猪2型链球菌体内诱导抗原的筛选、鉴定和功能研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
猪链球菌是一种重要的人畜共患病,能引起猪的脑膜炎、败血症、关节炎和急性死亡,每年给养猪业造成重大的经济损失。根据链球菌的荚膜可分为35个血清型,32和34血清型后来被证明实际上是属于Streptococcus orisratti链球菌。其中,2型链球菌的毒力最强,危害最大。近年来,也不乏猪链球菌感染人的报道,主要因为接触到感染的猪或组织。人感染链球菌后,会引起脑膜炎、心内膜炎、败血症和永久性失聪,严重时能引起人的死亡。
     目前对猪链球菌的控制仍然止步于对其致病机制知之甚少,缺少有效地疫苗和诊断方法。尽管猪已经鉴定出猪2型链球菌的一些毒力因子,但其入侵和破坏宿主的致病机理还很不明了。为进一步了解链球菌与宿主相互作用的关系,本研究利用体内诱导抗原技术鉴定了链球菌感染宿主过程中表达的蛋白,并对部分基因的功能做了进一步的研究。
     1.猪2型链球菌体内抗原的筛选和鉴定
     本研究使用体内诱导抗原技术去挖掘猪链球菌感染过程中活动的蛋白。使用pET28a, b, c载体构建了基因组猪2型链球菌的基因组表达文库,库容分别为8000,12000,11000,达到了基因覆盖率为99.9%的要求。收集了实验感染与临床采集的康复血清,采用膜吸附法,依次吸附了康复血清里的菌体表面抗体、菌体裂解物的抗体以及与大肠杆菌交叉反应的抗体,获得了体内表达抗体的探针。使用探针筛选基因组表达文库大于12000个克隆,经第二轮第三轮筛选鉴定,最终获得了包括已知毒力因子溶血素在内20种体内诱导。功能包括代谢、细胞分离的酶类,转运相关基因,细胞表面蛋白及其他未知功能的蛋白。选取不同亚细胞定位的5个基因,一个细胞壁蛋白(sspA),3个细胞质蛋白(secA, mod and moeA)和一个未知结构的蛋白(orf28)使用实时荧光定量PCR技术,通过比较感染小鼠体内与体外培养细菌的基因表达差异,发现验证的5个基因均有不同程度的上调表达。也从另一方面验证了体内诱导抗原技术的可靠性。这些鉴定出的蛋白值得更进一步的研究其对致病的作用。
     2.猪2型链球菌枯草菌素样丝氨酸蛋白酶(Subtilisin-like serine protease, SspA)的鉴定和致病功能研究
     SspA是通过体内诱导抗原技术筛选出来的,其与康复血清的反应性最强。表达纯化了SspA基因内部不同的片段ssp328-1624, sspA1610-2800,sspA3655-4470,使用点杂交的方法验证了SspA确实只在康复血清中存在抗体,而免疫血清中抗体检测为阴性。进一步使用荧光定量PCR方法验证了sspA基因在感染猪体内的上调表达。
     使用软件InterProScan预测SspA蛋白属于枯草杆菌素家族,含有motifⅠ(Asp 251), motifⅡ(His 311), and motifⅢ(Ser 649)。并使用间接免疫荧光的方法证实了含有LPXTG结构的SspA蛋白位于细胞的表面,为细胞壁相关蛋白。分析了SspA的参考菌株和临床菌株中存在情况,发现在参考菌株中,有29株存在sspA基因,同时使用间接免疫荧光方法验证该基因在参考菌株表面的表达。在扩增的112株2型分离株和53株其他血清型菌株中(包括1/2,1,7,9,4,11,13,12,19,21,23,25,28,6,10,14,15和20,结果都为PCR阳性。该基因在链球菌中相对保守。构建了sspA的基因突变株与恢复突变株。发现突变株的生长曲线、溶血性以及亚细胞结构并没有明显的改变。将突变株、野生菌株与基因回复突变株以同样的剂量感染本动物猪后,突变株的毒力相对于野生菌株大大减弱,而回复突变株的毒力与野生菌株相当。表明是SspA单基因缺失导致的毒力变化,提示了该基因在猪2型链球菌致病中发挥一定的作用。以突变株与野生菌株混合,感染本动物猪,比较它们在组织定植的能力。结果发现,突变株仍然可以在猪的扁桃体中定植,但扩散至深层组织形成感染的能力降低。突变株不具备与野生菌株竞争在扁桃体定植的能力。这些数据表明细菌表面蛋白SspA是一种保守的毒力因子,参与猪链球菌的致病过程。
Streptococcus suis is an important cause of meningitis, septicaemia, arthritis and sudden death in pigs. So far,35 serotypes were described based on variation of the capsular polysaccharide (CPS). S. suis infections especially the serotype 2, caused great economic loss in pig industry worldwide every year. Moreover, S. suis can infect humans, mainly associated with exposure to infected pigs or tissues. A recent outbreak in China caused by a serotype 2 strain resulted in 38 deaths among 215 infected humans, an 18% mortality rate. The bacterium has caused sporadic human illness in other countries as well, including the United Kingdom, and has been identified as a leading cause of bacterial meningitis in Hong Kong Special Administrative Region and Vietnam. S. suis infections raised considerable international concerns among the public health professionals.
