Molecular and genomic investigation unveils Pseudomonas putida as an emerging multidrug-resistant pathogen linked to bovine clinical mastitis

IF 3.5 3区 医学 Q3 IMMUNOLOGY Microbial pathogenesis Pub Date : 2025-06-01 Epub Date: 2025-03-08 DOI:10.1016/j.micpath.2025.107461
Tima Tisa Mallick , Md Morshedur Rahman , Naim Siddique , Khaled Hassan Shuvo , Kh Yeashir Arafat , Syeda Fowzia Homa , Salma Akter , Md Robiul Karim , Ziban Chandra Das , M. Nazmul Hoque
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Abstract

Pseudomonas putida is one of the emerging pathogens responsible causing mastitis in lactating animals. This study investigated the prevalence, antimicrobial resistance (AMR), genetic diversity and virulence factor genes (VFGs) to highlight the pathogenic potentials of P. putida strains isolated from milk, feces and farm soil of dairy cows diagnosed with clinical mastitis (CM). A total of 110 samples were collected and analyzed, revealing an overall prevalence of P. putida in dairy farms at 40.90 %, with specific prevalence rates of 42.22 % in milk, 26.67 % in feces, and 31.11 % in farm soil. In vitro antimicrobial assays demonstrated that 76.0 % P. putida isolates exhibited multidrug resistance (MDR, resistance to ≥ 3 antibiotics), particularly showing high resistance to oxacillin, ampicillin, nalidixic acid, and aztreonam. Conversely, P. putida isolates showed the highest susceptibility against imipenem. The genome analysis of three MDR P. putida strains 11CM-M1 (milk), 11CM-F1 (feces) and 11CM-S1 (farm soil), showed a close evolutionary relationship with different strains of Pseudomonas spp. isolated from bovine mastitis milk and feces samples, human stool, and samples sourced from hospital environment. The assembled genomes of three P. putida strains encoded nine antibiotic resistance genes (ARGs), 36 VFGs, and 367 metabolic subsystems, highlighting a complex functional profile and potential for pathogenicity. The detailed analysis of these ARGs and VFGs demonstrated that P. putida strains employ distinct mechanisms of resistance (e.g., efflux pumps), biofilm formation, and virulence factors, including adhesins, secreted toxins, and lipopolysaccharides, which contribute to their pathogenic potential. Given the lack of reports linking P. putida strains to bovine mastitis in Bangladesh, the increasing trend of AMR, along with the presence of significant ARGs and VFGs in the studied strains, underscores the need for more intensive research, including animal model experiment, to better elucidate the pathogenesis and inform treatment decisions for mastitis in dairy animals.
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分子和基因组研究揭示恶臭假单胞菌是一种与牛临床乳腺炎相关的新兴多重耐药病原体。
恶臭假单胞菌是引起哺乳动物乳腺炎的新兴病原体之一。本研究通过对牛临床乳腺炎(CM)乳汁、粪便和农场土壤中分离的恶臭杆菌(P. putida)的流行病学、抗微生物药物耐药性(AMR)、遗传多样性和毒力因子基因(vfg)的研究,揭示恶臭杆菌的致病潜力。共采集110份样本进行分析,结果显示,猪场恶臭假单胞菌总体流行率为40.90%,其中牛奶、粪便和土壤的具体流行率分别为42.22%、26.67%和31.11%。体外抗菌试验表明,76.0%的恶臭p.p . putida分离株表现出多药耐药(MDR,对≥3种抗生素耐药),特别是对oxacillin、氨苄西林、萘啶酸和氨曲南具有高耐药性。相反,恶臭假单胞菌对亚胺培南的敏感性最高。通过对3株耐多药恶臭假单胞菌菌株11CM-M1(乳)、11CM-F1(粪便)和11CM-S1(农场土壤)的基因组分析,发现它们与牛乳腺炎乳和粪便、人类粪便和医院环境中分离的假单胞菌菌株有密切的进化关系。3株恶臭p.p . putida菌株组装的基因组编码9个抗生素耐药基因(ARGs)、36个vfg和367个代谢子系统,突出了复杂的功能谱和潜在的致病性。对这些ARGs和vfg的详细分析表明,恶臭假单胞菌菌株具有不同的抗性机制(例如外排泵)、生物膜形成和毒力因子(包括粘附素、分泌毒素和脂多糖),这些都有助于其致病潜力。鉴于在孟加拉国缺乏将腐臭假单胞菌菌株与牛乳腺炎联系起来的报道,AMR的增加趋势以及在所研究菌株中存在显著的ARGs和vfg,强调需要进行更深入的研究,包括动物模型实验,以更好地阐明乳腺炎的发病机制并为治疗决策提供信息。
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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