家养和野生动物分离的化脓性真芽孢菌的基因组和代谢特征。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2025-01-31 Epub Date: 2024-12-31 DOI:10.1128/aem.01725-24
Gabriela Magossi, Katherine E Gzyl, Devin B Holman, T G Nagaraja, Raghavendra Amachawadi, Samat Amat
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引用次数: 0

摘要

化脓性true eperella pypygenes是一种重要的细菌病原体,与家畜和野生动物的乳腺炎、子宫炎、肺炎和肝脓肿等感染以及人类的心内膜炎和假体关节感染有关。了解使化脓螺旋体在宿主体内不同解剖部位定植的基因组和代谢特征,以及其在王国间的传播和存活,对于有效控制这种病原体具有重要意义。我们采用全基因组测序、表型微阵列和抗菌药物敏感性测试来鉴定从不同家畜、伴侣和野生动物中恢复的化脓性单胞菌的基因组、代谢和表型特征以及抗微生物药物耐药性(AMR)基因。为了进行比较基因组分析,我们对83个化脓性结核杆菌基因组进行了评估,其中包括目前研究中分离到的60个基因组和23个公开的基因组。这些基因组代表了来自11种不同动物宿主(如牛、猪、羊、鹿、野牛、马、羚羊和猫)的16个不同身体部位的化脓性乳杆菌菌株。此外,49株化脓性结核杆菌分离株(牛、羊、鹿、猪和猫)采用圆盘扩散法进行表型AMR评估,并使用生物GENIII微孔板进行代谢谱分析。发现化脓性芽孢杆菌菌株不具有宿主或身体部位特异性。保守毒力基因(plo和fimA)以及基因型和表型AMR的存在可能有助于化脓性T.引起牲畜、野生动物和宠物感染的能力。大多数被测试的分离株代谢不同的碳源和化合物,表明这种代谢的多样性可能提高了化脓性结核杆菌的生存、竞争力和致病潜力。化脓性真佩尔菌是一种具有人畜共患潜力的重要动物病原体,由于其能够引起不同动物宿主物种和组织的感染,对动物和人类都构成重大的健康问题。目前对这种病原体的适应性和生存机制的了解是有限的。在这里,我们评估了从11种不同动物宿主(家畜、伴侣和野生动物)的16个不同身体部位回收的化脓性单胞杆菌的基因组、毒力、代谢和抗微生物药物耐药性(AMR)特征。我们发现了多个抗菌素耐药性和毒力基因,这些基因可能使化脓性结核杆菌持续感染和传播。此外,化脓性乳杆菌菌株表现出代谢的多功能性,这也有助于其在不同环境中茁壮成长的能力。了解化脓性单胞菌在宿主体内不同解剖部位定植及其在不同动物物种间传播的基因组、代谢和抗菌素耐药性特征,对于有效控制该病原体具有重要意义。
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Genomic and metabolic characterization of Trueperella pyogenes isolated from domestic and wild animals.

Trueperella pyogenes is an important bacterial pathogen implicated in infections such as mastitis, metritis, pneumonia, and liver abscesses in both domestic and wild animals, as well as endocarditis and prosthetic joint infections in humans. Understanding the genomic and metabolic features that enable T. pyogenes to colonize different anatomical sites within a host and its inter-kingdom transmission and survival is important for the effective control of this pathogen. We employed whole-genome sequencing, phenotype microarrays, and antimicrobial susceptibility testing to identify genomic, metabolic and phenotypic features, and antimicrobial resistance (AMR) genes in T. pyogenes recovered from different livestock, companion, and wildlife animals. For comparative genomic analysis, 83 T. pyogenes genomes, including 60 isolated in the current study and 23 publicly available genomes were evaluated. These genomes represented T. pyogenes strains originating from 16 different body sites of 11 different animal hosts (e.g., cattle, swine, ovine, deer, bison, horse, chamois, and cat). Additionally, 49 T. pyogenes isolates (cattle, sheep, deer, swine, and cats) were evaluated for phenotypic AMR using disk diffusion, and for metabolic profiling using the Biology GENIII MicroPlates. The T. pyogenes strains were found not to be host- or body site-specific. The presence of conserved virulence genes (plo and fimA), as well as genotypic and phenotypic AMR may contribute to the ability of T. pyogenes to cause infections in livestock, wildlife, and pets. Most of the tested isolates metabolized diverse carbon sources and chemical compounds, suggesting that this metabolic versatility may enhance the survival, competitiveness, and pathogenic potential of T. pyogenes.IMPORTANCETrueperella pyogenes is an important animal pathogen with zoonotic potential, posing a significant health concern to both animals and humans due to its ability to cause infections across different animal host species and tissues. Current understanding of this pathogen's adaptability and survival mechanisms is limited. Here, we evaluated the genomic, virulence, metabolic, and antimicrobial resistance (AMR) characteristics of T. pyogenes recovered from 16 different body sites of 11 different animal hosts (livestock, companion, and wild animals). We identified multiple AMR and virulence genes that may enable T. pyogenes for sustained infection and transmission. Additionally, T. pyogenes strains displayed metabolic versatility which could also contribute to its ability to thrive in diverse environments. Understanding the genomic and metabolic, and AMR characteristics that enable T. pyogenes to colonize different anatomical sites within a host and its transmission between different animal species is important for the effective control of this pathogen.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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