首页> 外文期刊>Poultry Science >Quantitative real-time PCR study of the expression and regulation of the tetracycline resistance gene in Riemerella anatipestifer.
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Quantitative real-time PCR study of the expression and regulation of the tetracycline resistance gene in Riemerella anatipestifer.

机译:实时定量PCR研究厌食里氏杆菌四环素抗性基因的表达和调控。

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摘要

Riemerella anatipestifer (RA) is one of the most important pathogens of 1- to 8-wk-old ducklings that severely affects the development of the duck industry in China. Every year, antibiotic medicines including tetracycline and doxycycline are used in the duck industry. Few reports compare the expression of multidrug-resistant genes in RA before and after addition of chemical drugs. With this in mind, the direct effects of gradient concentration of tetracyclines on the expression of tetracycline resistance genes (TETr) in RA at the cDNA level were studied by using a quantitative real-time PCR method. The expression of TETr, tetA, tetC, and tetM was investigated in ATCC11845 and in 30 RA isolated from different samples. Using a range of doxycycline concentrations up to 50% of the minimum inhibitory concentration (MIC), the optimal induction concentration of 0.0625 micro g/mL was selected. Under the optimal inducible expression, concentrations of TETr, tetC, and tetM cDNA were detected in all isolates, and the highest mRNA expression level of TETr genes was shown. Additionally, the expression levels of 3 TETr genes in RA14 (tetA and tetC) and RA17 (tetM and tetC) were compared. Both tetC and tetA found in isolate RA14 was found to express both tetC and tetA, and tetC cDNA was detected in isolate RA17 at all doxycycline concentrations tested, whereas tetM cDNA was not detected at any concentration. We can conclude that resistance pump is the main mechanism of tetracycline antibiotic resistance, and under the action of drug resistance pump tetC, the expression of tetM was not activated in RA17. These data suggest that the mRNA expression level of TETr genes was correlated with the MIC values, indicating that the degree of drug resistance is determined by the expression levels of TETr genes. Also, the induction of TETr is the major tetracycline resistance mechanism in RA, especially the resistance pump. However, lower concentrations of doxycycline induced higher TETr expression, and higher concentrations inhibited TETr expression. Maybe that is the reason for selection mutation to make tolerated bacteria survive.
机译:鸭嘴黎氏菌(Riemerella anatipestifer,RA)是1至8周龄小鸭最重要的病原体之一,严重影响了中国鸭业的发展。每年,鸭业都使用抗生素药物,包括四环素和强力霉素。很少有报道比较化学药物添加前后RA中多药耐药基因的表达。考虑到这一点,使用定量实时PCR方法研究了四环素梯度浓度对RA在cDNA水平上RA中四环素抗性基因(TETr)表达的直接影响。在ATCC11845和从不同样品中分离出的30 RA中研究了TETr,tetA,tetC和tetM的表达。使用高达最小抑菌浓度(MIC)50%的强力霉素浓度范围,选择最佳诱导浓度0.0625 micro g / mL。在最佳诱导表达下,在所有分离物中检测到TETr,tetC和tetM cDNA的浓度,并显示出TETr基因的最高mRNA表达水平。此外,比较了RA14(tetA和tetC)和RA17(tetM和tetC)中3个TETr基因的表达水平。发现在分离株RA14中发现的tetC和tetA都表达tetC和tetA,并且在所有测试的强力霉素浓度下,在分离株RA17中都检测到tetC cDNA,而在任何浓度下均未检测到tetM cDNA。可以得出结论,耐药泵是四环素类抗生素耐药的主要机制,在耐药泵tetC的作用下,RA17中tetM的表达未被激活。这些数据表明,TETr基因的mRNA表达水平与MIC值相关,表明耐药性的程度由TETr基因的表达水平决定。另外,TETr的诱导是RA中主要的四环素抗性机制,尤其是电阻泵。但是,较低的强力霉素浓度会诱导较高的TETr表达,而较高的浓度会抑制TETr表达。也许这就是选择突变使耐受细菌存活的原因。

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