Effects of Bacillus in Pectobacterium quorum quenching: A survey of two different acyl-homoserine lactonases

被引:1
|
作者
Yamchi, Ahad [1 ]
Rahimi, Maryam [2 ]
Akbari, Ramin [3 ]
Ghobadi, Cyrus [4 ]
Aryapour, Hassan [5 ]
机构
[1] Gorgan Univ Agr Sci & Nat Resources, Dept Plant Biotechnol, Gorgan, Iran
[2] Univ Zabol, Dept Hort, Zabol, Iran
[3] Isfahan Univ Technol, Dept Agr Biotechnol, Esfahan, Iran
[4] Isfahan Univ Technol, Dept Hort Sci, Esfahan, Iran
[5] Golestan Univ, Fac Sci, Dept Biol, Gorgan, Iran
关键词
Pectobacterium carotovorum; Quorum sensing; Acyl-homoserine lactone; Virulence genes; Molecular dynamic modeling; III SECRETION SYSTEM; PARTICLE MESH EWALD; PSEUDOMONAS-AERUGINOSA; TWITCHING MOTILITY; MOLECULAR-DYNAMICS; BIOFILM FORMATION; VIRULENCE; POINT; AIIA;
D O I
10.1007/s12223-024-01139-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Numerous functions in pathogenic Pectobacterium are regulated by quorum sensing (QS). Two different aiiA genes isolated from Bacillus sp. A24(aiiA(A24)) and Bacillus sp. DMS133(aiiA(DMS133)) were used. Both genes encode acyl-homoserine lactonase (AiiA), which disrupts QS in Pectobacterium. To investigate the effect of different AiiAs on the inhibition of Pectobacterium carotovorum pathogenicity, two aiiA genes from different Bacillus strains were cloned and the resulting plasmids pME6863 (aiiA(A24)) and pME7080 (aiiAD(MS133)) were transformed into P. carotovorum EMPCC cells. The effects of different lactonases on virulence features such as enzymatic activity, twitching and swimming motilities, and production of pellicle and biofilm formation were investigated. In EMPCC/pME6863, twitching and swimming motilities, and pellicle production were significantly reduced compared with EMPCC/pME7080. Quantitative real-time PCR (qRT-PCR) was used to measure virulence gene expression in transformed cells compared with expression levels in wild-type EMPCC. The expression of peh and hrpL genes was greatly reduced in EMPCC/pME6863 compared with EMPCC/pME7080. The sequence alignment and molecular dynamic modeling of two different AiiA(A24 )and AiiADMS133 proteins suggested that the replacement of proline 210 from AiiA(A24) to serine in AiiA(DMS133) caused the reduction of enzyme activity in AiiADMS133.
引用
收藏
页码:913 / 926
页数:14
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