期刊文献+

一株精氨酸支原体的分离培养及分子生物学鉴定

Isolation,Cultivation and Molecular Identification of a Strain of Mycoplasma arginine
在线阅读 下载PDF
导出
摘要 【目的】旨在探究新疆哈密市伊州区某养殖户羊发病死亡的原因。【方法】采集病死羊的肺组织,进行分离培养、实时荧光定量PCR鉴定、普通PCR扩增以及基因测序分析。【结果】在改良的PPLO固体培养基上培养出了支原体;实时荧光定量PCR检测结果为支原体感染阳性;普通PCR扩增及基因测序,分离菌株与GenBank数据库中的精氨酸支原体同源性高达100%。【结论】研究结果表明,该养殖户羊发病死亡是由精氨酸支原体感染导致。 【Objective】In order to investigate the causes of illness and death of sheep in a household in Yizhou district,Hami City.【Methods】Lung tissue samples of dead sheep were collected,and bacterial isolation and cultivation,real-time fluorescent quantitative PCR,conventional PCR as well as gene sequencing and analysis were performed.【Results】Mycoplasma was cultured successfully on the surface of improved PPLO solid medium.Positive results of Mycoplasma infection were found by real-time fluorescent quantitative PCR.According to PCR amplification and gene sequencing results,the sequence of the isolate had 100% homology with that of Mycoplasma arginine registered in GenBank database.【Conclusion】A Hami strain of Mycoplasma arginine was successfully isolated.
作者 杨康 马春江 李海利 杨夷平 段进刚 古丽巴哈尔·卡德尔 陈建豪 张国新 杨帆 YANG Kang;MA Chunjiang;LI Haili;YANG Yiping;DUAN Jingang;GURI BAHAR·Cardle;CHEN Jianhao;ZHANG Guoxin;YANG Fan(Hami Animal Disease Prevention and Control Center,Hami,Xinjiang 839000,China)
出处 《草食家畜》 2025年第2期20-27,共8页 Grass-Feeding Livestock
基金 新疆维吾尔自治区“三农”骨干人才培养项目“新疆哈密市牛羊常见病标准化防控技术的推广与应用”(2022SNGGNT032)。
关键词 精氨酸支原体 分离培养 PCR 16SrRNA 基因测序 Mycoplasma arginine isolation and cultivation PCR 16S rRNA gene sequencing
  • 相关文献

参考文献5

二级参考文献56

  • 1Concalves R,Mariano I,Nunez A, et al. Atypical non progressive in goats[J]. Vet J , 2010,83(2) : 219-221.
  • 2Dassanayake R P, Shanthalingam S, Herndon C N, et al. Mycoplasma ovipneumoniae can predispose big- horn sheep to fatal Mannheimia haemolytica pneumo- nia[J]. Vet Microbiol, 2010,145 (3-4) : 354-359.
  • 3Mcauliffe L, Hatchell F M, Ayling R D, et al. Detec- tion of Mycoplasma ovipneumoniae in Pasteurella- vaccinated sheep flocks with respiratory disease in England[J]. Vet Rec ,2003,153(22) :687-688.
  • 4Kilic A, Kalender H, Eroksuz H, et al. Identification by culture, PCR, and immunohistorchemistry of My coplasma and their molecular typing in sheep and lamb lungs with pneumonia in Easter Turkey[J]. Trop Anim Health Prod ,2013,45(7) : 1525-1531.
  • 5Thirkell D, Spooner P K,Jones G E, et al. Cross-reacting antigens between Mycoplasma ovipneumoniae and other species of Mycoplasma of animal origin, shown by ELISA and immunoblotting with reference antisera[J]. Veterinary Microbiology, 1991,26 (3) : 249-261.
  • 6Sikdar A, Uppalp K. Antibiogram of respiratory My- coplasma of caprine and ovine origin[J]. Indian Joural of Animal Heal, 1996,35(2) : 185-187.
  • 7Weiser G C, Drew M L, Cassirer E F, et al. Detection of Mycoplasma ovipneumoniae and M. arginini in bighorn sheep using enrichment culture coupled with genus- and species-specific polymerase chain reaction[J]. Journal of Wildlife Diseases ,2012,48(2) :449-453.
  • 8储岳峰,高鹏程,赵萍,贺英,郭晗,逯忠新,赵海燕.应用双重PCR方法检测羊支原体肺炎病原[J].畜牧与兽医,2009(12):23-26. 被引量:12
  • 9沈志强,王金良,郭显坡,王晓虎,汪明,赵德明.SYBR GreenⅠ实时荧光定量PCR检测猪细小病毒方法的建立及初步应用[J].中国兽医学报,2011,31(1):11-15. 被引量:13
  • 10王华,杨发龙,王永,汤承.山羊支原体性肺炎流行病学调查[J].中国畜牧兽医,2011,38(1):210-214. 被引量:42

共引文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部