DNA-based methodologies for rapid detection, quantification, and species- or strain-level identification of respiratory pathogens (Mycobacteria and Pseudomonads) in metalworking fluids.

Jagjit S Yadav, Izhar U H Khan, Farnaz Fakhari, Mathew B Soellner
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引用次数: 34

Abstract

Mycobacteria and pseudomonads occurring in modern metalworking fluids (MWF) have been implicated in occupational health hazards as causal agents for hypersensitivity pneumonitis (HP) and other respiratory illnesses in machine workers exposed to these fluids and their aerosols. Unlike the conventional cultural and biochemical methods, which are often slow and ambiguous and detect only culturable cells, DNA-based methods offer a time-saving alternative for reliable detection and identification of both culturable and nonculturable bacteria in MWF and for selective quantification of individual genera of pathogens of interest in these fluids. This is the first report on DNA-based direct detection of mycobacteria and pseudomonads in MWF without culturing. Genus-specific PCR approach was successfully applied for screening of field MWF samples originating from different industrial users for detection of mycobacteria or pseudomonads including both culturable and nonculturable cells. PCR in combination with amplicon DNA sequencing led to the identification of Mycobacterium chelonae, Pseudomonas nitroreducens, and an undefined Pseudomonas species from these fluids. Genome fingerprinting by pulsed-field gel electrophoresis (PFGE) on Mycobacterium isolates further showed that the isolates represented three strains of M. chelonae although the possibility of one of the strains being clonal with M. immunogenum cannot be excluded. In parallel efforts, a quantitative competitive PCR method developed based on the Pseudomonas-specific PCR was applied to quantify total P. fluorescens cells in contaminated metalworking fluid and MWF aerosol without culturing. The DNA-based protocols developed in this study will allow rapid screening of field MWF samples for the presence of both culturable and nonculturable cells and thus facilitate effective fluid management and timely exposure assessment.

金属加工液中呼吸道病原体(分枝杆菌和假单胞菌)快速检测、定量和种或菌株水平鉴定的基于dna的方法。
在现代金属加工液(MWF)中发生的分枝杆菌和假单胞菌作为接触这些液体及其气溶胶的机器工人的过敏性肺炎(HP)和其他呼吸道疾病的致病因子,与职业健康危害有关。与传统的培养和生化方法不同,传统的培养和生化方法通常速度缓慢且含糊不清,只能检测可培养的细胞,而基于dna的方法提供了一种节省时间的替代方法,可以可靠地检测和鉴定MWF中可培养和不可培养的细菌,并对这些液体中感兴趣的单个属病原体进行选择性定量。这是首次在不培养的情况下,利用dna直接检测MWF中的分枝杆菌和假单胞菌。采用属特异性PCR方法成功筛选了来自不同工业用户的现场MWF样品,用于检测分枝杆菌或假单胞菌,包括可培养和不可培养的细胞。PCR与扩增子DNA测序相结合,从这些液体中鉴定出了chelonae分枝杆菌、硝化假单胞菌和一种未定义的假单胞菌。利用脉冲场凝胶电泳(PFGE)对分离的分枝杆菌进行基因组指纹图谱分析,进一步表明分离的分枝杆菌为3株龟分枝杆菌,但不能排除其中一株与免疫原分枝杆菌克隆的可能性。同时,在假单胞菌特异性PCR的基础上开发了一种定量竞争PCR方法,用于在未培养的情况下定量污染金属加工液和MWF气溶胶中的荧光假单胞菌总细胞。本研究开发的基于dna的方案将允许快速筛选现场MWF样品,以确定可培养细胞和不可培养细胞的存在,从而促进有效的流体管理和及时的暴露评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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