Characterization of Staphylococcus aureus strains associated with food poisoning outbreaks in France
Enterotoxins produced by Staphylococcus aureus are responsible for staphylococcal food-poisoning outbreaks (SFPO). In France, SFPO are the second cause of food-borne diseases after Salmonella. However, very little is known about the strains involved. The objective of this study was to characterize t...
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Veröffentlicht in: | International journal of food microbiology 2007-04, Vol.115 (3), p.369-375 |
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Zusammenfassung: | Enterotoxins produced by
Staphylococcus aureus are responsible for staphylococcal food-poisoning outbreaks (SFPO). In France, SFPO are the second cause of food-borne diseases after
Salmonella. However, very little is known about the strains involved. The objective of this study was to characterize the staphylococcal strains related to these SFPO through phenotypic and genotypic analyses. A total of 178 coagulase-positive staphylococcal isolates recovered from 31 SFPO (1981–2002) were screened through biotyping. Thirty-three strains representative of the different biotypes in each SFPO were further examined for
SmaI macrorestriction-type, phage-type, resistance to various antimicrobial drugs, presence of staphylococcal enterotoxin (
se) genes
sea to
sei, and production of enterotoxins SEA to SED. All these 33 strains were identified as
S. aureus species: 27 were of human biotypes and six ovine or non-host-specific biotypes. Most (74.1%) strains reacted with group III phages. Eleven strains were resistant to at least two classes of antibiotics and among them, two were resistant to methicillin. Twenty-nine strains carried one or several of the eight
se genes tested; the gene
sea was most common (
n
=
23), and often linked to
sed (
n
=
12) or
seh (
n
=
5). The novel
se genes
seg-i were in all cases associated with
se genes
sea to
sed except for one strain which carried only
seg and
sei. Pulsed-Field Gel Electrophoresis (PFGE) of
SmaI macrorestriction digests of the 33 strains discriminated 32 PFGE patterns grouped into nine biotype-specific clusters. All five strains carrying
sea and
seh were grouped together into the same sub-cluster. Three of the four
se-gene-negative strains were in one PFGE cluster: all four should be tested for
se genes not included in this study and, if negative, be further investigated for the presence of unidentified SEs. |
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ISSN: | 0168-1605 1879-3460 |
DOI: | 10.1016/j.ijfoodmicro.2006.10.050 |