Literature DB >> 16182591

Neutral-red reaction is related to virulence and cell wall methyl-branched lipids in Mycobacterium tuberculosis.

P-J Cardona1, C Y Soto, C Martín, B Giquel, G Agustí, Núria Andreu, E Guirado, T Sirakova, P Kolattukudy, E Julián, M Luquin.   

Abstract

Searching for virulence marking tests for Mycobacterium tuberculosis, Dubos and Middlebrook reported in 1948 that in an alkaline aqueous solution of neutral-red, the cells of the virulent H37Rv M. tuberculosis strain fixed the dye and became red in color, whereas the cells of the avirulent H37Ra M. tuberculosis strain remained unstained. In the 1950 and 1960s, fresh isolates of M. tuberculosis were tested for this neutral-red cytochemical reaction and it was reported that they were neutral-red positive, whereas other mycobacteria of diverse environmental origins that were non-pathogenic for guinea pigs were neutral-red negative. However, neutral-red has not really been proven to be a virulence marker. To test if virulence is in fact correlated to neutral-red, we studied a clinical isolate of M. tuberculosis that was originally neutral-red positive but, after more than 1 year passing through culture mediums, turned neutral-red negative. We found that, in comparison to the original neutral-red positive strain, this neutral-red negative variant was attenuated in two murine models of experimental tuberculosis. Lipid analysis showed that this neutral-red negative natural mutant lost the capacity to synthesize pthiocerol dimycocerosates, a cell wall methyl-branched lipid that has been related to virulence in M. tuberculosis. We also studied the neutral-red of different gene-targeted M. tuberculosis mutants unable to produce pthiocerol dimycocerosates or other cell wall methyl-branched lipids such as sulfolipids, and polyacyltrehaloses. We found a negative neutral-red reaction in mutants that were deficient in more than one type of methyl-branched lipids. We conclude that neutral-red is indeed a marker of virulence and it indicates important perturbations in the external surface of M. tuberculosis cells.

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Year:  2005        PMID: 16182591     DOI: 10.1016/j.micinf.2005.06.011

Source DB:  PubMed          Journal:  Microbes Infect        ISSN: 1286-4579            Impact factor:   2.700


  15 in total

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Journal:  J Biol Chem       Date:  2010-09-02       Impact factor: 5.157

2.  The value of comparative genomics in understanding mycobacterial virulence: Mycobacterium tuberculosis H37Ra genome sequencing - a worthwhile endeavour.

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Journal:  J Biosci       Date:  2007-03       Impact factor: 1.826

3.  DevR-mediated adaptive response in Mycobacterium tuberculosis H37Ra: links to asparagine metabolism.

Authors:  Vandana Malhotra; Jaya Sivaswami Tyagi; Josephine E Clark-Curtiss
Journal:  Tuberculosis (Edinb)       Date:  2009-02-13       Impact factor: 3.131

4.  Rapid and spontaneous loss of phthiocerol dimycocerosate (PDIM) from Mycobacterium tuberculosis grown in vitro: implications for virulence studies.

Authors:  Pilar Domenech; Michael B Reed
Journal:  Microbiology (Reading)       Date:  2009-08-06       Impact factor: 2.777

5.  Genetics of Capsular Polysaccharides and Cell Envelope (Glyco)lipids.

Authors:  Mamadou Daffé; Dean C Crick; Mary Jackson
Journal:  Microbiol Spectr       Date:  2014

6.  The impact of mouse passaging of Mycobacterium tuberculosis strains prior to virulence testing in the mouse and guinea pig aerosol models.

Authors:  Paul J Converse; Kathleen D Eisenach; Sue A Theus; Eric L Nuermberger; Sandeep Tyagi; Lan H Ly; Deborah E Geiman; Haidan Guo; Scott T Nolan; Nicole C Akar; Lee G Klinkenberg; Radhika Gupta; Shichun Lun; Petros C Karakousis; Gyanu Lamichhane; David N McMurray; Jacques H Grosset; William R Bishai
Journal:  PLoS One       Date:  2010-04-21       Impact factor: 3.240

7.  A point mutation in the two-component regulator PhoP-PhoR accounts for the absence of polyketide-derived acyltrehaloses but not that of phthiocerol dimycocerosates in Mycobacterium tuberculosis H37Ra.

Authors:  Marie-Laure Chesne-Seck; Nathalie Barilone; Frédéric Boudou; Jesús Gonzalo Asensio; Pappachan E Kolattukudy; Carlos Martín; Stewart T Cole; Brigitte Gicquel; Deshmukh N Gopaul; Mary Jackson
Journal:  J Bacteriol       Date:  2007-12-07       Impact factor: 3.490

Review 8.  The mycobacterial cell envelope-lipids.

Authors:  Mary Jackson
Journal:  Cold Spring Harb Perspect Med       Date:  2014-08-07       Impact factor: 6.915

9.  The Mycobacterium tuberculosis phoPR operon is positively autoregulated in the virulent strain H37Rv.

Authors:  Jesús Gonzalo-Asensio; Carlos Y Soto; Ainhoa Arbués; Javier Sancho; María del Carmen Menéndez; María J García; Brigitte Gicquel; Carlos Martín
Journal:  J Bacteriol       Date:  2008-08-29       Impact factor: 3.490

10.  Transcription of genes involved in sulfolipid and polyacyltrehalose biosynthesis of Mycobacterium tuberculosis in experimental latent tuberculosis infection.

Authors:  Jimmy E Rodríguez; Ana S Ramírez; Laura P Salas; Cecilia Helguera-Repetto; Jorge Gonzalez-y-Merchand; Carlos Y Soto; Rogelio Hernández-Pando
Journal:  PLoS One       Date:  2013-03-05       Impact factor: 3.240

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