de Oliveira Edmar Justo, Rabinovitch Leon, Monnerat Rose Gomes, Passos Liana Konovaloff Jannotti, Zahner Viviane
Laboratory of Bacterial Physiology, Department of Bacteriology, Oswaldo Cruz Institute-Fiocruz, Rio de Janeiro, Brazil.
Appl Environ Microbiol. 2004 Nov;70(11):6657-64. doi: 10.1128/AEM.70.11.6657-6664.2004.
Thirty-three strains of Brevibacillus laterosporus, including three novel strains isolated from Brazilian soil samples, were examined for genetic variability by the use of different PCR-based methods. Molecular markers that could characterize bacterial strains with regards to their pathogenic potential were investigated. In addition, toxicity was assessed by the use of insects belonging to the orders Lepidoptera and Coleoptera and the mollusk Biomphalaria glabrata. Among the targets tested, Biomphalaria glabrata demonstrated the highest degree of sensitivity to B. laterosporus, with some strains inducing 90 to 100% mortality in snails aged 3 and 12 days posteclosion. Larvae of the coleopteron Anthonomus grandis were also susceptible, presenting mortality levels of between 33 and 63%. Toxicity was also noted towards the lepidopteron Anticarsia gemmatalis. In contrast, no mortality was recorded among test populations of Tenebrio molitor or Spodoptera frugiperda. The application of intergenic transcribed spacer PCR and BOX-PCR generated 15 and 17 different genotypes, respectively. None of the molecular techniques allowed the identification of a convenient marker that was associated with any entomopathogenic phenotype. However, a 1,078-bp amplicon was detected for all strains of B. laterosporus when a primer for amplification of the BOXA1R region was used. Similarly, a 900-bp amplicon was generated from all isolates by use of the primer OPA-11 for randomly amplified polymorphic DNA analysis. These amplicons were not detected for other phenotypically related Brevibacillus species, indicating that they represent markers that are specific for B. laterosporus, which may prove useful for the isolation and identification of new strains of this species.
对33株短芽孢杆菌(Brevibacillus laterosporus)进行了研究,其中包括从巴西土壤样本中分离出的3株新菌株,采用了不同的基于聚合酶链反应(PCR)的方法检测其遗传变异性。研究了能够根据致病潜力对细菌菌株进行表征的分子标记。此外,通过使用鳞翅目和鞘翅目昆虫以及软体动物光滑双脐螺(Biomphalaria glabrata)评估了毒性。在所测试的靶标中,光滑双脐螺对短芽孢杆菌表现出最高的敏感性,一些菌株在孵化后3天和12天的蜗牛中可导致90%至100%的死亡率。鞘翅目大谷象(Anthonomus grandis)的幼虫也易感,死亡率在33%至63%之间。对鳞翅目豆蚀叶野螟(Anticarsia gemmatalis)也观察到了毒性。相比之下,黄粉虫(Tenebrio molitor)或草地贪夜蛾(Spodoptera frugiperda)的测试种群中未记录到死亡情况。基因间转录间隔区PCR和BOX-PCR分别产生了15种和17种不同的基因型。没有一种分子技术能够鉴定出与任何昆虫致病表型相关的便捷标记。然而,当使用用于扩增BOXA1R区域的引物时,所有短芽孢杆菌菌株均检测到一个1078 bp的扩增子。同样,通过使用用于随机扩增多态性DNA分析的引物OPA-11,从所有分离株中产生了一个900 bp的扩增子。其他表型相关的短芽孢杆菌物种未检测到这些扩增子,表明它们代表了短芽孢杆菌特有的标记,这可能对该物种新菌株的分离和鉴定有用。