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PLOS ONE  2012 

Characterization of the Promoter, MxiE Box and 5′ UTR of Genes Controlled by the Activity of the Type III Secretion Apparatus in Shigella flexneri

DOI: 10.1371/journal.pone.0032862

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Abstract:

Activation of the type III secretion apparatus (T3SA) of Shigella flexneri, upon contact of the bacteria with host cells, and its deregulation, as in ipaB mutants, specifically increases transcription of a set of effector-encoding genes controlled by MxiE, an activator of the AraC family, and IpgC, the chaperone of the IpaB and IpaC translocators. Thirteen genes carried by the virulence plasmid (ospB, ospC1, ospD2, ospD3, ospE1, ospE2, ospF, ospG, virA, ipaH1.4, ipaH4.5, ipaH7.8 and ipaH9.8) and five genes carried by the chromosome (ipaHa-e) are regulated by the T3SA activity. A conserved 17-bp MxiE box is present 5′ of most of these genes. To characterize the promoter activity of these MxiE box-containing regions, similar ~67-bp DNA fragments encompassing the MxiE box of 14 MxiE-regulated genes were cloned 5′ of lacZ in a promoter probe plasmid; β-galactosidase activity detected in wild-type and ipaB strains harboring these plasmids indicated that most MxiE box-carrying regions contain a promoter regulated by the T3SA activity and that the relative strengths of these promoters cover an eight-fold range. The various MxiE boxes exhibiting up to three differences as compared to the MxiE box consensus sequence were introduced into the ipaH9.8 promoter without affecting its activity, suggesting that they are equally efficient in promoter activation. In contrast, all nucleotides conserved among MxiE boxes were found to be involved in MxiE-dependent promoter activity. In addition, we present evidence that the 5′ UTRs of four MxiE-regulated genes enhance expression of the downstream gene, presumably by preventing degradation of the mRNA, and the 5′ UTRs of two other genes carry an ancillary promoter.

