Black shank-mediated alteration of the community assembly of rhizosphere soil bacteria in tobacco.

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1428284
Junchi Ma, Jili Chen, Qing Zhang, Yumei Dong, Zhihua Li, Junqiu Xie, Dongmei Yang, Lequn Zhou, Dahao Yan, Bo Zhou, Tao Liu
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Abstract

Introduction: There is a close and complex interaction between the elements in the aboveground-underground ecosystem during the growth and development of plants. Specifically, when the aboveground part of plants is infected by pathogens, it induces the plant rhizosphere to synthesize specific root exudates. Consequently, a group of beneficial rhizosphere soil bacteria is recruited to help plants resist diseases. However, the changes in the rhizosphere soil bacterial community of plants under infection by oomycete pathogens remain unknown.

Methods: Three experimental treatments were set up in this experiment: soils inoculated with P. nicotianae, no-inoculation with P. nicotianae, and a control. The control treatment was composed of soils without transplanted tobacco plants, with the pathogen inoculated twice at an interval of eight days to ensure a successful P. nicotianae infection. P. nicotianae inoculation treatments were designed using the hyphal block inoculation method. In the non-inoculation treatment, tobacco plants were grown normally without pathogen inoculation. The tobacco plants were grown in a greenhouse.

Results: This study demonstrates that tobacco plants recruit microorganisms at the rhizosphere level as a defense mechanism against disease after infection by the oomycete pathogen Phytophthora nicotianae. Specific rhizosphere soil bacteria were screened in vitro to promote tobacco growth in a biofilm-forming manner, which induced the systemic resistance of the plants to P. nicotianae. The recruitment of rhizosphere soil bacteria to the inter-root zone of tobacco plants after infection by P. nicotianae can help subsequently cultivated tobacco plants in the same soil resist pathogen infestation.

Discussion: In conclusion, the present study confirms that infestation caused by oomycete pathogens alters the composition of the plant rhizosphere soil bacterial community and recruits a specific group of beneficial microorganisms that induce disease resistance and promote plant growth, thereby maximizing the protection of progeny grown in the same soil against the disease.

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黑柄介导的烟草根瘤土壤细菌群落组合的改变。
引言在植物的生长发育过程中,地上地下生态系统中的各要素之间存在着密切而复杂的相互作用。具体来说,当植物的地上部分受到病原体感染时,会诱导植物根圈合成特定的根渗出物。因此,一群有益的根圈土壤细菌被招募进来,帮助植物抵抗病害。然而,在卵菌病原体感染下,植物根圈土壤细菌群落的变化仍然未知:本实验设置了三个实验处理:接种烟粉虱的土壤、未接种烟粉虱的土壤和对照。对照处理由没有移栽烟草植株的土壤组成,病原体接种两次,每次间隔八天,以确保烟粉虱成功感染。烟粉虱接种处理采用菌丝块接种法。在非接种处理中,烟草植株正常生长,不接种病原体。烟草植物在温室中生长:本研究表明,烟草植物在受到卵菌病原体烟草根瘤蚜感染后,会在根瘤层招募微生物作为病害防御机制。体外筛选出的特定根圈土壤细菌能以形成生物膜的方式促进烟草生长,从而诱导烟草植株对烟粉虱产生系统抗性。烟粉虱感染烟草后,根圈土壤细菌会被引入烟草植株的根际区,这有助于随后在同一土壤中栽培的烟草植株抵御病原体的侵袭:总之,本研究证实,卵菌病原体侵染会改变植物根圈土壤细菌群落的组成,并招募一组特定的有益微生物,诱导抗病性并促进植物生长,从而最大限度地保护在同一土壤中生长的后代免受病害侵染。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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