Operational Technical Nucleus (Microbiology), Hermes Pardini Institute, Vespasiano, Minas Gerais, Brazil.
Department of Microbiology, Immunology and Parasitology, Rio de Janeiro State University, Rio de Janeiro, Rio de Janeiro, Brazil.
Braz J Microbiol. 2023 Sep;54(3):1325-1334. doi: 10.1007/s42770-023-01086-z. Epub 2023 Aug 19.
Diphtheria is an infectious disease potentially fatal that constitutes a threat to global health security, with possible local and systemic manifestations that result mainly from the production of diphtheria toxin (DT). In the present work, we report a case of infection by Corynebacterium diphtheriae in a cutaneous lesion of a fully immunized individual and provided an analysis of the complete genome of the isolate. The clinical isolate was first identified by MALDI-TOF Mass Spectrometry. The commercial strip system and mPCR performed phenotypic and genotypic characterization, respectively. The antimicrobial susceptibility profile was determined by the disk diffusion method. Additionally, genomic DNA was sequenced and analyzed for species confirmation and sequence type (ST) determination. Detection of resistance and virulence genes was performed by comparisons against ResFinder and VFDB databases. The isolate was identified as a nontoxigenic C. diphtheriae biovar Gravis strain. Its genome presented a size of 2.46 Mbp and a G + C content of 53.5%. Ribosomal Multilocus Sequence Typing (rMLST) allowed the confirmation of species as C. diphtheriae with 100% identity. DDH in silico corroborated this identification. Moreover, MLST analyses revealed that the isolate belongs to ST-536. No resistance genes were predicted or mutations detected in antimicrobial-related genes. On the other hand, virulence genes, mostly involved in iron uptake and adherence, were found. Presently, we provided sufficient clinical data regarding the C. diphtheriae cutaneous infection in addition to the phenotypic and genomic data of the isolate. Our results indicate a possible circulation of ST-536 in Brazil, causing cutaneous infection. Considering that cases of C. diphtheriae infections, as well as diphtheria outbreaks, have still been reported in several regions of the world, studies focusing on taxonomic analyzes and predictions of resistance genes may help to improve the diagnosis and to monitor the propagation of resistant clones. In addition, they can contribute to understanding the association between variation in genetic factors and resistance to antimicrobials.
白喉是一种具有潜在致命性的传染病,对全球卫生安全构成威胁,可能表现为局部和全身症状,主要是由白喉毒素 (DT) 产生的。在本工作中,我们报告了一例完全免疫个体的皮肤损伤中 Corynebacterium diphtheriae 感染,并对分离株的全基因组进行了分析。临床分离株首先通过 MALDI-TOF 质谱鉴定。商业条带系统和 mPCR 分别进行表型和基因型特征分析。通过纸片扩散法测定抗菌药物敏感性谱。此外,还对基因组 DNA 进行测序和分析,以确认物种和序列型 (ST)。通过与 ResFinder 和 VFDB 数据库的比较检测耐药和毒力基因。分离株被鉴定为非产毒株 Corynebacterium diphtheriae biovar Gravis 菌株。其基因组大小为 2.46 Mbp,G+C 含量为 53.5%。核糖体多位点序列分型 (rMLST) 证实该物种为 Corynebacterium diphtheriae,同源性为 100%。DDH 证实了这一鉴定。此外,MLST 分析表明该分离株属于 ST-536。未预测到耐药基因,也未在抗菌相关基因中检测到突变。另一方面,发现了许多与铁摄取和黏附相关的毒力基因。目前,我们提供了关于 Corynebacterium diphtheriae 皮肤感染的充分临床数据,以及分离株的表型和基因组数据。我们的结果表明,ST-536 可能在巴西传播,引起皮肤感染。鉴于世界上几个地区仍有 Corynebacterium diphtheriae 感染和白喉暴发的报告,对分类分析和耐药基因预测的研究可能有助于提高诊断水平,并监测耐药克隆的传播。此外,它们还可以帮助我们了解遗传因素的变异与对抗生素的耐药性之间的关系。