCI, representing the stomach pH reported for newborns and infants. Moreover, bacterial growth in LB broth supplemented with 1% (w/v) glucose gave rise to a stationary-phase ATR which resulted in enhanced survival against a subsequent acid challenge at pH 3.0.A transposon mutagenesis approach was used to shed light on some of the molecular mechanisms involved in the response C sakazakii DPC6529 to normally lethal acid exposures. The data suggests that repairing damage in proteins and nucleic acids, posttranscriptional modification of tRNA molecules and maintenance of the integrity of the cellular envelope are key processes in the defence against acid stress. Clones carrying transposon insertions in genes encoding the envelope stress response regulators CpxR and OmpR were identified as acid-sensitive mutants. Further analyses of the ompR defective mutant and its complemented counterpart evidenced that OmpR is a key player in the response of C. sakazakii to acid stress, although it was not essential to mount an active stationary-phase ATR, at least under the tested conditions. The ability of C sakazakii DPC6529 to grow in acid environments and to develop an adaptive stationary-phase ATR may allow for its survival or even proliferation within the infant gastrointestinal tract after consumption of contaminated milk formulae. (c) 2014 Elsevier B.V. All rights reserved.}},
   = {10.1016/j.ijfoodmicro.2014.03.001},
  source = {IRIS}
}
AUTHORSAlvarez-Ordonez, A,Cummins, C,Deasy, T,Clifford, T,Begley, M,Hill, C
YEAR2014
MONTHMay
JOURNAL_CODEInternational Journal of Food Microbiology
TITLEAcid stress management by Cronobacter sakazakii
STATUSValidated
TIMES_CITEDAltmetric: 1 ()
SEARCH_KEYWORDC. sakazakii Acid stress Powdered infant formula Transposon mutagenesis ompR Acid tolerance response POWDERED INFANT FORMULA ENTERICA SEROVAR TYPHIMURIUM RNA WOBBLE POSITIONS ESCHERICHIA-COLI ENTEROBACTER-SAKAZAKII TOLERANCE RESPONSE BIOFILM FORMATION PRETERM INFANTS ORGANIC-ACIDS SPP.
VOLUME178
ISSUE
START_PAGE21
END_PAGE28
ABSTRACTCronobacter sakazakii is a foodborne pathogenic microorganism associated with sporadic cases of neonatal meningitis, necrotising enterocolitis, septicaemia, bloody diarrhoea and brain abscesses acquired through the consumption of contaminated powdered infant formula (PIF). This study aimed to investigate the growth of C sakazakii DPC6529, a particularly stress tolerant clinical isolate, in acidified laboratory media and PIF. The possibility of a stationary-phase acid tolerance response (ATR) was also investigated. C. sakazakii DPC6529 grew in LB broth acidified to pH 4.2 with hydrochloric acid (HCl) and was capable of relatively fast growth in PIF acidified to pH 5.0 with HCI, representing the stomach pH reported for newborns and infants. Moreover, bacterial growth in LB broth supplemented with 1% (w/v) glucose gave rise to a stationary-phase ATR which resulted in enhanced survival against a subsequent acid challenge at pH 3.0.A transposon mutagenesis approach was used to shed light on some of the molecular mechanisms involved in the response C sakazakii DPC6529 to normally lethal acid exposures. The data suggests that repairing damage in proteins and nucleic acids, posttranscriptional modification of tRNA molecules and maintenance of the integrity of the cellular envelope are key processes in the defence against acid stress. Clones carrying transposon insertions in genes encoding the envelope stress response regulators CpxR and OmpR were identified as acid-sensitive mutants. Further analyses of the ompR defective mutant and its complemented counterpart evidenced that OmpR is a key player in the response of C. sakazakii to acid stress, although it was not essential to mount an active stationary-phase ATR, at least under the tested conditions. The ability of C sakazakii DPC6529 to grow in acid environments and to develop an adaptive stationary-phase ATR may allow for its survival or even proliferation within the infant gastrointestinal tract after consumption of contaminated milk formulae. (c) 2014 Elsevier B.V. All rights reserved.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINK10.1016/j.ijfoodmicro.2014.03.001
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