Kałuzewski S, Gierczyński R, Szych J, Jagielski M
Zakład Bakteriologii PZH w Warszawie.
Med Dosw Mikrobiol. 1997;49(3-4):177-86.
The study was performed on 137 Y. enterocolitica strains belonging to various serological groups, including 75 03 group strains isolated form human clinical material. The agglutination test on slides was carried out on this strains using Mangifera indica extract of own production. Agglutinating preparation obtained from the seeds of M. indica agglutinated Y. enterocolitica organisms possessing the pVY plasmid and CRMOX+ phenotype in dilutions to 1.56 micrograms/ml. In identification tests conducted parallelly agglutination solution was used in concentrations of 100 and 10 micrograms/ml. All clones of Y. enterocolitica from O3 group from cultures at 37 degrees C and with CRMOX+ phenotype possessing the pVY plasmid were agglutinated by the extract. Agglutination failed to develop in the cultures of these clones incubated at 25 degrees C. Yersinia clones not containing the pVY plasmid with CRMOX- phenotype were resistant to agglutination. The virulence plasmid was found in 44 out of 75 strains of Y. enterocolitica O3 and was identified by restriction analysis after plasmid DNA digestion with Eco RI enzyme. The obtained results agreed with those of Wauters et al. in 1995 and confirmed the opinion of these authors on the usefulness of the test with M. indica agglutinin for the identification of virulent Y. enterocolitica strains.
该研究对137株属于不同血清群的小肠结肠炎耶尔森氏菌菌株进行了检测,其中包括从人类临床材料中分离出的75株03群菌株。使用自行制备的芒果提取物对这些菌株进行玻片凝集试验。从芒果种子中获得的凝集制剂在稀释至1.56微克/毫升时,能凝集具有pVY质粒和CRMOX+表型的小肠结肠炎耶尔森氏菌。在平行进行的鉴定试验中,使用浓度为100和10微克/毫升的凝集溶液。所有来自O3群、在37℃培养且具有CRMOX+表型并拥有pVY质粒的小肠结肠炎耶尔森氏菌克隆均被该提取物凝集。在25℃培养的这些克隆培养物中未出现凝集现象。不含有pVY质粒且具有CRMOX-表型的耶尔森氏菌克隆对凝集具有抗性。在75株小肠结肠炎耶尔森氏菌O3菌株中,有44株发现了毒力质粒,并在用Eco RI酶消化质粒DNA后通过限制性分析进行了鉴定。所得结果与1995年Wauters等人的结果一致,并证实了这些作者关于用芒果凝集素试验鉴定有毒力的小肠结肠炎耶尔森氏菌菌株的有用性的观点。