The inhibitory effect of Bacillus amyloliquefaciens L1 on Aeromonas hydrophila and its mechanism
文献类型： 外文期刊
作者： Li, Letian 1 ; Hu, Kun 2 ; Hong, Baohua 1 ; Lu, Xiandong 3 ; Liu, Yanhong 3 ; Xie, Jiasong 1 ; Jin, Shan 1 ; Zhou, Suming 1 ;
作者机构： 1.Ningbo Univ, Sch Marine Sci, Ningbo 315211, Peoples R China
2.Shanghai Ocean Univ, Shanghai 201306, Peoples R China
3.Ningbo Aigene Technol Co LTD, Ningbo 315211, Peoples R China
4.Chinese Acad Fishery Sci, Beijing 100141, Peoples R China
5.Shandong Key Lab Dis Control Mariculture, Qingdao 266237, Peoples R China
关键词： Bacillus amyloliquefaciens; Aeromonas hydrophila; Bacteriostasis; Transcriptome; Mechanistic pathway
期刊名称：AQUACULTURE （ 影响因子：3.224； 五年影响因子：3.591 ）
ISSN： 0044-8486
年卷期： 2021 年 539 卷
页码：
收录情况： SCI
摘要： Aeromonas hydrophila is an important aquatic pathogen, and the use of probiotics is an alternative way of controlling this bacterium. In this study, we evaluated the bacteriostatic effects of the fermentation broth, supernatant, and broken bacteria of Bacillus amyloliquefaciens strain L1 on A. hydrophila T1, X1, and W1 isolated from different sources. The results demonstrated that B. amyloliquefaciens L1 has a general bacteriostatic effect on A. hydrophila; the main bacteriostatic substance was found in the B. amyloliquefaciens L1 supernatant and was associated with an extracellular product. The effects of the B. amyloliquefaciens L1 supernatant on A. hydrophila W1 were analyzed at the transcriptome level to study the antibacterial mechanism. Six normalized cDNA libraries were constructed using RNA from a control group and the B. amyloliquefaciens L1 supernatant treatment group. A total of 103,491,644 clean reads were obtained. Further analysis identified 828 significantly differentially expressed genes (DEGs, including 434 up-regulated and 394 down-regulated genes) in A. hydrophila W1 after treatment with the supernatant of B. amyloliquefaciens L1. In a KEGG pathway analysis, six KEGG pathways were found to be significantly enriched. Among them, the Ribosome pathway was enriched only by significantly up-regulated DEGs. The other pathways, including the TCA cycle pathway, carbon fixation pathways in prokaryotes, pyruvate metabolism pathway, butanoate metabolism pathway, and oxidative phosphorylation pathway were enriched, mostly by down-regulated genes. Moreover, an ipath analysis showed that the ribosome regulatory pathway was annotated by up-regulated genes. Bacterial chemotaxis and the phosphotransferase system were annotated by down-regulated genes.
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