1887

Abstract

is a bacterial pathogen that causes ventilator-associated pneumonia and ocular infections. The FlhD and FlhC proteins complex to form a heteromeric transcription factor whose regulon, in , regulates genes for the production of flagellum, phospholipase A and the cytolysin ShlA. The previously identified mutation, , resulted in highly elevated expression of the operon. The mutant was observed to be more cytotoxic to human airway and ocular surface epithelial cells than the wild-type bacteria and the present study sought to identify the mechanism underlying the increased cytotoxicity phenotype.

Although FlhC and FlhD have been implicated as virulence determinants, the mechanisms by which these proteins regulate bacterial cytotoxicity to different cell types remains unclear.

This study aimed to evaluate the mechanisms of FlhDC-mediated cytotoxicity to human epithelial cells by .

Wild-type and mutant bacteria and bacterial secretomes were used to challenge airway and ocular surface cell lines as evaluated by resazurin and calcein AM staining. Pathogenesis was further tested using a infection model.

The increased cytotoxicity of bacteria and secretomes to both cell lines was eliminated by mutation of and . Mutation of the flagellin gene had no impact on cytotoxicity under any tested condition. Elimination of the phospholipase gene, , had no effect on bacteria-induced cytotoxicity to either cell line, but reduced cytotoxicity caused by secretomes to airway epithelial cells. Mutation of and , but not , reduced bacterial killing of larvae.

This study indicates that the FlhDC-regulated secreted proteins PhlA and ShlA, but not flagellin, are cytotoxic to airway and ocular surface cells and demonstrates differences in human epithelial cell susceptibility to PhlA.

Funding
This study was supported by the:
  • Research to Prevent Blindness (Award N/A)
    • Principle Award Recipient: NotApplicable
  • National Institutes of Health (Award EY08098)
    • Principle Award Recipient: NotApplicable
  • National Eye Institute (NIH) (Award EY027331)
    • Principle Award Recipient: RobertM. Q. Shanks
  • Eye and Ear Foundation of Pittsburgh (Award N/A)
    • Principle Award Recipient: NotApplicable
Loading

Article metrics loading...

/content/journal/jmm/10.1099/jmm.0.001292
2020-12-10
2024-04-16
Loading full text...

Full text loading...

/deliver/fulltext/jmm/70/2/jmm001292.html?itemId=/content/journal/jmm/10.1099/jmm.0.001292&mimeType=html&fmt=ahah

