Microbial Endocrinology

Lyte M., Microbial endocrinology and infectious disease in the 21st century, Trends in Micro., 2004, 12, 14–20 Freestone P.P., Sandrini S.M., Haigh R.D., Lyte M., Microbial endocrinology: how stress influences susceptibility to infection, Trends in Micro., 2008, 16, 55–64 Freestone P.P.E., Lyte M., Microbial endocrinology: experimental design issues in the study of interkingdom signalling in infectious disease, Adv. Appl. Micro., 2009, 64, 75–105 Lyte M., Freestone P.P.E., Microbial Endocrinology comes of age, Microbe, 2009, 4, 169–175 Freestone P.P.E, Lyte M. Stress and microbial endocrinology: prospects for ruminant nutrition, Animal 2010, 4, 1248–1257 Lyte M., Freestone P.P.E., Microbial Endocrinology: inter-kingdom signalling in health and infectious disease, Springer Publishers, 2010, ISBN, 978-1-4419-5575-3 Reiche E.M., Nunes S.O., Morimoto H.K., Stress, depression, the immune system, and cancer, Lancet Oncology, 2004, 5, 617–625 Furness J.B., The Enteric Nervous System, Blackwell Pub, 2006, Malden, MA Freestone P.P.E, Lyte M., Haigh R.D., Williams P.H., Stimulation of bacterial growth by heat-stable norepinephrine-induced autoinducers, FEMS Micro. Letts., 1999, 172, 53–60 Alverdy J., Holbrook C., Rocha F., Seiden L., Wu R.L., Musch M., et al., Gut-derived sepsis occurs when the right pathogen with the right virulence genes meets the right host: evidence for in vivo virulence expression in Pseudomonas aeruginosa, Ann. Surg., 2000, 232, 480–489 Anderson M., Armstrong S.K., The Bordetella Bfe system: Growth and transcriptional response to siderophores, catechols, and neuroendocrine catecholamines, J. Bact., 2006, 188, 5731–5740 Bansal T., Englert D, Lee J., Hegde M., Wood T.K., Jayaraman A., Differential effects of epinephrine, norepinephrine, and indole on Escherichia coli O157:H7 chemotaxis, colonization and gene expression, Infect. Immun., 2007, 75, 4597–4607 Chen C., Brown D.R., Xie Y., Green B.T., Lyte M., Catecholamines modulate Escherichia coli O157:H7 adherence to murine cecal mucosa, Shock, 2003, 20, 183–188 Cogan T.A., Thomas A.O., Rees L.E., Taylor A.H., Jepson M.A., Williams P.H., et al., Norepinephrine increases the pathogenic potential of Campylobacter jejuni, Gut, 2007, 56, 1060–1065 Coulanges V., Andre P., Vidon D.J., Effect of siderophores, catecholamines, and catechol compounds on Listeria spp. growth in ironcomplexed medium, Biochem. Biophys. Res. Commun., 1997, 249, 526–530 Doherty N.C., Tobias A., Watson S., Atherton J.C., The effect of the human gut-signalling hormone, norepinephrine, on the growth of the gastric pathogen Helicobacter pylori, Helicobacter, 2009, 14, 223–30 Dowd S.E., Escherichia coli O157:H7 gene expression in the presence of catecholamine norepinephrine, FEMS Micro.Letts., 2007, 273, 214–223 Freestone P.P.E., Williams P.H., Haigh R.D., Maggs A.F., Neal C.P., Lyte, M., Growth stimulation of intestinal commensal Escherichia coli by catecholamines: a possible contributory factor in trauma-induced sepsis, Shock, 2002, 18, 465–470 Kinney K.S., Austin C.E., Morton D.S., Sonnenfeld, G., Catecholamine enhancement of Aeromonas hydrophila growth, Micro. Pathogen., 1999, 26, 85–91 Lacoste A., Jalabert F., Malham S.K., Cueff A., Poulet, S.A., Stress and stress-induced neuroendocrine changes increase the susceptibility of juvenile oysters (Crassostrea gigas) to Vibrio splendidus, Appl. Environ. Micro. 2001, 67, 2304–2309 Lyte M., Freestone P.P., Neal C.P., Olson B.A., Haigh R.D., Bayston R., et al., Stimulation of Staphylococcus epidermidis growth and biofilm formation by catecholamine inotropes, Lancet, 2003, 361, 130–135 Nakano M., Takahashi A., Sakai Y., Nakaya Y., Modulation of pathogenicity with norepinephrine related to the type III secretion system of Vibrio parahaemolyticus, J. Inf. Dis. 2007, 195, 1353–1360 Neal C.P., Freestone P.P., Maggs A.F., Haigh R.D., Williams P.H., Lyte M., Catecholamine inotropes as growth factors for Staphylococcus epidermidis and other coagulase-negative staphylococci, FEMS Micro. Letts., 2001, 194, 163–169 O’Donnell P.M., Aviles H., Lyte M., Sonnenfeld, G., Enhancement of in vitro growth of pathogenic bacteria by norepinephrine: importance of inoculum density and role of transferrin, Appl. Environ. Micro., 2006, 72, 5097–5099 O’Neal M.J., Schafer E.R., Madsen M.L. Minion F.C., Global transcriptional analysis of Mycoplasma hyponeumoniae following exposure to norepinephrine, Microbiology, 2008, 154, 2581–2588. Roberts, A., Matthews, J., Socransky, S,. Freestone, P., Williams, P., and Chapple, I., Stress