     Currently, attempts to control the diseases caused by S. suis are still hampered by insufficient knowledge of pathogenesis mechanism, and a lack of effective vaccines and sensitive diagnostic methods. Althogh a set of virulence traits was identified. Knoledge about he molecular mechanism of invasion and damage of the host tissue by the bacteria is still limited. In order to put an insight to the interaction of host and pathogen, we use in vivo induced antigen technology to identify of Streptococcus suis serotype 2 antigens which were uniquely expressed during infection.
     1. Identification of Streptococcus suis antigenic determinants specifically expressed during infection
     Streptococcus suis is an important swine and human pathogen with adhesive and invasive properties. Pathogenesis mechanism of S. suis infection has not been completely defined due to limited information on its virulence factors. In this study, in vivo antigen technology (IVIAT) was used to identify S. suis antigens expressed during pig infection. In total,20 in vivo induced (ivi) genes were identified, including suilysin, a known putative virulence factor; enzymes function in metabolism/housekeeping, cell division/replication and cell wall degradation, transporting related genes, cell wall-associated proteins, and hypothetical proteins of unknown function. Five genes were selected to test the in vivo expression by relative real-time PCR in mice. SecA, putative modification enzyme (mod), moeA and orf28 were apparently upregulated in vivo. Of the twenty ivi genes, three parts of a subtilisin-like serine protease (ssp) gene were identified. The three segments (sspN, sspM and sspC) were expressed and purified. The anti-SSP antibodies in various phages after infection were evaluated. It was found that the antibody developed as early as at the first week post infection. Such proteins might be explored as markers of S. suis infection. S. suis antigens identified by IVIAT warrant further evaluation on their contributions to pathogenesis, and may probably be developed for diagnostc and preventive applications.
     2. Identification of a cell wall-associated subtilisin-like serine protease involved in the pathogenesis of Streptococcus suis serotype 2
     Streptococcus suis is an important swine and human pathogen, and also an emerging zoonotic agent. A surface-associated subtilisin-like serine protease (SspA) of S. suis was identified by screening a genomic expression library as fragments of this protein reacted most strongly with convalescent-phase pig sera. The sspA gene is present in 29 of 33 S. suis serotypes reference strains and is expressed on the surface of S. suis. Relative real-time quantitive PCR assay demonstrated that sspA mRNA expression in vivo was several thousand fold of that in vitro. A sspA- mutant was generated from a S. suis serotype 2 strain SC19 by allelic exchange. The mutant was not different from the wild type strain in subcellular structures and in hemolytic phenotype. However, the virulence of the sspA mutant was markedly lower than the wild type in pigs as demonstrated in experimental infections. These data indicated that the surface associated protein SspA is a conserved virulence factor of S. suis and is involved in the pathogenesis of S. suis.
引文
1.白雪梅,张亚兰,孙娜,周永运,叶长芸,郑瀚,杜华茂,徐建国.100株猪链球菌的生化检测及药物敏感性分析.中国人畜共患病学报,2006,22:396-398
    2.陈师勇,莫照兰,张振冬,邹玉霞,徐永立,张培军.细菌毒力基因体内表达检测技术研究进展.遗传,2005,27:505-511
    3.陈国强,姚火春,陆承平.2型猪链球菌溶血毒素的产生条件及其特性分析.南京农业大学学报,2000,23(03):71-75
    4. Aarestrup F M, Rasmussen S R, Artursson K, et al. Trends in the resistance to antimicrobial agents of Streptococcus suis isolates from Denmark and Sweden. Vet Microbiol,1998,63:71-80
    5. Akerley B J, Rubin E J, Camilli A, et al. Systematic identification of essential genes by in vitro mariner mutagenesis. Proc Natl Acad Sci U S A,1998,95:8927-8932
    6. Allen A G, Bolitho S, Lindsay H, et al. Generation and characterization of a defined mutant of Streptococcus suis lacking suilysin. Infect Immun,2001,69:2732-2735
    7. Amass S F, SanMiguel P and Clark L K. Demonstration of vertical transmission of Streptococcus suis in swine by genomic fingerprinting. J Clin Microbiol,1997,35: 1595-1596
    8. Anderson D, Shapiro L and Skalka A M. In situ immunoassays for translation products. Methods Enzymol,1979,68:428-436
