• 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

在伊朗西部洛雷斯坦省库赫达什特市使用显微镜和分子方法检测人类、山羊和绵羊中的感染情况。

Detection of infection among human, goats and sheep using microscopic and molecular methods in the city of Kuhdasht in Lorestan Province, West of Iran.

作者信息

Naderi Arash, Nayebzadeh Hassan, Gholami Shirzad

机构信息

Department of Parasitology, Science and Research BranchIslamic Azad University, Boroujerd, Iran.

Department of Parasitology, Faculty of Veterinary MedicineLorestan University, Khorramabad, Iran.

出版信息

J Parasit Dis. 2017 Sep;41(3):837-842. doi: 10.1007/s12639-017-0899-1. Epub 2017 Feb 28.

DOI:10.1007/s12639-017-0899-1
PMID:28848288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5555943/
Abstract

is a lethal protozoan disease, responsible for the loss of livestock in Iran and in the world. The purpose of the current study was to detect and identify spp. infection using microscopic and molecular methods in human, sheep and goats in Kuhdasht region, in the Lorestan Province, west of Iran. During 2013, a total of 384 blood smear samples were collected from 51 goats, 306 sheep suspected of infection and 27 humans from Kuhdasht region. The blood samples were fixed, stained and under light microscopic examined. DNA samples were extracted and amplified by polymerase chain reaction of 18S-rRNA gene. PCR and the semi-nested PCR were performed to identify to and to differentiate genus of and spp. The results of microscopic examination indicated that a total of 47 (12.2%) samples were positive for spp. infection: 38 (9.9%) belonging to sheep and 9 to goats (2.3%). No was observed in human samples. The PCR showed a band size of 389 bp, of spp. and the semi-nested PCR detected with a band size of 186 bp. By molecular method, 16 (4.2%) sheep and 2 (0.5%) goat blood samples were infected by . Totally, 18 samples (4.7%) were observed to have a, while no infection was found in human. Thus, the results of our study have shown sheep and goats could be vulnerable to spp., especially in Lorestan Province, Iran. Therefore, studies on the status of the animal especially are recommended.

摘要

是一种致命的原生动物疾病,在伊朗乃至全世界都导致了牲畜的损失。本研究的目的是利用显微镜和分子方法,在伊朗西部洛雷斯坦省库赫达什特地区的人类、绵羊和山羊中检测和鉴定 属物种感染情况。2013年期间,共从库赫达什特地区的51只山羊、306只疑似感染的绵羊和27名人类身上采集了384份血涂片样本。血样经固定、染色后进行光学显微镜检查。提取DNA样本并通过18S - rRNA基因的聚合酶链反应进行扩增。进行PCR和半巢式PCR以鉴定 并区分 属和 属物种。显微镜检查结果表明,共有47份(12.2%)样本 属物种感染呈阳性:38份(9.9%)属于绵羊,9份属于山羊(2.3%)。在人类样本中未观察到 。PCR显示 属物种的条带大小为389 bp,半巢式PCR检测到 的条带大小为186 bp。通过分子方法,16份(4.2%)绵羊和2份(0.5%)山羊血样感染了 。总共观察到18份样本(4.7%)感染了 ,而在人类中未发现感染。因此,我们的研究结果表明绵羊和山羊可能易受 属物种感染,尤其是在伊朗洛雷斯坦省。因此,建议对动物 尤其是 的状况进行研究。

