Department of Infection Control and Prevention, Faculty of Nursing, Toho University, 4-16-20, Omori-nishi, Ota-ku, Tokyo 143-0015, Japan.
J Antimicrob Chemother. 2022 Feb 2;77(2):364-373. doi: 10.1093/jac/dkab390.
The ceftriaxone-resistant Neisseria gonorrhoeae FC428 clone was first discovered in Japan in 2015.
We investigated the possibility of horizontal gene transfer from Neisseria subflava harbouring the mosaic-like PBP-2 in the emergence of the FC428 clone. We also analysed whether there were fitness costs associated with the sustained international dissemination of the clone.
Sequencing of the penA gene in ceftriaxone-resistant N. subflava strains was performed. For transformation experiments between donor N. subflava and ciprofloxacin-resistant wild-type penA N. gonorrhoeae recipient, the full-length PCR amplification product of the penA gene, including DUS regions, was used as the donor DNA. Biological fitness of the transformants was measured by growth competition assays. The impact of QRDR and mtrR mutations, which have been reported as compensatory mutations, on fitness was also assessed.
The penA mosaic allele of the FC428 clone showed 100%, 91.8%, and 89.8% homology, respectively, with penA genes of three ceftriaxone-resistant N. subflava strains, No. 30, No. 9 and No. 14. Results were consistent with homologous recombination with the donated penA mosaic allele. In co-cultures with the parent strain, transformants showed comparable growth indicating that a gyrA mutation compensates for the fitness cost of mosaic penA alleles.
Our findings support the hypothesis that the FC428 clone was generated by transformation of the mosaic penA allele from oropharyngeal N. subflava to N. gonorrhoeae. Furthermore, it suggests that mutations in the gyrA QRDR region compensate for fitness costs and contribute to the continued transmission of the FC428 clone.
耐头孢曲松淋病奈瑟菌 FC428 克隆于 2015 年在日本首次发现。
我们研究了携带镶嵌型 PBP-2 的口腔奈瑟氏菌向 FC428 克隆转移的可能性,并分析了该克隆持续国际传播是否存在适应度代价。
对耐头孢曲松的口腔奈瑟氏菌菌株的 penA 基因进行测序。在供体口腔奈瑟氏菌和环丙沙星耐药野生型 penA 淋病奈瑟氏菌受体内进行转化实验时,使用全长 PCR 扩增产物作为供体 DNA,包括 DUS 区。通过生长竞争实验测量转化体的生物适应性。还评估了 QRDR 和 mtrR 突变(已报道为补偿突变)对适应性的影响。
FC428 克隆的 penA 镶嵌等位基因与三种耐头孢曲松的口腔奈瑟氏菌菌株 No.30、No.9 和 No.14 的 penA 基因分别具有 100%、91.8%和 89.8%的同源性。结果与捐赠的 penA 镶嵌等位基因的同源重组一致。在与亲本菌株的共培养中,转化体的生长情况相似,表明 gyrA 突变补偿了镶嵌 penA 等位基因的适应性代价。
我们的研究结果支持以下假设:FC428 克隆是通过来自口腔奈瑟氏菌的镶嵌型 penA 等位基因向淋病奈瑟氏菌的转化而产生的。此外,它表明 gyrA QRDR 区的突变补偿了适应性代价,并有助于 FC428 克隆的持续传播。