Key Laboratory of Emerging Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
University of Chinese Academy of Sciences, Beijing, China.
J Appl Microbiol. 2018 Jun;124(6):1580-1588. doi: 10.1111/jam.13730. Epub 2018 Mar 13.
Isolation and characterization of pectolytic bacteria associated with soft rot disease of potatoes in Nakuru, Kenya, to provide the basis for the development of disease control measures.
Potato tubers showing symptoms of soft rot were collected from different farms in Molo and Mau Narok regions within Nakuru county. Isolation was done using crystal violet pectate medium (CVPM). Out of the 71 isolates that showed growth on CVPM, pathogenicity tests revealed that 36 of them had the ability to macerate tissues of potato tubers. All the isolates yielded a fragment of approximately 1500 bp after 16S rDNA amplification. Using the BIOLOG microbial identification system, 20 bacterial isolates were identified as Pectobacterium carotovorum subsp. carotovorum, 7 were Pseudomonas fluorescens B while 9 were Ps. fluorescens A. Y1/Y2 primers successfully amplified pectate lyase-encoding (pel) gene, approximately 434 bp, in all the 20 P. carotovorum species. The virulence of the isolated strains to cause disease, according to pectinolytic tests, varied with change in incubation temperature of the test samples. Pectobacterium carotovorum strains were the most virulent at 30°C while disease severity due to infection by Ps. fluorescens A strains was high at 20°C compared to the other isolates.
This study reveals the identity of pectolytic bacterial species from two genera, Pectobacterium and Pseudomonas, as causative agents of potato soft rot in Nakuru, Kenya.
Research findings from this study will aid in developing suitable risk mitigation methods for adoption by farmers to prevent losses due to soft rot.
从肯尼亚纳库鲁的马铃薯软腐病中分离和鉴定果胶分解细菌,为制定病害防治措施提供依据。
从纳库鲁县莫洛和毛纳罗克地区的不同农场收集出现软腐病症状的马铃薯块茎。使用结晶紫果胶培养基(CVPM)进行分离。在 CVPM 上生长的 71 个分离株中,有 36 个具有使马铃薯块茎组织溃烂的能力。所有分离株在 16S rDNA 扩增后均产生约 1500bp 的片段。使用 BIOLOG 微生物鉴定系统,20 个细菌分离株被鉴定为胡萝卜软腐果胶杆菌亚种胡萝卜软腐果胶杆菌,7 个为荧光假单胞菌 B,9 个为荧光假单胞菌 A。Y1/Y2 引物成功扩增了所有 20 个胡萝卜软腐果胶杆菌种的果胶裂解酶编码(pel)基因,约 434bp。根据果胶酶试验,分离株引起疾病的毒力随试验样品的孵育温度变化而变化。在 30°C 时,胡萝卜软腐果胶杆菌菌株的毒力最强,而在 20°C 时,感染荧光假单胞菌 A 菌株导致的病害严重程度高于其他分离株。
本研究揭示了来自两个属,果胶杆菌属和假单胞菌属的果胶分解细菌种是肯尼亚纳库鲁马铃薯软腐病的病原体。
本研究的研究结果将有助于制定适合农民采用的适当风险缓解方法,以防止因软腐病造成的损失。