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Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed

BACKGROUND: Several mutations have been described as responsible for rifampicin resistance in Neisseria meningitidis. However, the intriguing question on why these strains are so rare remains open. The aim of this study was to investigate the protein content and to identify differential expression i...

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Autores principales: Neri, Arianna, Mignogna, Giuseppina, Fazio, Cecilia, Giorgi, Alessandra, Schininà, Maria Eugenia, Stefanelli, Paola
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955632/
https://www.ncbi.nlm.nih.gov/pubmed/20868485
http://dx.doi.org/10.1186/1471-2180-10-246
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author Neri, Arianna
Mignogna, Giuseppina
Fazio, Cecilia
Giorgi, Alessandra
Schininà, Maria Eugenia
Stefanelli, Paola
author_facet Neri, Arianna
Mignogna, Giuseppina
Fazio, Cecilia
Giorgi, Alessandra
Schininà, Maria Eugenia
Stefanelli, Paola
author_sort Neri, Arianna
collection PubMed
description BACKGROUND: Several mutations have been described as responsible for rifampicin resistance in Neisseria meningitidis. However, the intriguing question on why these strains are so rare remains open. The aim of this study was to investigate the protein content and to identify differential expression in specific proteins in two rifampicin resistant and one susceptible meningococci using two-dimensional electrophoresis (2-DE) combined with mass spectrometry. RESULTS: In our experimental conditions, able to resolve soluble proteins with an isoelectric point between 4 and 7, twenty-three proteins have been found differentially expressed in the two resistant strains compared to the susceptible. Some of them, involved in the main metabolic pathways, showed an increased expression, mainly in the catabolism of pyruvate and in the tricarboxylic acid cycle. A decreased expression of proteins belonging to gene regulation and to those involved in the folding of polypeptides has also been observed. 2-DE analysis showed the presence of four proteins displaying a shift in their isoelectric point in both resistant strains, confirmed by the presence of amino acid changes in the sequence analysis, absent in the susceptible. CONCLUSIONS: The analysis of differentially expressed proteins suggests that an intricate series of events occurs in N. meningitidis rifampicin resistant strains and the results here reported may be considered a starting point in understanding their decreased invasion capacity. In fact, they support the hypothesis that the presence of more than one protein differentially expressed, having a role in the metabolism of the meningococcus, influences its ability to infect and to spread in the population. Different reports have described and discussed how a drug resistant pathogen shows a high biological cost for survival and that may also explain why, for some pathogens, the rate of resistant organisms is relatively low considering the widespread use of a particular drug. This seems the case of rifampicin resistant meningococci.
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spelling pubmed-29556322010-10-16 Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed Neri, Arianna Mignogna, Giuseppina Fazio, Cecilia Giorgi, Alessandra Schininà, Maria Eugenia Stefanelli, Paola BMC Microbiol Research Article BACKGROUND: Several mutations have been described as responsible for rifampicin resistance in Neisseria meningitidis. However, the intriguing question on why these strains are so rare remains open. The aim of this study was to investigate the protein content and to identify differential expression in specific proteins in two rifampicin resistant and one susceptible meningococci using two-dimensional electrophoresis (2-DE) combined with mass spectrometry. RESULTS: In our experimental conditions, able to resolve soluble proteins with an isoelectric point between 4 and 7, twenty-three proteins have been found differentially expressed in the two resistant strains compared to the susceptible. Some of them, involved in the main metabolic pathways, showed an increased expression, mainly in the catabolism of pyruvate and in the tricarboxylic acid cycle. A decreased expression of proteins belonging to gene regulation and to those involved in the folding of polypeptides has also been observed. 2-DE analysis showed the presence of four proteins displaying a shift in their isoelectric point in both resistant strains, confirmed by the presence of amino acid changes in the sequence analysis, absent in the susceptible. CONCLUSIONS: The analysis of differentially expressed proteins suggests that an intricate series of events occurs in N. meningitidis rifampicin resistant strains and the results here reported may be considered a starting point in understanding their decreased invasion capacity. In fact, they support the hypothesis that the presence of more than one protein differentially expressed, having a role in the metabolism of the meningococcus, influences its ability to infect and to spread in the population. Different reports have described and discussed how a drug resistant pathogen shows a high biological cost for survival and that may also explain why, for some pathogens, the rate of resistant organisms is relatively low considering the widespread use of a particular drug. This seems the case of rifampicin resistant meningococci. BioMed Central 2010-09-24 /pmc/articles/PMC2955632/ /pubmed/20868485 http://dx.doi.org/10.1186/1471-2180-10-246 Text en Copyright ©2010 Neri et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Neri, Arianna
Mignogna, Giuseppina
Fazio, Cecilia
Giorgi, Alessandra
Schininà, Maria Eugenia
Stefanelli, Paola
Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title_full Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title_fullStr Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title_full_unstemmed Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title_short Neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
title_sort neisseria meningitidis rifampicin resistant strains: analysis of protein differentially expressed
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955632/
https://www.ncbi.nlm.nih.gov/pubmed/20868485
http://dx.doi.org/10.1186/1471-2180-10-246
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