Rieu Aurélie, Lemaître Jean-Paul, Guzzo Jean, Piveteau Pascal
Laboratoire de Recherche En Vigne et Vin REVV, Université de Bourgogne, IUVV, F-21000 Dijon, France.
Int J Food Microbiol. 2008 Aug 15;126(1-2):76-82. doi: 10.1016/j.ijfoodmicro.2008.05.006. Epub 2008 May 15.
Six environmental isolates of Staphylococcus aureus and one collection strain were investigated for their ability to form monospecies biofilms and dual species biofilms with Listeria monocytogenes EGD-e on stainless steel coupons. All isolates were able to grow as biofilms but their ability to form monospecies biofilms differed. The population of L. monocytogenes EGD-e in dual species biofilms was not affected by the presence of S. aureus isolates except for strain CIP 53.156. The effect of L. monocytogenes EGD-e on the population of S. aureus was strain dependent: S. aureus population either increased or decreased or was not affected in the presence of L. monocytogenes EGD-e in dual species biofilms. Dual species biofilms were grown with L. monocytogenes EGD-e and the strain CIP 53.156 of S. aureus on stainless steel coupons under batch and dynamic conditions. Higher sessile populations of L. monocytogenes EGD-e were observed in the presence of S. aureus CIP 53.156. Microscope observations by scanning electron microscopy (SEM) revealed an intimate association of L. monocytogenes EGD-e and S. aureus CIP 53.156 in dual species biofilms. An increase of the number of L. monocytogenes EGD-e cells was observed in the presence of S. aureus CIP 53.156 cell-free supernatant. This activity was retained after ultrafiltation (<3 kDa), was heat stable but was lost after proteinase K treatment.
对6株金黄色葡萄球菌环境分离株和1株保藏菌株进行了研究,以考察它们在不锈钢试片上形成单菌种生物膜以及与单核细胞增生李斯特菌EGD-e形成双菌种生物膜的能力。所有分离株均能形成生物膜,但它们形成单菌种生物膜的能力有所不同。除了CIP 53.156菌株外,双菌种生物膜中单核细胞增生李斯特菌EGD-e的数量不受金黄色葡萄球菌分离株存在的影响。单核细胞增生李斯特菌EGD-e对金黄色葡萄球菌数量的影响因菌株而异:在双菌种生物膜中,金黄色葡萄球菌的数量在单核细胞增生李斯特菌EGD-e存在的情况下要么增加,要么减少,要么不受影响。在分批和动态条件下,在不锈钢试片上用单核细胞增生李斯特菌EGD-e和金黄色葡萄球菌的CIP 53.156菌株培养双菌种生物膜。在金黄色葡萄球菌CIP 53.156存在的情况下,观察到单核细胞增生李斯特菌EGD-e的附着菌数量更高。通过扫描电子显微镜(SEM)进行的显微镜观察显示,在双菌种生物膜中,单核细胞增生李斯特菌EGD-e和金黄色葡萄球菌CIP 53.156紧密相连。在金黄色葡萄球菌CIP 53.156无细胞上清液存在的情况下,观察到单核细胞增生李斯特菌EGD-e细胞数量增加。这种活性在超滤(<3 kDa)后仍保留,具有热稳定性,但在蛋白酶K处理后丧失。