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在资源有限的环境中,对用于旅行者腹泻诊断应用的不同粪便保存介质进行前瞻性评估,采用多重PCR BioFire FilmArray技术。

Prospective evaluation of different faecal preservation media for travellers' diarrhoea diagnostic application with multiplex PCR BioFire FilmArray in resource-limited settings.

作者信息

Toriro R, Woolley S D, Hale I, Bennett C J, Phelps C J, Nevin W D, Burns D S, Edwards T, Beeching N J, O'Shea M K, Fletcher T E

机构信息

Department of Clinical Sciences, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool, Merseyside, L3 5QA, UK.

Royal Centre for Defence Medicine, Mindelsohn Way, Queen Elizabeth Hospital, Edgbaston, Birmingham, B15 2WB, UK.

出版信息

J Med Microbiol. 2025 Jan;74(1). doi: 10.1099/jmm.0.001954.

Abstract

Immediate identification of travellers' diarrhoea-causing pathogens may not be possible in remote settings, but samples can be stored for epidemiological and related research. We collected pilot data to evaluate the utility of three different preservation media for testing stored faecal samples compared to immediate testing of fresh samples using the BioFire FilmArray multiplex PCR gastrointestinal panel (bioMérieux). No previous studies have demonstrated the utility of testing faecal samples directly by PCR BioFire FilmArray following prolonged storage and transportation in OMNIgene, DNA shield and FTA cards. To evaluate the reliability of OMNIgene, DNA shield and FTA card faecal storage and transport media in parallel, compared to initial testing of fresh faeces obtained from the same individuals at the time of presentation with diarrhoea in the field compare the results of faecal samples stored and transported at ambient temperature in OMNIgene, DNA shield and FTA cards then tested using PCR BioFire FilmArray 6-18 months later with those obtained from fresh faecal samples during a diarrhoea outbreak. Fresh faecal samples were obtained from British military personnel who developed diarrhoea during deployment to Kenya between February-April 2022. Unpreserved fresh samples were tested onsite using PCR BioFire FilmArray and corresponding samples were stored at ambient temperature in OMNIgene200 (DNAgenotek), DNA/RNA shield DX (Zymo Research) and Whatman FTA™ Elute cards (GE Healthcare) then repatriated to the UK for direct testing by PCR BioFire FilmArray, 6-18 months later. The most common enteropathogens evaluated were: spp., Enteroaggregative (; EAEC), Enteropathogenic (EPEC), Shiga toxin-producing (STEC) and spp. Test results for the three storage modalities were compared to the fresh sample tests as a reference standard. Samples from 60 individuals [80% male; median (interquartile range) age 24 (22-28) years] were analysed. Test sensitivity for spp. and EAEC was high across all three storage modalities (86.4-100%). OMNIgene200 and DNA/RNA shield showed significant concordance with the reference standard test for other pathogens, but FTA Elute card tests had low sensitivity for STEC and poor specificity for spp. Agreement between FTA Elute cards and the reference standard test was low-moderate (kappa coefficient ≤0-0.49) for all enteropathogens. This study demonstrates successful PCR BioFire FilmArray utility in testing samples stored in different media and is the first to compare the use of OMNIgene200, DNA/RNA shield and FTA Elute cards simultaneously with the results of clinical samples. Stored samples were tested up to 18 months later with significant concordance observed in OMNIgene200 and DNA/RNA shield compared to reference standard testing. The distorted performance of FTA Elute card testing requires further optimisation. Testing of samples stored in these media is suitable for research studies, but their applicability with other molecular diagnostic platforms, or clinical diagnostics, requires confirmation.

摘要

在偏远地区可能无法立即识别导致旅行者腹泻的病原体,但样本可以储存起来用于流行病学及相关研究。我们收集了试点数据,以评估三种不同保存介质在检测储存粪便样本方面的效用,并与使用BioFire FilmArray多重PCR胃肠道检测板(生物梅里埃公司)对新鲜样本进行即时检测进行比较。此前尚无研究证明在通过OMNIgene、DNA Shield和FTA卡进行长时间储存和运输后,直接用PCR BioFire FilmArray检测粪便样本的效用。为了并行评估OMNIgene、DNA Shield和FTA卡粪便储存和运输介质的可靠性,将其与在现场出现腹泻时从同一人获取的新鲜粪便的初始检测结果进行比较,比较在常温下储存在OMNIgene、DNA Shield和FTA卡中然后在6至18个月后使用PCR BioFire FilmArray检测的粪便样本结果与腹泻暴发期间从新鲜粪便样本获得的结果。新鲜粪便样本取自2022年2月至4月在肯尼亚部署期间出现腹泻的英国军事人员。未保存的新鲜样本在现场使用PCR BioFire FilmArray进行检测,相应样本在常温下储存在OMNIgene200(DNAgenotek公司)、DNA/RNA Shield DX(Zymo Research公司)和Whatman FTA™洗脱卡(通用电气医疗集团)中,然后运回英国在6至18个月后通过PCR BioFire FilmArray进行直接检测。评估的最常见肠道病原体为: 属、肠聚集性 (;EAEC)、肠致病性 (EPEC)、产志贺毒素 (STEC)和 属。将三种储存方式的检测结果与作为参考标准的新鲜样本检测结果进行比较。分析了来自60个人的样本[80%为男性;年龄中位数(四分位间距)为24(22 - 28)岁]。对于 属和EAEC,所有三种储存方式的检测灵敏度都很高(86.4 - 100%)。OMNIgene二百和DNA/RNA Shield与其他病原体的参考标准检测显示出显著一致性,但FTA洗脱卡检测对STEC的灵敏度较低,对 属的特异性较差。对于所有肠道病原体,FTA洗脱卡与参考标准检测之间的一致性为低至中度(kappa系数≤0 - 0.49)。本研究证明了PCR BioFire FilmArray在检测储存在不同介质中的样本方面的成功效用,并且是首次同时比较OMNIgene200、DNA Shield和FTA洗脱卡的使用情况与临床样本结果。储存的样本在18个月后进行检测,与参考标准检测相比,OMNIgene200和DNA/RNA Shield中观察到显著一致性。FTA洗脱卡检测的性能失真需要进一步优化。在这些介质中储存的样本检测适用于研究,但它们在其他分子诊断平台或临床诊断中的适用性需要确认。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a1/11784588/37e877904204/jmm-74-01954-g001.jpg

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