Maugeri Teresa L, Carbone Maria, Fera Maria T, Gugliandolo Concetta
Dipartimento di Biologia Animale ed Ecologia Marina, Università di Messina, Salita Sperone 31, 98166 Messina, Italy.
Res Microbiol. 2006 Mar;157(2):194-200. doi: 10.1016/j.resmic.2005.06.007. Epub 2005 Aug 8.
Vibrio vulnificus, a human and animal pathogen, is present in low numbers in the Mediterranean Sea. Seawater and plankton samples were collected from a marine coastal zone of the Straits of Messina in the Mediterranean Sea (Italy) in order to investigate V. vulnificus as free-living (>0.2 microm) and associated with small (>64 microm) and large plankton (>200 microm) utilizing cultural and molecular techniques. Characteristic colonies, grown on thiosulfate, citrate, bile salts and sucrose agar plates, were identified using a biochemical protocol system. A PCR assay was used to confirm isolates and to directly detect V. vulnificus in environmental concentrated samples. Specific primers were used to target the structural cytotoxin/hemolysin gene and the variable regions of 16S rRNA species-specific for V. vulnificus. In addition, a tri-primer PCR of 16S rRNA was used for the differentiation of V. vulnificus strains. Direct detection in marine samples was more frequent than isolation of culturable forms. All isolates were assigned to V. vulnificus biotype 1, 16S rRNA type B. These results confirm the low incidence of V. vulnificus in Mediterranean coastal waters. The isolation of cultivable forms is limited to the warmest months. 16S rRNA primers were the most sensitive molecular tool as they allowed detection of V. vulnificus in 79.1% of samples. Due to the low incidence of V. vulnificus in the Mediterranean coastal environment, its detection requires a molecular approach. The occurrence of V. vulnificus as plankton-associated confirms the role of plankton as a potential reservoir for this pathogen.
创伤弧菌是一种人畜共患病原体,在地中海中的数量较少。为了利用培养和分子技术研究作为自由生活状态(>0.2微米)以及与小型(>64微米)和大型浮游生物(>200微米)相关联的创伤弧菌,从地中海(意大利)墨西拿海峡的一个海洋沿岸区域采集了海水和浮游生物样本。在硫代硫酸盐、柠檬酸盐、胆盐和蔗糖琼脂平板上生长的特征性菌落,使用生化检测系统进行鉴定。采用聚合酶链反应(PCR)检测来确认分离株,并直接检测环境浓缩样本中的创伤弧菌。使用特异性引物靶向创伤弧菌特异性的结构细胞毒素/溶血素基因和16S rRNA的可变区。此外,16S rRNA的三引物PCR用于区分创伤弧菌菌株。在海洋样本中的直接检测比可培养形式的分离更为频繁。所有分离株均属于创伤弧菌生物型1、16S rRNA B型。这些结果证实了创伤弧菌在地中海沿岸水域的低发生率。可培养形式的分离仅限于最温暖的月份。16S rRNA引物是最敏感的分子工具,因为它们能在79.1%的样本中检测到创伤弧菌。由于创伤弧菌在地中海沿岸环境中的发生率较低,其检测需要采用分子方法。创伤弧菌与浮游生物相关的存在证实了浮游生物作为该病原体潜在储存库的作用。