Department of Microbiology and Biotechnology, Max Rubner-Institute, Federal Research Institute of Nutrition and Food, 24103 Kiel, Germany.
Department of Microbiology and Biotechnology, Max Rubner-Institute, Federal Research Institute of Nutrition and Food, 24103 Kiel, Germany.
J Dairy Sci. 2022 Oct;105(10):7951-7958. doi: 10.3168/jds.2022-21941. Epub 2022 Aug 12.
Cheese, especially ripened varieties, harbor a very complex and heterogeneous microbiota. In addition to the desired microorganisms (starter cultures) added during cheese production, potentially harmful bacteria may also enter the production chain. Regarding the latter, the focus of this study was on coagulase-negative staphylococci (CNS) and Macrococcuscaseolyticus. Both are known to harbor a variety of genes coding for antibiotic resistance, including mecA, mecB, mecC, and mecD. Coagulase-negative staphylococci or macrococci carrying such genes or other virulence factors should not be present in cheese. Cheese samples (101 in total) were collected from retail sources. Coagulase-negative staphylococci and M. caseolyticus were isolated utilizing selective agars, and species were identified by phenotypical tests and partial sequencing of the sodA gene. The results allowed identification of 53 CNS strains and 19 M. caseolyticus strains. Among the CNS, 11 isolates of Staphylococcus saprophyticus and one Staphylococcus epidermidis isolate were obtained. Both species are potential human pathogens and may thus adversely affect the safety of these food products. Screening for antimicrobial resistance was performed by application of disc diffusion tests, a gradient strip-test, and 14 different PCR tests. Evidence for methicillin resistance (by either positive disc diffusion assay for cefoxitin or by mec PCR) was found in CNS isolates and M. caseolyticus (9 isolates each). Regarding other virulence factors, no genetic determinants for coagulase or the most common staphylococcal enterotoxins sea, seb, sec, sed, and see were detected in any of the CNS or M. caseolyticus isolates by PCR testing. In conclusion, the presence of facultatively pathogenic CNS and carriers of genes for antibiotic resistance in both groups of microorganisms, especially mec genes, and the respective food safety issues need further evaluation and surveillance.
奶酪,尤其是成熟的奶酪,含有非常复杂和异质的微生物群。除了在奶酪生产过程中添加的所需微生物(起始培养物)外,潜在的有害细菌也可能进入生产链。关于后者,本研究的重点是凝固酶阴性葡萄球菌(CNS)和巨球菌属。已知两者都携带有多种编码抗生素抗性的基因,包括 mecA、mecB、mecC 和 mecD。不应该在奶酪中存在携带这些基因或其他毒力因子的凝固酶阴性葡萄球菌或巨球菌。从零售来源采集了 101 个奶酪样本。利用选择性琼脂分离出凝固酶阴性葡萄球菌和巨球菌属,并通过表型试验和 sodA 基因的部分测序鉴定物种。结果鉴定出 53 株 CNS 菌株和 19 株 M. caseolyticus 菌株。在 CNS 中,获得了 11 株表皮葡萄球菌和 1 株表皮葡萄球菌分离株。这两种物种都是潜在的人类病原体,因此可能会对这些食品的安全性产生不利影响。通过应用圆盘扩散试验、梯度条带试验和 14 种不同的 PCR 试验进行了抗菌药物耐药性筛选。在 CNS 菌株和 M. caseolyticus(各 9 株)中发现了耐甲氧西林的证据(头孢西丁的阳性圆盘扩散试验或 mec PCR)。关于其他毒力因子,通过 PCR 试验未在任何 CNS 或 M. caseolyticus 分离株中检测到凝固酶或最常见的葡萄球菌肠毒素 sea、seb、sec、sed 和 see 的遗传决定因素。总之,需进一步评估和监测兼性致病 CNS 的存在以及这两组微生物中抗生素耐药基因的携带者,尤其是 mec 基因,以及各自的食品安全问题。