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A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in hum...

A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in hum...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3069178367

A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in human macrophages and in a mouse model of infection

About this item

Full title

A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in human macrophages and in a mouse model of infection

Publisher

United States: Public Library of Science

Journal title

PLoS biology, 2024-04, Vol.22 (4), p.e3002259-e3002259

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Antituberculosis drugs, mostly developed over 60 years ago, combined with a poorly effective vaccine, have failed to eradicate tuberculosis. More worryingly, multiresistant strains of
Mycobacterium tuberculosis
(MTB) are constantly emerging. Innovative strategies are thus urgently needed to improve tuberculosis treatment. Recently, host-direc...

Alternative Titles

Full title

A host-directed oxadiazole compound potentiates antituberculosis treatment via zinc poisoning in human macrophages and in a mouse model of infection

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_3069178367

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_3069178367

Other Identifiers

ISSN

1545-7885,1544-9173

E-ISSN

1545-7885

DOI

10.1371/journal.pbio.3002259

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