意大利两个养猪场分离的胸膜肺炎放线杆菌对氟苯尼考的新抗药性。

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY
A. Brenciani , S.N. Coccitto , L. Cucco , M. Ustulin , E. Albini , M. Paniccià , D. Vio , M. Cinthi , E. Giovanetti , F.R. Massacci , C.F. Magistrali
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引用次数: 0

摘要

胸膜肺炎放线杆菌是猪胸膜肺炎的元凶,这是一种传染性极强的肺部感染。这种呼吸道疾病的控制仍然严重依赖抗生素,酚类抗生素是养猪业使用的主要抗生素种类之一。在本研究中,我们描述了从意大利的两个养猪场分离出的三个胸膜肺炎甲虫(B2278、B2176 和 B2177),它们对氟苯尼考(因含有 floR 基因)具有抗药性。氟苯尼考药敏试验表明,B2176 表现出中等药敏性,而 B2177 和 B2278 具有抗药性。这三个分离株都属于血清 6 型,其 floR 基因检测呈阳性。全基因组测序分析表明,分离物 B2176、B2177 和 B2278 含有编码毒素 ApxII 和 ApxIII 的基因,这是具有中等毒力菌株的特征。此外,系统进化分析表明,这些分离株关系密切,单核苷酸多态性(SNPs)从 8 个到 19 个不等。floR 基因位于一个 5588 bp 的新型质粒上,该质粒被命名为 pAp-floR。BLASTN 分析表明,pAp-floR 质粒与来自猪源变异曼氏菌 MVSCS1 的 pMVSCS1 质粒(5621 bp)具有很高的核苷酸同一性(99%)和覆盖率(60%)。此外,至少在实验室条件下,pAp-floR 即使在没有直接选择压力的情况下也能稳定地维持,这表明它不会带来适应性成本。我们的研究强调了在未来几年中监测耐氟苯尼考胸膜肺炎甲虫分离物扩散的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging resistance to florfenicol in Actinobacillus pleuropneumoniae isolates on two Italian pig farms

Actinobacillus pleuropneumoniae is responsible for porcine pleuropneumonia, a highly contagious lung infection. The control of this respiratory disease remains heavily reliant on antibiotics, with phenicols being one of the primary classes of antibiotics used in pig farming. In the present study, we describe three isolates (B2278, B2176 and B2177) of A. pleuropneumoniae resistant to florfenicol attributed to the presence of the floR gene, which were obtained from two pig farms in Italy. Florfenicol susceptibility tests indicated that B2176 exhibited an intermediate susceptibility profile, while B2177 and B2278 were resistant. All three isolates belonged to serovar 6 and tested positive for the presence of the floR gene. Whole genome sequencing analysis revealed that isolates B2176, B2177 and B2278 harbored genes encoding the toxins ApxII and ApxIII, characteristic of strains with moderate virulence. Moreover, phylogenetic analysis demonstrated that these isolates were closely related, with single nucleotide polymorphisms (SNPs) ranging from 8 to 19. The floR gene was located on a novel 5588 bp plasmid, designated as pAp-floR. BLASTN analysis showed that the pAp-floR plasmid had high nucleotide identity (99 %) and coverage (60 %) with the pMVSCS1 plasmid (5621 bp) from Mannheimia varigena MVSCS1 of porcine origin. Additionally, at least under laboratory conditions, pAp-floR was stably maintained even in the absence of direct selective pressure, suggesting that it does not impose a fitness cost. Our study underscores the necessity of monitoring the spread of florfenicol-resistant A. pleuropneumoniae isolates in the coming years.

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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
期刊介绍: Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal. Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge. Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.
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