Laboratory of Food Microbiology and Food Preservation, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium.
Food Microbiol. 2011 Sep;28(6):1117-23. doi: 10.1016/j.fm.2011.03.001. Epub 2011 Mar 10.
In the present study, we evaluate the recommended ISO 10272:2006 versus alternative procedures for Campylobacter enumeration and enrichment in naturally contaminated chicken meat samples (n = 49). Three enrichment media were evaluated; Bolton broth, Preston broth and CampyFood broth(®) (bioMérieux SA, Marcy l'Etoile, France). In addition, three selective plating agars were compared; modified charcoal cefoperazone deoxycholate agar (mCCDA), CampyFood agar(®) (CFA; bioMérieux SA) and Brilliance CampyCount agar(®) (BCC; Oxoid, Basingstoke, England). Direct plating on CFA provided the highest number of Campylobacter positive samples (17/49); however this was not statistically different (P > 0.05) from numbers of positive samples recovered by direct plating on mCCDA (15/49) or BCC agars (14/49). Also, there was no significant difference between Campylobacter counts on the three compared media (P > 0.05). The coloured colonies of Campylobacter on CFA and BCC were easier to record and count than those on mCCDA. Enrichment of chicken meat samples in Bolton broth for 48 h and subsequent plating on CFA provided significantly higher (P < 0.05) Campylobacter detection compared to the other broth-agar combinations. Enrichment in Preston broth for 24 h followed by plating on mCCDA gave a higher number of positive samples (20/49) than 48 h enrichment in Bolton broth and plating on mCCDA (15/49). Enrichment in Bolton broth for 48 h followed by plating on CFA recovered 35% of samples below the limit for quantifications (<10 CFU/g, n = 34), as identified by direct plating on mCCDA. Compared to the current ISO method, some alternative combinations of enrichment and agar media could provide significantly better detection and enumeration of Campylobacter in chicken meat.
在本研究中,我们评估了推荐的 ISO 10272:2006 与替代程序,用于在自然污染的鸡肉样本中计数和富集弯曲杆菌(n=49)。评估了三种增菌培养基:Bolton 肉汤、Preston 肉汤和 CampyFood 肉汤(bioMérieux SA,法国马西-勒-埃托勒)。此外,还比较了三种选择性平板琼脂:改良炭头孢哌酮去氧胆酸盐琼脂(mCCDA)、CampyFood 琼脂(CFA;bioMérieux SA)和辉煌弯曲杆菌计数琼脂(BCC;Oxoid,英国贝辛斯托克)。直接在 CFA 平板上接种可获得最多的弯曲杆菌阳性样本(17/49);但这与直接在 mCCDA(15/49)或 BCC 琼脂上接种的阳性样本数量无统计学差异(P>0.05)。此外,三种比较培养基上的弯曲杆菌计数之间也没有显著差异(P>0.05)。CFA 和 BCC 上的弯曲杆菌彩色菌落比 mCCDA 上的更容易记录和计数。在 Bolton 肉汤中富集鸡肉样品 48 小时,随后在 CFA 平板上接种,与其他肉汤-琼脂组合相比,弯曲杆菌的检测率显著提高(P<0.05)。在 Preston 肉汤中富集 24 小时,然后在 mCCDA 平板上接种,比在 Bolton 肉汤中富集 48 小时和在 mCCDA 平板上接种的阳性样本数量(20/49)更高。在 Bolton 肉汤中富集 48 小时,然后在 CFA 平板上接种,可恢复 35%低于定量限(<10 CFU/g,n=34)的样品,如直接在 mCCDA 平板上接种所确定的。与现行的 ISO 方法相比,一些替代的增菌和琼脂培养基组合可以显著提高鸡肉中弯曲杆菌的检测和计数。