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Elevated levels of VCA0117 ( VasH ) in response to external signals activate the type VI secretion system of Vibrio cholerae O1 El Tor A1552

Henrik Seibt; Kyaw Min Aung; Takahiko Ishikawa; Annika Sjöström; Martin Gullberg; Gemma Catherine Atkinson; Sun Nyunt Wai; Victoria Shingler
Environmental Microbiology · Vol. 22, Issue 10 · pp. 4409-4423 · 2020

Abstract

Summary The type VI nanomachine is critical for Vibrio cholerae to establish infections and to thrive in niches co‐occupied by competing bacteria. The genes for the type VI structural proteins are encoded in one large and two small auxiliary gene clusters. VCA0117 (VasH) – a σ 54 ‐transcriptional activator – is strictly required for functionality of the type VI secretion system since it controls production of the structural protein Hcp. While some strains constitutively produce a functional system, others do not and require specific growth conditions of low temperature and high osmolarity for expression of the type VI machinery. Here, we trace integration of these regulatory signals to the promoter activity of the large gene cluster in which many components of the machinery and VCA0117 itself are encoded. Using in vivo and in vitro assays and variants of VCA0117, we show that activation of the σ 54 ‐promoters of the auxiliary gene clusters by elevated VCA0117 levels are all that is required to overcome the need for specialized growth conditions. We propose a model in which signal integration via the large operon promoter directs otherwise restrictive levels of VCA0117 that ultimately dictates a sufficient supply of Hcp for completion of a functional type VI secretion system.

Bibliographic Information

JournalEnvironmental Microbiology
PublisherWiley
Publication Date2020-10-01
Publication Year2020
Volume22
Issue10
Pages4409-4423
Document TypeJournal Article
Print ISSN1462-2912
eISSN1462-2920
DOI10.1111/1462-2920.15141
SubjectMicrobial Ecology

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NARA Access Coverage1999-01-01~Current
Journal Homepagehttps://onlinelibrary.wiley.com/loi/14622920
Publisher PageOpen Publisher Page
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