RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI

Аbstract. Gene fragments encoding N-terminal and central parts of group B streptococci (GBS) C5a peptidase were cloned in E. coli M15. The appropriate recombinant SCPB1a and SCPB3a polypeptides with molecular masses of, resp., 12.0±0.5 kDa and 11.0±0.5 kDa, were subject to expression and affinity pu...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: N. V. Duplik, I. V. Koroleva, K. B. Grabovskaya, A. N. Suvorov
Formato: article
Lenguaje:RU
Publicado: SPb RAACI 2014
Materias:
Acceso en línea:https://doaj.org/article/ce7d1775d31a4a5b87e916777d8ff4d1
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ce7d1775d31a4a5b87e916777d8ff4d1
record_format dspace
spelling oai:doaj.org-article:ce7d1775d31a4a5b87e916777d8ff4d12021-11-18T08:03:39ZRECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI1563-06252313-741X10.15789/1563-0625-2011-1-41-48https://doaj.org/article/ce7d1775d31a4a5b87e916777d8ff4d12014-07-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/281https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XАbstract. Gene fragments encoding N-terminal and central parts of group B streptococci (GBS) C5a peptidase were cloned in E. coli M15. The appropriate recombinant SCPB1a and SCPB3a polypeptides with molecular masses of, resp., 12.0±0.5 kDa and 11.0±0.5 kDa, were subject to expression and affinity purification. Both polypeptides  induced  specific  antibodies  production  upon  subcutaneous  immunization  of  mice.  A more pronounced immune response was detected with SCPB3a injection. Antimicrobial properties of anti-SCPB1a and anti-SCPB3a antibodies have been investigated in vitro (by opsonophagocytosis test) and in vivo (a model of generalized GBS infection in mice). N-terminal and central segments of C5a peptidase molecule have been shown to contain epitopes inducing humoral immune response with production of class G antibodies that efficiently opsonize GBS, whereas recombinant SCPB1a and SCPB3a polypeptides can be recommended for  future  implications  in  development  of  a  polycomponent  vaccine  against  GBS.  (Med.  Immunol.,  2011, vol. 13, N 1, pp 41-48)N. V. DuplikI. V. KorolevaK. B. GrabovskayaA. N. SuvorovSPb RAACIarticlegroup b streptococcic5a peptidaserecombinant polypeptidesimmunogenicityopsonophagocytosisImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 13, Iss 1, Pp 41-48 (2014)
institution DOAJ
collection DOAJ
language RU
topic group b streptococci
c5a peptidase
recombinant polypeptides
immunogenicity
opsonophagocytosis
Immunologic diseases. Allergy
RC581-607
spellingShingle group b streptococci
c5a peptidase
recombinant polypeptides
immunogenicity
opsonophagocytosis
Immunologic diseases. Allergy
RC581-607
N. V. Duplik
I. V. Koroleva
K. B. Grabovskaya
A. N. Suvorov
RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
description Аbstract. Gene fragments encoding N-terminal and central parts of group B streptococci (GBS) C5a peptidase were cloned in E. coli M15. The appropriate recombinant SCPB1a and SCPB3a polypeptides with molecular masses of, resp., 12.0±0.5 kDa and 11.0±0.5 kDa, were subject to expression and affinity purification. Both polypeptides  induced  specific  antibodies  production  upon  subcutaneous  immunization  of  mice.  A more pronounced immune response was detected with SCPB3a injection. Antimicrobial properties of anti-SCPB1a and anti-SCPB3a antibodies have been investigated in vitro (by opsonophagocytosis test) and in vivo (a model of generalized GBS infection in mice). N-terminal and central segments of C5a peptidase molecule have been shown to contain epitopes inducing humoral immune response with production of class G antibodies that efficiently opsonize GBS, whereas recombinant SCPB1a and SCPB3a polypeptides can be recommended for  future  implications  in  development  of  a  polycomponent  vaccine  against  GBS.  (Med.  Immunol.,  2011, vol. 13, N 1, pp 41-48)
format article
author N. V. Duplik
I. V. Koroleva
K. B. Grabovskaya
A. N. Suvorov
author_facet N. V. Duplik
I. V. Koroleva
K. B. Grabovskaya
A. N. Suvorov
author_sort N. V. Duplik
title RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
title_short RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
title_full RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
title_fullStr RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
title_full_unstemmed RECOMBINANT POLYPEPTIDES BASED ON C5A PEPTIDASE AS POTENTIAL VACCINE COMPONENTS AGAINST GROUP B STREPTOCOCCI
title_sort recombinant polypeptides based on c5a peptidase as potential vaccine components against group b streptococci
publisher SPb RAACI
publishDate 2014
url https://doaj.org/article/ce7d1775d31a4a5b87e916777d8ff4d1
work_keys_str_mv AT nvduplik recombinantpolypeptidesbasedonc5apeptidaseaspotentialvaccinecomponentsagainstgroupbstreptococci
AT ivkoroleva recombinantpolypeptidesbasedonc5apeptidaseaspotentialvaccinecomponentsagainstgroupbstreptococci
AT kbgrabovskaya recombinantpolypeptidesbasedonc5apeptidaseaspotentialvaccinecomponentsagainstgroupbstreptococci
AT ansuvorov recombinantpolypeptidesbasedonc5apeptidaseaspotentialvaccinecomponentsagainstgroupbstreptococci
_version_ 1718422569457025024