    9. Angelichio M J and Camilli A. In vivo expression technology. Infect Immun,2002, 70:6518-6523
    10. Areschoug T, Carlsson F, Stalhammar-Carlemalm M, et al. Host-pathogen interactions in Streptococcus pyogenes infections, with special reference to puerperal fever and a comment on vaccine development. Vaccine,2004,22 Suppl 1:S9-S14
    11. Bartilson M, Marra A, Christine J, et al. Differential fluorescence induction reveals Streptococcus pneumoniae loci regulated by competence stimulatory peptide. Mol Microbiol,2001,39:126-135
    12. Bateman A and Rawlings N D. The CHAP domain:a large family of amidases including GSP amidase and peptidoglycan hydrolases. Trends Biochem Sci,2003, 28:234-237
    13. Baums C G, Kaim U, Fulde M, et al. Identification of a novel virulence determinant with serum opacification activity in Streptococcus suis. Infect Immun, 2006,74:6154-6162
    14. Bensaid T, Bonnefoi-Kyriacou B, Dupel-Pottier C, et al. [Streptococcus suis meningitis following wild boar hunting]. Presse Med,2003,32:1077-1078
    15. Berthelot-Herault F, Morvan H, Keribin A M, et al. Production of muraminidase-released protein (MRP), extracellular factor (EF) and suilysin by field isolates of Streptococcus suis capsular types 2,1/2,9,7 and 3 isolated from swine in France. Vet Res,2000,31:473-479
    16. Bumann D and Valdivia R H. Identification of host-induced pathogen genes by differential fluorescence induction reporter systems. Nat Protoc,2007,2:770-777
    17. Cao S L, Progulske-Fox A, Hillman J D, et al. In vivo induced antigenic determinants of Actinobacillus actinomycetemcomitans. FEMS Microbiol Lett, 2004,237:97-103
    18. Chanter N, Jones P W and Alexander T J. Meningitis in pigs caused by Streptococcus suis--a speculative review. Vet Microbiol,1993,36:39-55
    19. Charland N, Harel J, Kobisch M, et al. Streptococcus suis serotype 2 mutants deficient in capsular expression. Microbiology,1998,144 (Pt 2):325-332
    20. Charland N, Kobisch M, Martineau-Doize B, et al. Role of capsular sialic acid in virulence and resistance to phagocytosis of Streptococcus suis capsular type 2. FEMS Immunol Med Microbiol,1996,14:195-203
    21. Charland N, Nizet V, Rubens C E, et al. Streptococcus suis serotype 2 interactions with human brain microvascular endothelial cells. Infect Immun,2000,68: 637-643
    22. Chatellier S, Gottschalk M, Higgins R, et al. Relatedness of Streptococcus suis serotype 2 isolates from different geographic origins as evaluated by molecular fingerprinting and phenotyping. J Clin Microbiol,1999,37:362-366
    23. Chen C, Tang J, Dong W, et al. A glimpse of streptococcal toxic shock syndrome from comparative genomics of S. suis 2 Chinese isolates. PLoS ONE,2007,2: e315
    24. Cheng S, Clancy C J, Checkley M A, et al. Identification of Candida albicans genes induced during thrush offers insight into pathogenesis. Mol Microbiol,2003, 48:1275-1288
    25. Chiang S L and Mekalanos J J. Use of signature-tagged transposon mutagenesis to identify Vibrio cholerae genes critical for colonization. Mol Microbiol,1998,27: 797-805
    26. Cleary P P, Prahbu U, Dale J B, et al. Streptococcal C5a peptidase is a highly specific endopeptidase. Infect Immun,1992,60:5219-5223
    27. Clifton-Hadley F A. Streptococcus suis type 2 infections. Br Vet J,1983,139:1-5
    28. Clifton-Hadley F A, Alexander T J, Enright M R, et al. Monitoring herds for Streptococcus suis type 2 by sampling tonsils of slaughter pigs. Vet Rec,1984a, 115:562-564
    29. Clifton-Hadley F A, Alexander T J, Upton I, et al. Further studies on the subclinical carrier state of Streptococcus suis type 2 in pigs. Vet Rec,1984b,114: 513-518
    30. Clifton-Hadley R S, Bucke D and Richards R H. Economic importance of proliferative kidney disease of salmonid fish in England and Wales. Vet Rec,1986, 119:305-306
    31. Cloutier G, D'Allaire S, Martinez G, et al. Epidemiology of Streptococcus suis serotype 5 infection in a pig herd with and without clinical disease. Vet Microbiol, 2003,97:135-151
    32. Costa A T, Lobato F C, Abreu V L, et al. Serotyping and evaluation of the virulence in mice of Streptococcus suis strains isolated from diseased pigs. Rev Inst Med Trop Sao Paulo,2005,47:113-115
