Journalartikel

Occurrence of mutations impairing sigma factor B (SigB) function upon inactivation of Listeria monocytogenes genes encoding surface proteins


AutorenlisteQuereda, Juan J.; Graciela Pucciarelli, M.; Botello-Morte, Laura; Calvo, Enrique; Carvalho, Filipe; Bouchier, Christiane; Vieira, Ana; Mariscotti, Javier F.; Chakraborty, Trinad; Cossart, Pascale; Hain, Torsten; Cabanes, Didier; Garcia-del Portillo, Francisco

Jahr der Veröffentlichung2013

Seiten1328-1339

ZeitschriftMicrobiology

Bandnummer159

ISSN1350-0872

eISSN1465-2080

Open Access StatusGreen

DOI Linkhttps://doi.org/10.1099/mic.0.067744-0

VerlagMicrobiology Society


Abstract
Bacteria of the genus Listeria contain the largest family of LPXTG surface proteins covalently anchored to the peptidoglycan. The extent to which these proteins may function or be regulated cooperatively is at present unknown. Because of their unique cellular location, we reasoned that distinct LPXTG proteins could act as elements contributing to cell wall homeostasis or influencing the stability of other surface proteins bound to peptidoglycan. To test this hypothesis, we used proteomics to analyse mutants of the intracellular pathogen Listeria monocytogenes lacking distinct LPXTG proteins implicated in pathogen host interactions, such as InIA, InIF, InIG, InIH, LapB and Vip. Changes in the cell wall proteome were found in inIG and vip mutants, which exhibited reduced levels of the LPXTG proteins InIH, Lmo0610, Lmo0880 and Lmo2085, all regulated by the stress-related sigma factor SigB. The ultimate basis of this alteration was uncovered by genome sequencing, which revealed that these inIG and vip mutants carried loss-of-function mutations in the rsbS, rsbU and rsbV genes encoding regulatory proteins that control SigB activity. Attempts to recapitulate this negative selection of SigB in a large series of new inIG or vip mutants constructed for this purpose were, however, unsuccessful. These results indicate that inadvertent secondary mutations affecting SigB functionality can randomly arise in L. monocytogenes when using common genetic procedures or during subculturing. Testing of SigB activity could be therefore valuable when manipulating genetically L. monocytogenes prior to any subsequent phenotypic analysis. This test may be even more justified when generating deletions affecting cell envelope components.



Zitierstile

Harvard-ZitierstilQuereda, J., Graciela Pucciarelli, M., Botello-Morte, L., Calvo, E., Carvalho, F., Bouchier, C., et al. (2013) Occurrence of mutations impairing sigma factor B (SigB) function upon inactivation of Listeria monocytogenes genes encoding surface proteins, Microbiology, 159, pp. 1328-1339. https://doi.org/10.1099/mic.0.067744-0

APA-ZitierstilQuereda, J., Graciela Pucciarelli, M., Botello-Morte, L., Calvo, E., Carvalho, F., Bouchier, C., Vieira, A., Mariscotti, J., Chakraborty, T., Cossart, P., Hain, T., Cabanes, D., & Garcia-del Portillo, F. (2013). Occurrence of mutations impairing sigma factor B (SigB) function upon inactivation of Listeria monocytogenes genes encoding surface proteins. Microbiology. 159, 1328-1339. https://doi.org/10.1099/mic.0.067744-0



Schlagwörter


COORDINATE REGULATIONEGDEUKARYOTIC CELLSPRFAvirulence factor


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