Solymosi Norbert, Tóth Adrienn Gréta, Nagy Sára Ágnes, Csabai István, Feczkó Csongor, Reibling Tamás, Németh Tibor
Centre for Bioinformatics, University of Veterinary Medicine, Budapest, Hungary.
Department of Physics of Complex Systems, Eötvös Loránd University, Budapest, Hungary.
PeerJ. 2025 Jan 28;13:e18802. doi: 10.7717/peerj.18802. eCollection 2025.
Antimicrobial resistance (AMR) is one of our greatest public health challenges. Targeted use of antibiotics (ABs) can reduce the occurrence and spread of AMR and boost the effectiveness of treatment. This requires knowledge of the AB susceptibility of the pathogens involved in the disease. Therapeutic recommendations based on classical AB susceptibility testing (AST) are based on the analysis of only a fraction of the bacteria present in the disease process. Next and third generation sequencing technologies allow the identification of antimicrobial resistance genes (ARGs) present in a bacterial community. Using this metagenomic approach, we can map the antimicrobial resistance potential (AMRP) of a complex, multi-bacterial microbial sample. To understand the interpretiveness of AMRP, the concordance between phenotypic AMR properties and ARGs was investigated by analyzing data from 574 strains of five different studies. The overall results show that for 44% of the studied ABs, phenotypically resistant strains are genotypically associated with a 90% probability of resistance, while for 92% of the ABs, the phenotypically susceptible strains are genotypically susceptible with a 90% probability. ARG detection showed a phenotypic prediction with at least 90% confidence in 67% of ABs. The probability of detecting a phenotypically susceptible strain as resistant based on genotype is below 5% for 92% of ABs. While the probability of detecting a phenotypically resistant strain as susceptible based on genotype is below 5% for 44% of ABs. We can assume that these strain-by-strain concordance results are also true for bacteria in complex microbial samples, and conclude that AMRP obtained from metagenomic ARG analysis can help choose efficient ABs. This is illustrated using AMRP by a canine external otitis sample.
抗菌药物耐药性(AMR)是我们面临的最大公共卫生挑战之一。有针对性地使用抗生素(ABs)可以减少AMR的发生和传播,并提高治疗效果。这需要了解疾病中所涉及病原体的AB敏感性。基于经典AB敏感性测试(AST)的治疗建议仅基于对疾病过程中存在的一小部分细菌的分析。第二代和第三代测序技术能够鉴定细菌群落中存在的抗菌药物耐药基因(ARGs)。使用这种宏基因组学方法,我们可以绘制复杂的多细菌微生物样本的抗菌药物耐药潜力(AMRP)图谱。为了了解AMRP的解释性,通过分析来自五项不同研究的574株菌株的数据,研究了表型AMR特性与ARGs之间的一致性。总体结果表明,对于44%的研究ABs,表型耐药菌株在基因型上有90%的概率与耐药相关,而对于92%的ABs,表型敏感菌株在基因型上有90%的概率为敏感。ARG检测显示,在67%的ABs中,表型预测的置信度至少为90%。对于92%的ABs,基于基因型将表型敏感菌株检测为耐药的概率低于5%。而对于44%的ABs,基于基因型将表型耐药菌株检测为敏感的概率低于5%。我们可以假设,这些逐菌株的一致性结果对于复杂微生物样本中的细菌也是成立的,并得出结论,从宏基因组ARG分析获得的AMRP有助于选择有效的ABs。通过犬外耳炎样本的AMRP对此进行了说明。