    33. De Bolle X, Bayliss C D, Field D, et al. The length of a tetranucleotide repeat tract in Haemophilus influenzae determines the phase variation rate of a gene with homology to type Ⅲ DNA methyltransferases. Mol Microbiol,2000,35:211-222
    34. de Greeff A, Buys H, van Alphen L, et al. Response regulator important in pathogenesis of Streptococcus suis serotype 2. Microb Pathog,2002a,33:185-192
    35. de Greeff A, Buys H, Verhaar R, et al. Contribution of fibronectin-binding protein to pathogenesis of Streptococcus suis serotype 2. Infect Immun,2002b,70: 1319-1325
    36. de Vries N, Duinsbergen D, Kuipers E J, et al. Transcriptional phase variation of a type Ⅲ restriction-modification system in Helicobacter pylori. J Bacteriol,2002, 184:6615-6623
    37. Deb D K, Dahiya P, Srivastava K K, et al. Selective identification of new therapeutic targets of Mycobacterium tuberculosis by IVIAT approach. Tuberculosis (Edinb),2002,82:175-182
    38. Dee S A, Carlson A R, Winkelman N L, et al. Effect of management practices on the Streptococcus suis carrier rate in nursery swine. J Am Vet Med Assoc,1993, 203:295-299
    39. Devriese L A, Haesebrouck F, de Herdt P, et al. Streptococcus suis infections in birds. Avian Pathol,1994,23:721-724
    40. Devriese L A, Sustronck B, Maenhout T, et al. Streptococcus suis meningitis in a horse. Vet Rec,1990,127:68
    41. Erickson E D, Doster A R and Pokorny T S. Isolation of Streptococcus suis from swine in Nebraska. J Am Vet Med Assoc,1984,185:666-668
    42. Etz H, Minh D B, Henics T, et al. Identification of in vivo expressed vaccine candidate antigens from Staphylococcus aureus. Proc Natl Acad Sci U S A,2002, 99:6573-6578
    43. Fittipaldi N, Sekizaki T, Takamatsu D, et al. Significant contribution of the pgdA gene to the virulence of Streptococcus suis. Mol Microbiol,2008a,70:1120-1135
    44. Fittipaldi N, Sekizaki T, Takamatsu D, et al. D-alanylation of lipoteichoic acid contributes to the virulence of Streptococcus suis. Infect Immun,2008b,76: 3587-3594
    45. Fontaine M C, Perez-Casal J and Willson P J. Investigation of a novel DNase of Streptococcus suis serotype 2. Infect Immun,2004,72:774-781
    46. Fox K L, Dowideit S J, Erwin A L, et al. Haemophilus influenzae phasevarions have evolved from type Ⅲ DNA restriction systems into epigenetic regulators of gene expression. Nucleic Acids Res,2007,35:5242-5252
    47. Francois B, Gissot V, Ploy M C, et al. Recurrent septic shock due to Streptococcus suis. J Clin Microbiol,1998,36:2395
    48. Galina L, Collins J E and Pijoan C. Porcine Streptococcus suis in Minnesota. J Vet Diagn Invest,1992,4:195-196
    49. Galina L, Pijoan C, Sitjar M, et al. Interaction between Streptococcus suis serotype 2 and porcine reproductive and respiratory syndrome virus in specific pathogen-free piglets. Vet Rec,1994,134:60-64
    50. Galina L, Vecht U, Wisselink H J, et al. Prevalence of various phenotypes of Streptococcus suis isolated from swine in the U.S.A. based on the presence of muraminidase-released protein and extracellular factor. Can J Vet Res,1996,60: 72-74
    51. Ge J, Feng Y, Ji H, et al. Inactivation of dipeptidyl peptidase Ⅳ attenuates the virulence of Streptococcus suis serotype 2 that causes streptococcal toxic shock syndrome. Curr Microbiol,2009,59:248-255
    52. Gogolewski R P, Cook R W and O'Connell C J. Streptococcus suis serotypes associated with disease in weaned pigs. Aust Vet J,1990,67:202-204
    53. Gottschalk M and Segura M. The pathogenesis of the meningitis caused by Streptococcus suis:the unresolved questions. Vet Microbiol,2000,76:259-272
    54. Gottschalk M G, Lacouture S and Dubreuil J D. Characterization of Streptococcus suis capsular type 2 haemolysin. Microbiology,1995,141 (Pt 1):189-195
    55. Handfield M, Brady L J, Progulske-Fox A, et al. IVIAT:a novel method to identify microbial genes expressed specifically during human infections. Trends Microbiol,2000a,8:336-339
    56. Handfield M, Lehoux D E, Sanschagrin F, et al. In vivo-induced genes in Pseudomonas aeruginosa. Infect Immun,2000b,68:2359-2362
    57. Handfield M and Levesque R C. Strategies for isolation of in vivo expressed genes from bacteria. FEMS Microbiol Rev,1999,23:69-91
    58. Handfield M, Seifert T and Hillman J D. In vivo expression of bacterial genes during human infections. Methods Mol Med,2003,71:225-242
