Recent Evolution of Susceptibility to Beta-Lactams in Neisseria meningitidis

被引:7
|
作者
Deghmane, Ala-Eddine [1 ]
Hong, Eva [1 ]
Taha, Muhamed-Kheir [1 ]
机构
[1] Univ Paris Cite, Inst Pasteur, Invas Bacterial Infect Unit, F-75724 Paris, France
来源
ANTIBIOTICS-BASEL | 2023年 / 12卷 / 06期
关键词
Neisseria meningitidis; beta-lactams; antimicrobial resistance; penA gene sequence; three-dimensional structure; PENICILLIN-BINDING PROTEIN-2; RESISTANT STRAINS; ANTIBIOTICS; GONORRHOEAE; MECHANISM;
D O I
10.3390/antibiotics12060992
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Beta-lactams are the main antibiotics for the treatment of invasive meningococcal disease. However, reduced susceptibility to penicillin G is increasingly reported in Neisseria meningitidis and reduced susceptibility to third-generation cephalosporines (3GC) and the rare acquisition of ROB-1 beta-lactamase were also described. Modifications of penicillin-binding protein 2 (PBP2) encoded by the penA gene are the main described mechanism for the reduced susceptibility to penicillin and to other beta-lactams. penA modifications were analyzed using the sequences of all penA genes from cultured isolates between 2017-2021 in France (n = 1255). Data showed an increasing trend of reduced susceptibility to penicillin from 36% in 2017 to 58% in 2021. Reduced susceptibility to 3GC remained limited at 2.4%. We identified 74 different penA alleles and penA1 was the most frequent wild-type allele and represented 29% of all alleles while penA9 was the most frequently altered allele and represented 17% of all alleles. Reduced susceptibility to 3GC was associated with the penA327 allele. The amino acid sequences of wild-type and altered PBP2 were modeled. The critical amino acid substitutions were shown to change access to the active S310 residue and hence hinder the binding of beta-lactams to the active site of PBP2.
引用
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页数:9
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