| Literature DB >> 32648938 |
Lu Dai1, Bock-Gie Jung2, Jungang Chen1, Buka Samten2, James Craig Forrest3, Steven R Post1, Zhiqiang Qin1.
Abstract
Kaposi's sarcoma-associated herpesvirus (KSHV) causes several human cancers, including Kaposi's sarcoma (KS) and primary effusion lymphoma, which are mostly seen in immunocompromised patients, such as human immunodefeciency virus (HIV)+ individuals. Tuberculosis (TB), caused by the bacterial pathogen Mycobacterium tuberculosis (Mtb), remains one of the deadliest infectious diseases in the world. The risk of developing TB is dramatically higher in people living with HIV than among those without HIV infection. Case reports link cutaneous or pulmonary KS in HIV+ patients with mycobacterial co-infections, however, impacts of Mtb infection or its products on KSHV-infected cells are not known. We report here that ESAT-6, a secreted Mtb virulence factor, induces viral reactivation from KSHV-infected cells. KSHV-infected pulmonary endothelial cells were resistant to ESAT-6 induced inhibition of cell growth. Our data demonstrate that Mtb virulence factors influence the biology of KSHV-infected cells, highlighting the need to study the interactions between these two pathogens commonly found in people living with HIV.Entities:
Keywords: ESAT-6; HIV; KSHV; Kaposi's sarcoma; mycobacterium tuberculosis
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Year: 2020 PMID: 32648938 PMCID: PMC7796979 DOI: 10.1002/jmv.26291
Source DB: PubMed Journal: J Med Virol ISSN: 0146-6615 Impact factor: 20.693