    59. Hang L, John M, Asaduzzaman M, et al. Use of in vivo-induced antigen technology (IVIAT) to identify genes uniquely expressed during human infection with Vibrio cholerae. Proc Natl Acad Sci U S A,2003,100:8508-8513
    60. Hansen K, Bangsborg J M, Fjordvang H, et al. Immunochemical characterization of and isolation of the gene for a Borrelia burgdorferi immunodominant 60-kilodalton antigen common to a wide range of bacteria. Infect Immun,1988, 56:2047-2053
    61. Harris J B, Baresch-Bernal A, Rollins S M, et al. Identification of in vivo-induced bacterial protein antigens during human infection with Salmonella enterica serovar Typhi. Infect Immun,2006,74:5161-5168
    62. Heath P J and Hunt B W. Streptococcus suis serotypes 3 to 28 associated with disease in pigs. Vet Rec,2001,148:207-208
    63. Heath P J, Hunt B W, Duff J P, et al. Streptococcus suis serotype 14 as a cause of pig disease in the UK. Vet Rec,1996,139:450-451
    64. Hensel M, Shea J E, Gleeson C, et al. Simultaneous identification of bacterial virulence genes by negative selection. Science,1995,269:400-403
    65. Higgins R and Gottschalk M. Distribution of Streptococcus suis capsular types in 1999. Can Vet J,2000,41:414
    66. Higgins R and Gottschalk M. Distribution of Streptococcus suis capsular types in 2000. Can Vet J,2001,42:223
    67. Hill J E, Gottschalk M, Brousseau R, et al. Biochemical analysis, cpn60 and 16S rDNA sequence data indicate that Streptococcus suis serotypes 32 and 34, isolated from pigs, are Streptococcus orisratti. Vet Microbiol,2005,107:63-69
    68. Holt M E, Enright M R and Alexander T J. Immunisation of pigs with killed cultures of Streptococcus suis type 2. Res Vet Sci,1990a,48:23-27
    69. Holt M E, Enright M R and Alexander T J. Immunisation of pigs with live cultures of Streptococcus suis type 2. Res Vet Sci,1988,45:349-352
    70. Holt M E, Enright M R and Alexander T J. Protective effect of sera raised against different fractions of Streptococcus suis type 2. J Comp Pathol,1990b,103:85-94
    71. Hu X, Zhu F, Wang H, et al. [Studies on human streptococcal infectious syndrome caused by infected pigs]. Zhonghua Yu Fang Yi Xue Za Zhi,2000,34:150-152
    72. Huang R, Lin Y, Shi Q, et al. Enhanced protein profiling arrays with ELISA-based amplification for high-throughput molecular changes of tumor patients' plasma. Clin Cancer Res,2004,10:598-609
    73. Huang Y T, Teng L J, Ho S W, et al. Streptococcus suis infection. J Microbiol Immunol Infect,2005,38:306-313
    74. Hui A C, Ng K C, Tong P Y, et al. Bacterial meningitis in Hong Kong:10-years' experience. Clin Neurol Neurosurg,2005,107:366-370
    75. Jackson R W and Giddens S R. Development and application of in vivo expression technology (IVET) for analysing microbial gene expression in complex environments. Infect Disord Drug Targets,2006,6:207-240
    76. Jacobs A A, Loeffen P L, van den Berg A J, et al. Identification, purification, and characterization of a thiol-activated hemolysin (suilysin) of Streptococcus suis. Infect Immun,1994,62:1742-1748
    77. Jacobs A A, van den Berg A J, Baars J C, et al. Production of suilysin, the thiol-activated haemolysin of Streptococcus suis, by field isolates from diseased pigs. Vet Rec,1995,137:295-296
    78. Jobin M C and Grenier D. Identification and characterization of four proteases produced by Streptococcus suis. FEMS Microbiol Lett,2003,220:113-119
    79. Jobin M C, Martinez G, Motard J, et al. Cloning, purification, and enzymatic properties of dipeptidyl peptidase IV from the swine pathogen Streptococcus suis. J Bacteriol,2005,187:795-799
    80. John M, Kudva I T, Griffin R W, et al. Use of in vivo-induced antigen technology for identification of Escherichia coli O157:H7 proteins expressed during human infection. Infect Immun,2005,73:2665-2679
    81. Juarez Z E and Stinson M W. An extracellular protease of Streptococcus gordonii hydrolyzes type IV collagen and collagen analogues. Infect Immun,1999,67: 271-278
    82. Kataoka Y, Yoshida T and Sawada T. A 10-year survey of antimicrobial susceptibility of streptococcus suis isolates from swine in Japan. J Vet Med Sci, 2000,62:1053-1057
    83. Kilic A O, Vijayakumar M N and al-Khaldi S F. Identification and nucleotide sequence analysis of a transfer-related region in the streptococcal conjugative transposon Tn5252. J Bacteriol,1994,176:5145-5150
