What role do biocontrol agents with Mg 2+ play in the fate of antibiotic resistome and pathogenic bacteria in the phyllosphere?

Author:

Zhi Qiqi12ORCID,Tan Ge3,Wu Shaolong4,Ma Qianqian5,Fan Jianqiang6,Chen Yiqiang6,Li Jingjing6,Hu Zhengrong4,Xiao Yansong7,Li Liangzhi12ORCID,Liu Zhenghua12,Yang Zhaoyue12,Yang Zhendong8,Meng Delong12,Yin Huaqun12ORCID,Tang Qianjun5ORCID,Liu Tianbo4ORCID

Affiliation:

1. School of Minerals Processing and Bioengineering, Central South University, Changsha, China

2. Key Laboratory of Biometallurgy, Ministry of Education, Changsha, China

3. China Tobacco Hunan Industrial Co., Ltd., Changsha, China

4. Tobacco Research Institute of Hunan Province, Changsha, China

5. College of Plant Protection, Hunan Agricultural University, Changsha, China

6. Technology Center, China Tobacco Fujian Industrial Co., Ltd, Xiamen, Fujian, China

7. Chenzhou Tobacco Company of Hunan Province, Chenzhou, China

8. School of Architecture and Civil Engineering, Chengdu University, Chengdu, Sichuan, China

Abstract

ABSTRACT The contamination of the plant phyllosphere with antibiotics and antibiotic resistance genes (ARGs), caused by application of antibiotics, is a significant environmental issue in agricultural management. Alternatively, biocontrol agents are environmentally friendly and have attracted a lot of interest. However, the influence of biocontrol agents on the phyllosphere resistome remains unknown. In this study, we applied biocontrol agents to control the wildfire disease in the Solanaceae crops and investigated their effects on the resistome and the pathogen in the phyllosphere by using metagenomics. A total of 250 ARGs were detected from 15 samples, which showed a variation in distribution across treatments of biocontrol agents (BA), BA with Mg 2+ (T1), BA with Mn 2+ (T2), and kasugamycin (T3) and nontreated (CK). The results showed that the abundance of ARGs under the treatment of BA-Mg 2+ was lower than that in the CK group. The abundance of cphA3 (carbapenem resistance), PME-1 (carbapenem resistance), tcr3 (tetracycline antibiotic resistance), and AAC (3)-VIIIa (aminoglycoside antibiotic resistance) in BA-Mg 2+ was significantly higher than that in BA-Mn 2+ ( P < 0.05). The abundance of cphA3 , PME_1, and tcr3 was significantly negatively related to the abundance of the phyllosphere pathogen Pseudomonas syringae ( P < 0.05). We also found that the upstream and downstream regions of cphA3 were relatively conserved, in which rpl , rpm, and rps gene families were identified in most sequences (92%). The Ka/Ks of cphA3 was 0 in all observed sequences, indicating that under the action of purifying selection, nonsynonymous substitutions are often gradually eliminated in the population. Overall, this study clarifies the effect of biocontrol agents with Mg 2+ on the distribution of the phyllosphere resistome and provides evolutionary insights into the biocontrol process. IMPORTANCE Our study applied metagenomics analysis to examine the impact of biocontrol agents (BAs) on the phyllosphere resistome and the pathogen. Irregular use of antibiotics has led to the escalating dissemination of antibiotic resistance genes (ARGs) in the environment. The majority of BA research has focused on the effect of monospecies on the plant disease control process, the role of the compound BA with nutrition elements in the phyllosphere disease, and the resistome is still unknown. We believe BAs are eco-friendly alternatives for antibiotics to combat the transfer of ARGs. Our results revealed that BA-Mg 2+ had a lower relative abundance of ARGs compared to the CK group, and the phyllosphere pathogen Pseudomonas syringae was negatively related to three specific ARGs, cphA3 , PME-1, and tcr3 . These three genes also present different Ka/Ks. We believe that the identification of the distribution and evolution modes of ARGs further elucidates the ecological role and facilitates the development of BAs, which will attract general interest in this field.

Publisher

American Society for Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3