Unit for Environment Science and Management, Microbiology, North-West University, Potchefstroom campus, Private Bag X6001, Potchefstroom, 2520, South Africa.
Unit for Environment Science and Management, Microbiology, North-West University, Mahikeng campus, Private Bag X2046, Mahikeng, 2745, South Africa.
BMC Genomics. 2023 Dec 7;24(1):755. doi: 10.1186/s12864-023-09867-4.
Citrobacter species are Gram-negative opportunistic pathogens commonly reported in nosocomial-acquired infections. This study characterised four Citrobacter species that were isolated from surface water in the North West Province, South Africa.
Phenotypic antimicrobial susceptibility profiles of the isolates demonstrated their ability to produce the extended-spectrum β-lactamase (ESBL). Whole genomes were sequenced to profile antibiotic resistance and virulence genes, as well as mobile genetic elements. In silico taxonomic identification was conducted by using multi-locus sequence typing and average nucleotide identity. A pangenome was used to determine the phylogenomic landscape of the Citrobacter species by using 109 publicly available genomes. The strains S21 and S23 were identified as C. braakii, while strains S24 and S25 were C. murliniae and C. portucalensis, respectively. Comparative genomics and sequenced genomes of the ESBL-producing isolates consisted of n = 91; 83% Citrobacter species in which bla- (n = 19; 32,2%) and bla- (n = 12; 38,7%) were prevalent in C. braakii, and C. portucalensis strains, respectively. Macrolide (acrAB-TolC, and mdtG) and aminoglycoside (acrD) efflux pumps genes were identified in the four sequenced Citrobacter spp. isolates. The quinolone resistance gene, qnrB13, was exclusive to the C. portucalensis S25 strain. In silico analysis detected plasmid replicon types IncHI1A, IncP, and Col(VCM04) in C. murliniae S24 and C. portucalensis S25, respectively. These potentially facilitate the T4SS secretion system in Citrobacter species. In this study, the C. braakii genomes could be distinguished from C. murliniae and C. portucalensis on the basis of gene encoding for cell surface localisation of the CPS (vexC) and identification of genes involved in capsule polymer synthesis (tviB and tviE). A cluster for the salmochelin siderophore system (iro-BCDEN) was found in C. murliniae S24. This is important when it comes to the pathogenicity pathway that confers an advantage in colonisation.
The emerging and genomic landscapes of these ESBL-producing Citrobacter species are of significant concern due to their dissemination potential in freshwater systems. The presence of these ESBL and multidrug-resistant (MDR) pathogens in aquatic environments is of One Health importance, since they potentially impact the clinical domain, that is, in terms of human health and the agricultural domain, that is, in terms of animal health and food production as well as the environmental domain.
柠檬酸杆菌属是一种革兰氏阴性机会性病原体,通常在医院获得性感染中报告。本研究对南非西北省地表水分离出的 4 种柠檬酸杆菌属进行了特征描述。
分离株的表型抗菌药物敏感性谱表明它们能够产生扩展谱β-内酰胺酶(ESBL)。对全基因组进行测序以分析抗生素耐药性和毒力基因以及移动遗传元件。通过多位点序列分型和平均核苷酸同一性进行了基于基因组的分类学鉴定。通过使用 109 个公开可用的基因组,泛基因组用于确定柠檬酸杆菌属的系统基因组景观。菌株 S21 和 S23 被鉴定为 C. braakii,而菌株 S24 和 S25 分别为 C. murliniae 和 C. portucalensis。比较基因组学和产生 ESBL 的分离株的测序基因组由 n = 91 组成;83%的柠檬酸杆菌属中,bla-(n = 19;32.2%)和 bla-(n = 12;38.7%)在 C. braakii 和 C. portucalensis 菌株中较为常见。在四个测序的柠檬酸杆菌属分离株中鉴定出大环内酯(acrAB-TolC 和 mdtG)和氨基糖苷(acrD)外排泵基因。喹诺酮耐药基因 qnrB13 仅存在于 C. portucalensis S25 菌株中。基于基因组的分析检测到 C. murliniae S24 和 C. portucalensis S25 中的 IncHI1A、IncP 和 Col(VCM04)质粒复制子类型。这些质粒可能有助于柠檬酸杆菌属的 T4SS 分泌系统。在这项研究中,C. braakii 基因组可以基于 CPS(vexC)的细胞表面定位编码基因和参与荚膜聚合物合成的基因(tviB 和 tviE)的鉴定与 C. murliniae 和 C. portucalensis 区分开来。在 C. murliniae S24 中发现了沙门氏菌属铁载体系统(iro-BCDEN)簇。这对于赋予定植优势的致病性途径很重要。
由于这些产生 ESBL 的柠檬酸杆菌属在淡水系统中的传播潜力,它们的出现和基因组景观令人严重关切。这些 ESBL 和多药耐药(MDR)病原体在水生环境中的存在对“同一健康”具有重要意义,因为它们可能会影响临床领域,即人类健康,以及农业领域,即动物健康和食品生产以及环境领域。