    84. Kim Y R, Lee S E, Kim C M, et al. Characterization and pathogenic significance of Vibrio vulnificus antigens preferentially expressed in septicemic patients. Infect Immun,2003,71:5461-5471
    85. King S J, Heath P J, Luque I, et al. Distribution and genetic diversity of suilysin in Streptococcus suis isolated from different diseases of pigs and characterization of the genetic basis of suilysin absence. Infect Immun,2001,69:7572-7582
    86. Larsson C, Stalhammar-Carlemalm M and Lindahl G. Protection against experimental infection with group B streptococcus by immunization with a bivalent protein vaccine. Vaccine,1999,17:454-458
    87. Larsson C, Stalhammar-Carlemalm M and Lindahl G. Vaccination with highly purified cell surface proteins confers protection against experimental group B streptococcal infection. Adv Exp Med Biol,1997,418:851-853
    88. Li M, Wang C, Feng Y, et al. SalK/SalR, a two-component signal transduction system, is essential for full virulence of highly invasive Streptococcus suis serotype 2. PLoS ONE,2008,3:e2080
    89. Li Y, Gottschalk M, Esgleas M, et al. Immunization with recombinant Sao protein confers protection against Streptococcus suis infection. Clin Vaccine Immunol, 2007,14:937-943
    90. Li Y, Martinez G, Gottschalk M, et al. Identification of a surface protein of Streptococcus suis and evaluation of its immunogenic and protective capacity in pigs. Infect Immun,2006,74:305-312
    91. Livak K J and Schmittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods,2001, 25:402-408
    92. Mahan M J, Heithoff D M, Sinsheimer R L, et al. Assessment of bacterial pathogenesis by analysis of gene expression in the host. Annu Rev Genet,2000, 34:139-164
    93. Mahan M J, Slauch J M and Mekalanos J J. Selection of bacterial virulence genes that are specifically induced in host tissues. Science,1993,259:686-688
    94. Mai N T, Hoa N T, Nga T V, et al. Streptococcus suis meningitis in adults in Vietnam. Clin Infect Dis,2008,46:659-667
    95. McKellar Q A, Baxter P, Taylor D, et al. Penicillin therapy of spontaneous streptococcal meningitis in pigs. Vet Rec,1987,121:347-350
    96. Mei J M, Nourbakhsh F, Ford C W, et al. Identification of Staphylococcus aureus virulence genes in a murine model of bacteraemia using signature-tagged mutagenesis. Mol Microbiol,1997,26:399-407
    97. Mogollon J D, Pijoan C, Murtaugh M P, et al. Identification of epidemic strains of Streptococcus suis by genomic fingerprinting. J Clin Microbiol,1991,29:782-787
    98. Norton P M, Rolph C, Ward P N, et al. Epithelial invasion and cell lysis by virulent strains of Streptococcus suis is enhanced by the presence of suilysin. FEMS Immunol Med Microbiol,1999,26:25-35
    99. Osaki M, Takamatsu D, Shimoji Y, et al. Characterization of Streptococcus suis genes encoding proteins homologous to sortase of gram-positive bacteria. J Bacteriol,2002,184:971-982
    100. Pan X, Ge J, Li M, et al. The Orphan Response Regulator CovR: a Globally Negative Modulator of Virulence in Streptococcus suis Serotype 2. J Bacteriol, 2009:
    101. Pedroli S, Kobisch M, Beauchet O, et al. [Streptococcus suis bacteremia]. Presse Med,2003,32:599-601
    102. Perch B, Pedersen K B and Henrichsen J. Serology of capsulated streptococci pathogenic for pigs:six new serotypes of Streptococcus suis. J Clin Microbiol, 1983,17: 993-996
    103. Pozzi G, Contorni M, Oggioni M R, et al. Delivery and expression of a heterologous antigen on the surface of streptococci. Infect Immun,1992,60: 1902-1907
    104. Purushothaman S S, Park H S and Cleary P P. Promotion of fibronectin independent invasion by C5a peptidase into epithelial cells in group A Streptococcus. Indian J Med Res,2004,119 Suppl:44-47
    105. Reams R Y, Glickman L T, Harrington D D, et al. Streptococcus suis infection in swine:a retrospective study of 256 cases. Part I. Epidemiologic factors and antibiotic susceptibility patterns. J Vet Diagn Invest,1993,5:363-367
    106. Reams R Y, Harrington D D, Glickman L T, et al. Fibrinohemorrhagic pneumonia in pigs naturally infected with Streptococcus suis. J Vet Diagn Invest, 1995,7:406-408
    107. Reams R Y, Harrington D D, Glickman L T, et al. Multiple serotypes and strains of Streptococcus suis in naturally infected swine herds. J Vet Diagn Invest,1996,8: 119-121
