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Fecal shedding of Clostridioides difficile in calves in Sao Paulo state, Brazil.巴西圣保罗州犊牛艰难梭菌的粪便排出。
Anaerobe. 2024 Aug;88:102861. doi: 10.1016/j.anaerobe.2024.102861. Epub 2024 May 9.
2
in calves, cattle and humans from Dutch dairy farms: Predominance of PCR ribotype 695 (clade 5, sequence type 11) in cattle.来自荷兰奶牛场的犊牛、牛和人类:牛中PCR核糖体分型695(进化枝5,序列类型11)占主导地位。
One Health. 2024 Apr 24;18:100739. doi: 10.1016/j.onehlt.2024.100739. eCollection 2024 Jun.
3
Laboratory diagnosis of Clostridioides (Clostridium) difficile infection in domestic animals: A short review.家畜艰难梭菌(梭状芽孢杆菌)感染的实验室诊断:简短综述。
Anaerobe. 2022 Jun;75:102574. doi: 10.1016/j.anaerobe.2022.102574. Epub 2022 Apr 25.
4
Performance of commercial PCR assays to detect toxigenic Clostridioides difficile in the feces of puppies.商业 PCR 检测试剂盒在幼犬粪便中检测产毒艰难梭菌的性能。
Vet Med Sci. 2021 Sep;7(5):1536-1541. doi: 10.1002/vms3.567. Epub 2021 Jul 3.
5
Clostridioides difficile on dairy farms and potential risk to dairy farm workers.奶牛场艰难梭菌及其对奶牛场工人的潜在风险。
Anaerobe. 2021 Jun;69:102353. doi: 10.1016/j.anaerobe.2021.102353. Epub 2021 Feb 25.
6
Comparative Study of Clinical Detection Methods in Patients with Diarrhoea.腹泻患者临床检测方法的比较研究
Can J Infect Dis Med Microbiol. 2020 Jan 21;2020:8753284. doi: 10.1155/2020/8753284. eCollection 2020.
7
() in animals.()在动物中。
J Vet Diagn Invest. 2020 Mar;32(2):213-221. doi: 10.1177/1040638719899081. Epub 2020 Jan 6.
8
Development of a rapid-viability PCR method for detection of Clostridioides difficile spores from environmental samples.开发一种快速活力 PCR 方法,用于从环境样本中检测艰难梭菌孢子。
Anaerobe. 2020 Feb;61:102077. doi: 10.1016/j.anaerobe.2019.102077. Epub 2019 Jul 19.
9
A Laboratory Medicine Best Practices Systematic Review and Meta-analysis of Nucleic Acid Amplification Tests (NAATs) and Algorithms Including NAATs for the Diagnosis of () in Adults.一项关于核酸扩增检测(NAATs)和包括 NAATs 在内的算法在诊断成人()中的实验室医学最佳实践系统评价和荟萃分析。
Clin Microbiol Rev. 2019 May 29;32(3). doi: 10.1128/CMR.00032-18. Print 2019 Jun 19.
10
Quantification of Clostridioides (Clostridium) difficile in feces of calves of different age and determination of predominant Clostridioides difficile ribotype 033 relatedness and transmission between family dairy farms using multilocus variable-number tandem-repeat analysis.不同年龄犊牛粪便中艰难梭菌的定量分析,以及使用多位点可变数目串联重复序列分析确定主要的艰难梭菌核糖体分型033在家庭奶牛场之间的相关性和传播情况。
BMC Vet Res. 2018 Oct 1;14(1):298. doi: 10.1186/s12917-018-1616-8.

比较检测牛粪便中艰难梭菌的厌氧培养方法。

Comparison of Anaerobic Culture Methods for Detecting Clostridioides difficile in Bovine Faeces.

机构信息

Clinical Studies - New Bolton Center, School of Veterinary Medicine, University of Pennsylvania, Kennett Square, Pennsylvania, USA.

Roberts Center for Pediatric Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.

出版信息

Vet Med Sci. 2025 Jan;11(1):e70085. doi: 10.1002/vms3.70085.

DOI:10.1002/vms3.70085
PMID:39611384
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11605475/
Abstract

BACKGROUND

The study of the epidemiology of Clostridioides difficile in populations is greatly facilitated by the ability to isolate and further characterize individual organisms, which requires effective culture protocols. In cattle, where little is known about the epidemiology of C. difficile, no studies have assessed or compared the performance of different assays for detecting C. difficile.

OBJECTIVES

This study compared two culture protocols for detecting C. difficile in bovine faeces from 121 gestating cows and 70 of their neonatal calves, while situating results obtained with each protocol relative to those obtained with shotgun metagenomic sequencing.

METHODS

Protocol 1 involved direct plating enrichment onto taurocholine-cycloserine-cefoxitin-fructose agar (TCCFA), while Protocol 2 included an ethanol shock step before plating on CCFA/ChromID agar. For both protocols, one aliquot underwent broth enrichment prior to plating, while the other aliquot did not.

RESULTS

Clostridioides difficile was detected following broth enrichment in two of the same calf samples using both protocols, and an additional cow sample was found to be positive with Protocol 2, though the difference in detection rates was not statistically significant (p = 1.0).

CONCLUSIONS

The detection of C. difficile in a much high number of these samples by shotgun metagenomics, albeit at low levels of relative abundance, suggests that neither of these culture protocols is sensitive when levels of abundance are low.

摘要

背景

通过分离和进一步鉴定个体生物的能力,极大地促进了对人群中艰难梭菌流行病学的研究,这需要有效的培养方案。在对艰难梭菌的流行病学知之甚少的牛群中,尚无研究评估或比较过用于检测艰难梭菌的不同检测方法的性能。

目的

本研究比较了两种从 121 头妊娠奶牛及其 70 头新生牛犊的粪便中检测艰难梭菌的培养方案,同时将每种方案的结果与 shotgun 宏基因组测序的结果进行比较。

方法

方案 1 涉及直接在牛磺胆酸钠-环丝氨酸-头孢西丁-果糖琼脂(TCCFA)上进行直接平板增菌,而方案 2 则在 CCFA/ChromID 琼脂上进行平板增菌之前包括乙醇冲击步骤。对于两种方案,一种样品进行了肉汤增菌,而另一种样品则没有。

结果

使用两种方案的肉汤增菌后,在两个相同牛犊样本中均检测到了艰难梭菌,并且方案 2 还检测到了一个牛犊样本和一个奶牛样本呈阳性,但检测率的差异无统计学意义(p = 1.0)。

结论

尽管 shotgun 宏基因组学检测到的这些样本中艰难梭菌的相对丰度较低,但检测到的样本数量大大增加,这表明当丰度较低时,这两种培养方案都不敏感。