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Studies on antimicrobial resistance transfer in vitro and existent selectivity of avian antimicrobial-resistant enterobacteriaccae in vivo.

机译:禽类耐药性肠杆菌在体内的体外耐药性转移和存在选择性研究。

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Increasing antimicrobial resistance (AR) has become a severe problem of public health in the world, whereas control of the AR of bacteria will be based on investigation of the AR mechanism. Furthermore, understanding the existent selectivity of AR organisms from animals can prevent the emergence and diffusion of AR effectively. PCR amplifications of gyrA and parC genes have been performed for detecting fluoroquinolones-resistance (FR) genes. A conjugational transfer test has been carried out using a donor which is resistant to tetracycline (TE), ampicillin (AMP), sulfamethoxazole-trimethoprim (SXT), and a recipient which is sensitive to TE, AMP, and SXT. The AR strains have been passed 20 passages. Two groups of chicken inoculated multi-AR Escherichia coli (E. coli) and multi-AR Salmonella, respectively, are mix-fed. The result shows that amino acid codons of Ser-83 and Asp-87 are mutations from gyrA and there are no mutations from parC genes in all the FR strains. Resistance to TE, AM, and SXT can transfer among E. coli and the conjugal transfer frequency of TE is 3x10-7. AR can inherit in 20 passages at least. The multi-AR E. coli and Salmonella can be isolated from all chickens three days after inoculation but CIP-resistant strains decrease during the time run out and disappear at 23 days after inoculation. The results indicate that the mutations of gene gyrA are correlative with the FR phenotype. AR genes that are not connected to the chromosome can transfer horizontally and vertically. AR bacteria can diffuse quickly and eliminate naturally from the host if the chicken is not under the pressure of this antibiotic.
机译:抗菌素耐药性(AR)的增加已成为世界公共卫生的严重问题,而细菌AR的控制将基于对AR机制的研究。此外,了解动物AR生物的存在选择性可以有效防止AR的出现和扩散。gyrA 和 parC 基因的 PCR 扩增已被用于检测氟喹诺酮类药物耐药 (FR) 基因。使用对四环素 (TE)、氨苄西林 (AMP)、磺胺甲噁唑-甲氧苄啶 (SXT) 耐药的供体和对 TE、AMP 和 SXT 敏感的受体进行了共轭转移试验。AR 菌株已通过 20 次传代。两组鸡分别接种多 AR 大肠杆菌 (E. coli) 和多 AR 沙门氏菌,混合喂养。结果表明,Ser-83和Asp-87的氨基酸密码子均为gyrA突变,所有FR菌株均无parC基因突变。对TE、AM和SXT的抗性可以在大肠杆菌之间转移,TE的共生转移频率为3x10-7。AR 至少可以继承 20 个段落。接种后3天,可以从所有鸡中分离出多AR大肠杆菌和沙门氏菌,但CIP耐药菌株在接种时间内减少,并在接种后23天消失。结果表明,gyrA基因的突变与FR表型相关。未与染色体相连的AR基因可以水平和垂直转移。如果鸡没有受到这种抗生素的压力,AR细菌可以迅速扩散并自然地从宿主中排出。

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