Feng Yanling, Xue Guanhua, Feng Junxia, Yan Chao, Cui Jinghua, Gan Lin, Zhang Rui, Zhao Hanqin, Xu Wenjian, Li Nannan, Liu Shiyu, Du Shuheng, Zhang Weiwei, Yao Hailan, Tai Jun, Ma Lijuan, Zhang Ting, Qu Dong, Wei Yongxiang, Yuan Jing
Capital Institute of Pediatrics, Beijing, China.
Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing, China.
Front Microbiol. 2021 Jul 22;12:691289. doi: 10.3389/fmicb.2021.691289. eCollection 2021.
New Delhi metallo-β-lactamase, a metallo-β-lactamase carbapenemase type, mediates resistance to most β-lactam antibiotics including penicillins, cephalosporins, and carbapenems. Therefore, it is important to detect genes in children's clinical samples as quickly as possible and analyze their characteristics. Here, a recombinase-aided amplification (RAA) assay, which operates in a single one-step reaction tube at 39°C in 5-15 min, was established to target genes in children's clinical samples. The analytical sensitivity of the RAA assay was 20 copies, and the various bacterial types without genes did not amplify. This method was used to detect genes in 112 children's stool samples, 10 of which were tested positive by both RAA and standard PCR. To further investigate the characteristics of carbapenem-resistant bacteria carrying in children, 15 carbapenem-resistant bacteria (, , , , , , and ) were isolated from the 10 samples. Notably, more than one bacterial type was isolated from three samples. Most of these isolates were resistant to cephalosporins, cefoperazone-sulbactam, piperacillin-tazobactam, ticarcillin-clavulanic acid, aztreonam, co-trimoxazole, and carbapenems. and were the two main types in these samples. These data show that the RAA assay has potential to be a sensitive and rapid gene screening test for clinical samples. The common existence of and multi-drug resistance genes presents major challenges for pediatric treatment.
新德里金属β-内酰胺酶是一种金属β-内酰胺酶类碳青霉烯酶,介导对包括青霉素、头孢菌素和碳青霉烯类在内的大多数β-内酰胺抗生素的耐药性。因此,尽快检测儿童临床样本中的基因并分析其特征非常重要。在此,建立了一种重组酶辅助扩增(RAA)检测方法,该方法在单个一步反应管中于39℃下5 - 15分钟内运行,以靶向儿童临床样本中的基因。RAA检测的分析灵敏度为20个拷贝,无基因的各种细菌类型均未扩增。该方法用于检测112份儿童粪便样本中的基因,其中10份经RAA和标准PCR检测均为阳性。为进一步研究儿童携带碳青霉烯耐药菌的特征,从这10份样本中分离出15株碳青霉烯耐药菌(、、、、、、和)。值得注意的是,从三份样本中分离出了不止一种细菌类型。这些分离株大多对头孢菌素、头孢哌酮 - 舒巴坦、哌拉西林 - 他唑巴坦、替卡西林 - 克拉维酸、氨曲南、复方新诺明和碳青霉烯类耐药。和是这些样本中的两种主要类型。这些数据表明,RAA检测方法有潜力成为一种针对临床样本的灵敏且快速的基因筛查检测方法。和多重耐药基因的普遍存在给儿科治疗带来了重大挑战。