ISOLATION, CHARACTERIZATION AND MANAGEMENT OF Alternaria solani CAUSING EARLY BLIGHT IN TOMATO THROUGH DIFFERENT BACTERIAL STRAINS

Q4 Agricultural and Biological Sciences
M. N. Subhani, F. Ali, Shaista Nasir, A. A. Shahid
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Abstract

Tomato is grown widely in almost 140 countries having annual production of 151 million tons and is mostly grown in South America. Pure culture of Alternaria solani isolated from twig and leaf samples was prepared. The fungal colonies were cultured in Broth of MEA and PDA for 5-7 days at 25oC. Cetyl-trimethyl-ammonium-bromide (CTAB) extraction technique was applied for DNA extraction of A. solani with little modification. Molecular identification with ITS primers of isolated fungi was undertaken and a 594bp size of the band was obtained. The DNA sequence was submitted to Gen Bank having Gene Bank no. MN200940. The sequenced data was 100% similar to the Alternaria isolate Alt-C81 of Gen Bank accession code MN044802. Biological control agents were applied and data were collected at an interval of 3, 5, 7 and 10 days. The maximum inhibition percentage after 3 days (84.23%) was recorded by Azospirillum lipoferum (RB-38) while the lowest inhibition (44.84%) was recorded by Bacillus subtilis (RB-59). After 7 days of incubation, the highest inhibition (89.13%) was observed by using A. lipoferum (RB-38) and the lowest (60.57%) by Bacillus spp. (RB-43), respectively. After 10 days of incubation, the highest inhibition percentage (95.91%) was recorded by B. subtilis (RB-59) and the lowest by Bacillus thuringiensis (RB-16) with PI of 13.71% respectively. These results suggest that the bacterial isolates studied have a good potential to be used as biocontrol agents of A. solani in tomato plants for the sustainable production of tomatoes without using fungicides. It not gives a good perspective for sustainability and also reduce the environmental pollution.  
番茄早疫病病菌的分离、鉴定及防治
番茄在近140个国家广泛种植,年产量1.51亿吨,主要种植在南美洲。制备了从枝条和叶片样品中分离得到的茄格孢的纯培养物。真菌菌落在MEA和PDA的肉汤中在25℃下培养5-7天。采用十六烷基三甲基溴化铵(CTAB)提取技术对龙葵DNA进行了提取,并对其进行了微改性。用分离真菌的ITS引物进行分子鉴定,获得594bp大小的条带。将DNA序列提交给基因库编号为MN200940的Gen Bank。测序数据与Gen Bank登录代码MN044802的Alternaria分离株Alt-C81 100%相似。施用生物对照剂,并每隔3、5、7和10天收集数据。3天后的最大抑制率(84.23%)由硫铁氮螺菌(RB-38)记录,而最低抑制率(44.84%)由枯草芽孢杆菌(RB-59)记录。孵育7天后,使用A.lipoferum(RB-38)观察到最高的抑制作用(89.13%),使用Bacillus spp.(RB-43)分别观察到最低的(60.57%)。培养10天后,枯草芽孢杆菌(RB-59)和苏云金芽孢杆菌(RB-16)的抑制率最高(95.91%),PI分别为13.71%。这些结果表明,所研究的细菌分离株在不使用杀菌剂的情况下,具有良好的潜力,可作为番茄植株中茄尼a.solani的生物防治剂,用于番茄的可持续生产。它没有为可持续发展提供一个良好的视角,也没有减少环境污染。
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来源期刊
Plant Cell Biotechnology and Molecular Biology
Plant Cell Biotechnology and Molecular Biology Agricultural and Biological Sciences-Horticulture
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