Centre for Biosecurity and One Health, Harry Butler Institute, Murdoch University, Murdoch, Western Australia, Australia.
Communicable Disease Control Directorate, WA Department of Health, East Perth, Western Australia, Australia.
Microb Genom. 2024 May;10(5). doi: 10.1099/mgen.0.001232.
infection (CDI) remains a significant public health threat globally. New interventions to treat CDI rely on an understanding of the evolution and epidemiology of circulating strains. Here we provide longitudinal genomic data on strain diversity, transmission dynamics and antimicrobial resistance (AMR) of ribotypes (RTs) 014/020 (=169), 002 (=77) and 056 (=36), the three most prominent strains causing CDI in Australia. Genome scrutiny showed that AMR was uncommon in these lineages, with resistance-conferring alleles present in only 15/169 RT014/020 strains (8.9 %), 1/36 RT056 strains (2.78 %) and none of 77 RT002 strains. Notably, ~90 % of strains were resistant to MLS agents , but only ~5.9 % harboured known resistance alleles, highlighting an incongruence between AMR genotype and phenotype. Core genome analyses revealed all three RTs contained genetically heterogeneous strain populations with limited evidence of clonal transmission between CDI cases. The average number of pairwise core genome SNP (cgSNP) differences within each RT group ranged from 23.3 (RT056, ST34, =36) to 115.6 (RT002, ST8, =77) and 315.9 (RT014/020, STs 2, 13, 14, 49, =169). Just 19 clonal groups (encompassing 40 isolates), defined as isolates differing by ≤2 cgSNPs, were identified across all three RTs (RT014/020, =14; RT002, =3; RT056, =2). Of these clonal groups, 63 % (12/19) comprised isolates from the same Australian State and 37 % (7/19) comprised isolates from different States. The low number of plausible transmission events found for these major RTs (and previously documented populations in animal and environmental sources/reservoirs) points to widespread and persistent community sources of diverse strains as opposed to ongoing nationwide healthcare outbreaks dominated by a single clone. Together, these data provide new insights into the evolution of major lineages causing CDI in Australia and highlight the urgent need for enhanced surveillance, and for public health interventions to move beyond the healthcare setting and into a One Health paradigm to effectively combat this complex pathogen.
在全球范围内,感染(CDI)仍然是一个重大的公共卫生威胁。治疗 CDI 的新干预措施依赖于对循环菌株的进化和流行病学的理解。在这里,我们提供了关于引起澳大利亚 CDI 的三个最主要菌株 014/020 型(RT014/020)(169 型)、002 型(RT002)(77 型)和 056 型(RT056)(36 型)的菌株多样性、传播动态和抗生素耐药性(AMR)的纵向基因组数据。基因组分析表明,这些谱系中的 AMR 并不常见,只有 15/169 株 RT014/020 菌株(8.9%)、36 株 RT056 菌株中的 1 株(2.78%)和 77 株 RT002 菌株中没有任何一株携带耐药等位基因。值得注意的是,大约 90%的菌株对 MLS 制剂有耐药性,但只有约 5.9%的菌株携带已知的耐药等位基因,这表明 AMR 基因型和表型之间存在不一致。核心基因组分析显示,所有三种 RT 都包含遗传上异质的菌株群体,在 CDI 病例之间几乎没有证据表明克隆传播。在每个 RT 组内,平均成对核心基因组 SNP(cgSNP)差异数范围为 23.3(RT056,ST34,=36)至 115.6(RT002,ST8,=77)和 315.9(RT014/020,STs 2、13、14、49、=169)。在所有三种 RT 中,只发现了 19 个克隆群(定义为差异≤2 个 cgSNP 的分离株)(RT014/020,=14;RT002,=3;RT056,=2)。在这些克隆群中,63%(12/19)由来自同一澳大利亚州的分离株组成,37%(7/19)由来自不同州的分离株组成。对于这些主要 RT 来说,发现的可传播事件数量很少(以及以前在动物和环境来源/储库中记录的种群)表明,社区中有广泛而持久的不同菌株来源,而不是由单一克隆主导的全国性医疗保健疫情。总之,这些数据为澳大利亚引起 CDI 的主要谱系的进化提供了新的见解,并强调了迫切需要加强监测,并将公共卫生干预措施从医疗保健领域扩展到一个健康的范式,以有效应对这种复杂的病原体。