Zhou Gang, Wang Ying-Si, Peng Hong, Li Su-Juan, Sun Ting-Li, Shen Peng-Fei, Xie Xiao-Bao, Shi Qing-Shan
Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, State Key Laboratory of Applied Microbiology Southern China, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou, Guangdong, 510070, People's Republic of China.
Appl Microbiol Biotechnol. 2021 Apr;105(7):2841-2854. doi: 10.1007/s00253-020-11057-1. Epub 2021 Mar 25.
The genus Citrobacter is commonly found in environmental and industrial settings, some members of which have been used for bioremediation of heavy metals owing to the absorption ability of their biofilms. Although our previous studies have found that the outer membrane protein A (OmpA) contributes to the process of Citrobacter werkmanii biofilm formation, the underlying mechanisms remain elusive. Therefore, we deleted ompA from the genome of C. werkmanii and investigated its phenotypes in comparison to the wild type strain (WT) and the complementary strain using biochemical and molecular techniques including RNA-Seq. Our results demonstrated that the deletion of ompA led to an increase in biofilm formation on both polystyrene and glass surfaces due to upregulation of some biofilm formation related genes. Meanwhile, swimming ability, which is mediated by activation of flagellar assembly genes, was increased on semi-solid plates in the ∆ompA strain when compared with WT. Additionally, inactivation of ompA also caused increased 1,2-benzisothiazolin-3-one (BIT) resistance, differential responses to Ca stress, curli protein expression and cellulose production. Finally, ∆ompA caused differential expression of a total of 1470 genes when compared with WT, of which 146 were upregulated and 1324 were downregulated. These genes were classified into different Gene Ontology (GO) and KEGG pathways. In summary, ompA in C. werkmanii contributes to a variety of biological functions and may act as a target site to modulate biofilm formation. KEY POINTS: • ompA is a negative regulator for biofilm formation by C. werkmanii. • ompA inhibits swimming motility of C. werkmanii. • ompA deletion causes different expression profiles in C. werkmanii.
柠檬酸杆菌属常见于环境和工业环境中,其中一些成员因其生物膜的吸收能力而被用于重金属的生物修复。尽管我们之前的研究发现外膜蛋白A(OmpA)有助于韦氏柠檬酸杆菌生物膜的形成过程,但其潜在机制仍不清楚。因此,我们从韦氏柠檬酸杆菌基因组中删除了ompA,并使用包括RNA测序在内的生化和分子技术,与野生型菌株(WT)和互补菌株相比,研究了其表型。我们的结果表明,ompA的缺失导致在聚苯乙烯和玻璃表面上生物膜形成增加,这是由于一些生物膜形成相关基因的上调。同时,与WT相比,在半固体平板上,由鞭毛组装基因激活介导的游动能力在∆ompA菌株中有所增加。此外,ompA的失活还导致对1,2-苯并异噻唑啉-3-酮(BIT)的抗性增加、对钙胁迫的不同反应、卷曲蛋白表达和纤维素产生。最后,与WT相比,∆ompA导致总共1470个基因的差异表达,其中146个上调,1324个下调。这些基因被分类到不同的基因本体论(GO)和KEGG途径中。总之,韦氏柠檬酸杆菌中的ompA有助于多种生物学功能,可能作为调节生物膜形成的靶位点。要点:•ompA是韦氏柠檬酸杆菌生物膜形成的负调节因子。•ompA抑制韦氏柠檬酸杆菌的游动能力。•ompA缺失导致韦氏柠檬酸杆菌中不同的表达谱。