<p>The biocontrol efficacy of probiotics <i>Bacillus velezensis</i> B31 against fusarium wilt is contingent upon its successful colonization in the plant rhizosphere. This study aimed to develop a quantitative detection method for probiotics strain B31 and to monitor its rhizosphere dynamics. Utilizing comparative genomics, a specific gene in strain B31 was identified, which facilitated the design of precise primers and a Taqman probe. The resulting real-time PCR assay demonstrated high specificity to strain B31 and high sensitivity with detection limit of 28 copies/µL of the genome. Comparative analysis with regular PCR methods revealed a strong correlation, yet highlighted the superior sensitivity and rapidity of the real-time PCR technique. The temporal colonization profile of strain B31, post root-inoculation, was charted using this assay. An initial rhizosphere population of 7.2 × 10<sup>7</sup>&#xa0;CFU&#xa0;g<sup>−1</sup> was observed, which then tapered to 10<sup>5</sup>&#xa0;CFU&#xa0;g<sup>−1</sup> over 14&#xa0;days. These dynamics corresponded with the observed control effect, where a higher initial population correlated with enhanced disease suppression. This study underscores the potential of real-time PCR as a robust tool for biocontrol agents’ monitoring, offering insights into the microbial interactions within the rhizosphere.</p>

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Development and Utilization of Quantitative Detection for Probiotics Bacillus velezensis B31 with Potential Protection Against Tomato Fusarium Wilt

  • Zhenhe Su,
  • Yanan Gao,
  • Lemeng Dong,
  • Yunzhuan He,
  • Qinggang Guo,
  • Ping Ma

摘要

The biocontrol efficacy of probiotics Bacillus velezensis B31 against fusarium wilt is contingent upon its successful colonization in the plant rhizosphere. This study aimed to develop a quantitative detection method for probiotics strain B31 and to monitor its rhizosphere dynamics. Utilizing comparative genomics, a specific gene in strain B31 was identified, which facilitated the design of precise primers and a Taqman probe. The resulting real-time PCR assay demonstrated high specificity to strain B31 and high sensitivity with detection limit of 28 copies/µL of the genome. Comparative analysis with regular PCR methods revealed a strong correlation, yet highlighted the superior sensitivity and rapidity of the real-time PCR technique. The temporal colonization profile of strain B31, post root-inoculation, was charted using this assay. An initial rhizosphere population of 7.2 × 107 CFU g−1 was observed, which then tapered to 105 CFU g−1 over 14 days. These dynamics corresponded with the observed control effect, where a higher initial population correlated with enhanced disease suppression. This study underscores the potential of real-time PCR as a robust tool for biocontrol agents’ monitoring, offering insights into the microbial interactions within the rhizosphere.