Effect of Acetic Acid on Biofilm Formation in Paracidovorax citrulli, Causal Agent of Bacterial Fruit Blotch.

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Jincheng Yang, Liang Mao, Yousaf Gulfam, Muhammad Zeeshan, Xiaodong Wang, Ting Fan
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引用次数: 0

Abstract

The unique tissue structure of pathogenic bacteria biofilm plays an important role in its pathogenicity and bactericide resistance. Inhibition or destruction of biofilm formation of pathogenic bacteria is of great significance for the control of plant bacterial diseases. In this study, Paracidovorax citrulli was inoculated into KB medium containing acetic acid, and after shaking at 28°C and 55 r/min for 48 h, it was found that the content of extracellular polysaccharide, extracellular protein and extracellular DNA (eDNA) decreased with the increase of acetic acid concentration, which resulted in the decrease of biofilm formation, it is not even possible to form biofilms on plastic slides. When the final concentration of acetic acid in the culture medium was greater than or equal to 0.5 mg/mL, there was no biofilm on the plastic slides. Therefore, the use of acetic acid as an inhibitor of P. citrulli has a good potential for control of bacterial fruit blotch.

醋酸对果实细菌性斑点病病原菌 Paracidovorax citrulli 生物膜形成的影响
病原菌生物膜独特的组织结构对其致病性和对杀菌剂的抗性起着重要作用。抑制或破坏病原菌生物膜的形成对植物细菌病害的防治具有重要意义。本研究将 Paracidovorax citrulli 接种到含醋酸的 KB 培养基中,在 28℃、55 r/min 条件下振荡 48 h 后发现,随着醋酸浓度的增加,胞外多糖、胞外蛋白和胞外 DNA(eDNA)含量减少,导致生物膜形成减少,甚至无法在塑料载玻片上形成生物膜。当培养基中醋酸的最终浓度大于或等于 0.5 毫克/毫升时,塑料载玻片上没有生物膜。因此,使用醋酸作为柠檬褐斑病菌的抑制剂在控制细菌性果斑病方面具有良好的潜力。
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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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