• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于分子诊断的高传染性家畜和禽类病毒(包括甲型流感病毒和新城疫病毒)的灭活

Inactivation of highly transmissible livestock and avian viruses including influenza A and Newcastle disease virus for molecular diagnostics.

作者信息

Welch Jennifer L, Shrestha Ram, Hutchings Heather, Pal Narinder, Levings Randall, Robbe-Austerman Suelee, Palinski Rachel, Shanmuganatham Karthik K

机构信息

National Veterinary Services Laboratories, Veterinary Services, Animal and Plant Health Inspection Service, United States Department of Agriculture, Ames, IA, United States.

出版信息

Front Vet Sci. 2024 Mar 7;11:1304022. doi: 10.3389/fvets.2024.1304022. eCollection 2024.

DOI:10.3389/fvets.2024.1304022
PMID:38515532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10955088/
Abstract

There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.

摘要

迫切需要一种灭活方法,该方法能在样本采集时完全灭活病原体,同时保持诊断性PCR检测所需的核酸质量。这种灭活方法有助于减轻对传播风险的担忧,将运输复杂性和成本降至最低,并能在较低防护水平的实验室进行检测,从而通过缩短周转时间来加强疾病诊断。本研究评估了一组代表高致病性动物疾病的10种替代病毒。结果表明,一种商用的PrimeStore®分子运输介质(PSMTM)能使所有测试病毒的灭活率超过99.99%,这是通过感染性和连续传代试验确定的。然而,在PSMTM和对照处理条件下,通过qRT-PCR检测病毒核酸的结果相当。当分别在血清和泄殖腔拭子等生物材料存在的情况下评估病毒,以模拟非禽病毒和禽病毒的诊断样本条件时,结果是一致的。本研究结果可供诊断检测实验室用于检测影响动物和人类群体的高致病性病原体。这些结果可用于修订特定病原体诊断检测和感染性物质运输的指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/f2ab9567d8b3/fvets-11-1304022-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/804e6f7e7fc9/fvets-11-1304022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/a82d0095b961/fvets-11-1304022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/d258da0cf72c/fvets-11-1304022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/cfeab1c1aff7/fvets-11-1304022-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/f2ab9567d8b3/fvets-11-1304022-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/804e6f7e7fc9/fvets-11-1304022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/a82d0095b961/fvets-11-1304022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/d258da0cf72c/fvets-11-1304022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/cfeab1c1aff7/fvets-11-1304022-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbc4/10955088/f2ab9567d8b3/fvets-11-1304022-g005.jpg

相似文献

1
Inactivation of highly transmissible livestock and avian viruses including influenza A and Newcastle disease virus for molecular diagnostics.用于分子诊断的高传染性家畜和禽类病毒(包括甲型流感病毒和新城疫病毒)的灭活
Front Vet Sci. 2024 Mar 7;11:1304022. doi: 10.3389/fvets.2024.1304022. eCollection 2024.
2
Inactivation of Viable Surrogates for the Select Agents Virulent Newcastle Disease Virus and Highly Pathogenic Avian Influenza Virus Using Either Commercial Lysis Buffer or Heat.使用商业裂解缓冲液或加热法使新城疫病毒强毒株和高致病性禽流感病毒的替代活毒株失活
Appl Biosaf. 2019 Dec 1;24(4):189-199. doi: 10.1177/1535676019888920.
3
Optimal specimen collection and transport methods for the detection of avian influenza virus and Newcastle disease virus.用于检测禽流感病毒和新城疫病毒的最佳样本采集和运输方法。
BMC Vet Res. 2013 Feb 22;9:35. doi: 10.1186/1746-6148-9-35.
4
Biosafety Recommendations for Work with Influenza Viruses Containing a Hemagglutinin from the A/goose/Guangdong/1/96 Lineage.含有 A/goose/Guangdong/1/96 谱系血凝素的流感病毒工作的生物安全建议。
MMWR Recomm Rep. 2013 Jun 28;62(RR-06):1-7.
5
Evaluation of different inactivation methods for high and low pathogenic avian influenza viruses in egg-fluids for antigen preparation.用于抗原制备的蛋液中高致病性和低致病性禽流感病毒不同灭活方法的评估。
J Virol Methods. 2015 Sep 15;222:28-33. doi: 10.1016/j.jviromet.2015.05.004. Epub 2015 May 18.
6
Inactivation of the novel avian influenza A (H7N9) virus under physical conditions or chemical agents treatment.新型甲型禽流感病毒(H7N9)在物理条件或化学试剂处理下的灭活
Virol J. 2013 Sep 15;10:289. doi: 10.1186/1743-422X-10-289.
7
Evaluation and clinical validation of an alcohol-based transport medium for preservation and inactivation of respiratory viruses.评估并验证一种基于酒精的运输介质,用于保存和灭活呼吸道病毒。
J Clin Microbiol. 2011 Jun;49(6):2138-42. doi: 10.1128/JCM.00327-11. Epub 2011 Apr 20.
8
Viral infection detection using metagenomics technology in six poultry farms of eastern China.利用宏基因组学技术在中国东部六个家禽养殖场进行病毒感染检测。
PLoS One. 2019 Feb 20;14(2):e0211553. doi: 10.1371/journal.pone.0211553. eCollection 2019.
9
Comparison of commercial influenza A virus assays in detecting avian influenza H7N9 among poultry cloacal swabs, China.比较商业流感 A 病毒检测方法在中国禽类泄殖腔拭子中检测 H7N9 禽流感病毒。
J Clin Virol. 2014 Apr;59(4):242-5. doi: 10.1016/j.jcv.2014.01.009. Epub 2014 Jan 24.
10
Avian influenza surveillance reveals presence of low pathogenic avian influenza viruses in poultry during 2009-2011 in the West Bengal State, India.禽流感监测显示,2009-2011 年期间印度西孟加拉邦家禽中存在低致病性禽流感病毒。
Virol J. 2012 Aug 7;9:151. doi: 10.1186/1743-422X-9-151.

