首页> 美国卫生研究院文献>Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians Inc >Comparison of detection methods for Salmonella enterica shedding among reptilian patients at a veterinary teaching hospital
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Comparison of detection methods for Salmonella enterica shedding among reptilian patients at a veterinary teaching hospital

机译:兽医教学院爬行动物患者沙门氏菌肠道检测方法的比较

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摘要

In the United States, ~1.4 million sporadic human Salmonella enterica infections occur annually, with an estimated 6% attributable to reptile exposure. Detection of Salmonella in reptiles can be challenging given the limitations among detection methods. We evaluated sampling and detection methods for S. enterica in a cross-sectional study of reptilian patients (n = 45) over the course of 13 mo. Two sampling methods (cloacal swabs, electrostatic cloth body-feet samples) and 3 detection methods (enriched culture, lateral flow immunoassay [LFI], real-time PCR) were compared using McNemar and Fisher exact tests. Results varied by species, sample type, and detection method. In total, 14 of 45 (33%) patients were positive by culture, 10 of 45 (22%), and/or 13 of 45 (29%) by rtPCR. Among rtPCR-positive results, cloacal swabs (12 of 45 [27%]) resulted in a higher detection than body-feet wipes (4 of 45 [9%]; p = 0.01). Among culture-positive results, shedding was most commonly detected after additional incubation at room temperature when testing cloacal swabs (9 of 45 [20%]). However, there was significant disagreement between sampling methods (cloacal vs. body-feet; p = 0.03). No samples were positive by LFI. In general, cloacal swabs yielded the highest test-positive rates, irrespective of testing method. Our study highlights the importance of using detection methods optimized for the sample being tested.
机译:在美国,每年〜140万孢状体人类沙门氏菌肠道感染,估计可归因于爬行动物暴露的6%。鉴于检测方法的局限性,爬行动物中的沙门氏菌的检测可能是挑战。我们在13月的过程中评估了肠系肠道肠杆菌(N = 45)的横截面研究中的肠溶和检测方法。使用McNemar和Fisher精确测试比较了两种取样方法(克隆拭子,静电布体脚样品)和3种检测方法(富集培养,横向流动免疫测定[LFI],实时PCR)。结果因物种,样品类型和检测方法而变化。总共,45个(33%)患者的培养阳性为阳性,10例45(22%),和/或通过RTPCR的13个(29%)。在rtpcr阳性结果中,延长拭子(124%]的12个)导致较高的检测,比体脚湿润(4个,45%]; p = 0.01)。在培养阳性结果中,在测试核酸拭子(940%)的室温下额外孵育后,最常检测到脱落。然而,取样方法(克隆与体脚; P = 0.03)之间存在显着的分歧。 LFI没有样品阳性。通常,无论检测方法如何,癌拭子都会产生最高的试验阳性率。我们的研究突出了使用对正在测试的样品进行优化的检测方法的重要性。

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