Parvathi Ammini, Kumar H Sanath, Karunasagar Indrani, Karunasagar Iddya
Department of Fishery Microbiology, University of Agricultural Sciences, College of Fisheries, Kankanady, Mangalore, India.
Environ Microbiol. 2005 Jul;7(7):995-1002. doi: 10.1111/j.1462-2920.2005.00770.x.
The pathogenic bacterium Vibrio vulnificus is widely distributed in estuarine waters throughout the world. In this study, the presence of V. vulnificus in oysters was studied both by conventional culture and DNA-based molecular technique. Following enrichment in alkaline peptone water (APW), the bacteria were lysed and a nested polymerase chain reaction (PCR) for vvhA gene was performed. The effect of duration of enrichment on the sensitivity of detection by PCR was evaluated. The organism was isolated from 43% of samples after 18 h enrichment in APW by conventional culture method. Nested PCR amplifying a fragment of vvhA gene detected the organism in 11%, 60% and 81% of samples following 0, 6 and 18 h of enrichment. All the biochemically identified V. vulnificus strains possessed vvhA gene and belonged to biotype 1. The genetic relatedness among the strains was studied by randomly amplified polymorphic DNA (RAPD) PCR and gyrB sequence analysis. The results suggest the presence of two distinct clonal groups of V. vulnificus in oysters in India. The study demonstrates, for the first time that gyrB sequence analysis could be used to study the genetic diversity of V. vulnificus.
致病性创伤弧菌广泛分布于世界各地的河口水域。在本研究中,采用传统培养法和基于DNA的分子技术对牡蛎中创伤弧菌的存在情况进行了研究。在碱性蛋白胨水(APW)中富集后,裂解细菌并进行vvhA基因的巢式聚合酶链反应(PCR)。评估了富集时间对PCR检测灵敏度的影响。通过传统培养方法,在APW中富集18小时后,从43%的样本中分离出该菌。巢式PCR扩增vvhA基因片段,在富集0、6和18小时后的样本中分别检测到该菌的比例为11%、60%和81%。所有经生化鉴定的创伤弧菌菌株均具有vvhA基因,属于生物型1。通过随机扩增多态性DNA(RAPD)PCR和gyrB序列分析研究了菌株之间的遗传相关性。结果表明,印度牡蛎中存在两个不同的创伤弧菌克隆群。该研究首次证明,gyrB序列分析可用于研究创伤弧菌的遗传多样性。