Laboratory of Microbiology of Food and Sanitizes, INCQS/Fiocruz, Brazil.
Laboratory of Reference Microorganisms, INCQS/Fiocruz, Brazil.
Food Res Int. 2017 Dec;102:61-67. doi: 10.1016/j.foodres.2017.09.083. Epub 2017 Sep 28.
Several Cronobacter species are opportunistic pathogens that cause infections in humans. This study evaluated the phenotypic characteristics of 57 Cronobacter strains (C. sakazakii n=41, C. malonaticus n=10, C. dublinensis n=4, and C. muytjensii n=2) isolated from food (n=54) and clinical specimens (n=3) in Brazil. These strains included sequence types (ST): ST395-ST398, ST402, ST413 and ST433-ST439, isolated from food samples, and three C. malonaticus clinical strains previous isolated from an outbreak which were ST394 (n=1) and ST440 (n=2). Strains were tested for capsule production, biofilm formation, protease activity, hemolytic activity, cell-cell aggregation, and desiccation resistance. Capsule formation was observed with all Cronobacter strains. Forty-four (77.2%) strains showed proteolytic activity on milk agar. All strains showed β-hemolysis against erythrocytes from guinea pig, horse and rabbit. Using erythrocytes from sheep, the majority of strains (53/57; 92.9%) showed α-hemolysis and the remaining, β-hemolysis. All Cronobacter strains produced weak biofilms in microtiters polystyrene plates, which were independent of temperature (4, 25 and 37°C) and/or growth conditions. In glass tubes, formation of either a moderate or strong biofilm was observed in 15/57 (26.3%), 19/57 (33.3%) and 27/57 (47.4%), at 4, 25 and 37°C, respectively. Desiccation treatment decreased Cronobacter viability by 1.55 to >3.87LogCFU/mL. Cell-cell aggregation was observed in 17 (29.8%) strains. This study showed that the Cronobacter species evaluated showed differing phenotypes, independent of their origin (clinical or not) and ST. Further studies are necessary to elucidate the factors affecting phenotype expression. This may identify novel bacterial targets that could be useful in the development of strategies to control Cronobacter in food chain and to prevent cases of infections.
几种克罗诺杆菌属物种是机会性病原体,可导致人类感染。本研究评估了 57 株克罗诺杆菌属菌株(41 株阪崎克罗诺杆菌、10 株马尔他克罗诺杆菌、4 株都柏林克罗诺杆菌和 2 株穆氏克罗诺杆菌)的表型特征,这些菌株分别从巴西的食品(54 株)和临床标本(3 株)中分离得到。这些菌株包括序列类型(ST):ST395-ST398、ST402、ST413 和 ST433-ST439,这些 ST 类型分离自食品样本,而 3 株马尔他克罗诺杆菌临床菌株之前从一次暴发中分离得到,其 ST 类型为 ST394(1 株)和 ST440(2 株)。对菌株进行了荚膜生成、生物膜形成、蛋白酶活性、溶血活性、细胞-细胞聚集和干燥抗性检测。所有克罗诺杆菌属菌株均形成荚膜。44 株(77.2%)菌株在牛奶琼脂上显示出蛋白酶活性。所有菌株对豚鼠、马和兔的红细胞均显示β-溶血。使用绵羊的红细胞,大多数菌株(53/57;92.9%)显示α-溶血,其余菌株显示β-溶血。所有克罗诺杆菌属菌株在聚苯乙烯微量滴定板上产生弱生物膜,其不受温度(4、25 和 37°C)和/或生长条件的影响。在玻璃管中,在 4、25 和 37°C 下,分别有 15/57(26.3%)、19/57(33.3%)和 27/57(47.4%)的菌株形成中度或强生物膜。干燥处理使克罗诺杆菌属的活菌数减少了 1.55 至>3.87LogCFU/mL。在 17 株(29.8%)菌株中观察到细胞-细胞聚集。本研究表明,评估的克罗诺杆菌属物种表现出不同的表型,而与它们的来源(临床或非临床)和 ST 无关。需要进一步的研究来阐明影响表型表达的因素。这可能确定新的细菌靶标,这些靶标可用于开发控制食品链中克罗诺杆菌属和预防感染病例的策略。