Cook David W, Oleary Paul, Hunsucker Jeff C, Sloan Edna M, Bowers John C, Blodgett Robert J, Depaola Angelo
Gulf Coast Seafood Laboratory, Food and Drug Administration, Dauphin Island, Alabama 36528, USA.
J Food Prot. 2002 Jan;65(1):79-87. doi: 10.4315/0362-028x-65.1.79.
From June 1998 to July 1999, 370 lots of oysters in the shell were sampled at 275 different establishments (71%, restaurants or oyster bars; 27%, retail seafood markets: and 2%, wholesale seafood markets) in coastal and inland markets throughout the United States. The oysters were harvested from the Gulf (49%). Pacific (14%), Mid-Atlantic (18%), and North Atlantic (11%) Coasts of the United States and from Canada (8%). Densities of Vibrio vulnificus and Vibrio parahaemolyticus were determined using a modification of the most probable number (MPN) techniques described in the Food and Drug Administration's Bacteriological Analytical Manual. DNA probes and enzyme immunoassay were used to identify suspect isolates and to determine the presence of the thermostable direct hemolysin gene associated with pathogenicity of V. parahaemolyticus. Densities of both V. vulnifcus and V. parahaemolyticus in market oysters from all harvest regions followed a seasonal distribution, with highest densities in the summer. Highest densities of both organisms were observed in oysters harvested from the Gulf Coast, where densities often exceeded 10,000 MPN/g. The majority (78%) of lots harvested in the North Atlantic, Pacific, and Canadian Coasts had V. vulnificus densities below the detectable level of 0.2 MPN/g; none exceeded 100 MPN/g. V. parahaemolyticus densities were greater than those of V. vulnificus in lots from these same areas, with some lots exceeding 1,000 MPN/g for V. parahaemolyticus. Some lots from the Mid-Atlantic states exceeded 10,000 MPN/g for both V. vulnificus and V. parahaemolyicus. Overall, there was a significant correlation between V. vulificus and V. parahaemolyticus densities (r = 0.72, n = 202, P < 0.0001), but neither density correlated with salinity. Storage time significantly affected the V. vulnificus (10% decrease per day) and V. parahaemolyticus (7% decrease per day) densities in market oysters. The thermostable direct hemolysin gene associated with V parahaemolyticus virulence was detected in 9 of 3,429 (0.3%) V. parahaemolyticus cultures and in 8 of 198 (4.0%) lots of oysters. These data can be used to estimate the exposure of raw oyster consumers to V. vulnificus and V. parahaemolyticus.
1998年6月至1999年7月,在美国沿海和内陆市场的275个不同场所(71%为餐馆或牡蛎吧;27%为海鲜零售市场;2%为海鲜批发市场)采集了370批带壳牡蛎样本。这些牡蛎采自美国的海湾(49%)、太平洋(14%)、中大西洋(18%)和北大西洋(11%)海岸以及加拿大(8%)。采用对美国食品药品管理局《细菌学分析手册》中所述的最可能数(MPN)技术进行改良的方法,测定创伤弧菌和副溶血性弧菌的密度。使用DNA探针和酶免疫测定法来鉴定可疑分离株,并确定与副溶血性弧菌致病性相关的耐热直接溶血素基因的存在情况。所有收获区域的市售牡蛎中,创伤弧菌和副溶血性弧菌的密度均呈季节性分布,夏季密度最高。在从墨西哥湾沿岸收获的牡蛎中观察到这两种菌的密度最高,其密度常常超过10,000 MPN/g。在北大西洋、太平洋和加拿大海岸收获的大部分(78%)批次的牡蛎中,创伤弧菌密度低于可检测水平0.2 MPN/g;没有超过100 MPN/g的。在这些相同区域的批次中,副溶血性弧菌的密度高于创伤弧菌,有些批次的副溶血性弧菌超过1,000 MPN/g。来自中大西洋各州的一些批次的创伤弧菌和副溶血性弧菌密度均超过10,000 MPN/g。总体而言,创伤弧菌和副溶血性弧菌密度之间存在显著相关性(r = 0.72,n = 202,P < 0.0001),但两种菌的密度均与盐度无关。储存时间显著影响市售牡蛎中创伤弧菌(每天降低10%)和副溶血性弧菌(每天降低7%)的密度。在3429株副溶血性弧菌培养物中的9株(0.3%)以及198批牡蛎中的8批(4.0%)中检测到了与副溶血性弧菌毒力相关的耐热直接溶血素基因。这些数据可用于估计生食牡蛎的消费者接触创伤弧菌和副溶血性弧菌的情况。