以丙氨酸消旋酶为靶点抑制L和d氨基酸形成空肠弯曲菌生物膜

Biofilms Pub Date : 2020-07-01 DOI:10.5194/biofilms9-137
Bassam A. Elgamoudi, T. Taha, V. Korolik
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引用次数: 0

摘要

细菌病原体形成生物膜的能力是与其发病机制和传播有关的重要毒力机制。生物膜在不利的环境条件下生存起着至关重要的作用,是微生物污染和抗生素耐药性的宿主。对于肠道病原体空肠弯曲杆菌,生物膜被认为是通过食物链传播的一个促成因素,目前还没有已知的干预方法。在这里,我们提出了一种通过应用D-氨基酸(DA)和L-氨基酸(LA)来减少空肠弯曲菌生物膜形成的非常规方法。我们发现,除Lalanine外,DA(而非LA)可减少高达70%的生物膜形成。DAs处理空肠弯曲菌细胞改变了生物膜结构,减少了淀粉样原纤维的出现。此外,与单独的DCS治疗相比,DA的混合物将D-环丝氨酸(DCS)的抗菌功效提高了32%。出乎意料的是,D-丙氨酸能够逆转其他DA以及DCS的抑制作用。此外,L-丙氨酸和D-色氨酸降低了丙氨酸外消旋酶(alr)和D-丙氨酸-D-丙氨酸连接酶(ddlA)的转录水平。我们的研究结果表明,DAs的组合可以减少空肠弯曲菌的生物膜形成、活力和持久性。
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Alanine racemase as target to inhibit the Campylobacter jejuni biofilm formation by L and D-amino acids
The ability of bacterial pathogens to form biofilm is an important virulence mechanism in relation to its pathogenesis and transmission. Biofilms play a crucial role in survival in unfavourable environmental conditions, act as reservoirs of microbial contamination and antibiotic resistance. For intestinal pathogen Campylobacter jejuni, biofilms are considered to be a contributing factor in transmission through the food chain and currently, there are no known methods for intervention. Here we present an unconventional approach to reducing biofilm formation by C. jejuni by the application of D-amino acids (DAs), and L-amino acids (LAs). We found that DAs not LAs, except Lalanine, reduced biofilm formation by up to 70%. The treatment of C. jejuni cells with DAs changed the biofilm architecture and reduced the appearance of amyloid-like fibrils. In addition, a mixture of DAs enhanced antimicrobial efficacy of D-Cycloserine (DCS) up to 32% as compared with DCS treatment alone. Unexpectedly, D-alanine was able to reverse the inhibitory effect of other DAs as well as DCS. Furthermore, L-alanine and D-tryptophan decreased transcript levels of alanine racemase (alr) and D-alanine-D-alanine ligase (ddlA). Our findings suggest that a combination of DAs could reduce biofilm formation, viability and persistence of C. jejuni.
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