3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis

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3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis. / Hu, Y; van der Geize, R; Besra, Gurdyal; Gurcha, Sudagar; Liu, A; Rohde, M; Singh, M; Coates, A.

In: Molecular Microbiology, Vol. 75, No. 1, 01.01.2010, p. 107-121.

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Hu, Y ; van der Geize, R ; Besra, Gurdyal ; Gurcha, Sudagar ; Liu, A ; Rohde, M ; Singh, M ; Coates, A. / 3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis. In: Molecular Microbiology. 2010 ; Vol. 75, No. 1. pp. 107-121.

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@article{6380956f33e04986ac28dcd8920d97f4,
title = "3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis",
abstract = "Mycobacterium tuberculosis H37Rv contains the kshA (Rv3526) and kshB (Rv3571) genes, encoding 3-ketosteroid 9a-hydroxylase (KSH). Consistent with their predicted roles, the Delta kshA and Delta kshB deletion mutants of M. tuberculosis H37Rv were unable to use cholesterol and 4-androstene-3,17-dione as primary carbon and energy sources. Interestingly, Delta kshA and Delta kshB mutants were also unable to metabolize the steroid substrate 5 alpha-androstane-3,17-dione, whereas wild-type M. tuberculosis H37Rv could. The deletion of either of these genes lead to rapid death of the microorganism in murine infection models and in macrophages, showing that kshA and kshB are essential factors for M. tuberculosis pathogenesis. Penta-acylated trehalose (PAT) biosynthesis was altered in the Delta kshB mutant, but not the Delta kshA mutant. The Delta kshB mutant synthesizes all other types of lipids. The Delta kshB mutant had a thickened outer layer in its cell wall. KshB thus appears to be involved in multiple processes, probably as a reductase of different oxygenases. We conclude that an impaired 3-ketosteroid 9 alpha-hydroxylase activity is the cause of the highly attenuated phenotype of our M. tuberculosis H37Rv mutants.",
author = "Y Hu and {van der Geize}, R and Gurdyal Besra and Sudagar Gurcha and A Liu and M Rohde and M Singh and A Coates",
year = "2010",
month = jan,
day = "1",
doi = "10.1111/j.1365-2958.2009.06957.x",
language = "English",
volume = "75",
pages = "107--121",
journal = "Molecular Microbiology",
issn = "0950-382X",
publisher = "Wiley",
number = "1",

}

RIS

TY - JOUR

T1 - 3-Ketosteroid 9 alpha-hydroxylase is an essential factor in the pathogenesis of Mycobacterium tuberculosis

AU - Hu, Y

AU - van der Geize, R

AU - Besra, Gurdyal

AU - Gurcha, Sudagar

AU - Liu, A

AU - Rohde, M

AU - Singh, M

AU - Coates, A

PY - 2010/1/1

Y1 - 2010/1/1

N2 - Mycobacterium tuberculosis H37Rv contains the kshA (Rv3526) and kshB (Rv3571) genes, encoding 3-ketosteroid 9a-hydroxylase (KSH). Consistent with their predicted roles, the Delta kshA and Delta kshB deletion mutants of M. tuberculosis H37Rv were unable to use cholesterol and 4-androstene-3,17-dione as primary carbon and energy sources. Interestingly, Delta kshA and Delta kshB mutants were also unable to metabolize the steroid substrate 5 alpha-androstane-3,17-dione, whereas wild-type M. tuberculosis H37Rv could. The deletion of either of these genes lead to rapid death of the microorganism in murine infection models and in macrophages, showing that kshA and kshB are essential factors for M. tuberculosis pathogenesis. Penta-acylated trehalose (PAT) biosynthesis was altered in the Delta kshB mutant, but not the Delta kshA mutant. The Delta kshB mutant synthesizes all other types of lipids. The Delta kshB mutant had a thickened outer layer in its cell wall. KshB thus appears to be involved in multiple processes, probably as a reductase of different oxygenases. We conclude that an impaired 3-ketosteroid 9 alpha-hydroxylase activity is the cause of the highly attenuated phenotype of our M. tuberculosis H37Rv mutants.

AB - Mycobacterium tuberculosis H37Rv contains the kshA (Rv3526) and kshB (Rv3571) genes, encoding 3-ketosteroid 9a-hydroxylase (KSH). Consistent with their predicted roles, the Delta kshA and Delta kshB deletion mutants of M. tuberculosis H37Rv were unable to use cholesterol and 4-androstene-3,17-dione as primary carbon and energy sources. Interestingly, Delta kshA and Delta kshB mutants were also unable to metabolize the steroid substrate 5 alpha-androstane-3,17-dione, whereas wild-type M. tuberculosis H37Rv could. The deletion of either of these genes lead to rapid death of the microorganism in murine infection models and in macrophages, showing that kshA and kshB are essential factors for M. tuberculosis pathogenesis. Penta-acylated trehalose (PAT) biosynthesis was altered in the Delta kshB mutant, but not the Delta kshA mutant. The Delta kshB mutant synthesizes all other types of lipids. The Delta kshB mutant had a thickened outer layer in its cell wall. KshB thus appears to be involved in multiple processes, probably as a reductase of different oxygenases. We conclude that an impaired 3-ketosteroid 9 alpha-hydroxylase activity is the cause of the highly attenuated phenotype of our M. tuberculosis H37Rv mutants.

U2 - 10.1111/j.1365-2958.2009.06957.x

DO - 10.1111/j.1365-2958.2009.06957.x

M3 - Article

C2 - 19906176

VL - 75

SP - 107

EP - 121

JO - Molecular Microbiology

JF - Molecular Microbiology

SN - 0950-382X

IS - 1

ER -