首页> 外文期刊>Journal of Veterinary Diagnostic Investigation >A new variant of Actinobacillus pleuropneumoniae serotype 3 lacking the entire apxII operon.
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A new variant of Actinobacillus pleuropneumoniae serotype 3 lacking the entire apxII operon.

机译:缺少整个apxII操纵子的胸膜肺炎放线杆菌血清型3的新变体。

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Actinobacillus pleuropneumoniae is an important respiratory pathogen causing pleuropneumonia in pig. The species is genetically characterized by the presence of 4 RTX (Repeats in the Structural ToXin) toxin genes: apxI, apxII, and apxIII genes are differentially present in various combinations among the different serotypes, thereby defining pathogenicity; the apxIV gene is present in all serotypes. Polymerase chain reaction (PCR)-based apx gene typing is done in many veterinary diagnostic laboratories, especially reference laboratories. The present report describes the isolation of atypical A. pleuropneumoniae from 4 independent cases from 2 countries. All isolates were beta-nicotinamide adenine dinucleotide (beta-NAD) dependent and nonhemolytic but showed strong co-hemolysis with the sphingomyelinase of Staphylococcus aureus on sheep blood agar. Classical biochemical tests as well as Matrix-assisted laser desorption ionization time-of-flight mass spectrometry and sequence-based analysis (16S ribosomal RNA [rRNA] and rpoB genes) identified them as A. pleuropneumoniae. Apx-toxin gene typing using 2 different PCR systems showed the presence of apxIV and only the apxIII operon (apxIIICABD). None of the apxI or apxII genes were present as confirmed by Southern blot analysis. The 16S rRNA and rpoB gene analyses as well as serotype-specific PCR indicate that the isolates are variants of serotype 3. Strains harboring only apxIV and the apxIII operon are possibly emerging types of A. pleuropneumoniae and should therefore be carefully monitored for epidemiological reasons. Copyright 2011 The Author(s)CAS Registry/EC Number/Name of Substance 0 (ApxII toxin, bacteria). 0 (Bacterial Proteins). 0 (Hemolysin Proteins).
机译:胸膜肺炎放线杆菌是引起猪胸膜肺炎的重要呼吸道病原体。该物种的遗传学特征是存在4种RTX(结构毒素中的重复)毒素基因:apxI,apxII和apxIII基因在不同血清型之间以不同组合的形式存在差异,从而确定了致病性。 apxIV基因存在于所有血清型中。在许多兽医诊断实验室,尤其是参考实验室中,都进行了基于聚合酶链反应(PCR)的apx基因分型。本报告介绍了从2个国家的4例独立病例中分离出非典型胸膜肺炎放线杆菌的情况。所有分离株都是β-烟酰胺腺嘌呤二核苷酸(β-NAD)依赖性且非溶血性的,但在绵羊血琼脂上与金黄色葡萄球菌的鞘磷脂酶显示强烈的共溶血作用。经典的生化测试以及基质辅助激光解吸电离飞行时间质谱分析和基于序列的分析(16S核糖体RNA [rRNA]和rpoB基因)均将它们鉴定为胸膜肺炎放线杆菌。使用2种不同的PCR系统进行的Apx-毒素基因分型显示,存在apxIV,仅存在apxIII操纵子(apxIIICABD)。如通过Southern印迹分析所证实的,不存在apxI或apxII基因。 16S rRNA和rpoB基因分析以及血清型特异性PCR表明,分离株是血清型3的变体。仅携带apxIV和apxIII操纵子的菌株可能是胸膜肺炎放线杆菌的新兴类型,因此应基于流行病学原因进行仔细监测。版权所有2011作者CAS登记号/ EC物质编号0(ApxII毒素,细菌)。 0(细菌蛋白)。 0(溶血素蛋白)。

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