A novel virulence gene, cviA1 of Clavibacter michiganensis for necrosis development in the Nicotiana benthamiana plant

烟草 生物 米氏棒杆菌 毒力 基因 微生物学 病毒学 植物 遗传学 病菌
作者
In‐Sul Hwang,Eom‐Ji Oh,Chang‐Sik Oh
出处
期刊:Microbiological Research [Elsevier BV]
卷期号:285: 127743-127743
标识
DOI:10.1016/j.micres.2024.127743
摘要

Clavibacter michiganensis is a Gram-positive bacterium that causes diverse disease symptoms in tomatoes and Nicotiana benthamiana, a surrogate host plant, including canker, blister lesions, and wilting. Previously, we reported that C. michiganensis also causes necrosis in N. benthamiana leaves. Here, to identify novel virulence genes of C. michiganensis required for necrosis development in N. benthamiana leaves, we screened 1,862 transposon-inserted mutants and identified a mutant strain that exhibited weak and delayed necrosis, whereas there was no discernible difference in blister lesions, canker, or wilting symptoms. Notably, this mutant caused canker similar to that of the wild-type strain, but caused mild wilting in tomato. This mutant carried a transposon in a chromosomal gene, called Clavibactervirulence gene A1 (cviA1). CviA1 encodes a 180-amino acid protein with a signal peptide (SP) at the N-terminus and two putative transmembrane domains (TMs) at the C-terminus. Interestingly, deletion of the SP or the C-terminus, including the two putative TMs, in CviA1 failed to restore full necrosis in the mutant, highlighting the importance of protein secretion and the putative TMs for necrosis. A paralog of cviA1, cviA2 is located on the large plasmid pCM2 of C. michiganensis. Despite its high similarity to cviA1, the introduction of cviA2 into the cviA1 mutant strain did not restore virulence. Similarly, the introduction of cviA1 into the Clavibacter capsici type strain PF008, which initially lacks cviA1, did not enhance necrosis symptoms. These results reveals that the chromosomal cviA1 gene in C. michiganensis plays an important role in necrosis development in N. benthamiana leaves.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Horizon应助朱朱看文献采纳,获得10
刚刚
难过的尔丝完成签到,获得积分10
刚刚
FashionBoy应助lawang采纳,获得10
刚刚
刚刚
科目三应助lawang采纳,获得10
刚刚
bkagyin应助lawang采纳,获得10
刚刚
情怀应助lawang采纳,获得10
刚刚
完美世界应助lawang采纳,获得10
1秒前
李爱国应助lawang采纳,获得30
1秒前
领导范儿应助lawang采纳,获得10
1秒前
英俊的铭应助lawang采纳,获得10
1秒前
CipherSage应助lawang采纳,获得10
1秒前
研友_VZG7GZ应助桃子采纳,获得10
1秒前
研友_VZG7GZ应助wgm采纳,获得10
2秒前
chen发布了新的文献求助10
2秒前
加油小天鹅完成签到,获得积分10
3秒前
Alaiiif应助daxixi采纳,获得10
3秒前
香蕉觅云应助辣条采纳,获得10
3秒前
充电宝应助章鱼采纳,获得10
4秒前
4秒前
传奇3应助无辜曼冬采纳,获得10
4秒前
芊芊完成签到,获得积分10
5秒前
6秒前
owldan发布了新的文献求助10
6秒前
彭于晏应助哇哦采纳,获得10
7秒前
汉堡包应助傻傻的哈密瓜采纳,获得10
7秒前
小豆豆完成签到,获得积分10
7秒前
科研通AI6.4应助自由枕头采纳,获得30
8秒前
小智0921完成签到,获得积分10
8秒前
9秒前
搜集达人应助wgm采纳,获得10
10秒前
深情安青应助哈哈采纳,获得30
10秒前
欢呼书包完成签到,获得积分20
11秒前
11秒前
owldan完成签到,获得积分10
12秒前
jam完成签到,获得积分10
12秒前
无霜完成签到,获得积分10
12秒前
12秒前
13秒前
是个小刺儿完成签到,获得积分10
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Cronologia da história de Macau 5000
咳嗽・喀痰の診療ガイドライン第2版2025 800
Petrology and Plate Tectonics 800
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
The globalisation of real estate: the politics and practice of foreign real estate investment 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 光电子学 物理化学 电极 基因 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 6999842
求助须知:如何正确求助?哪些是违规求助? 8675256
关于积分的说明 18394052
捐赠科研通 6476405
什么是DOI,文献DOI怎么找? 3100296
关于科研通互助平台的介绍 2164794
邀请新用户注册赠送积分活动 2076674