Research and Production Center of Microbiology and Virology" LLP, Almaty, Kazakhstan.
Kazakh Research Institute of Plant Protection and Quarantine named after Zh. Zhyembayev, LLP, Almaty, Kazakhstan.
Braz J Biol. 2024 Aug 5;84:e285493. doi: 10.1590/1519-6984.285493. eCollection 2024.
The paper presents data on phytosanitary monitoring of garden cenoses for fire blight in the Turkestan, Zhambyl, and Almaty regions of Kazakhstan. The purpose of this study is to assess the phytosanitary situation in various regions of Kazakhstan, determine the extent of fire blight spread, and isolate and identify the fire blight pathogen. During the study, methods such as hypersensitivity, pathogenicity, and fluorescent simplification-based specific hybridization polymerase chain reaction (FLASH-PCR) were used. It was found that in all the surveyed areas, disease foci were identified. For the first time, the fire blight pathogen was detected on fruit crops such as plum, peach, cherry plum, and quince, as well as on wild apricots. 274 plant samples were collected from which microorganisms were isolated. Isolates related to the fire blight pathogen Erwinia amylovora were identified by methods of hypersensitivity, pathogenicity, and FLASH-PCR diagnostics. Of the 156 isolates of microorganisms isolated from apple tree plant samples, 21 inhibited the in vitro growth of E. amylovora to varying degrees. Isolates 16.2 and 19.2 with maximum antagonistic activity were selected, where the pathogen growth inhibition zones were 52.2 ± 2.58 mm and 45.6 ± 0.55 mm, respectively. Based on the obtained sequence of nucleotides of the 16SpRNA gene site, it was found that the selected isolates with high antagonistic activity belonged to the Pseudomonas genus. In the future, based on these isolates, a new biological product for fire blight control can be created and adapted to the natural and climatic conditions of Kazakhstan.
本文介绍了哈萨克斯坦突厥斯坦、江布尔和阿拉木图地区花园生物群落梨火疫病植物检疫监测的数据。本研究的目的是评估哈萨克斯坦不同地区的植物检疫情况,确定梨火疫病的传播范围,分离和鉴定梨火疫病病原菌。在研究过程中,使用了过敏反应、致病性和基于荧光简化的特异性杂交聚合酶链反应(FLASH-PCR)等方法。结果发现,在所调查的所有地区都发现了病源。首次在李、桃、樱桃李和榅桲等水果作物以及野生杏树上检测到了梨火疫病病原菌。从 274 个植物样本中采集了微生物进行分离。通过过敏反应、致病性和 FLASH-PCR 诊断方法鉴定出与梨火疫病病原菌欧文氏菌属相关的分离物。从苹果树植物样本中分离出的 156 个微生物分离物中,有 21 个对 E. amylovora 的体外生长有不同程度的抑制作用。选择具有最大拮抗活性的分离物 16.2 和 19.2,其对病原菌的生长抑制带分别为 52.2±2.58mm 和 45.6±0.55mm。根据获得的 16SpRNA 基因位点的核苷酸序列,发现具有高拮抗活性的所选分离物属于假单胞菌属。未来,可以基于这些分离物,为梨火疫病防治创造一种新的生物制剂,并适应哈萨克斯坦的自然和气候条件。