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Quantification of hydrogen cyanide and 2-aminoacetophenone in the headspace of Pseudomonas aeruginosa cultured under biofilm and planktonic conditions

机译:在生物膜和浮游条件下培养的铜绿假单胞菌顶空中氰化氢和2-氨基苯乙酮的定量

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Hydrogen cyanide (HCN) and 2-aminoacetophenone (2-AA; H2NC6H4COCH3) are possible biomarkers of pulmonary Pseudomonas aeruginosa (PA) infection that could be used in an exhaled breath test. All factors affecting their production need to be investigated, including the culture conditions: planktonic (free-floating) or biofilm (non-motile communities attached to a solid surface). In vivo, the change from planktonic to biofilm growth is signalled when a certain population density is reached. Using selected ion flow tube mass spectrometry, SIFT-MS, we have analysed HCN and 2-AA produced by 12 genotyped PA samples, cultured under both planktonic and biofilm conditions after 24, 48, 72 and 96 hours of incubation. The 12 samples included 3 different strains (genotypes), 50% of which had a mucoid phenotype and 50% had a non-mucoid phenotype. All samples produced significant concentrations of HCN; median (25th to 75th percentiles, IQR) concentration: 144 (61-512) parts-per-billion by volume (ppbv). Multivariate analysis showed HCN production varied dependent on genotype (p = 0.0014), culture duration (p = 0.005) and phenotype (p < 0.001) but not culture conditions (planktonic/biofilm). Much smaller concentrations of 2-AA were detected, median (IQR) concentration 1.8 (1.3-3) ppbv, despite which, multivariate analysis showed production was affected by genotype (p < 0.001) and culture duration (p = 0.007) but not phenotype or culture conditions. These data show that biofilm formation does not affect HCN production by PA and supports its use as a biomarker of PA infection. The concentrations of 2-AA are much lower than previous studies have shown. The reason for this is unclear but it raises questions about its suitability as a biomarker of PA infection.
机译:氰化氢(HCN)和2-氨基苯乙酮(2-AA; H2NC6H4COCH3)可能是肺铜绿假单胞菌(PA)感染的生物标志物,可用于呼气呼气试验。需要调查影响生产的所有因素,包括培养条件:浮游生物(自由漂浮)或生物膜(附着在固体表面的非运动群落)。在体内,当达到一定的种群密度时,就指示了从浮游生物向生物膜生长的变化。使用选定的离子流管质谱仪SIFT-MS,我们分析了在孵育24、48、72和96小时后在浮游生物膜和生物膜条件下培养的12个基因型PA样品产生的HCN和2-AA。这12个样本包括3个不同的菌株(基因型),其中50%具有粘液表型,50%具有非粘液表型。所有样品均产生高浓度的六氯化萘。中位数(25至75个百分位数,IQR)浓度:按体积(ppbv)计算的十亿分之144(61-512)。多变量分析显示,HCN的产生取决于基因型(p = 0.0014),培养时间(p = 0.005)和表型(p <0.001),而与培养条件(浮游生物/生物膜)无关。尽管检测到的2-AA浓度要小得多,中值(IQR)浓度为1.8(1.3-3)ppbv,但多变量分析表明产量受基因型(p <0.001)和培养时间(p = 0.007)的影响,而不受表型的影响或文化条件。这些数据表明生物膜的形成不会影响PA产生HCN,并支持将其用作PA感染的生物标记。 2-AA的浓度远低于以前的研究结果。其原因尚不清楚,但是引起了关于其作为PA感染生物标志物的适用性的疑问。

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