Staley T E, Colwell R R
J Bacteriol. 1973 Jun;114(3):916-27. doi: 10.1128/jb.114.3.916-927.1973.
Polynucleotide sequence relationships between two reference Vibrio parahaemolyticus strains isolated from Japanese and American gastroenteritis patients were investigated by use of (32)P-DNA/DNA reassociation in free solution. In addition, these strains were similarly compared with 22 other strains of estuarine and marine vibrios, including 11 strains previously identified as V. parahaemolyticus (2 Japanese, 1 of unknown location, and 8 American strains obtained from diverse geographical locations and sources in North America), 3 strains of V. alginolyticus, and 8 of Vibrio spp. Deoxyribonucleic acid (DNA) from the Japanese and American gastroenteritis isolates showed high relative levels of intraspecific duplex formation (92 to 93%) when reassociated, reciprocally, at 60 C. Heterologous DNA duplexes exhibited thermal elution midpoint [Tm(e)] values comparable to those obtained from homologous duplexes (88.0) when thermally eluted from hydroxyapatite, thus indicating high base-pair complementarity. Other V. parahaemolyticus strains showed DNA homologies of 85% or greater, with correspondingly high Tm(e) values (86.0 to 88.0) for the heteroduplexes formed. DNA of two of three V. alginolyticus strains (ATCC 17749 and 166-70) was 55 to 60% homologous to reference V. parahaemolyticus DNA preparations; Vibrio sp. strain 5144 (originally classified as V. parahaemolyticus biotype 2 and subsequently as V. alginolyticus strain 5144) showed only 24 to 26% DNA homology to the same reference DNA. These data provide evidence that Vibrio sp. strain 5144 is genetically distinct from the other V. alginolyticus strains used in this study. Three bioluminescent strains thought to be closely related to V. parahaemolyticus demonstrated only 24 to 31% DNA homology to the reference V. parahaemolyticus DNA. These data firmly establish the existence in some Atlantic and Gulf Coast estuaries of organisms genetically very similar to V. parahaemolyticus, the causative agent of "shirasu" food poisoning in Japan.
利用自由溶液中的(32)P-DNA/DNA重结合技术,研究了从日本和美国肠胃炎患者中分离出的两株副溶血性弧菌参考菌株之间的多核苷酸序列关系。此外,还将这些菌株与其他22株河口和海洋弧菌进行了类似比较,其中包括11株先前鉴定为副溶血性弧菌的菌株(2株日本菌株、1株来源不明菌株以及8株从北美不同地理位置和来源获得的美国菌株)、3株溶藻弧菌菌株和8株弧菌属菌株。当在60℃下相互重结合时,来自日本和美国肠胃炎分离株的脱氧核糖核酸(DNA)显示出较高水平的种内双链体形成(92%至93%)。当从羟基磷灰石上进行热洗脱时,异源DNA双链体的热洗脱中点[Tm(e)]值与同源双链体(88.0)相当,这表明碱基对互补性较高。其他副溶血性弧菌菌株显示出85%或更高的DNA同源性,形成的异源双链体相应地具有较高的Tm(e)值(86.0至88.0)。三株溶藻弧菌菌株中的两株(ATCC 17749和166 - 70)的DNA与副溶血性弧菌参考DNA制剂的同源性为55%至60%;弧菌属菌株5144(最初分类为副溶血性弧菌生物型2,随后重新分类为溶藻弧菌菌株5144)与相同参考DNA的DNA同源性仅为24%至26%。这些数据证明弧菌属菌株5144在遗传上与本研究中使用的其他溶藻弧菌菌株不同。三株被认为与副溶血性弧菌密切相关的发光菌株与副溶血性弧菌参考DNA的DNA同源性仅为24%至31%。这些数据有力地证明了在一些大西洋和墨西哥湾沿岸河口存在与副溶血性弧菌在遗传上非常相似的生物,副溶血性弧菌是日本“白身鱼”食物中毒的病原体。