    108. Rediers H, Rainey P B, Vanderleyden J, et al. Unraveling the secret lives of bacteria: use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression. Microbiol Mol Biol Rev,2005,69:217-261
    109. Robertson I D and Blackmore D K. Occupational exposure to Streptococcus suis type 2. Epidemiol Infect,1989,103:157-164
    110. Rosenkranz M, Elsner H A, Sturenburg H J, et al. Streptococcus suis meningitis and septicemia contracted from a wild boar in Germany. J Neurol,2003,250: 869-870
    111. Salim K Y, Cvitkovitch D G, Chang P, et al. Identification of group A Streptococcus antigenic determinants upregulated in vivo. Infect Immun,2005,73: 6026-6038
    112. Saukkonen K, Sande S, Cioffe C, et al. The role of cytokines in the generation of inflammation and tissue damage in experimental gram-positive meningitis. J Exp Med,1990,171:439-448
    113. Segura M, Stankova J and Gottschalk M. Heat-killed Streptococcus suis capsular type 2 strains stimulate tumor necrosis factor alpha and interleukin-6 production by murine macrophages. Infect Immun,1999,67:4646-4654
    114. Segura M A, Cleroux P and Gottschalk M. Streptococcus suis and group B Streptococcus differ in their interactions with murine macrophages. FEMS Immunol Med Microbiol,1998,21:189-195
    115. Siezen R J. Multi-domain, cell-envelope proteinases of lactic acid bacteria. Antonie Van Leeuwenhoek,1999,76:139-155
    116. Skalka A and Shapiro L. In situ immunoassays for gene translation products in phage plaques and bacterial colonies. Gene,1976,1:65-79
    117. Slauch J M and Camilli A. IVET and RIVET:use of gene fusions to identify bacterial virulence factors specifically induced in host tissues. Methods Enzymol, 2000,326:73-96
    118. Smith H E, Buijs H, de Vries R R, et al. Environmentally regulated genes of Streptococcus suis:identification by the use of iron-restricted conditions in vitro and by experimental infection of piglets. Microbiology,2001,147:271-280
    119. Smith H E, Damman M, van der Velde J, et al. Identification and characterization of the cps locus of Streptococcus suis serotype 2:the capsule protects against phagocytosis and is an important virulence factor. Infect Immun,1999,67: 1750-1756
    120. Smith H E, de Vries R, van't Slot R, et al. The cps locus of Streptococcus suis serotype 2:genetic determinant for the synthesis of sialic acid. Microb Pathog, 2000,29:127-134
    121. Smith H E, Vecht U, Gielkens A L, et al. Cloning and nucleotide sequence of the gene encoding the 136-kilodalton surface protein (muramidase-released protein) of Streptococcus suis type 2. Infect Immun,1992,60:2361-2367
    122. Smith H E, Vecht U, Wisselink H J, et al. Mutants of Streptococcus suis types 1 and 2 impaired in expression of muramidase-released protein and extracellular protein induce disease in newborn germfree pigs. Infect Immun,1996,64: 4409-4412
    123. Smith V, Botstein D and Brown P O. Genetic footprinting:a genomic strategy for determining a gene's function given its sequence. Proc Natl Acad Sci U S A,1995, 92:6479-6483
    124. Sriskandan S and Slater J D. Invasive disease and toxic shock due to zoonotic Streptococcus suis:an emerging infection in the East? PLoS Med,2006,3:e187
    125. Staats J J, Feder I, Okwumabua O, et al. Streptococcus suis:past and present. Vet Res Commun,1997,21:381-407
    126. Takamatsu D, Osaki M and Sekizaki T. Thermosensitive suicide vectors for gene replacement in Streptococcus suis. Plasmid,2001,46:140-148
    127. Takezaki T, Inoue M, Kataoka H, et al. Diet and lung cancer risk from a 14-year population-based prospective study in Japan: with special reference to fish consumption. Nutr Cancer,2003,45:160-167
    128. Tamura G S, Hull J R, Oberg M D, et al. High-affinity interaction between fibronectin and the group B streptococcal C5a peptidase is unaffected by a naturally occurring four-amino-acid deletion that eliminates peptidase activity. Infect Immun,2006,74:5739-5746
    129. Tan C, Fu S, Liu M, et al. Cloning, expression and characterization of a cell wall surface protein, 6-phosphogluconate-dehydrogenase, of Streptococcus suis serotype 2. Vet Microbiol,2008,130:363-370
    130. Tan C, Liu M, Jin M, et al. The key virulence-associated genes of Streptococcus suis type 2 are upregulated and differentially expressed in vivo. FEMS Microbiology Letters, In press:
    131. Tang J, Wang C, Feng Y, et al. Streptococcal toxic shock syndrome caused by Streptococcus suis serotype 2. PLoS Med,2006,3:e151
    132. Tarradas C, Borge C, Arenas A, et al. Suilysin production by Streptococcus suis strains isolated from diseased and healthy carrier pigs in Spain. Vet Rec,2001, 148:183-184
    133. Thanawongnuwech R, Brown G B, Halbur P G, et al. Pathogenesis of porcine reproductive and respiratory syndrome virus-induced increase in susceptibility to Streptococcus suis infection. Vet Pathol,2000,37:143-152
    134. Turgeon P L, Higgins R, Gottschalk M, et al. Antimicrobial susceptibility of Streptococcus suis isolates. Br Vet J,1994,150:263-269
    135. Vadeboncoeur N, Segura M, Al-Numani D, et al. Pro-inflammatory cytokine and chemokine release by human brain microvascular endothelial cells stimulated by Streptococcus suis serotype 2. FEMS Immunol Med Microbiol,2003,35:49-58
    136. Valdivia R H and Falkow S. Bacterial genetics by flow cytometry:rapid isolation of Salmonella typhimurium acid-inducible promoters by differential fluorescence induction. Mol Microbiol,1996,22:367-378
    137. Vanier G, Sekizaki T, Dominguez-Punaro M C, et al. Disruption of srtA gene in Streptococcus suis results in decreased interactions with endothelial cells and extracellular matrix proteins. Vet Microbiol,2008,127:417-424
    138. Vecht U, van Leengoed L A and Verheijen E R. Streptococcus suis infections in pigs in the Netherlands (Part I). Vet Q,1985,7:315-321
    139. Vecht U, Wisselink H J, Jellema M L, et al. Identification of two proteins associated with virulence of Streptococcus suis type 2. Infect Immun,1991,59: 3156-3162
    140. Vela A I, Goyache J, Tarradas C, et al. Analysis of genetic diversity of Streptococcus suis clinical isolates from pigs in Spain by pulsed-field gel electrophoresis. J Clin Microbiol,2003,41:2498-2502
    141. Vitalis T Z, Keicho N, Itabashi S, et al. A model of latent adenovirus 5 infection in the guinea pig (Cavia porcellus). Am J Respir Cell Mol Biol,1996,14:225-231
    142. Wang C, Li M, Feng Y, et al. The involvement of sortase A in high virulence of STSS-causing Streptococcus suis serotype 2. Arch Microbiol,2009,191:23-33
    143. Wangkaew S, Chaiwarith R, Tharavichitkul P, et al. Streptococcus suis infection: a series of 41 cases from Chiang Mai University Hospital. J Infect,2006,52: 455-460
    144. Watkins E J, Brooksby P, Schweiger M S, et al. Septicaemia in a pig-farm worker. Lancet,2001,357:38
    145. Wei Z, Li R, Zhang A, et al. Characterization of Streptococcus suis isolates from the diseased pigs in China between 2003 and 2007. Vet Microbiol,2009,137: 196-201
    146. Wertheim H F, Nghia H D, Taylor W, et al. Streptococcus suis:an emerging human pathogen. Clin Infect Dis,2009a,48:617-625
    147. Wertheim H F, Nguyen H N, Taylor W, et al. Streptococcus suis, an important cause of adult bacterial meningitis in northern Vietnam. PLoS One,2009b,4: e5973
    148. Williams A E and Blakemore W F. Pathogenesis of meningitis caused by Streptococcus suis type 2. J Infect Dis,1990,162:474-481
    149. Wilson T L, Jeffers J, Rapp-Gabrielson V J, et al. A novel signature-tagged mutagenesis system for Streptococcus suis serotype 2. Vet Microbiol,2007,122: 135-145
    150. Wisselink H J, Smith H E, Stockhofe-Zurwieden N, et al. Distribution of capsular types and production of muramidase-released protein (MRP) and extracellular factor (EF) of Streptococcus suis strains isolated from diseased pigs in seven European countries. Vet Microbiol,2000,74:237-248
    151. Yoo J Y, Kim H C, Zhu W, et al. Identification of Tannerella forsythia antigens specifically expressed in patients with periodontal disease. FEMS Microbiol Lett, 2007,275:344-352
    152. Yu H, Jing H, Chen Z, et al. Human Streptococcus suis outbreak, Sichuan, China. Emerg Infect Dis,2006,12:914-920
    153. Zhang A, Xie C, Chen H, et al. Identification of immunogenic cell wall-associated proteins of Streptococcus suis serotype 2. Proteomics,2008,8: 3506-3515
    154. Zysk G, Bongaerts R J, ten Thoren E, et al. Detection of 23 immunogenic pneumococcal proteins using convalescent-phase serum. Infect Immun,2000,68: 3740-3743

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700