相似文献

1
Detection of infection among human, goats and sheep using microscopic and molecular methods in the city of Kuhdasht in Lorestan Province, West of Iran.在伊朗西部洛雷斯坦省库赫达什特市使用显微镜和分子方法检测人类、山羊和绵羊中的感染情况。
J Parasit Dis. 2017 Sep;41(3):837-842. doi: 10.1007/s12639-017-0899-1. Epub 2017 Feb 28.
2
Molecular identification of Theileria and Babesia in sheep and goats in the Black Sea Region in Turkey.土耳其黑海地区绵羊和山羊中泰勒虫和巴贝斯虫的分子鉴定。
Parasitol Res. 2013 Aug;112(8):2817-24. doi: 10.1007/s00436-013-3452-x. Epub 2013 May 21.
3
Molecular Characterization and Phylogenetic Analysis of Theileria spp. and Babesia spp. Isolated from Various Ticks in Southeastern and Northwestern Regions of Iran.从伊朗东南部和西北部不同蜱虫中分离出的泰勒虫属和巴贝斯虫属的分子特征及系统发育分析
Vector Borne Zoonotic Dis. 2018 Nov;18(11):595-600. doi: 10.1089/vbz.2018.2271. Epub 2018 Jul 9.
4
Semi-nested polymerase chain reaction-based detection of spp. in small ruminants from Northwest of Iran.基于半巢式聚合酶链反应检测伊朗西北部小反刍动物中的 spp.。
Vet World. 2018 Mar;11(3):268-273. doi: 10.14202/vetworld.2018.268-273. Epub 2018 Mar 3.
5
Development of a polymerase chain reaction method for diagnosis of Babesia ovis infection in sheep and goats.一种用于诊断绵羊和山羊巴贝斯虫感染的聚合酶链反应方法的开发。
Vet Parasitol. 2005 Nov 5;133(4):277-81. doi: 10.1016/j.vetpar.2005.05.057.
6
Molecular detection of Theileria spp. and Babesia spp. in sheep and ixodid ticks from the northeast of Iran.伊朗东北部绵羊和硬蜱中泰勒虫属和巴贝斯虫属的分子检测
J Parasitol. 2013 Feb;99(1):77-81. doi: 10.1645/GE-3202.1. Epub 2012 Aug 27.
7
Molecular and Parasitological Survey of Ovine Piroplasmosis, Including the First Report of Theileria annulata (Apicomplexa: Theileridae) in Sheep and Goats from Turkey.绵羊梨形虫病的分子和寄生虫学调查,包括土耳其绵羊和山羊环形泰勒虫(顶复门:泰勒科)的首次报道
J Med Entomol. 2017 Jan;54(1):212-220. doi: 10.1093/jme/tjw134. Epub 2016 Aug 23.
8
Determination of Prevalence and Risk Factors of Infection with Babesia ovis in Small Ruminants from West Azerbaijan Province, Iran by Polymerase Chain Reaction.通过聚合酶链反应测定伊朗西阿塞拜疆省小反刍动物巴贝斯虫感染率及危险因素
J Arthropod Borne Dis. 2015 Mar 11;9(2):246-52. eCollection 2015 Dec.
9
Molecular detection and genetic characterization of Babesia, Theileria and Anaplasma amongst apparently healthy sheep and goats in the central region of Turkey.土耳其中部地区表面健康的绵羊和山羊中巴贝斯虫、泰勒虫和无形体的分子检测与基因特征分析
Ticks Tick Borne Dis. 2017 Feb;8(2):246-252. doi: 10.1016/j.ttbdis.2016.11.006. Epub 2016 Nov 16.
10
Determination of prevalence and risk factors for infection with Babesia ovis in small ruminants from Turkey by polymerase chain reaction.采用聚合酶链反应法测定土耳其小反刍动物中绵羊巴贝斯虫感染的患病率及危险因素。
Parasitol Res. 2007 Mar;100(4):797-802. doi: 10.1007/s00436-006-0345-2. Epub 2006 Nov 10.

