Department of Entomology and Plant Pathology, Auburn University, Auburn, AL, United States of America.
Crop Science Division, Biologics, Bayer, West Sacramento, CA, United States of America.
PLoS One. 2018 Feb 15;13(2):e0193119. doi: 10.1371/journal.pone.0193119. eCollection 2018.
Bacillus amyloliquefaciens QST713 and B. firmus I-1582 are bacterial strains which are used as active ingredients of commercially-available soil application and seed treatment products Serenade® and VOTiVO®, respectively. These bacteria colonize plant roots promoting plant growth and offering protection against pathogens/pests. The objective of this study was to develop a qPCR protocol to quantitate the dynamics of root colonization by these two strains under field conditions. Primers and TaqMan® probes were designed based on genome comparisons of the two strains with publicly-available and unpublished bacterial genomes of the same species. An optimized qPCR protocol was developed to quantify bacterial colonization of corn roots after seed treatment. Treated corn seeds were planted in non-sterile soil in the greenhouse and grown for 28 days. Specific detection of bacteria was quantified weekly, and showed stable colonization between ~104-105 CFU/g during the experimental period for both bacteria, and the protocol detected as low as 103 CFU/g bacteria on roots. In a separate experiment, streptomycin-resistant QST713 and rifampicin-resistant I-1582 strains were used to compare dilution-plating on TSA with the newly developed qPCR method. Results also indicated that the presence of natural microflora and another inoculated strain does not affect root colonization of either one of these strains. The same qPCR protocol was used to quantitate root colonization by QST713 and I-1582 in two corn and two soybean varieties grown in the field. Both bacteria were quantitated up to two weeks after seeds were planted in the field and there were no significant differences in root colonization in either bacteria strain among varieties. Results presented here confirm that the developed qPCR protocol can be successfully used to understand dynamics of root colonization by these bacteria in plants growing in growth chamber, greenhouse and the field.
解淀粉芽胞杆菌 QST713 和 B. firmus I-1582 是两种细菌菌株,分别作为市售土壤施用和种子处理产品 Serenade®和 VOTiVO®的有效成分。这些细菌定殖在植物根部,促进植物生长,并提供对病原体/害虫的保护。本研究的目的是开发一种 qPCR 协议,以定量研究这两种菌株在田间条件下根系定殖的动态。基于两种菌株与同一物种的公开和未公开细菌基因组的基因组比较,设计了引物和 TaqMan®探针。开发了一种优化的 qPCR 协议,用于定量玉米种子处理后根系细菌定殖。将处理过的玉米种子种植在温室中的非无菌土壤中,并生长 28 天。每周定量检测细菌的特异性检测,结果表明,在实验期间,两种细菌的根际定殖均稳定在 104-105 CFU/g 之间,该协议可检测到低至 103 CFU/g 的细菌。在另一个实验中,使用链霉素抗性 QST713 和利福平抗性 I-1582 菌株,将其与新开发的 qPCR 方法进行比较稀释平板法。结果还表明,天然微生物群落和另一种接种菌株的存在并不影响这两种菌株中任何一种的根际定殖。该 qPCR 协议还用于定量田间种植的两种玉米和两种大豆品种中 QST713 和 I-1582 的根际定殖。在田间种植种子后两周内,两种细菌均被定量检测到,并且在不同品种中,两种细菌的根际定殖均无显著差异。本文结果证实,所开发的 qPCR 协议可成功用于了解这些细菌在生长室、温室和田间生长的植物中根系定殖的动态。