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NafA negatively con...
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Kuwae, AsaomiStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
(author)
NafA negatively controls Neisseria meningitidis piliation
- Article/chapterEnglish2011
Publisher, publication year, extent ...
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2011-07-01
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Public Library of Science (PLoS),2011
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:su-63671
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https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-63671URI
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https://doi.org/10.1371/journal.pone.0021749DOI
Supplementary language notes
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Language:English
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Summary in:English
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
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Bacterial auto-aggregation is a critical step during adhesion of N. meningitidis to host cells. The precise mechanisms and functions of bacterial auto-aggregation still remain to be fully elucidated. In this work, we characterize the role of a meningococcal hypothetical protein, NMB0995/NMC0982, and show that this protein, here denoted NafA, acts as an anti-aggregation factor. NafA was confirmed to be surface exposed and was found to be induced at a late stage of bacterial adherence to epithelial cells. A NafA deficient mutant was hyperpiliated and formed bundles of pili. Further, the mutant displayed increased adherence to epithelial cells when compared to the wild-type strain. In the absence of host cells, the NafA deficient mutant was more aggregative than the wild-type strain. The in vivo role of NafA in sepsis was studied in a murine model of meningococcal disease. Challenge with the NafA deficient mutant resulted in lower bacteremia levels and mortality when compared to the wild-type strain. The present study reveals that meningococcal NafA is an anti-aggregation factor with strong impact on the disease outcome. These data also suggest that appropriate bacterial auto-aggregation is controlled by both aggregation and anti-aggregation factors during Neisseria infection in vivo.
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Sjölinder, HongStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi(Swepub:su)misj
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Eriksson, JensStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi(Swepub:su)jerik
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Eriksson, SaraStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi(Swepub:su)saer5592
(author)
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Chen, YaoStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi
(author)
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Jonsson, Ann-BethStockholms universitet,Institutionen för genetik, mikrobiologi och toxikologi(Swepub:su)anjons
(author)
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Stockholms universitetInstitutionen för genetik, mikrobiologi och toxikologi
(creator_code:org_t)
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In:PLOS ONE: Public Library of Science (PLoS)6:7, s. e21749-1932-6203
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