A beta-galactosidase negative E. coli isolated from a raw milk sample leading to atypical colonies on RAPID'E.coli 2 agar

作者：Johler Sophia; Moser Mirjam; Corti Sabrina; Stephan Roger^*

来源：Archiv für Lebensmittelhygiene, 2012, 63(6): 179-181.

DOI：10.2376/0003-925X-63-179

• beta-galactosidase
• E. coli
• chromogenic agar
• atypical colonies

In recent years, the use of chromogenic media for detection of coliforms and E. coli increases as they allow fast identification of colonies directly on the plate without further confirmation steps. We obtained an atypical strain. from a raw milk sample forming bright red colonies on RAPID'E.coli 2 agar, as opposed to the violet coloration characteristic for E. coli, or blue/green coloration characteristic for coliforms. API32E and MALDI-TOF analysis were used to identify isolate 2099 as E. coli. While API ID 32 E analysis resulted in a biochemical profile characteristic for E. coli, isolate 2099 was found to be phenotypically beta-glucuronidase positive but g-galactosidase negative, which resulted in atypical red coloration of its colonies on RAPID'E.coli 2 agar. In order to elucidate possible causes of the beta-galactosidase negative phenotype, we sequenced the lacZ gene encoding beta-galactosidase. A mutation leading to a premature stop codon at amino acid position 774 was identified, rendering the polypeptide abnormally short and most likely not functional. Considering our findings, not only beta-glucuronidase, but also beta-galactosidase negative E. coli represent a challenge to routine diagnostic procedures screening for E. coli with chromogenic media that rely on detection of beta-glucuronidase and beta-galactosidase activity.

• 出版日期2012-12