Household transmission of non-toxigenic diphtheria toxin gene-bearing Corynebacterium diphtheriae following a cluster of cutaneous cases in a specialist outpatient setting.

IF 2.4 4区 医学 Q3 MICROBIOLOGY Journal of medical microbiology Pub Date : 2023-06-01 DOI:10.1099/jmm.0.001722
Norman K Fry, Ellen Pringle, William Newsholme, Margot Nicholls, Jim Stephenson, Rachel Thorn Heathcock, Charlotte Gower, Joanne Lacy, Shennae O'Boyle, David J Litt, Carmen Sheppard, Natalie Groves, Joshua D'Aeth, Katie L Hopkins, Danièle Meunier, Aruni De Zoysa, Androulla Efstratiou, Colin Brown, Meera Chand, Gayatri Amirthalingam
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引用次数: 1

Abstract

Introduction. Combination of PCR and Elek testing to identify toxigenic corynebacteria has revealed organisms described as non-toxigenic toxin-gene bearing (NTTB) Corynebacterium diphtheriae or C. ulcerans (i.e. PCR tox positive; Elek negative). These organisms carry part or all of tox, but are unable to express diphtheria toxin (DT) and present a challenge to clinical and public health case management.Gap analysis/Hypothesis. There are few data on the theoretical risk of NTTB reversion to toxigenicity. This unique cluster and subsequent epidemiologically linked isolates allowed the opportunity to determine any change in DT expression status.Aim. To characterize a cluster of infections due to NTTB in a skin clinic and subsequent cases in two household contacts.Methodology. Epidemiological and microbiological investigations were carried out according to existing national guidance at the time. Susceptibility testing used gradient strips. The tox operon analysis and multi-locus sequence typing (MLST) was derived from whole-genome sequencing. Alignment of the tox operon and phylogenetic analyses were performed using clustalW, mega, the public core-genome MLST (cgMLST) scheme and an in-house bioinformatic single nucleotide polymorphism (SNP) typing pipeline.Results. Isolates of NTTB C. diphtheriae were recovered from four cases (cases 1 to 4) with epidermolysis bullosa attending the clinic. Two further isolates were subsequently recovered from case 4, >18 months later, and from two household contacts (cases 5 and 6) after a further 18 months and 3.5 years, respectively. All eight strains were NTTB C. diphtheriae biovar mitis, belonged to the same sequence type (ST-336) with the same deletion in tox. Phylogenetic analysis showed relatively high diversity between the eight strains with 7-199 SNP and 3-109 cgMLST loci differences between them. The number of SNPs between the three isolates from case 4 and two household contacts (cases 5 and 6) was 44-70 with 28-38 cgMLST loci differences.Conclusions. We report a cluster of NTTB C. diphtheriae cases in a skin clinic and evidence of onward household transmission. We conclude the deletion in the tox was responsible for the non-expression of DT. There was no evidence of reversion to DT expression over the 6.5 year period studied. These data informed revision to guidance in the management of NTTB cases and their contacts in the UK.

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非产毒性白喉毒素基因携带白喉链杆菌的家庭传播继在一个专科门诊设置皮肤病例。
介绍。结合PCR和Elek检测来鉴定产毒杆状菌,已经发现了被描述为非产毒毒素基因携带(NTTB)的白喉杆状杆菌或溃疡杆菌(即PCR毒素阳性;Elek负)。这些生物携带部分或全部毒素,但不能表达白喉毒素(DT),这对临床和公共卫生病例管理提出了挑战。差距分析/假说。关于NTTB还原为毒性的理论风险的数据很少。这个独特的集群和随后的流行病学相关分离株允许有机会确定DT表达状态的任何变化。在皮肤诊所和随后的两个家庭接触者的NTTB感染的聚集性特征。流行病学和微生物学调查是根据当时现有的国家指导进行的。药敏试验采用梯度试纸。tox操纵子分析和多位点序列分型(MLST)来源于全基因组测序。使用clustalW、mega、公共核心基因组MLST (cgMLST)方案和内部生物信息学单核苷酸多态性(SNP)分型管道进行tox操纵子比对和系统发育分析。从就诊的4例(病例1 ~ 4)大疱性表皮松解症患者中分离出NTTB白喉分枝杆菌。病例4在18个月后又分离出两株,病例5和病例6分别在18个月和3.5年后从两名家庭接触者(病例5和病例6)中分离出两株。8株均为NTTB白喉支原体生物变种,属同一序列型(ST-336),毒素缺失相同。系统发育分析表明,8株菌株间存在较高的多样性,SNP位点差异为7-199个,cgMLST位点差异为3-109个。病例4与2例家庭接触者(病例5和病例6)分离株的snp数为44 ~ 70个,cgMLST位点差异为28 ~ 38个。我们在皮肤诊所报告了一组NTTB c白喉病例和家庭传播的证据。我们得出结论,毒素的缺失是DT不表达的原因。在研究的6.5年期间,没有证据表明DT表达恢复。这些数据为修订英国NTTB病例及其接触者管理指南提供了依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of medical microbiology
Journal of medical microbiology 医学-微生物学
CiteScore
5.50
自引率
3.30%
发文量
143
审稿时长
4.5 months
期刊介绍: Journal of Medical Microbiology provides comprehensive coverage of medical, dental and veterinary microbiology, and infectious diseases. We welcome everything from laboratory research to clinical trials, including bacteriology, virology, mycology and parasitology. We publish articles under the following subject categories: Antimicrobial resistance; Clinical microbiology; Disease, diagnosis and diagnostics; Medical mycology; Molecular and microbial epidemiology; Microbiome and microbial ecology in health; One Health; Pathogenesis, virulence and host response; Prevention, therapy and therapeutics
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