Snel G G M, Malvisi M, Pilla R, Piccinini R
Department of Veterinary Science and Public Health, University of Milan, Via Celoria 10, 20133 Milan, Italy.
Department of Veterinary Science and Public Health, University of Milan, Via Celoria 10, 20133 Milan, Italy.
Vet Microbiol. 2014 Dec 5;174(3-4):489-495. doi: 10.1016/j.vetmic.2014.09.020. Epub 2014 Oct 5.
It was hypothesized that biofilm could play an important role in the establishment of chronic Staphylococcus aureus bovine mastitis. The in vitro evaluation of biofilm formation can be performed either in closed/static or in flow-based systems. Efforts have been made to characterize the biofilm-forming ability of S. aureus mastitis isolates, however most authors used static systems and matrices other than UHT milk. It is not clear whether such results could be extrapolated to the mammary gland environment. Therefore, the present study aimed to investigate the biofilm-forming ability of S. aureus strains from subclinical bovine mastitis using the static method and a flow-based one. One hundred and twelve strains were tested by the classic tissue culture plate assay (TCP) and 30 out of them were also tested by a dynamic semi-quantitative assay using commercial UHT milk as culture medium (Milk Flow Culture, MFC) or Tryptic Soy Broth as control medium (TS Flow Culture, TSFC). Only 6 (20%) strains formed biofilm in milk under flow conditions, while 36.6% were considered biofilm-producers in TCP, and 93.3% produced biofilm in TSFC. No agreement was found between TCP, MFC and TSFC results. The association between strain genetic profile, determined by microarray, and biofilm-forming ability in milk was evaluated. Biofilm formation in MFC was significantly associated with the presence of those genes commonly found in bovine-associated strains, assigned to clonal complexes typically detected in mastitis. Based on our results, biofilm-forming potential of bovine strains should be critically analysed and tested applying conditions similar to mammary environment.
据推测,生物膜可能在金黄色葡萄球菌引起的慢性牛乳腺炎的发病过程中发挥重要作用。生物膜形成的体外评估可以在封闭/静态系统或基于流动的系统中进行。人们已经努力对金黄色葡萄球菌乳腺炎分离株的生物膜形成能力进行表征,然而大多数作者使用的是静态系统以及超高温瞬时灭菌牛奶以外的基质。目前尚不清楚这些结果是否可以外推至乳腺环境。因此,本研究旨在使用静态方法和基于流动的方法研究来自亚临床牛乳腺炎的金黄色葡萄球菌菌株的生物膜形成能力。通过经典的组织培养板检测法(TCP)对112株菌株进行了检测,其中30株还通过动态半定量检测法进行了检测,该检测法使用商业超高温瞬时灭菌牛奶作为培养基(牛奶流动培养,MFC)或胰蛋白胨大豆肉汤作为对照培养基(TS流动培养,TSFC)。在流动条件下,只有6株(20%)菌株在牛奶中形成了生物膜,而在TCP检测中有36.6%的菌株被认为是生物膜产生菌,在TSFC检测中有93.3%的菌株产生了生物膜。在TCP、MFC和TSFC的检测结果之间未发现一致性。评估了通过微阵列确定的菌株基因谱与牛奶中生物膜形成能力之间的关联。在MFC中生物膜的形成与牛相关菌株中常见的那些基因的存在显著相关,这些基因属于乳腺炎中通常检测到的克隆复合体。基于我们的结果,对于牛源菌株的生物膜形成潜力应进行严格分析,并在类似于乳腺环境的条件下进行测试。