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脆弱拟杆菌中克林霉素耐药性的转移

Clindamycin resistance transfer in Bacteroides fragilis.

作者信息

Teng L J, Liaw S J, Luh K T, Ho S W

机构信息

Department of Laboratory Medicine, National Taiwan University Hospital, Taipei, R.O.C.

出版信息

Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi. 1994 Nov;27(4):186-95.

PMID:9747348
Abstract

Clindamycin is one of the antimicrobial agents most commonly used against anaerobes. Resistance to clindamycin in Bacteroides fragilis has been increasing recently. Thirty strains of clindamycin-resistant (including multi-resistant) B. fragilis were collected for study of cross-resistance to beta-lactam agents and beta-lactam--beta-lactamase inhibitor and resistance transferability. Imipenem was the most active drug against these 30 isolates. Resistance to clindamycin was transferred to a recipient in 12 out of 30 donor strains by using filter-mating. Of 12 transconjugants, only three had detectable plasmids by alkaline lysis method and the remaining nine strains lacked plasmids. The transfer frequencies ranged from 10(-4) to 10(-6). The role of plasmid in the resistance transfer was not certain. However, the results suggest that non-plasmid-mediated transfer accounted for the majority of the transfers of clindamycin-resistance of B. fragilis in this study. Tetracycline resistance was co-transferred from six donors. There was no evidence of co-transference of beta-lactam resistance under the selection marker of clindamycin, beta-lactam, or both. Therefore, non-plasmid-mediated transfer may play an important role in dissemination of resistance transfer in B. fragilis in Taiwan.

摘要

克林霉素是最常用于抗厌氧菌的抗菌药物之一。脆弱拟杆菌对克林霉素的耐药性近来一直在增加。收集了30株克林霉素耐药(包括多重耐药)的脆弱拟杆菌菌株,用于研究对β-内酰胺类药物和β-内酰胺-β-内酰胺酶抑制剂的交叉耐药性以及耐药转移性。亚胺培南是对这30株分离株活性最强的药物。通过滤膜交配法,30株供体菌株中有12株的克林霉素耐药性转移至受体菌。在12株接合子中,只有3株通过碱裂解法可检测到质粒,其余9株缺乏质粒。转移频率范围为10^(-4)至10^(-6)。质粒在耐药性转移中的作用尚不确定。然而,结果表明在本研究中,非质粒介导的转移在脆弱拟杆菌克林霉素耐药性转移中占大多数。6株供体菌的四环素耐药性发生了共转移。在克林霉素、β-内酰胺或两者的选择标记下,没有证据表明β-内酰胺耐药性会发生共转移。因此,非质粒介导的转移可能在台湾脆弱拟杆菌耐药性转移传播中起重要作用。

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