{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T16:53:13Z","timestamp":1787503993218,"version":"build-2736575974"},"reference-count":36,"publisher":"Microbiology Society","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2005,5,1]]},"abstract":"<jats:p>\n                    <jats:italic>Enterococcus faecalis divIVA<\/jats:italic>\n                    (\n                    <jats:italic>divIVA<\/jats:italic>\n                    <jats:sub>Ef<\/jats:sub>\n                    ) is an essential gene implicated in cell division and chromosome segregation. This gene was disrupted by insertional inactivation creating\n                    <jats:italic>E. faecalis<\/jats:italic>\n                    JHSR1, which was viable only when a wild-type copy of\n                    <jats:italic>divIVA<\/jats:italic>\n                    <jats:sub>Ef<\/jats:sub>\n                    was expressed\n                    <jats:italic>in trans<\/jats:italic>\n                    , confirming the essentiality of the gene. The absence of DivIVA\n                    <jats:sub>Ef<\/jats:sub>\n                    in\n                    <jats:italic>E. faecalis<\/jats:italic>\n                    JHSR1 inhibited proper cell division, which resulted in abnormal cell clusters possessing enlarged cells of altered shape instead of the characteristic diplococcal morphology of enterococci. The lower viability of the\n                    <jats:italic>divIVA<\/jats:italic>\n                    <jats:sub>Ef<\/jats:sub>\n                    mutant is caused by improper nucleoid segregation and impaired septation within the numerous cells generated in each cluster. Overexpression of DivIVA\n                    <jats:sub>Ef<\/jats:sub>\n                    in\n                    <jats:italic>Escherichia coli<\/jats:italic>\n                    KJB24 resulted in enlarged cells with disrupted cell division, suggesting that this round\n                    <jats:italic>E. coli<\/jats:italic>\n                    mutant strain could be used as an indicator for functionality of DivIVA\n                    <jats:sub>Ef<\/jats:sub>\n                    . A\n                    <jats:italic>Bacillus subtilis divIVA<\/jats:italic>\n                    mutant was not complemented by DivIVA\n                    <jats:sub>Ef<\/jats:sub>\n                    , indicating that this protein does not recognize DivIVA-specific target sites in\n                    <jats:italic>B. subtilis<\/jats:italic>\n                    , or that it does not interact with other proteins of the cell division machinery of this micro-organism. DivIVA\n                    <jats:sub>Ef<\/jats:sub>\n                    also failed to complement a\n                    <jats:italic>Streptococcus pneumoniae divIVA<\/jats:italic>\n                    mutant, supporting the phylogenetic distance between\n                    <jats:italic>Enterococcus<\/jats:italic>\n                    and\n                    <jats:italic>Streptococcus<\/jats:italic>\n                    . Our results indicate that DivIVA is a species-specific multifunctional protein implicated in cell division and chromosome segregation in\n                    <jats:italic>E. faecalis<\/jats:italic>\n                    .\n                  <\/jats:p>","DOI":"10.1099\/mic.0.27718-0","type":"journal-article","created":{"date-parts":[[2005,5,3]],"date-time":"2005-05-03T17:28:21Z","timestamp":1115141301000},"page":"1381-1393","source":"Crossref","is-referenced-by-count":56,"title":["Enterococcus faecalis divIVA: an essential gene involved in cell division, cell growth and chromosome segregation"],"prefix":"10.1099","volume":"151","author":[{"given":"Sandra","family":"Ramirez-Arcos","sequence":"first","affiliation":[{"name":"Centre for Research in Biopharmaceuticals and Biotechnology, University of Ottawa, Ottawa, ON, Canada K1H 8M5"},{"name":"Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON, Canada K1H 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