Chen Xiu P, Ali Liaqat, Wu Li-Yun, Liu Can, Gang Chen X, Huang Qi F, Ruan Jing H, Bao Song Y, Rao Yun P, Yu DaoJin
Fujian Key Laboratory of Traditional Chinese Veterinary Medicine and Animal Health, Fujian Agriculture and Forestry University, Fuzhou, China.
Department of Biosciences, Faculty of Sciences, COMSATS Institute of Information Technology, Islamabad, Pakistan.
Front Microbiol. 2018 Mar 2;9:367. doi: 10.3389/fmicb.2018.00367. eCollection 2018.
In this study, microcosms were established to determine the effect of nitrogen (N) and phosphorus (P) on the multidrug resistance and biofilm-forming abilities of . The expression of biofilm-formation-related genes was detected to establish correlations between genotype and phenotype. Different concentrations of N and P were added to make one control group and four treatment groups. The glass tube method was used to determine biofilm-forming capabilities. Real-time PCR was used to detect the mRNA abundance of six biofilm-formation-related genes in . . No resistant strains were isolated from the control group; meanwhile, multidrug resistance rates were high in the treatment groups. Expression of the biofilm-associated genes , and was detected in all treatment groups; however, there was no expression of . The expression of , and significantly correlated with the concentration of N and P, as well as with the appearance and duration of multidrug resistance in different groups. Overall, the results of this study suggest that biofilm-forming ability plays a key role in the formation of multidrug resistance in . after the addition of N and P to a microcosm.
在本研究中,构建了微宇宙来确定氮(N)和磷(P)对[具体研究对象]的多药耐药性和生物膜形成能力的影响。检测生物膜形成相关基因的表达,以建立基因型与表型之间的相关性。添加不同浓度的N和P,设置一个对照组和四个处理组。采用玻璃管法测定生物膜形成能力。运用实时荧光定量PCR检测[具体研究对象]中六个生物膜形成相关基因的mRNA丰度。对照组未分离出耐药菌株;同时,处理组的多药耐药率较高。在所有处理组中均检测到生物膜相关基因[具体基因名称]、[具体基因名称]和[具体基因名称]的表达;然而,[具体基因名称]未表达。[具体基因名称]、[具体基因名称]和[具体基因名称]的表达与N和P的浓度以及不同组中多药耐药的出现和持续时间显著相关。总体而言,本研究结果表明,在微宇宙中添加N和P后,生物膜形成能力在[具体研究对象]多药耐药性的形成中起关键作用。