References

  1. Young GM, Schmiel DH, Miller VL. A new pathway for the secretion of virulence factors by bacteria: the flagellar export apparatus functions as a protein-secretion system. Proc Natl Acad Sci U S A 1999; 96:6456–6461 [View Article][PubMed]
    [Google Scholar]
  2. Chilcott GS, Hughes KT. Coupling of flagellar gene expression to flagellar assembly in Salmonella enterica serovar typhimurium and Escherichia coli . Microb Mol Biol Rev 2000; 64:694–708 [View Article][PubMed]
    [Google Scholar]
  3. Morgenstein RM, Szostek B, Rather PN. Regulation of gene expression during swarmer cell differentiation in Proteus mirabilis . FEMS Microbiol Rev 2010; 34:753–763 [View Article][PubMed]
    [Google Scholar]
  4. Xu T, Su Y, Xu Y, He Y, Wang B et al. Mutations of flagellar genes fliC12, fliA and flhDC of Edwardsiella tarda attenuated bacterial motility, biofilm formation and virulence to fish. J Appl Microbiol 2013
    [Google Scholar]
  5. Eichelberg K, Galán JE. The flagellar sigma factor FliA (sigma(28)) regulates the expression of Salmonella genes associated with the centisome 63 type III secretion system. Infect Immun 2000; 68:2735–2743 [View Article][PubMed]
    [Google Scholar]
  6. Sule P, Horne SM, Logue CM, Prüss BM. Regulation of cell division, biofilm formation, and virulence by FlhC in Escherichia coli O157:H7 grown on meat. Appl Environ Microbiol 2011; 77:3653–3662 [View Article][PubMed]
    [Google Scholar]
  7. Hung C, Zhou Y, Pinkner JS, Dodson KW, Crowley JR et al. Escherichia coli biofilms have an organized and complex extracellular matrix structure. mBio 2013; 4:e00645–00613 [View Article][PubMed]
    [Google Scholar]
  8. Schmiel DH, Wagar E, Karamanou L, Weeks D, Miller VL. Phospholipase A of Yersinia enterocolitica contributes to pathogenesis in a mouse model. Infect Immun 1998; 66:3941–3951 [View Article][PubMed]
    [Google Scholar]
  9. Schmiel DH, Young GM, Miller VL. The Yersinia enterocolitica phospholipase gene yplA is part of the flagellar regulon. J Bacteriol 2000; 182:2314–2320 [View Article][PubMed]
    [Google Scholar]
  10. Park D, Forst S. Co-regulation of motility, exoenzyme and antibiotic production by the EnvZ-OmpR-FlhDC-FliA pathway in Xenorhabdus nematophila . Mol Microbiol 2006; 61:1397–1412 [View Article][PubMed]
    [Google Scholar]
  11. Liu JH, Lai MJ, Ang S, Shu JC, Soo PC et al. Role of flhDC in the expression of the nuclease gene nucA, cell division and flagellar synthesis in Serratia marcescens . J Biomed Sci 2000; 7:475–483 [View Article][PubMed]
    [Google Scholar]
  12. Castelli ME, Fedrigo GV, Clementín AL, Ielmini MV, Feldman MF et al. Enterobacterial common antigen integrity is a checkpoint for flagellar biogenesis in Serratia marcescens . J Bacteriol 2008; 190:213–220 [View Article][PubMed]
    [Google Scholar]
  13. Givskov M, Eberl L, Christiansen G, Benedik MJ, Molin S. Induction of phospholipase- and flagellar synthesis in Serratia liquefaciens is controlled by expression of the flagellar master operon flhD . Mol Microbiol 1995; 15:445–454 [View Article][PubMed]
    [Google Scholar]
  14. Givskov M, Molin S. Expression of extracellular phospholipase from Serratia liquefaciens is growth-phase-dependent, catabolite-repressed and regulated by anaerobiosis. Mol Microbiol 1992; 6:1363–1374 [View Article][PubMed]
    [Google Scholar]
  15. Givskov M, Molin S. Secretion of Serratia liquefaciens phospholipase from Escherichia coli . Mol Microbiol 1993; 8:229–242 [View Article][PubMed]
    [Google Scholar]
  16. Lin CS, Horng JT, Yang CH, Tsai YH, Su L-H et al. RssAB-FlhDC-ShlBA as a major pathogenesis pathway in Serratia marcescens . Infect Immun 2010; 78:4870–4881 [View Article][PubMed]
    [Google Scholar]
  17. Song JK, Kim MK, Rhee JS. Cloning and expression of the gene encoding phospholipase A1 from Serratia sp. MK1 in Escherichia coli . J Biotechnol 1999; 72:103–114 [View Article][PubMed]
    [Google Scholar]
  18. Di Venanzio G, Stepanenko TM, García Véscovi E. Serratia marcescens ShlA pore-forming toxin is responsible for early induction of autophagy in host cells and is transcriptionally regulated by RcsB. Infect Immun 2014; 82:3542–3554 [View Article][PubMed]
