TY - JOUR
T1 - Characterization of Escherichia coli from raw poultry in Belgium and impact on the detection of Campylobacter jejuni using Bolton broth
AU - Jasson, Vicky
AU - Sampers, Imca
AU - Botteldoorn, Nadine
AU - López-Gálvez, Francisco
AU - Baert, Leen
AU - Denayer, Sarah
AU - Rajkovic, Andreja
AU - Habib, Ihab
AU - De Zutter, Lieven
AU - Debevere, Johan
AU - Uyttendaele, Mieke
PY - 2009/11/15
Y1 - 2009/11/15
N2 - A comparative study examining Bolton broth and Preston broth for enrichment and reliable detection of Campylobacter jejuni (both healthy and freeze stressed cells) was performed. Tested as pure cultures, Bolton broth enabled faster resuscitation and growth of C. jejuni compared to Preston broth. When C. jejuni was co-incubated with extended-spectrum-beta-lactamase (ESBL) producing Escherichia coli isolated from Belgian poultry meat preparations, the latter dominated in the Bolton enrichment broth and crowded the mCCDA plates. This resulted in the inability to recover C. jejuni by ISO 10272-1:2006 standard method. Preston broth did not support the growth of the ESBL E. coli isolates, but showed longer detection time of C. jejuni compared to Bolton broth. The use of the same antibiotic (sodium cefoperazone) in Bolton broth and in mCCDA plates may explain the problems encountered for detection of C. jejuni, as high numbers of ESBL E. coli present after enrichment in Bolton broth, also caused overgrowth and masked the few C. jejuni colonies present on the mCCDA plates. The use of Campylobacter spp. specific real-time PCR circumvented these problems and enabled rapid detection of the pathogen after 24 h enrichment in both Bolton and Preston broth, for both healthy and freeze stressed cells.
AB - A comparative study examining Bolton broth and Preston broth for enrichment and reliable detection of Campylobacter jejuni (both healthy and freeze stressed cells) was performed. Tested as pure cultures, Bolton broth enabled faster resuscitation and growth of C. jejuni compared to Preston broth. When C. jejuni was co-incubated with extended-spectrum-beta-lactamase (ESBL) producing Escherichia coli isolated from Belgian poultry meat preparations, the latter dominated in the Bolton enrichment broth and crowded the mCCDA plates. This resulted in the inability to recover C. jejuni by ISO 10272-1:2006 standard method. Preston broth did not support the growth of the ESBL E. coli isolates, but showed longer detection time of C. jejuni compared to Bolton broth. The use of the same antibiotic (sodium cefoperazone) in Bolton broth and in mCCDA plates may explain the problems encountered for detection of C. jejuni, as high numbers of ESBL E. coli present after enrichment in Bolton broth, also caused overgrowth and masked the few C. jejuni colonies present on the mCCDA plates. The use of Campylobacter spp. specific real-time PCR circumvented these problems and enabled rapid detection of the pathogen after 24 h enrichment in both Bolton and Preston broth, for both healthy and freeze stressed cells.
KW - Bolton
KW - C. jejuni
KW - E. coli
KW - ESBL
KW - Preston
KW - Real-time PCR
UR - http://www.scopus.com/inward/record.url?scp=70349776375&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70349776375&partnerID=8YFLogxK
U2 - 10.1016/j.ijfoodmicro.2009.09.007
DO - 10.1016/j.ijfoodmicro.2009.09.007
M3 - Article
C2 - 19786312
AN - SCOPUS:70349776375
SN - 0168-1605
VL - 135
SP - 248
EP - 253
JO - International Journal of Food Microbiology
JF - International Journal of Food Microbiology
IS - 3
ER -