Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, St Lucia, Queensland, Australia.
School of Chemistry and Molecular Biosciences, Australian Infectious Diseases Research Centre, Australian Centre for Ecogenomics, The University of Queensland, St Lucia, Queensland, Australia.
Microb Genom. 2020 Mar;6(3). doi: 10.1099/mgen.0.000346.
Fowl cholera, caused by continues to be a challenge in meat-chicken-breeder operations and has emerged as a problem for free-range meat chickens. Here, using whole-genome sequencing (WGS) and phylogenomic analysis, we investigate isolate relatedness during outbreaks of fowl cholera on a free-range meat chicken farm over a 5-year period. Our genomic analysis revealed that while all outbreak isolates were sequence type (ST) 20, they could be separated into two distinct clades (clade 1 and clade 2) consistent with difference in their lipopolysaccharide (LPS) type. The isolates from the earlier outbreaks (clade 1) were carrying LPS type L3 while those from the more recent outbreaks (clade 2) were LPS type L1. Additionally, WGS data indicated high inter- and intra-chicken genetic diversity during a single outbreak. Furthermore, we demonstrate that while a killed autogenous vaccine carrying LPS type L3 had been successful in protecting against challenge from L3 isolates it might have driven the emergence of the closely related clade 2, against which the vaccine was ineffective. The genomic results also revealed a 14 bp deletion in the galactosyltransferase gene in LPS type L3 isolates, which would result in producing a semi-truncated LPS in those isolates. In conclusion, our study clearly demonstrates the advantages of genomic analysis over the conventional PCR-based approaches in providing clear insights in terms of linkage of isolate within and between outbreaks. More importantly, it provides more detailed information than the multiplex PCR on the possible structure of outer LPS, which is very important in the case of strain selection for killed autogenous vaccines.
禽霍乱,由 引起,继续是肉种鸡养殖者的一个挑战,并且已成为自由放养肉用鸡的一个问题。在这里,我们使用全基因组测序(WGS)和系统发育基因组分析,在五年的时间里,研究了自由放养肉用鸡场禽霍乱爆发期间的分离株相关性。我们的基因组分析表明,虽然所有爆发分离株均为血清型 20(ST20),但它们可以分为两个不同的分支(分支 1 和分支 2),这与它们的脂多糖(LPS)型的差异一致。早期爆发(分支 1)的分离株携带 LPS 型 L3,而最近爆发(分支 2)的分离株携带 LPS 型 L1。此外,WGS 数据表明,在一次单一爆发中,鸡之间存在高度的种内和种间遗传多样性。此外,我们证明,虽然携带 LPS 型 L3 的灭活同源疫苗成功地保护了来自 L3 分离株的挑战,但它可能导致了密切相关的分支 2 的出现,而该疫苗对分支 2 无效。基因组结果还揭示了 LPS 型 L3 分离株中半乳糖基转移酶基因 中的 14bp 缺失,这将导致这些分离株产生半截断的 LPS。总之,我们的研究清楚地表明,与传统的基于 PCR 的方法相比,基因组分析在提供关于分离株在爆发内和爆发之间的关联的清晰见解方面具有优势。更重要的是,它提供了比多重 PCR 更详细的关于外 LPS 结构的信息,这在选择用于灭活同源疫苗的菌株时非常重要。