Emergence of plasmid-mediated fosfomycin resistance among Escherichia coli harboring fosA4, tet(X4), and mcr-1 genes in wild birds.

IF 4.6 2区 生物学 Q1 MICROBIOLOGY mSystems Pub Date : 2025-04-22 Epub Date: 2025-03-13 DOI:10.1128/msystems.01673-24
Asim Munir, Xiaoyu Lu, Farwa Humak, Cemil Kürekci, Muhammad Shahid Mahmood, Sehrish Gul, Zhiqiang Wang, Mashkoor Mohsin, Ruichao Li
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Abstract

Fosfomycin represents a last-line reserve antibiotic for the treatment of infections caused by multidrug-resistant (MDR) bacteria. Nevertheless, the advent of plasmid-mediated fosfomycin resistance among bacteria from humans and food animals incurs great concern. This study reports the detection and genomic portrait of the plasmid-mediated fosfomycin resistance gene, fosA4, amid Escherichia coli from wild birds co-harboring plasmid-mediated tigecycline resistance gene, tet(X4), and colistin resistance gene, mcr-1. A total of 100 samples from fecal droppings of wild birds in the urban parks in Faisalabad, Pakistan were subjected for the isolation and characterization of fosfomycin-resistant E. coli. The fosA4 gene was identified in 11 (11%) of the E. coli isolates, and all exhibited an MDR phenotype. Genome sequencing confirmed that all the fosA4-positive isolates also co-harbored the mobile tigecycline resistance tet(X4) gene on a large MDR IncFII plasmid. One isolate PKF8 belonging to ST48 also co-carried the colistin resistance gene mcr-1 on the IncHI2 plasmid. To the extent of our knowledge, this is the first discovery of E. coli isolates in wild birds co-harboring the mcr-1, fosA4, and tet(X4) genes. The emergence of these pivotal antimicrobial resistance genes in wild birds native to South Asia with their close association to humans and animals is alarming. Our findings highlight the urgent need for further surveillance of bacterial resistance to last-resort antibiotics in the clinics, animal farming, and environment with the One Health approach.

Importance: The global spread of the plasmid-mediated fosfomycin resistance gene fosA4 bearing Escherichia coli strains incurs a public health concern. However, research focusing on the pervasiveness of fosA4-positive isolates in wild birds is still rare, and to the best of our knowledge, this is the first documentation from South Asia highlighting the concurrent presence of the fosA4, mcr-1, and tet(X4) genes within E. coli isolates recovered from fecal samples of wild birds in Pakistan. This co-existence of ARGs along with phylogenetic analysis revealed that MDR plasmids carried by E. coli isolates have the ability to spread horizontally between wild birds, food animals, and humans. Co-existence of fosA4, tet(X4), and mcr-1-carrying plasmids is worrying and warrants further investigation.

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携带fosA4、tet(X4)和mcr-1基因的大肠杆菌在野生鸟类中出现质粒介导的磷霉素耐药。
磷霉素是治疗耐多药(MDR)细菌引起的感染的最后一线储备抗生素。然而,来自人类和食用动物的细菌中质粒介导的磷霉素耐药性的出现引起了极大的关注。本研究报道了质粒介导的磷霉素耐药基因fosA4的检测和基因组图谱,该基因在野生鸟类大肠杆菌中共携带质粒介导的替加环素耐药基因tet(X4)和粘菌素耐药基因mcr-1。从巴基斯坦费萨拉巴德城市公园的野生鸟类粪便中采集了100份样本,对耐磷菌素大肠杆菌进行了分离和鉴定。在11株(11%)大肠杆菌分离株中鉴定出fosA4基因,且均表现出耐多药表型。基因组测序证实,所有fosa4阳性分离株也在一个大的MDR IncFII质粒上共同携带移动替加环素耐药tet(X4)基因。一个属于ST48的分离物PKF8也在IncHI2质粒上共同携带粘菌素抗性基因mcr-1。据我们所知,这是首次在野生鸟类中发现大肠杆菌分离物同时携带mcr-1、fosA4和tet(X4)基因。这些关键的抗微生物药物耐药性基因在南亚原生野生鸟类中出现,与人类和动物密切相关,这令人震惊。我们的研究结果强调,迫切需要进一步监测诊所、动物养殖场和环境中采用“同一个健康”方法对最后手段抗生素的细菌耐药性。重要性:携带大肠杆菌菌株的质粒介导的磷霉素耐药基因fosA4的全球传播引起了公共卫生关注。然而,关注fosA4阳性分离株在野生鸟类中普遍存在的研究仍然很少,据我们所知,这是南亚首次强调在从巴基斯坦野生鸟类粪便样本中回收的大肠杆菌分离株中同时存在fosA4, mcr-1和tet(X4)基因。ARGs的共存以及系统发育分析表明,大肠杆菌分离株携带的耐多药质粒具有在野生鸟类、食用动物和人类之间水平传播的能力。携带fosA4、tet(X4)和mcr-1质粒的共存令人担忧,值得进一步研究。
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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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