期刊文献+

猪源多杀性巴氏杆菌荚膜分型及外膜蛋白H基因序列分析 被引量:4

Capsular Typing and Sequences Analysis of the ompH Gene of Pasteurella multocidafrom Swine
下载PDF
导出
摘要 为了解国内猪源多杀性巴氏杆菌外膜蛋白H基因的变异情况及与荚膜型之间的相关性,本试验采用PCR方法对44株猪源多杀性巴氏杆菌进行荚膜分型和ompH基因的扩增测序。结果显示,44株菌株中22株为荚膜A型,17株为荚膜B型,5株为荚膜D型;44株菌株的ompH基因开放阅读框在1 002~1 056bp之间;SignaIP 4.1预测结果显示,信号肽为N端20个氨基酸残基;ProtParam分析结果显示,成熟蛋白氨基酸残基数量在313~331aa之间,推测的分子质量在33.83~36.46ku之间。序列分析结果显示,44株菌株核苷酸同源性为86.2%~100.0%,氨基酸同源性为86.0%~100.0%;ompH基因核苷酸序列遗传进化树结果显示,荚膜A型、B型和D型菌株分别在不同的分支。试验结果表明,猪源多杀性巴氏杆菌ompH基因在不同血清型之间具有较高的同源性,与荚膜型之间存在相关性。 In order to understand the variation of outer membrane protein H(ompH)gene and the correlation with capsular type,the capsular typing and ompH gene of 44 strains of P.multocida were examined and anlalyzed by PCR method.The results showed that 22 strains were capsular type A,17 strains were capsular type B,5strains were identified as capsular type D.The open reading frames of ompH gene were from 1 002 to 1 056 bp.The predicted maturation proteins were composed of 313 to 331amino acids except the signal peptide including 20 amino acid residues in N terminal.The molecular weight of maturation proteins were from 33.83 to 36.46 ku.The alignment data indicated that the nucleotide sequence homologies were from 86.2% to100.0%,and the homology of amino acid were from 86.0% to 100.0%.The phylogenetic tree constructed by the ompH gene showed that capsular type A,B and D strains were in different branches.The sequence analysis results showed the ompH gene of P.multocidaisolated from swine had high homology among different serotypes.At the same time,there was a correlation between capsular type and the ompH gene.
出处 《中国畜牧兽医》 CAS 北大核心 2015年第1期32-37,共6页 China Animal Husbandry & Veterinary Medicine
基金 国家微生物资源平台(NIMR-5)
关键词 多杀性巴氏杆菌 荚膜分型 ompH基因 序列分析 Pasteurella multocida capsular type ompH gene sequence analysis
  • 相关文献

参考文献10

  • 1陆承平.兽医微生物学[M].第5版.北京:中国农业出版社,2012.
  • 2康立超,黄新,韩猛立,王正荣,何延华,谭鹏飞,薄新文,钟发刚,王新华.多杀性巴氏杆菌分离鉴定及序列分析[J].西北农业学报,2013,22(6):10-16. 被引量:8
  • 3李伟杰,赵耘,康凯,岂晓鑫,杜昕波,陈敏.红斑丹毒丝菌SpaA抗原基因的克隆、序列分析及蛋白结构预测[J].中国兽医学报,2011,31(11):1631-1634. 被引量:6
  • 4Townsend K M. Boyce J D,Chung J Y,et ah Genetic or-ganization of Pasteurella multocida cap loci and develop-ment of a multiplex capsular PCR typing system[J].Journal of Clinical Microbiology, 2001,39(3):924-929.
  • 5高明燕,徐步,龚建森,王鑫,俞燕,范建华,刘学贤.8株禽多杀性巴氏杆菌外膜蛋白H基因序列分析[J].中国畜牧兽医,2013,40(12):43-47. 被引量:3
  • 6Luo Y,Glisson J R,Jackwood M W,et al. Cloning andcharacterization of the major outer membrane proteingene ( ompH ) of Pasteurella multocida X-73 [ J ].Journal of Bacteriology ,1997,179(24) : 7856-7864.
  • 7Lee J,Kim Y B,Kwon M. Outer membrane protein Hfor protective immunity against Pasteurella multoci-da [J]. Journal of Microbiology, 2007, 45 ( 2 ):179-184.
  • 8Tan H Y,Nagoor N H ,Sekaran S D. Cloning, expres-sion and protective capacity of 37 kl)a outer mem-brane protein gene (ompH) of Pasteurella multocidaserotype B : 2 [ J], Tropical Biomedicine, 2010,27(3):430-441.
  • 9Sthitmatee N,Katao Y, Sawada T. Inhibition of cap-sular protein synthesis of Pasteurella multocida strainP-1059[J]. The Journal of Veterinary Medical Sci-e/ice,2011,73(11):1445-1451.
  • 10Sthitmatee N, Yano T, Lampang K N, et al. A 39~kDacapsular protein is a major cross-protection factor asdemonstrated by protection of chickens with a live at-tenuated Pasteurella multocida strain of P-1059[J].The Journal of Veterinary Medical Science , 2013.75(7);923-928.

二级参考文献25

  • 1吴斌,唐先春,陈焕春,王大鹏.猪源多杀性巴氏杆菌ompH基因的克隆、表达[J].畜牧兽医学报,2005,36(7):701-704. 被引量:11
  • 2To H, Nagai S. Genetic and antigenic diversity of the surface protective antigen proteins of Erysipelothrix rhu.ffopathiae [J]. Clin Vaccine Immunol, 2007,14 (7) : 813-820.
  • 3Takahashi T, Fujisawa T, Tamura Y, et al. DNA relat- edness among Erysipelothrix rhusiopathiae strains re- presenting all twenty-three serovars and Erysipelo thrix tonsillarum[J]. Int J Syst Evol Mierobiol, 1992, 42(3) :439-473.
  • 4Wood R L. Straw B E, D~Allaire S, et al. Diseases of swine[M]. 8th ed. Iowa State University Press, 1999: 419-430.
  • 5Galan J E, Timoney J F. Cloning and expression in Escherichia coli of a protective antigen of Erysipelo- thrix rhusiopathiae [J]. Infect Immun, 1990, 58 (9) : 3116-3121.
  • 6Makino S I, Yamamoto K, Murakami S, et al. Properties of repeat domain found in a novel protective antigen, SpaA,of Erysipelothricc rhusiopathiae [J]. Microbial Pathogenesis, 1998,25 (2) :101-109.
  • 7Makino S I, Yamamoto K, Asakura H, et al. Surface an tigen SpaA, of Erysipelothrix rhusiopathiae binds to Gram-positive bacterial cell surface[J].FEMS Micro biol Lett,2000,186:313-317.
  • 8Imada Y,Goji N, Ishikawa H, et al. Truncated surface protective antigen (SpaA) of Erysipelothrix rhusio- pathiae serotype la elicits protection against challenge with serotypes la and 2b in pigs[J]. Infect Immun, 1999,67(9) :4376-4382.
  • 9Shimoji Y, Mori Y, Fischetti V A. Immunological char- acterization of a protective antigen of Erysipelothrix rhusiopathiae identification of the region responsible for protective immunity[J]. Infect Immun, 1999,67: 1646-1651.
  • 10Cheun H I, Kawamoto K, Hiramatsu M,et al. Protec- tive immunity of SpaA-antigen producing Lactococcus lactis against Erysil)elothriz rhusiopathiae infection [J]. J Appl Microbiol,2004,96(6) :1347-1353.

共引文献16

同被引文献19

引证文献4

二级引证文献16

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