The three extra-cellular zinc metalloproteinases of Streptococcus pneumoniae have a different impact on virulence in mice -: art. no. 14

被引:53
作者
Chiavolini, D
Memmi, G
Maggi, T
Iannelli, F
Pozzi, G
Oggioni, MR
机构
[1] Dipartimento di Biologia Molecolare, Lab. di Microbiol. Molec./Biotecnol., Università di Siena, Siena
关键词
D O I
10.1186/1471-2180-3-14
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Streptococcus pneumoniae possesses large zinc metalloproteinases on its surface. To analyse the importance in virulence of three of these metalloproteinases, intranasal challenge of MFI outbred mice was carried out using a range of infecting doses of wild type and knock-out pneumococcal mutant strains, in order to compare mice survival. Results: Observation of survival percentages over time and detection of LD(50)s of knock out mutants in the proteinase genes in comparison to the type 4 TIGR4 wild type strain revealed two major aspects: i) Iga and ZmpB, present in all strains of S. pneumoniae, strongly contribute to virulence in mice; (ii) ZmpC, only present in about 25% of pneumococcal strains, has a lower influence on virulence in mice. Conclusions: These data suggest Iga, ZmpB and ZmpC as candidate surface proteins responsible for pneumococcal infection and potentially involved in distinct stages of pneumococcal disease.
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页码:1 / 9
页数:9
相关论文
共 38 条
[11]   Large-scale identificationof serotype 4 Streptococcus pneumoniae virulence factors [J].
Hava, D ;
Camilli, A .
MOLECULAR MICROBIOLOGY, 2002, 45 (05) :1389-1405
[12]   Genome of the bacterium Streptococcus pneumoniae strain R6 [J].
Hoskins, J ;
Alborn, WE ;
Arnold, J ;
Blaszczak, LC ;
Burgett, S ;
DeHoff, BS ;
Estrem, ST ;
Fritz, L ;
Fu, DJ ;
Fuller, W ;
Geringer, C ;
Gilmour, R ;
Glass, JS ;
Khoja, H ;
Kraft, AR ;
Lagace, RE ;
LeBlanc, DJ ;
Lee, LN ;
Lefkowitz, EJ ;
Lu, J ;
Matsushima, P ;
McAhren, SM ;
McHenney, M ;
McLeaster, K ;
Mundy, CW ;
Nicas, TI ;
Norris, FH ;
O'Gara, M ;
Peery, RB ;
Robertson, GT ;
Rockey, P ;
Sun, PM ;
Winkler, ME ;
Yang, Y ;
Young-Bellido, M ;
Zhao, GS ;
Zook, CA ;
Baltz, RH ;
Jaskunas, SR ;
Rosteck, PR ;
Skatrud, PL ;
Glass, JI .
JOURNAL OF BACTERIOLOGY, 2001, 183 (19) :5709-5717
[13]   Host cellular immune response to pneumococcal lung infection in mice [J].
Kadioglu, A ;
Gingles, NA ;
Grattan, K ;
Kerr, A ;
Mitchell, TJ ;
Andrew, PW .
INFECTION AND IMMUNITY, 2000, 68 (02) :492-501
[14]   Use of green fluorescent protein in visualisation of pneumococcal invasion of broncho-epithelial cells in vivo [J].
Kadioglu, A ;
Sharpe, JA ;
Lazou, I ;
Svanborg, C ;
Ockleford, C ;
Mitchell, TJ ;
Andrew, PW .
FEMS MICROBIOLOGY LETTERS, 2001, 194 (01) :105-110
[15]   Cellular function of elastase in Pseudomonas aeruginosa:: role in the cleavage of nucleoside diphosphate kinase and in alginate synthesis [J].
Kamath, S ;
Kapatral, V ;
Chakrabarty, AM .
MOLECULAR MICROBIOLOGY, 1998, 30 (05) :933-941
[16]   Variation in extracellular protease production among clinical isolates of Staphylococcus aureus due to different levels of expression of the protease repressor sarA [J].
Karlsson, A ;
Arvidson, S .
INFECTION AND IMMUNITY, 2002, 70 (08) :4239-4246
[17]   Biological significance of IgA1 proteases in bacterial colonization and pathogenesis: Critical evaluation of experimental evidence [J].
Kilian, M ;
Reinholdt, J ;
Lomholt, H ;
Poulsen, K ;
Frandsen, EVG .
APMIS, 1996, 104 (05) :321-338
[18]  
KORNFELD SJ, 1981, REV INFECT DIS, V3, P521
[19]   A functional genomic analysis of type 3 Streptococcus pneumoniae virulence [J].
Lau, GW ;
Haataja, S ;
Lonetto, M ;
Kensit, SE ;
Marra, A ;
Bryant, AP ;
McDevitt, D ;
Morrison, DA ;
Holden, DW .
MOLECULAR MICROBIOLOGY, 2001, 40 (03) :555-571
[20]   Molecular analysis of virulence factors of Streptococcus pneumoniae [J].
Mitchell, TJ ;
Alexander, JE ;
Morgan, PJ ;
Andrew, PW .
JOURNAL OF APPLIED MICROBIOLOGY, 1997, 83 :S62-S71