Department of Biological Sciences, Bowling Green State University, Bowling Green, OH, USA.
Department of Biology, Seton Hill University, Greensburg, PA, USA.
Microbiologyopen. 2017 Jun;6(3). doi: 10.1002/mbo3.435. Epub 2017 Jan 22.
The emergence of bacterial pathogens resistant to all known antibiotics is a global health crisis. Adding to this problem is that major pharmaceutical companies have shifted away from antibiotic discovery due to low profitability. As a result, the pipeline of new antibiotics is essentially dry and many bacteria now resist the effects of most commonly used drugs. To address this global health concern, citizen science through the Small World Initiative (SWI) was formed in 2012. As part of SWI, students isolate bacteria from their local environments, characterize the strains, and assay for antibiotic production. During the 2015 fall semester at Bowling Green State University, students isolated 77 soil-derived bacteria and genetically characterized strains using the 16S rRNA gene, identified strains exhibiting antagonistic activity, and performed an expanded SWI workflow using transposon mutagenesis to identify a biosynthetic gene cluster involved in toxigenic compound production. We identified one mutant with loss of antagonistic activity and through subsequent whole-genome sequencing and linker-mediated PCR identified a 24.9 kb biosynthetic gene locus likely involved in inhibitory activity in that mutant. Further assessment against human pathogens demonstrated the inhibition of Bacillus cereus, Listeria monocytogenes, and methicillin-resistant Staphylococcus aureus in the presence of this compound, thus supporting our molecular strategy as an effective research pipeline for SWI antibiotic discovery and genetic characterization.
细菌病原体对抗生素产生耐药性是全球健康危机。更糟糕的是,由于利润低,大型制药公司已不再专注于抗生素的研发。因此,新抗生素的供应几乎枯竭,许多细菌现在对大多数常用药物都具有耐药性。为了解决这一全球健康问题,公民科学组织 Small World Initiative(SWI)于 2012 年成立。作为 SWI 的一部分,学生们从当地环境中分离细菌,对菌株进行特征描述,并检测抗生素的产生。在 2015 年秋季的 Bowling Green State 大学,学生们从土壤中分离出 77 株细菌,通过 16S rRNA 基因进行遗传特征描述,鉴定出具有拮抗活性的菌株,并使用转座子诱变进行了扩展的 SWI 工作流程,以鉴定参与产毒化合物生产的生物合成基因簇。我们发现了一个失去拮抗活性的突变体,通过随后的全基因组测序和连接介导的 PCR,确定了一个可能与该突变体抑制活性相关的 24.9kb 的生物合成基因座。对人类病原体的进一步评估表明,该化合物可抑制蜡样芽孢杆菌、单核细胞增生李斯特菌和耐甲氧西林金黄色葡萄球菌,这支持了我们的分子策略,即作为 SWI 抗生素发现和遗传特征描述的有效研究途径。