    [Google Scholar]
  19. Shanks RM, Stella NA, Brothers KM, Polaski DM. Exploitation of a "hockey-puck" phenotype to identify pilus and biofilm regulators in Serratia marcescens through genetic analysis. Can J Microbiol 2016; 62:83–93 [View Article][PubMed]
    [Google Scholar]
  20. Hertle R. The family of Serratia type pore forming toxins. Curr Protein Pept Sci 2005; 6:313–325 [View Article][PubMed]
    [Google Scholar]
  21. Poole K, Braun V. Influence of growth temperature and lipopolysaccharide on hemolytic activity of Serratia marcescens . J Bacteriol 1988; 170:5146–5152 [View Article][PubMed]
    [Google Scholar]
  22. Hertle R, Hilger M, Weingardt-Kocher S, Walev I. Cytotoxic action of Serratia marcescens hemolysin on human epithelial cells. Infect Immun 1999; 67:817–825 [View Article][PubMed]
    [Google Scholar]
  23. Hertle R, Schwarz H. Serratia marcescens internalization and replication in human bladder epithelial cells. BMC Infect Dis 2004; 4:16 [View Article][PubMed]
    [Google Scholar]
  24. Shimuta K, Ohnishi M, Iyoda S, Gotoh N, Koizumi N et al. The hemolytic and cytolytic activities of Serratia marcescens phospholipase A (PhlA) depend on lysophospholipid production by PhlA. BMC Microbiol 2009; 9:261 [View Article][PubMed]
    [Google Scholar]
  25. Brothers KM, Callaghan JD, Stella NA, Bachinsky JM, AlHigaylan M et al. Blowing epithelial cell bubbles with GumB: ShlA-family pore-forming toxins induce blebbing and rapid cellular death in corneal epithelial cells. PLoS Pathog 2019; 15:e1007825 [View Article][PubMed]
    [Google Scholar]
  26. Aggarwal C, Paul S, Tripathi V, Paul B, Khan MA. Characterization of putative virulence factors of Serratia marcescens strain SEN for pathogenesis in Spodoptera litura . J Invertebr Pathol 2017; 143:115–123 [View Article][PubMed]
    [Google Scholar]
  27. Alexpandi R, Prasanth MI, Ravi AV, Balamurugan K, Durgadevi R et al. Protective effect of neglected plant Diplocyclos palmatus on quorum sensing mediated infection of Serratia marcescens and UV-A induced photoaging in model Caenorhabditis elegans . J Photochem Photobiol B 2019; 201:111637 [View Article][PubMed]
    [Google Scholar]
  28. González-Juarbe N, Mares CA, Hinojosa CA, Medina JL, Cantwell A et al. Requirement for Serratia marcescens cytolysin in a murine model of hemorrhagic pneumonia. Infect Immun 2015; 83:614–624 [View Article][PubMed]
    [Google Scholar]
  29. Tsaplina O, Bozhokina E, Mardanova A, Khaitlina S. Virulence factors contributing to invasive activities of Serratia grimesii and Serratia proteamaculans . Arch Microbiol 2015; 197:481–488 [View Article][PubMed]
    [Google Scholar]
  30. Brothers KM, Stella NA, Shanks RMQ. Biologically active pigment and ShlA cytolysin of Serratia marcescens induce autophagy in a human ocular surface cell line. BMC Ophthalmol 2020; 20:120 [View Article][PubMed]
    [Google Scholar]
  31. Di Venanzio G, Lazzaro M, Morales ES, Krapf D, García Véscovi E. A pore-forming toxin enables Serratia a nonlytic egress from host cells. Cell Microbiol 2017; 19:e12656 [View Article][PubMed]
    [Google Scholar]
  32. Fedrigo GV, Campoy EM, Di Venanzio G, Colombo MI, García Véscovi E. Serratia marcescens is able to survive and proliferate in autophagic-like vacuoles inside non-phagocytic cells. PLoS One 2011; 6:e24054 [View Article][PubMed]
    [Google Scholar]
  33. Soo PC, Horng YT, Wei JR, Shu JC, Lu C-C et al. Regulation of swarming motility and flhDC(Sm) expression by RssAB signaling in Serratia marcescens . J Bacteriol 2008; 190:2496–2504 [View Article][PubMed]
    [Google Scholar]
  34. Stella NA, Kalivoda EJ, O'Dee DM, Nau GJ, Shanks RM. Catabolite repression control of flagellum production by Serratia marcescens . Res Microbiol 2008; 159:562–568 [View Article][PubMed]
    [Google Scholar]
  35. Kalivoda EJ, Stella NA, Aston MA, Fender JE, Thompson PP et al. Cyclic AMP negatively regulates prodigiosin production by Serratia marcescens . Res Microbiol 2010; 161:158–167 [View Article][PubMed]
    [Google Scholar]
