Reyes-Ramirez Arturo, Ibarra Jorge E
Departamento de Biotecnología y Bioquímica, CINVESTAV, Apartado Postal 629, 36500 Irapuato, Guanajuato, Mexico.
Appl Environ Microbiol. 2005 Mar;71(3):1346-55. doi: 10.1128/AEM.71.3.1346-1355.2005.
A total of 119 Bacillus thuringiensis strains (83 type strains and 26 native isolates), as well as five B. cereus group species, were analyzed by repetitive extragenic palindromic sequence-based PCR analysis (Rep-PCR) fingerprinting. Primers Bc-REP-1 and Bc-REP-2 were specifically designed according to an extragenic 26-bp repeated sequence found in the six B. cereus group genomes reported. A total of 47 polymorphic bands were detected, and the patterns varied from 5 to 13 bands in number and from 0.2 to 3.8 kb in size. Virtually each type strain showed a distinctive B. cereus (Bc)-Rep-PCR pattern, except for B. thuringiensis serovars dakota (H serotype 15 [H15]) and sotto (H4a,4b), as well as serovars amagiensis (H29) and seoulensis (H35), which shared the same patterns. As expected, serovar entomocidus (H6) and its biovar subtoxicus showed an identical pattern; similarly, serovars sumiyoshiensis (H3a,3d) and fukuokaensis (H3a,3d,3e), which share two antigenic determinants, also showed identical Bc-Rep-PCR patterns. Interestingly, serovars israelensis (H14) and malaysiensis (H36), which share several phenotypic attributes, also showed identical Bc-Rep-PCR patterns. Native, coleopteran-active strains, including the self-agglutinated LBIT-74 strain, showed Bc-Rep-PCR patterns identical or very similar to that of the tenebrionis strain. Likewise, native mosquitocidal strains (including some self-agglutinated strains) also showed patterns identical or very similar to that of the serovar israelensis IPS-82 strain. Additionally, native beta-exotoxin-producing strains from serovar thuringiensis showed patterns identical to that of the B. thuringiensis type strain. The B. cereus group-specific Bc-Rep-PCR fingerprinting technique was shown to be highly discriminative, fast, easy, and able to identify B. thuringiensis serotypes, including nonflagellar and self-agglutinated strains.
通过基于重复外显子回文序列的聚合酶链反应分析(Rep-PCR)指纹图谱,对总共119株苏云金芽孢杆菌菌株(83株模式菌株和26株本地分离株)以及5种蜡样芽孢杆菌群物种进行了分析。引物Bc-REP-1和Bc-REP-2是根据已报道的6个蜡样芽孢杆菌群基因组中发现的一个26bp的外显子重复序列专门设计的。共检测到47条多态性条带,其条带数量从5条到13条不等,大小从0.2kb到3.8kb不等。实际上,除了苏云金芽孢杆菌达科他血清型(H血清型15 [H15])和 sotto血清型(H4a,4b),以及阿玛吉血清型(H29)和首尔血清型(H35)具有相同的图谱外,每种模式菌株都显示出独特的蜡样芽孢杆菌(Bc)-Rep-PCR图谱。正如预期的那样,昆虫血清型(H6)及其生物变种亚毒素型显示出相同的图谱;同样,具有两个抗原决定簇的sumiyoshiensis血清型(H3a,3d)和福冈血清型(H3a,3d,3e)也显示出相同的Bc-Rep-PCR图谱。有趣的是,具有几种表型特征的以色列血清型(H14)和马来西亚血清型(H36)也显示出相同的Bc-Rep-PCR图谱。包括自凝集LBIT-74菌株在内的本地鞘翅目活性菌株显示出与tenebrionis菌株相同或非常相似的Bc-Rep-PCR图谱。同样,本地杀蚊菌株(包括一些自凝集菌株)也显示出与以色列血清型IPS-82菌株相同或非常相似的图谱。此外,来自苏云金芽孢杆菌血清型的本地产β-外毒素菌株显示出与苏云金芽孢杆菌模式菌株相同的图谱。蜡样芽孢杆菌群特异性的Bc-Rep-PCR指纹图谱技术被证明具有高度的鉴别力、快速、简便,并且能够鉴定苏云金芽孢杆菌血清型,包括非鞭毛菌株和自凝集菌株。