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奈瑟菌属细菌在微观环境中青霉素耐药性的转移

Transfer of penicillin resistance between Neisseriae in microcosm.

作者信息

Orús P, Viñas M

机构信息

Microbiology Unit and Public Health Institute, University of Barcelona, Spain.

出版信息

Microb Drug Resist. 2000 Summer;6(2):99-104. doi: 10.1089/107662900419393.

Abstract

Horizontal gene transfer between commensal and pathogenic Neisseriae is the mechanism proposed to explain how pathogenic species acquire altered portions of the penA gene, which encodes penicillin binding protein 2. These changes resulted in a moderately penicillin-resistant phenotype in the meningococci, whose frequency of isolation in Spain increased at the end of the 1980s. Little has been published about the possibility of this gene transfer in nature or about its simulation in the laboratory. We designed a simple microcosm, formed by solid and liquid media, that partially mimics the upper human respiratory tract. In this microcosm, penicillin-resistant commensal strains and the fully susceptible meningococcus were co-cultivated. The efficiency of gene transfer between the strains depended on the phase of bacterial growth and the conditions of culture. Resistance of penicillin was acquired in different steps irrespective of the source of the DNA. The presence of DNase in the medium had no effect on gene transfer, but it was near zero when nicked DNA was used. Cell-to-cell contact or membrane blebs could explain these results. The analysis of sequences of the transpeptidase domain of PBP2 from transformants, and from donor and recipient strains demonstrated that the emergence of moderately resistant transformants was due to genetic exchange between the co-cultivated strains. Finally, mechanisms other than penA modification could be invoked to explain decreased susceptibility.

摘要

共生奈瑟菌和致病性奈瑟菌之间的水平基因转移是一种被提出的机制,用于解释致病菌种如何获得编码青霉素结合蛋白2的penA基因的变异部分。这些变化导致脑膜炎球菌出现中度耐青霉素表型,20世纪80年代末其在西班牙的分离频率有所增加。关于这种基因在自然环境中转移的可能性或在实验室中的模拟研究,相关报道较少。我们设计了一个由固体和液体培养基组成的简单微观模型,部分模拟了人类上呼吸道。在这个微观模型中,将耐青霉素的共生菌株和完全敏感的脑膜炎球菌共同培养。菌株间基因转移的效率取决于细菌生长阶段和培养条件。无论DNA来源如何,青霉素抗性都是在不同步骤中获得的。培养基中存在DNase对基因转移没有影响,但使用切口DNA时基因转移效率几乎为零。细胞间接触或膜泡可能解释了这些结果。对转化体以及供体和受体菌株的PBP2转肽酶结构域序列分析表明,中度抗性转化体的出现是由于共同培养菌株之间的基因交换。最后,可以调用除penA修饰以外的机制来解释敏感性降低的现象。

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