  36. Anderson MT, Mitchell LA, Sintsova A, Rice KA, Mobley HLT. Sulfur assimilation alters flagellar function and modulates the gene expression landscape of Serratia marcescens . mSystems 2019; 4:e00285-19 [View Article][PubMed]
    [Google Scholar]
  37. Ishii K, Adachi T, Imamura K, Takano S, Usui K et al. Serratia marcescens induces apoptotic cell death in host immune cells via a lipopolysaccharide- and flagella-dependent mechanism. J Biol Chem 2012; 287:36582–36592 [View Article][PubMed]
    [Google Scholar]
  38. Burke DDD, Stearns T. Methods In Yeast Genetics, A Cold Spring Harbor Laboratory Course Manual Plainview, NY: Cold Harbor laboratory Press; 2000
    [Google Scholar]
  39. Shanks RM, Caiazza NC, Hinsa SM, Toutain CM, O'Toole GA. Saccharomyces cerevisiae-based molecular tool kit for manipulation of genes from gram-negative bacteria. Appl Environ Microbiol 2006; 72:5027–5036 [View Article][PubMed]
    [Google Scholar]
  40. Shanks RM, Kadouri DE, MacEachran DP, O'Toole GA. New yeast recombineering tools for bacteria. Plasmid 2009; 62:88–97 [View Article][PubMed]
    [Google Scholar]
  41. Berlyn M, Rudd K, Chater K. Genetic nomenclature guide. bacteria. Trends Genet 1998; 14:s.1–s.4
    [Google Scholar]
  42. Garcia CJ, Pericleous A, Elsayed M, Tran M, Gupta S et al. Serralysin family metalloproteases protects Serratia marcescens from predation by the predatory bacteria Micavibrio aeruginosavorus . Sci Rep 2018; 8:14025 [View Article][PubMed]
    [Google Scholar]
  43. Giard DJ, Aaronson SA, Todaro GJ, Arnstein P, Kersey JH et al. In vitro cultivation of human tumors: establishment of cell lines derived from a series of solid tumors. J Natl Cancer Inst 1973; 51:1417–1423 [View Article][PubMed]
    [Google Scholar]
  44. Gipson IK, Spurr-Michaud S, Argüeso P, Tisdale A, Ng TF et al. Mucin gene expression in immortalized human corneal-limbal and conjunctival epithelial cell lines. Invest Ophthalmol Vis Sci 2003; 44:2496–2506 [View Article][PubMed]
    [Google Scholar]
  45. Shanks RM, Stella NA, Lahr RM, Wang S, Veverka TI et al. Serratamolide is a hemolytic factor produced by Serratia marcescens . PLoS One 2012; 7:e36398 [View Article][PubMed]
    [Google Scholar]
  46. O'Hara JA, Ambe LA, Casella LG, Townsend BM, Pelletier MR et al. Activities of vancomycin-containing regimens against colistin-resistant Acinetobacter baumannii clinical strains. Antimicrob Agents Chemother 2013; 57:2103–2108 [View Article][PubMed]
    [Google Scholar]
  47. Shanks RM, Stella NA, Hunt KM, Brothers KM, Zhang L et al. Identification of SlpB, a cytotoxic protease from Serratia marcescens . Infect Immun 2015; 83:2907–2916 [View Article][PubMed]
    [Google Scholar]
  48. Jander G, Rahme LG, Ausubel FM. Positive correlation between virulence of Pseudomonas aeruginosa mutants in mice and insects. J Bacteriol 2000; 182:3843–3845 [View Article][PubMed]
    [Google Scholar]
  49. Rhee SH, Im E, Riegler M, Kokkotou E, O'brien M et al. Pathophysiological role of Toll-like receptor 5 engagement by bacterial flagellin in colonic inflammation. Proc Natl Acad Sci U S A 2005; 102:13610–13615 [View Article][PubMed]
    [Google Scholar]
  50. Zeng H, Wu H, Sloane V, Jones R, Yu Y et al. Flagellin/TLR5 responses in epithelia reveal intertwined activation of inflammatory and apoptotic pathways. Am J Physiol Gastrointest Liver Physiol 2006; 290:G96–G108 [View Article][PubMed]
    [Google Scholar]
  51. Ryu JC, Kim MJ, Kwon Y, Oh J-H, Yoon SS et al. Neutrophil pyroptosis mediates pathology of P. aeruginosa lung infection in the absence of the NADPH oxidase NOX2. Mucosal Immunol 2017; 10:757–774 [View Article][PubMed]
    [Google Scholar]
  52. Zhao Y, Yang J, Shi J, Gong YN, Lu Q et al. The NLRC4 inflammasome receptors for bacterial flagellin and type III secretion apparatus. Nature 2011; 477:596–600 [View Article][PubMed]
    [Google Scholar]
  53. Gao N, Kumar A, Jyot J, Yu F-S. Flagellin-Induced corneal antimicrobial peptide production and wound repair involve a novel NF-kappaB-independent and EGFR-dependent pathway. PLoS One 2010; 5:e9351 [View Article][PubMed]
    [Google Scholar]