引用本文的文献

1
Evaluation of Spleen Swabs for Sensitive and High-Throughput Detection of Classical Swine Fever Virus.用于经典猪瘟病毒灵敏且高通量检测的脾脏拭子评估
Pathogens. 2025 Aug 3;14(8):767. doi: 10.3390/pathogens14080767.
2
Successful Inactivation of High-Consequence Pathogens in PrimeStore Molecular Transport Media.在PrimeStore分子转运介质中成功灭活高致病性病原体
Viruses. 2025 Apr 29;17(5):639. doi: 10.3390/v17050639.
3
Effect of stabilizers on the detection of swine influenza A virus (swIAV) in spiked oral fluids over time.

本文引用的文献

1
From cold chain to ambient temperature: transport of viral specimens- a review.从冷链到常温:病毒标本运输-综述。
Ann Med. 2023;55(2):2257711. doi: 10.1080/07853890.2023.2257711. Epub 2023 Sep 19.
2
Rapid evolution of A(H5N1) influenza viruses after intercontinental spread to North America.A(H5N1) 流感病毒在跨洲际传播至北美洲后迅速进化。
Nat Commun. 2023 May 29;14(1):3082. doi: 10.1038/s41467-023-38415-7.
3
African swine fever outbreaks in China led to gross domestic product and economic losses.中国的非洲猪瘟疫情导致了国内生产总值和经济损失。
稳定剂对随时间推移加标口腔液中甲型猪流感病毒(swIAV)检测的影响。
Porcine Health Manag. 2024 Nov 11;10(1):49. doi: 10.1186/s40813-024-00386-6.
4
Comparison of Extraction Methods for the Detection of Avian Influenza Virus RNA in Cattle Milk.比较牛初乳中检测禽流感病毒 RNA 的提取方法。
Viruses. 2024 Sep 10;16(9):1442. doi: 10.3390/v16091442.
Nat Food. 2021 Oct;2(10):802-808. doi: 10.1038/s43016-021-00362-1. Epub 2021 Sep 27.
4
The resurgence of Avian influenza and human infection: A brief outlook.禽流感的再度流行与人类感染:简要展望
New Microbes New Infect. 2023 Mar 30;53:101122. doi: 10.1016/j.nmni.2023.101122. eCollection 2023 Jun.
5
Disease control tools to secure animal and public health in a densely populated world.在人口密集的世界中保障动物和公共卫生的疾病控制工具。
Lancet Planet Health. 2022 Oct;6(10):e812-e824. doi: 10.1016/S2542-5196(22)00147-4.
6
African Swine Fever Vaccinology: The Biological Challenges from Immunological Perspectives.非洲猪瘟疫苗学:从免疫学角度看生物挑战。
Viruses. 2022 Sep 13;14(9):2021. doi: 10.3390/v14092021.
7
Modified Vaccinia Virus Ankara as a Potential Biosafety Level 2 Surrogate for African Swine Fever Virus in Disinfectant Efficacy Tests.在消毒剂效力测试中,安卡拉痘苗病毒作为非洲猪瘟病毒潜在的生物安全2级替代物
Pathogens. 2022 Mar 4;11(3):320. doi: 10.3390/pathogens11030320.
8
Virus viability in spiked swine bone marrow tissue during above-ground burial method and under in vitro conditions.在地上掩埋方法和体外条件下,刺猪骨髓组织中病毒的存活能力。
Transbound Emerg Dis. 2022 Sep;69(5):2987-2995. doi: 10.1111/tbed.14462. Epub 2022 Feb 19.
9
A Cold Chain-Independent Specimen Collection and Transport Medium Improves Diagnostic Sensitivity and Minimizes Biosafety Challenges of COVID-19 Molecular Diagnosis.一种无需冷链的标本采集和运输介质可提高 COVID-19 分子诊断的诊断灵敏度并降低生物安全挑战。
Microbiol Spectr. 2021 Dec 22;9(3):e0110821. doi: 10.1128/Spectrum.01108-21. Epub 2021 Dec 8.
10
Developing a Stabilizing Formulation of a Live Chimeric Dengue Virus Vaccine Dry Coated on a High-Density Microarray Patch.开发一种包被在高密度微阵列贴片上的活嵌合登革病毒疫苗的稳定制剂。
Vaccines (Basel). 2021 Nov 9;9(11):1301. doi: 10.3390/vaccines9111301.