Department of Medical Microbiology, Medical University of Warsaw, Warsaw, Poland.
Arch Microbiol. 2022 Jan 9;204(2):130. doi: 10.1007/s00203-021-02623-w.
Neisseria gonorrhoeae is an etiological agent of gonorrhea which remains a major public health problem the mechanisms that determine resistance to drugs of the beta-lactam class, which are recommended for the treatment of gonorrhea, are currently the most important problem in its treatment. Chromosomal mutations are responsible for resistance to ceftriaxone and cefepime. The possibility of mutations in the gene encoding beta-lactamase (bla) in the penicillinase plasmid may also turn out to be a serious threat.
The occurrence of resistance encoded on penicillinase plasmid has been investigated. For this purpose, the susceptibility of bacteria was determined and the gene for resistance to beta-lactams as well as the plasmids themselves was typed.
Of the 333 strains tested, 21 (6.3%) had the beta-lactamase gene and produced penicillinase. Two of the beta-lactamase: TEM-1 and TEM-135 occurred among the tested strains of N. gonorrhoeae. Most of the known penicillinase plasmid types of N. gonorrhoeae were demonstrated: the Asian, the African, the Toronto/Rio plasmids and Australian variants.
In the first 3 years, TEM-1 beta-lactamases dominated in N. gonorrhoeae, which were replaced by TEM-135 in the following years of the study. Not all molecular methods are capable of varying the types of penicillinase plasmids. A particularly noteworthy observation is the fact that the Australia-type of penicillinase plasmid (3270 bp) was identified for the first time in Europe, and the second time in the world.
淋病奈瑟菌是淋病的病因,淋病仍然是一个主要的公共卫生问题。确定对推荐用于治疗淋病的β-内酰胺类药物的耐药机制是目前治疗中的最重要问题。染色体突变导致对头孢曲松和头孢吡肟的耐药性。青霉素酶质粒中编码β-内酰胺酶(bla)的基因突变也可能成为一个严重的威胁。
研究了青霉素酶质粒上编码的耐药性的发生。为此,测定了细菌的敏感性,并对β-内酰胺类药物的耐药基因以及质粒本身进行了分型。
在 333 株测试菌株中,有 21 株(6.3%)具有β-内酰胺酶基因并产生青霉素酶。在测试的淋病奈瑟菌菌株中存在两种β-内酰胺酶:TEM-1 和 TEM-135。大多数已知的淋病奈瑟菌青霉素酶质粒类型都得到了证实:亚洲、非洲、多伦多/里约 plasmids 和澳大利亚变体。
在最初的 3 年中,TEM-1 型β-内酰胺酶在淋病奈瑟菌中占主导地位,随后在研究的后续几年中被 TEM-135 取代。并非所有分子方法都能够改变青霉素酶质粒的类型。一个特别值得注意的观察结果是,澳大利亚型青霉素酶质粒(3270 bp)首次在欧洲发现,也是世界上第二次发现。