  54. Kumar A, Gao N, Standiford TJ, Gallo RL, Yu F-SX. Topical flagellin protects the injured corneas from Pseudomonas aeruginosa infection. Microbes Infect 2010; 12:978–989 [View Article][PubMed]
    [Google Scholar]
  55. Kumar A, Hazlett LD, Yu F-SX. Flagellin suppresses the inflammatory response and enhances bacterial clearance in a murine model of Pseudomonas aeruginosa keratitis. Infect Immun 2008; 76:89–96 [View Article][PubMed]
    [Google Scholar]
  56. Anderson MT, Mitchell LA, Mobley HLT. Cysteine Biosynthesis controls Serratia marcescens phospholipase activity. J Bacteriol 2017; 199: [View Article][PubMed]
    [Google Scholar]
  57. Qu XD, Lehrer RI. Secretory phospholipase A2 is the principal bactericide for staphylococci and other gram-positive bacteria in human tears. Infect Immun 1998; 66:2791–2797 [View Article][PubMed]
    [Google Scholar]
  58. Saari KM, Aho V, Paavilainen V, Nevalainen TJ, Group II PLA. 2) content of tears in normal subjects. Invest Ophthalmol Vis Sci 2001; 42:318–320
    [Google Scholar]
  59. Hertle R. Serratia type pore forming toxins. Curr Protein Pept Sci 2000; 1:75–89 [View Article][PubMed]
    [Google Scholar]
  60. Shanks RM, Stella NA, Arena KE, Fender JE. Mutation of crp mediates Serratia marcescens serralysin and global secreted protein production. Res Microbiol 2013; 164:38–45 [View Article][PubMed]
    [Google Scholar]
  61. Wall E, Majdalani N, Gottesman S. The complex RCS regulatory cascade. Annu Rev Microbiol 2018; 72:111–139 [View Article][PubMed]
    [Google Scholar]
  62. Oñate-Garzón J, Manrique-Moreno M, Trier S, Leidy C, Torres R et al. Antimicrobial activity and interactions of cationic peptides derived from Galleria mellonella cecropin D-like peptide with model membranes. J Antibiot 2017; 70:238–245 [View Article][PubMed]
    [Google Scholar]
  63. Danese PN, Pratt LA, Kolter R. Exopolysaccharide production is required for development of Escherichia coli K-12 biofilm architecture. J Bacteriol 2000; 182:3593–3596 [View Article][PubMed]
    [Google Scholar]
  64. Richards MJ, Edwards JR, Culver DH, Gaynes RP. Nosocomial infections in coronary care units in the United States. National nosocomial infections surveillance system. Am J Cardiol 1998; 82:789–793 [View Article][PubMed]
    [Google Scholar]
  65. Cheng KH, Leung SL, Hoekman HW, Beekhuis WH, Mulder PG et al. Incidence of contact-lens-associated microbial keratitis and its related morbidity. Lancet 1999; 354:181–185 [View Article][PubMed]
    [Google Scholar]
  66. Alexandrakis G, Alfonso EC, Miller D. Shifting trends in bacterial keratitis in South Florida and emerging resistance to fluoroquinolones. Ophthalmology 2000; 107:1497–1502 [View Article][PubMed]
    [Google Scholar]
  67. Mah-Sadorra JH, Najjar DM, Rapuano CJ, Laibson PR, Cohen EJ. Serratia corneal ulcers: a retrospective clinical study. Cornea 2005; 24:793–800 [View Article][PubMed]
    [Google Scholar]
  68. Verhelst D, Koppen C, Van Looveren J, Meheus A, Tassignon MJ et al. Contact lens-related corneal ulcers requiring hospitalization: a 7-year retrospective study in Belgium. Acta Ophthalmol Scand 2006; 84:522–526 [View Article][PubMed]
    [Google Scholar]
  69. Mayo MS, Schlitzer RL, Ward MA, Wilson LA, Ahearn DG. Association of Pseudomonas and Serratia corneal ulcers with use of contaminated solutions. J Clin Microbiol 1987; 25:1398–1400 [View Article][PubMed]
    [Google Scholar]
  70. Póvoa HCC, Chianca GC, Iorio NLPP. COVID-19: an alert to ventilator-associated bacterial pneumonia. Infect Dis Ther 2020; 9:417–420 [View Article][PubMed]
    [Google Scholar]
  71. Quartuccio L, Sonaglia A, McGonagle D, Fabris M, Peghin M et al. Profiling COVID-19 pneumonia progressing into the cytokine storm syndrome: results from a single Italian centre study on tocilizumab versus standard of care. J Clin Virol 2020; 129:104444 [View Article][PubMed]
    [Google Scholar]
  72. Miller VL, Mekalanos JJ. A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR. J Bacteriol 1988; 170:2575–2583 [View Article][PubMed]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/jmm/10.1099/jmm.0.001292
Loading
/content/journal/jmm/10.1099/jmm.0.001292
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error