Botany Department, Faculty of Science, Assuit University, Assuit 71516, Egypt.
Folia Microbiol (Praha). 2010 Jan;55(1):47-52. doi: 10.1007/s12223-010-0008-7. Epub 2010 Mar 25.
Common bean seed lots collected from different seed dealers and Malawii agriculture station were screened for the presence of Xanthomonas axonopodis pv. phaseoli. In the laboratory the pathogen was isolated following the routine laboratory assay method, i.e. direct plating method using yeast extract-dextrose-calcium carbonate agar medium (YDC). Yellow, convex, mucoid colonies of Xanthomonas were consistently isolated on YDC from seed samples. The presumptive pathogen was confirmed by isolation on semiselective medium, such as mTBM and MD5A. Further, the pathogen was confirmed by biochemical, physiological and, finally, the pathogenicity tests. Five samples out of seven were positive for Xanthomonas. The isolates were found to cause common blight of 3-week-old common bean plants by 7 d after inoculation. Bacteria with the same characteristics as those inoculated were re-isolated from the infected plants.
从不同种子经销商和马拉维农业站收集的普通菜豆种子进行了筛选,以检测是否存在菜豆细菌性萎蔫病菌。在实验室中,按照常规实验室检测方法,即使用酵母提取物-葡萄糖-碳酸钙琼脂培养基(YDC)的直接平板法,分离出病原菌。从种子样品中,YDC 上始终分离出黄色、凸起、黏液状的黄单胞菌菌落。通过半选择性培养基(如 mTBM 和 MD5A)分离,可确认疑似病原菌。进一步通过生化、生理特性试验,最终进行致病性试验。7 个样本中有 5 个为黄单胞菌阳性。接种后 7 天,这些分离株可引起 3 周龄普通菜豆植物的普通疫病。从感染植物中重新分离出与接种物具有相同特征的细菌。