引用本文的文献

1
Infection by haemopathogens and tick infestation of sheep during summer season in Constantine region, Northeast Algeria.在阿尔及利亚东北部君士坦丁地区,夏季绵羊感染血液病原体和蜱虫。
Vet Med Sci. 2021 Sep;7(5):1769-1777. doi: 10.1002/vms3.551. Epub 2021 Jun 17.
2
Molecular detection of Theileria spp. and Babesia ovis Infection in Sheep in Baneh, Iran.伊朗巴内省绵羊感染泰勒虫属和绵羊巴贝斯虫的分子检测。
Arch Razi Inst. 2020 Jun;75(2):289-296. doi: 10.22092/ari.2019.125136.1297. Epub 2020 Jun 1.
3
Detection of incidence of spp. in sheep and goats by parasitological diagnostic techniques.通过寄生虫学诊断技术检测绵羊和山羊体内 spp. 的感染率。
J Parasit Dis. 2019 Sep;43(3):452-457. doi: 10.1007/s12639-019-01109-3. Epub 2019 Mar 30.

本文引用的文献

1
Genetic variability, phylogenetic evaluation and first global report of Theileria luwenshuni, T. buffeli, and T. ovis in sheepdogs in Iran.伊朗牧羊犬中鲁氏泰勒虫、水牛泰勒虫和绵羊泰勒虫的遗传变异性、系统发育评估及首次全球报告
Parasitol Res. 2016 May;115(5):2125-30. doi: 10.1007/s00436-016-5005-6. Epub 2016 Mar 21.
2
Human exposure to piroplasms in Central and Northern Italy.意大利中部和北部人群对梨形虫的暴露情况。
Vet Ital. 2014 Jan-Mar;50(1):41-7. doi: 10.12834/VetIt.1302.13.
3
Coinfection of sheep with Anaplasma, Theileria and Babesia species in the Kurdistan Region, Iraq.伊拉克库尔德地区绵羊中感染 Anaplasma、Theileria 和 Babesia 物种的情况。
Transbound Emerg Dis. 2013 Nov;60 Suppl 2:113-8. doi: 10.1111/tbed.12148.
4
A molecular study on Theileria and Babesia in cattle from Isfahan province, Central Iran.伊朗中部伊斯法罕省牛泰勒虫和巴贝斯虫的分子研究
J Parasit Dis. 2013 Oct;37(2):208-10. doi: 10.1007/s12639-012-0167-3. Epub 2012 Sep 15.
5
The use of different diagnostic tools for Babesia and Theileria parasites in cattle in Menofia, Egypt.埃及迈努菲亚省牛巴贝斯虫和泰勒虫属寄生虫的不同诊断工具的应用。
Parasitol Res. 2012 Sep;111(3):1019-24. doi: 10.1007/s00436-012-2926-6. Epub 2012 Apr 29.
6
Babesia ovis as the main causative agent of sheep babesiosis in Iran.巴贝斯虫属 ovis 是伊朗绵羊巴贝斯虫病的主要病原体。
Parasitol Res. 2012 Apr;110(4):1531-6. doi: 10.1007/s00436-011-2658-z.
7
Biometrical and genetical characterization of large Babesia ovis in Iran.伊朗大型绵羊巴贝斯虫的生物统计学和遗传学特征
Parasitol Res. 2008 Jun;103(1):217-21. doi: 10.1007/s00436-008-0960-1.
8
Simultaneous differentiation between Theileria spp. and Babesia spp. on stained blood smear using PCR.使用聚合酶链式反应(PCR)在染色血涂片上同时鉴别泰勒虫属和巴贝斯虫属。
Parasitol Res. 2005 Oct;97(4):281-6. doi: 10.1007/s00436-005-1434-3. Epub 2005 Jul 9.
9
Piroplasmosis in man; report of a case.人类梨形虫病;一例报告。
Doc Med Geogr Trop. 1957 Mar;9(1):11-6.
10
A fatal case of human babesiosis in Portugal: molecular and phylogenetic analysis.葡萄牙一例人巴贝斯虫病致死病例:分子与系统发育分析
Trop Med Int Health. 2003 Aug;8(8):760-4. doi: 10.1046/j.1365-3156.2003.01074.x.