Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, Canada.
Department of Large Animal Clinical Sciences, University of Saskatchewan, Saskatoon, Canada.
Appl Environ Microbiol. 2024 Jul 24;90(7):e0050224. doi: 10.1128/aem.00502-24. Epub 2024 Jun 12.
is a major contributor to bovine respiratory disease (BRD), which causes substantial economic losses to the beef industry, and there is an urgent need for rapid and accurate diagnostic tests to provide evidence for treatment decisions and support antimicrobial stewardship. Diagnostic sequencing can provide information about antimicrobial resistance genes in more rapidly than conventional diagnostics. Realizing the full potential of diagnostic sequencing requires a comprehensive understanding of the genetic markers of antimicrobial resistance. We identified genetic markers of resistance in to macrolide class antibiotics commonly used for control of BRD. Genome sequences were determined for 99 isolates with six different susceptibility phenotypes collected over 2 years from a feedlot in Saskatchewan, Canada. Known macrolide resistance genes , (E), and (E) were identified in most resistant isolates within predicted integrative and conjugative elements (ICEs). ICE sequences lacking antibiotic resistance genes were detected in 10 of 47 susceptible isolates. No resistance-associated polymorphisms were detected in ribosomal RNA genes, although previously unreported mutations in the L22 and L23 ribosomal proteins were identified in 12 and 27 resistant isolates, respectively. Pangenome analysis led to the identification of 79 genes associated with resistance to gamithromycin, of which 95% (75 of 79) had no functional annotation. Most of the observed phenotypic resistance was explained by previously identified antibiotic resistance genes, although resistance to the macrolides gamithromycin and tulathromycin was not explained in 39 of 47 isolates, demonstrating the need for continued surveillance for novel determinants of macrolide resistance.IMPORTANCEBovine respiratory disease is the costliest disease of beef cattle in North America and the most common reason for injectable antibiotic use in beef cattle. Metagenomic sequencing offers the potential to make economically significant reductions in turnaround time for diagnostic information for evidence-based selection of antibiotics for use in the feedlot. The success of diagnostic sequencing depends on a comprehensive catalog of antimicrobial resistance genes and other genome features associated with reduced susceptibility. We analyzed the genome sequences of isolates of , a major bovine respiratory disease pathogen, and identified both previously known and novel genes associated with reduced susceptibility to macrolide class antimicrobials. These findings reinforce the need for ongoing surveillance for markers of antimicrobial resistance to support improved diagnostics and antimicrobial stewardship.
是牛呼吸道疾病(BRD)的主要病原体,给牛肉行业造成了巨大的经济损失。因此,迫切需要快速、准确的诊断测试来为治疗决策提供依据,并支持抗生素管理。与传统诊断相比,诊断测序可以更快地提供关于抗生素耐药性基因的信息。要充分发挥诊断测序的潜力,需要全面了解抗生素耐药性的遗传标记。我们确定了 对用于控制 BRD 的大环内酯类抗生素的耐药性遗传标记。在加拿大萨斯喀彻温省一个饲养场的 2 年时间里,收集了 99 株具有 6 种不同药敏表型的分离株,并对其进行了基因组测序。在大多数耐药分离株中,预测的整合子和转座子(ICE)内发现了已知的大环内酯类抗生素耐药基因、(E)、和(E)。在 47 株敏感分离株中,有 10 株检测到缺乏抗生素耐药基因的 ICE 序列。核糖体 RNA 基因中未检测到耐药相关的多态性,但在 12 株和 27 株耐药分离株中分别鉴定到了以前未报道的 L22 和 L23 核糖体蛋白突变。全基因组分析导致了对加米霉素耐药的 79 个基因的鉴定,其中 95%(75/79)没有功能注释。虽然 39 株分离株对大环内酯类抗生素加米霉素和替拉霉素的耐药性无法用以前鉴定的抗生素耐药基因解释,但观察到的表型耐药性大部分可以用以前鉴定的抗生素耐药基因解释。这表明需要继续监测大环内酯类抗生素耐药性的新决定因素。重要性牛呼吸道疾病是北美肉牛最昂贵的疾病,也是肉牛中最常见的注射用抗生素使用原因。宏基因组测序有可能大大缩短基于证据的抗生素选择的诊断信息的周转时间,从而具有显著的经济效益。诊断测序的成功取决于对抗生素耐药性和其他与降低敏感性相关的基因组特征的全面目录。我们分析了 分离株的基因组序列,确定了与大环内酯类抗菌药物敏感性降低相关的以前已知和新的基因。这些发现强调了需要持续监测抗生素耐药性标志物,以支持改进的诊断和抗生素管理。