1887

Abstract

Cholix toxin (ChxA) is an ADP-ribosylating exotoxin produced by . However, to date, there is no quantitative assay available for ChxA, which makes it difficult to detect and estimate the level of ChxA produced by .

It is important to develop a reliable and specific quantitative assay to measure the production level of ChxA, which will help us to understand the role of ChxA in pathogenesis.

The aim of this study was to develop a bead-based sandwich ELISA (bead-ELISA) for the quantification of ChxA and to evaluate the importance of ChxA in the pathogenesis of infection.

Anti-rChxA was raised in New Zealand white rabbits, and Fab-horse radish peroxidase conjugate was prepared by the maleimide method to use in the bead-ELISA. This anti-ChxA bead-ELISA was applied to quantify the ChxA produced by various strains. The production of ChxA was examined in different growth media such as alkaline peptone water (APW), Luria-Bertani broth and AKI. Finally, the assay was evaluated using a mouse lethality assay with representative strains categorized as low to high ChxA-producers based on anti-ChxA bead-ELISA.

A sensitive bead-ELISA assay, which can quantify from 0.6 to 60 ng ml of ChxA, was developed. ChxA was mostly detected in the extracellular cell-free supernatant and its production level varied from 1.2 ng ml to 1.6 µg ml. The highest ChxA production was observed when strains were cultured in LB broth, but not in APW or AKI medium. The ChxA-producer strains showed 20–80 % lethality and only the high ChxA II-producer was statistically more lethal than a non-ChxA-producer, in the mice model assay. ChxA I and II production levels were not well correlated with mice lethality, and this could be due to the heterogeneity of the strains tested.

ChxA I to III was produced mostly extracellularly at various levels depending on strains and culture conditions. The bead-ELISA developed in this study is useful for the detection and quantification of ChxA in strains.

Funding
This study was supported by the:
  • Japan Society for the Promotion of Science (Award 26460533)
    • Principle Award Recipient: SHINJIYAMASAKI
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2021-04-08
2024-04-19
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References

  1. Yamai S, Okitsu T, Shimada T, Katsube Y. Distribution of serogroups of Vibrio cholerae non-O1 non-O139 with specific reference to their ability to produce cholera toxin and addition of novel serogroups. Kansenshogaku Zasshi 1997; 71:1037–1045 [View Article][PubMed]
    [Google Scholar]
  2. WHO (February 2014) Media centre, fact sheets, N°107 (Cholera). ( http://www.who.int/mediacentre/factsheets/fs107/en/).
  3. Sharma C, Thungapathra M, Ghosh A, Mukhopadhyay AK, Basu A et al. Molecular analysis of non-O1, non-O139 Vibrio cholerae associated with an unusual upsurge in the incidence of cholera-like disease in Calcutta, India. J Clin Microbiol 1998; 36:756–763 [View Article][PubMed]
    [Google Scholar]
  4. Faruque SM, Chowdhury N, Kamruzzaman M, Dziejman M, Rahman MH et al. Genetic diversity and virulence potential of environmental Vibrio cholerae population in a cholera-endemic area. Proc Natl Acad Sci U S A 2004; 101:2123–2128 [View Article][PubMed]
    [Google Scholar]
  5. Dziejman M, Serruto D, Tam VC, Sturtevant D, Diraphat P et al. Genomic characterization of non-O1, non-O139 Vibrio cholerae reveals genes for a type III secretion system. Proc Natl Acad Sci U S A 2005; 102:3465–3470 [View Article][PubMed]
    [Google Scholar]
  6. Pukatzki S, Ma AT, Sturtevant D, Krastins B, Sarracino D et al. Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system. Proc Natl Acad Sci U S A 2006; 103:1528–1533 [View Article][PubMed]
    [Google Scholar]
  7. Sarkar B, Bhattacharya T, Ramamurthy T, Shimada T, Takeda Y et al. Preferential association of the heat-stable enterotoxin gene (stn) with environmental strains of Vibrio cholerae belonging to the O14 serogroup. Epidemiol Infect 2002; 129:245–251 [View Article][PubMed]
    [Google Scholar]
  8. Ghosh A, Saha DR, Hoque KM, Asakuna M, Yamasaki S et al. Enterotoxigenicity of mature 45-kilodalton and processed 35-kilodalton forms of hemagglutinin protease purified from a cholera toxin gene-negative Vibrio cholerae non-O1, non-O139 strain. Infect Immun 2006; 74:2937–2946 [View Article][PubMed]
    [Google Scholar]
  9. Fasano A, Baudry B, Pumplin DW, Wasserman SS, Tall BD et al. Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions. Proc Natl Acad Sci U S A 1991; 88:5242–5246 [View Article][PubMed]
    [Google Scholar]
  10. Fasano A, Fiorentini C, Donelli G, Uzzau S, Kaper JB et al. Zonula occludens toxin modulates tight junctions through protein kinase C-dependent actin reorganization, in vitro . J Clin Invest 1995; 96:710–720 [View Article][PubMed]
    [Google Scholar]
  11. Jørgensen R, Purdy AE, Fieldhouse RJ, Kimber MS, Bartlett DH et al. Cholix toxin, a novel ADP-ribosylating factor from Vibrio cholerae . J Biol Chem 2008; 283:10671–10678 [View Article][PubMed]
    [Google Scholar]
  12. Awasthi SP, Asakura M, Chowdhury N, Neogi SB, Hinenoya A et al. Novel cholix toxin variants, ADP-ribosylating toxins in Vibrio cholerae non-O1/non-O139 strains, and their pathogenicity. Infect Immun 2013; 81:531–541 [View Article][PubMed]
    [Google Scholar]
  13. Awasthi SP, Asakura M, Neogi SB, Hinenoya A, Ramamurthy T et al. Development of a PCR-restriction fragment length polymorphism assay for detection and subtyping of cholix toxin variant genes of Vibrio cholerae . J Med Microbiol 2014; 63:667–673 [View Article][PubMed]
    [Google Scholar]
  14. Purdy AE, Balch D, Lizárraga-Partida ML, Islam MS, Martinez-Urtaza J et al. Diversity and distribution of cholix toxin, a novel ADP-ribosylating factor from Vibrio cholerae . Environ Microbiol Rep 2010; 2:198–207 [View Article][PubMed]
    [Google Scholar]
  15. Ouchterlony O. Antigen -antobody reactions in gel. Acta Pathologica Microbiologica Scandinavica 1949; 26:507–515 [View Article]
    [Google Scholar]
  16. Oku Y, Uesaka Y, Hirayama T, Takeda Y. Development of a highly sensitive bead-ELISA to detect bacterial protein toxins. Microbiol Immunol 1988; 32:807–816 [View Article][PubMed]
    [Google Scholar]
  17. Iwanaga M, Yamamoto K. New medium for the production of cholera toxin by Vibrio cholerae O1 biotype El Tor. J Clin Microbiol 1985; 22:405–408 [View Article][PubMed]
    [Google Scholar]
  18. Mekalanos JJ, Swartz DJ, Pearson GD, Harford N, Groyne F et al. Cholera toxin genes: nucleotide sequence, deletion analysis and vaccine development. Nature 1983; 306:551–557 [View Article][PubMed]
    [Google Scholar]
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