An assay to compare the infectivity of Mycobacterium tuberculosis isolates based on aerosol infection of guinea pigs and assessment of bacteriology

被引:20
作者
Williams, A [1 ]
James, BW [1 ]
Bacon, J [1 ]
Hatch, KA [1 ]
Hatch, GJ [1 ]
Hall, GA [1 ]
Marsh, PD [1 ]
机构
[1] Hlth Protect Agcy Porton Down, Salisbury SP4 0JG, Wilts, England
关键词
aerosol; guinea pig; infectivity; iron; oxygen;
D O I
10.1016/j.tube.2004.11.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim of this study was to establish an assay to compare Mycobacterium tuberculosis strains, and cells grown under different growth conditions, in terms of their ability to cause a lung infection and disseminate to the spleen. M. tuberculosis strains H37Rv, Erdman, South Indian (TMC120, SI) and H37Rv cells grown aerobically or under tow oxygen/iron limitation in a chemostat were assayed for infectivity. Groups of 8 animals were challenged with 3 different doses of each strain. Lung and spleen bacteriology was assessed at 16 days post-infection for all strains. Bacteriology and lung pathology at day 56 was studied for H37Rv, Erdman and SI. Strains H37Rv and Erdman had a statistically significantly higher pathogenic potential than SI and this was confirmed by analysis of lung pathology performed at 8 weeks post-infection, although the Erdman strain caused more extensive caseation without calcification and little encapsulation. The model could discriminate between cells grown under different growth conditions; low-oxygen/iron-limited cells had a significantly higher infectivity than those grown aerobically. This study presents a quick and reliable method for comparing with statistical confidence, the pathogenic potential of M. tuberculosis strains and the impact of in vitro growth conditions on the infectivity of M. tuberculosis in vivo. © 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:177 / 184
页数:8
相关论文
共 25 条
[1]   TB vaccines: progress and problems [J].
Andersen, P .
TRENDS IN IMMUNOLOGY, 2001, 22 (03) :160-168
[2]   The influence of reduced oxygen availability on pathogenicity and gene expression in Mycobacterium tuberculosis [J].
Bacon, J ;
James, BW ;
Wernisch, L ;
Williams, A ;
Morley, KA ;
Hatch, GJ ;
Mangan, JA ;
Hinds, J ;
Stoker, NG ;
Butcher, PD ;
Marsh, PD .
TUBERCULOSIS, 2004, 84 (3-4) :205-217
[3]   VIRULENCE OF MYCOBACTERIUM-TUBERCULOSIS FOR GUINEA-PIGS - A QUANTITATIVE MODIFICATION OF THE ASSAY DEVELOPED BY MITCHISON [J].
BALASUBRAMANIAN, V ;
GUOZHI, W ;
WIEGESHAUS, E ;
SMITH, D .
TUBERCLE AND LUNG DISEASE, 1992, 73 (05) :268-272
[4]  
BALASUBRAMANIAN V, 1994, IMMUNOBIOLOGY, V191, P4
[5]  
BHATIA AL, 1961, B WORLD HEALTH ORGAN, V25, P313
[6]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[8]   In vitro gene expression dissected:: chemostat surgery for Mycobacterium tuberculosis [J].
James, BW ;
Bacon, J ;
Hampshire, T ;
Morley, K ;
Marsh, PD .
COMPARATIVE AND FUNCTIONAL GENOMICS, 2002, 3 (04) :345-347
[9]   The physiology and pathogenicity of Mycobacterium tuberculosis grown under controlled conditions in a defined medium [J].
James, BW ;
Williams, A ;
Marsh, PD .
JOURNAL OF APPLIED MICROBIOLOGY, 2000, 88 (04) :669-677
[10]   Survival of mycobacterial species in aerosols generated from artificial saliva [J].
Lever, MS ;
Williams, A ;
Bennett, AM .
LETTERS IN APPLIED MICROBIOLOGY, 2000, 31 (03) :238-241