NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE

Abstract. Streptococcus agalactiae can cause variety of diseases of newborns and adults. For successful colonization of different human tissues and organs as well as for suppression of the host immune system S. agalactiae expresses numerous virulence factors. For coordinated expression of the virule...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: A. S. Rozhdestvenskaya, I. Santos-Sanches, A. V. Dmitriev
Formato: article
Lenguaje:RU
Publicado: Sankt-Peterburg : NIIÈM imeni Pastera 2014
Materias:
Acceso en línea:https://doaj.org/article/4d7b2ff5ea1f4641aafa66c3081b929f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:4d7b2ff5ea1f4641aafa66c3081b929f
record_format dspace
spelling oai:doaj.org-article:4d7b2ff5ea1f4641aafa66c3081b929f2021-11-22T07:09:46ZNATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE2220-76192313-739810.15789/2220-7619-2013-1-43-48https://doaj.org/article/4d7b2ff5ea1f4641aafa66c3081b929f2014-07-01T00:00:00Zhttps://www.iimmun.ru/iimm/article/view/122https://doaj.org/toc/2220-7619https://doaj.org/toc/2313-7398Abstract. Streptococcus agalactiae can cause variety of diseases of newborns and adults. For successful colonization of different human tissues and organs as well as for suppression of the host immune system S. agalactiae expresses numerous virulence factors. For coordinated expression of the virulence genes S. agalactiae employs regulatory molecules including regulatory proteins of two-component systems. Results of the present study demonstrated that in S. agalactiae strain A49V the natural mutation in the brgR gene encoding for BgrR regulatory protein, which is component of regulatory system BgrRS, resulted in the repression of Bac protein synthesis, a virulence factor of S. agalactiae. A single nucleotide deletion in the bgrR gene has caused a shift of the reading frame and the changes in the primary, secondary and tertiary structures of the BgrR protein. The loss of functional activity of BgrR protein in A49V strain and repression of Bac protein synthesis have increased virulence of the strain in experimental animal streptococcal infection.A. S. RozhdestvenskayaI. Santos-SanchesA. V. DmitrievSankt-Peterburg : NIIÈM imeni Pasteraarticlestreptococcus agalactiaebgrrs two-component regulatory systemprotein bacvirulenceInfectious and parasitic diseasesRC109-216RUInfekciâ i Immunitet, Vol 3, Iss 1, Pp 43-48 (2014)
institution DOAJ
collection DOAJ
language RU
topic streptococcus agalactiae
bgrrs two-component regulatory system
protein bac
virulence
Infectious and parasitic diseases
RC109-216
spellingShingle streptococcus agalactiae
bgrrs two-component regulatory system
protein bac
virulence
Infectious and parasitic diseases
RC109-216
A. S. Rozhdestvenskaya
I. Santos-Sanches
A. V. Dmitriev
NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
description Abstract. Streptococcus agalactiae can cause variety of diseases of newborns and adults. For successful colonization of different human tissues and organs as well as for suppression of the host immune system S. agalactiae expresses numerous virulence factors. For coordinated expression of the virulence genes S. agalactiae employs regulatory molecules including regulatory proteins of two-component systems. Results of the present study demonstrated that in S. agalactiae strain A49V the natural mutation in the brgR gene encoding for BgrR regulatory protein, which is component of regulatory system BgrRS, resulted in the repression of Bac protein synthesis, a virulence factor of S. agalactiae. A single nucleotide deletion in the bgrR gene has caused a shift of the reading frame and the changes in the primary, secondary and tertiary structures of the BgrR protein. The loss of functional activity of BgrR protein in A49V strain and repression of Bac protein synthesis have increased virulence of the strain in experimental animal streptococcal infection.
format article
author A. S. Rozhdestvenskaya
I. Santos-Sanches
A. V. Dmitriev
author_facet A. S. Rozhdestvenskaya
I. Santos-Sanches
A. V. Dmitriev
author_sort A. S. Rozhdestvenskaya
title NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
title_short NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
title_full NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
title_fullStr NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
title_full_unstemmed NATURAL MUTATION IN THE GENE OF RESPONSE REGULATOR BgrR RESULTING IN REPRESSION OF Bac PROTEIN SYNTHESIS, A PATHOGENICITY FACTOR OF STREPTOCOCCUS AGALACTIAE
title_sort natural mutation in the gene of response regulator bgrr resulting in repression of bac protein synthesis, a pathogenicity factor of streptococcus agalactiae
publisher Sankt-Peterburg : NIIÈM imeni Pastera
publishDate 2014
url https://doaj.org/article/4d7b2ff5ea1f4641aafa66c3081b929f
work_keys_str_mv AT asrozhdestvenskaya naturalmutationinthegeneofresponseregulatorbgrrresultinginrepressionofbacproteinsynthesisapathogenicityfactorofstreptococcusagalactiae
AT isantossanches naturalmutationinthegeneofresponseregulatorbgrrresultinginrepressionofbacproteinsynthesisapathogenicityfactorofstreptococcusagalactiae
AT avdmitriev naturalmutationinthegeneofresponseregulatorbgrrresultinginrepressionofbacproteinsynthesisapathogenicityfactorofstreptococcusagalactiae
_version_ 1718418039223877632