References

[1]  Cornelis GR (2006) The type III secretion injectisome. Nat Rev Microbiol 4: 811–825.
[2]  Galan JE, Wolf-Watz H (2006) Protein delivery into eukaryotic cells by type III secretion machines. Nature 444: 567–573.
[3]  Miller VL (2002) Connections between transcriptional regulation and type III secretion? Curr Opin Microbiol 5: 211–215.
[4]  Brutinel ED, Yahr TL (2008) Control of gene expression by type III secretory activity. Curr Opin Microbiol 11: 128–133.
[5]  Parsot C (2005) Shigella spp. and enteroinvasive Escherichia coli pathogenicity factors. Fems Microbiol Lett 252: 11–18.
[6]  Ashida H, Ogawa M, Mimuro H, Sasakawa C (2009) Shigella infection of intestinal epithelium and circumvention of the host innate defense system. Current Topics in Microbiology and Immunology 337: 231–255.
[7]  Buchrieser C, Glaser P, Rusniok C, Nedjari H, d'Hauteville H, et al. (2000) The virulence plasmid pWR100 and the repertoire of proteins secreted by the type III secretion apparatus of Shigella flexneri. Mol Microbiol 38: 760–771.
[8]  Buysse JM, Hartman AB, Strockbine N, Venkatesan M (1995) Genetic polymorphism of the ipaH multicopy antigen gene in Shigella spps and enteroinvasive Escherichia coli. Microb Pathogenesis 19: 335–349.
[9]  Ashida H, Toyotome T, Nagai T, Sasakawa C (2007) Shigella chromosomal IpaH proteins are secreted via the type III secretion system and act as effectors. Mol Microbiol 63: 680–693.
[10]  Adler B, Sasakawa C, Tobe T, Makino S, Komatsu K, et al. (1989) A Dual transcriptional activation system for the 230-kb plasmid genes coding for virulence-associated antigens of Shigella flexneri. Mol Microbiol 3: 627–635.
[11]  Dorman CJ, McKenna S, Beloin C (2001) Regulation of virulence gene expression in Shigella flexneri, a facultative intracellular pathogen. Int J Med Microbiol 291: 89–96.
[12]  Blocker A, Gounon P, Larquet E, Niebuhr K, Cabiaux V, et al. (1999) The tripartite type III secreton of Shigella flexneri inserts IpaB and IpaC into host membranes. J Cell Biol 147: 683–693.
[13]  Menard R, Sansonetti P, Parsot C (1994) The secretion of the Shigella flexneri Ipa invasins is activated by epithelial cells and controlled by IpaB and IpaD. Embo J 13: 5293–5302.
[14]  Bahrani FK, Sansonetti PJ, Parsot C (1997) Secretion of Ipa proteins by Shigella flexneri: inducer molecules and kinetics of activation. Infect Immun 65: 4005–4010.
[15]  Menard R, Sansonetti PJ, Parsot C (1993) Nonpolar mutagenesis of the ipa genes defines ipaB, ipaC, and ipaD as effectors of Shigella flexneri entry into epithelial cells. J Bacteriol 175: 5899–5906.
[16]  Mavris M, Page AL, Tournebize R, Demers B, Sansonetti P, et al. (2002) Regulation of transcription by the activity of the Shigella flexneri type III secretion apparatus. Mol Microbiol 43: 1543–1553.
[17]  Demers B, Sansonetti PJ, Parsot C (1998) Induction of type III secretion in Shigella flexneri is associated with differential control of transcription of genes encoding secreted proteins. Embo J 17: 2894–2903.
[18]  Le Gall T, Mavris M, Martino MC, Bernardini ML, Denamur E, et al. (2005) Analysis of virulence plasmid gene expression defines three classes of effectors in the type III secretion system of Shigella flexneri. Microbiology 151: 951–962.
[19]  Allaoui A, Sansonetti PJ, Parsot C (1993) MxiD, an outer-membrane protein necessary for the secretion of the Shigella flexneri Ipa invasins. Mol Microbiol 7: 59–68.
[20]  Penno C, Sansonetti P, Parsot C (2005) Frameshifting by transcriptional slippage is involved in production of MxiE, the transcription activator regulated by the activity of the type III secretion apparatus in Shigella flexneri. Mol Microbiol 56: 204–214.
[21]  Menard R, Sansonetti P, Parsot C, Vasselon T (1994) Extracellular association and cytoplasmic partitioning of the IpaB and IpaC invasins of Shigella flexneri. Cell 79: 515–525.
[22]  Parsot C, Ageron E, Penno C, Mavris M, Jamoussi K, et al. (2005) A secreted anti-activator, OspD1, and its chaperone, Spa15, are involved in the control of transcription by the type III secretion apparatus activity in Shigella flexneri. Mol Microbiol 56: 1627–1635.
[23]  Pilonieta MC, Munson GP (2008) The chaperone IpgC copurifies with the virulence regulator MxiE. J Bacteriol 190: 2249–2251.
[24]  Kane CD, Schuch R, Day WA, Maurelli AT (2002) MxiE regulates intracellular expression of factors secreted by the Shigella flexneri 2a type III secretion system. J Bacteriol 184: 4409–4419.
[25]  Mavris M, Sansonetti PJ, Parsot C (2002) Identification of the cis-acting site involved in activation of promoters regulated by activity of the type III secretion apparatus in Shigella flexneri. J Bacteriol 184: 6751–6759.
[26]  Kim DW, Lenzen G, Page AL, Legrain P, Sansonetti PJ, et al. (2005) The Shigella flexneri effector OspG interferes with innate immune responses by targeting ubiquitin-conjugating enzymes. P Natl Acad Sci USA 102: 14046–14051.
[27]  Allaoui A, Mounier J, Prevost MC, Sansonetti PJ, Parsot C (1992) IcsB, a Shigella flexneri virulence gene necessary for the lysis of protrusions during intercellular spread. Mol Microbiol 6: 1605–1616.
[28]  Sansonetti PJ, Kopecko DJ, Formal SB (1982) Involvement of a plasmid in the invasive ability of Shigella flexneri. Infect Immun 35: 852–860.
[29]  Jin Q, Yuan ZH, Xu JG, Wang Y, Shen Y, et al. (2002) Genome sequence of Shigella flexneri 2a: insights into pathogenicity through comparison with genomes of Escherichia coli K12 and O157. Nucleic Acids Res 30: 4432–4441.
[30]  Farinha MA, Kropinski AM (1990) Construction of broad-host-range plasmid vectors for easy visible selection and analysis of promoters. J Bacteriol 172: 3496–3499.
[31]  Platt T, Weber K, Ganem D, Miller JH (1972) Translational restarts: AUG reinitiation of a lac repressor fragment. Proc Natl Acad Sci USA 69: 897–901.
[32]  Mathews DH, Turner DH, Zuker M (2007) RNA secondary structure prediction. Curr Protoc in Nucleic Acid Chem, edited by Serge L Beaucage, Chapter 11: Unit 11 12.
[33]  Chen LH, Emory SA, Bricker AL, Bouvet P, Belasco JG (1991) Structure and function of a bacterial mRNA stabilizer: analysis of the 5′ untranslated region of ompA mRNA. J Bacteriol 173: 4578–4586.
[34]  Emory SA, Bouvet P, Belasco JG (1992) A 5′-terminal stem-loop structure can stabilize mRNA in Escherichia coli. Gene Dev 6: 135–148.
[35]  Bricker AL, Belasco JG (1999) Importance of a 5′ stem-loop for longevity of papA mRNA in Escherichia coli. J Bacteriol 181: 3587–3590.
[36]  Wong KK, Bouwer HG, Freitag NE (2004) Evidence implicating the 5′ untranslated region of Listeria monocytogenes actA in the regulation of bacterial actin-based motility. Cell Microbiol 6: 155–166.
[37]  Shen A, Higgins DE (2005) The 5′ untranslated region-mediated enhancement of intracellular listeriolysin O production is required for Listeria monocytogenes pathogenicity. Mol Microbiol 57: 1460–1473.
[38]  Stritzker J, Schoen C, Goebel W (2005) Enhanced synthesis of internalin A in aro mutants of Listeria monocytogenes indicates posttranscriptional control of the inlAB mRNA. J Bacteriol 187: 2836–2845.
[39]  Loh E, Gripenland J, Johansson J (2006) Control of Listeria monocytogenes virulence by 5′-untranslated RNA. Trends Microbiol 14: 294–298.

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