Affiliation:
1. Laboratory of Immunology and Microbial Pathogenesis, National Institute of Animal Biotechnology (NIAB), Hyderabad, Telangana, India
2. Regional Centre for Biotechnology (RCB), Faridabad, India
Abstract
ABSTRACT
Brucella
species are Gram-negative intracellular bacterial pathogens that cause the worldwide zoonotic disease brucellosis.
Brucella
can infect many mammals, including humans and domestic and wild animals.
Brucella
manipulates various host cellular processes to invade and multiply in professional and non-professional phagocytic cells. However, the host targets and their modulation by
Brucella
to facilitate the infection process remain obscure. Here, we report that the host ubiquitin-specific protease, USP8, negatively regulates the invasion of
Brucella
into macrophages through the plasma membrane receptor, CXCR4. Upon silencing or chemical inhibition of USP8, the membrane localization of the CXCR4 receptor was enriched, which augmented the invasion of
Brucella
into macrophages. Activation of USP8 through chemical inhibition of 14-3-3 protein affected the invasion of
Brucella
into macrophages.
Brucella
suppressed the expression of
Usp8
at its early stage of infection in the infected macrophages. Furthermore, we found that only live
Brucella
could negatively regulate the expression of
Usp8
, suggesting the role of secreted effector protein of
Brucella
in modulating the gene expression. Subsequent studies revealed that the
Brucella
effector protein, TIR-domain containing protein from
Brucella
, TcpB, plays a significant role in downregulating the expression of
Usp8
by targeting the cyclic-AMP response element-binding protein pathway. Treatment of mice with USP8 inhibitor resulted in enhanced survival of
B. melitensis,
whereas mice treated with CXCR4 or 14-3-3 antagonists showed a diminished bacterial load. Our experimental data demonstrate a novel role of
Usp8
in the host defense against microbial intrusion. The present study provides insights into the microbial subversion of host defenses, and this information may ultimately help to develop novel therapeutic interventions for infectious diseases.
Funder
Department of Biotechnology, Ministry of Science and Technology, India
Indian Council of Medical Research
University Grants Commission
Publisher
American Society for Microbiology
Cited by
1 articles.
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