and the periodontal diseases: effects of catecholamines on the growth of periodontal bacteria in vitro, Oral Micro. Immun., 2002, 17, 296–303 Roberts A., Matthews J., Socransky S., Freestone P., Williams P., Chapple I., Stress and the periodontal diseases: growth responses of periodontal bacteria to Escherichia coli stress-associated autoinducer and exogenous Fe, Oral Micro. Immun., 2005, 20, 147–153 Scheckelhoff M.R., Telford S.R., Wesley M., Hu L.T., Borrelia burgdorferi intercepts host hormonal signals to regulate expression of outer surface protein A, Proc. Natl. Acad. Sci. USA., 2007, 104, 7247–7252 Lucero M.T., Squires A., Catecholamine concentrations in rat nasal mucus are modulated by trigeminal stimulation of the nasal cavity, Brain Research, 1998, 807, 234–236 Freestone P.P.E., Haigh R.D., Lyte M. Catecholamine inotrope resuscitation of antibioticdamaged staphylococci and its blockade by specific receptor antagonists, J. Infect. Dis., 2008, 197, 2044–1052 Ratledge C, Dover LG., Iron metabolism in pathogenic bacteria, Ann. Rev. Micro., 2000, 54, 881–941 Krewulak K.D., Vogel H.J., Structural biology of bacterial iron uptake, Biochim. Biophys. Acta., 2008, 1778, 1781–1804 Freestone P.P., Lyte M., Neal C.P., Maggs A.F., Haigh R.D., Williams P.H., The mammalian neuroendocrine hormone norepinephrine supplies iron for bacterial growth in the presence of transferrin or lactoferrin, J. Bact., 2000, 182, 6091–6098 Sandrini S.M., Shergill R., Woodward J., Muralikuttan R., Haigh R.D., Lyte M., et al., Elucidation of the mechanism by which catecholamine stress hormones liberate iron from the innate immune defense proteins transferrin and lactoferrin, J. Bact., 2010, 192, 587–594 Freestone P.P., Haigh R.D., Williams P.H., Lyte M., Involvement of enterobactin in norepinephrinemediated iron supply from transferrin to enterohaemorrhagic Escherichia coli, FEMS Micro. Letts., 2003, 222, 39–43 Williams P.H., Rabsch W., Methner U., Voigt W., Tschäpe H., Reissbrodt R., Catecholate receptor proteins in Salmonella enterica: role in virulence and implications for vaccine development, Vaccine, 2006, 24, 840–3844 Lyte M., Frank C.D., Green, B.T., Production of an autoinducer of growth by norepinephrine cultured Escherichia coli O157:H7, FEMS Micro. Letts., 1996, 139, 155–159 Lyte M., Arulanandam B.P. Frank C.D., Production of Shiga-like toxins by Escherichia coli O157:H7 can be influenced by the neuroendocrine hormone norepinephrine, J. Lab. Clin. Med., 1996, 128, 392–398 Tarr P.I., Neill M.A., Escherichia coli O157:H7, Gastroenterol. Clin. North Am., 2001. 30, 735–751 Hendrickson B.A., Guo J., Laughlin R., Chen Y. Alverdy J.C., Increased type 1 fimbrial expression among commensal Escherichia coli isolates in the murine cecum following catabolic stress, Infect. Immun., 1999, 67, 745–753 Vlisidou I., Lyte M., Van Diemen P.M., Hawes P., Monaghan P., Wallis T.S., et al., The neuroendocrine stress hormone norepinephrine augments Escherichia coli O157:H7-induced enteritis and adherence in a bovine ligated ileal loop model of infection, Infect. Immun. 2004, 72, 5446–5451 Green B.T., Lyte M., Chen C., Xie Y., Casey M.A., Kulkarni-Narla A., et al., Adrenergic modulation of Escherichia coli O157:H7 adherence to the colonic mucosa, Am. J. Phys. — Gastrointest. Liver Physiol., 2004, 287, G1238–G1246 Toscano M.J, Stabel T.J., Bearson S.M., Bearson B.L., Lay Jr D.C., Cultivation of Salmonella enterica serovar Typhimurium in a norepinephrinecontaining medium alters in vivo tissue prevalence in swine, J. Exp. Animal Sci., 2007, 43, 329–338 Methner U., Rabsch W., Reissbrodt R., Williams P.H., Effect of norepinephrine on colonisation and systemic spread of Salmonella enterica in infected animals: Role of catecholate siderophore precursors and degradation products, Int. J. Med. Microbiol., 2008, 298, 429–439 Mishra S.K, Segal E., Gunter E., Kurup V.P., Mishra J., Murali P.S., et al., Stress, immunity and mycotic diseases, J. Med.Vet. Mycol., 1994, 32, 379–406 Schreiber K.L., Brown, D.R., Adrenocorticotrophic hormone modulates Escherichia coli O157:H7 adherence to porcine colonic mucosa, Stress, 2005, 8, 185–19. Bailey M.T., Engler H., Sheridan J.F., Stress induces the translocation of cutaneous and gastrointestinal microflora to secondary lymphoid organs of C57BL/6 mice, J.Neuroimmunol., 2006, 171, 29–37 Bailey M.T., Dowd S.E., Parry N.M., Galley J.D., Schauer D.B., Lyte, M., Stressor exposure disrupts commensal microbial populations in the intestines and leads to increased colonization by Citrobacter rodentium, Infect. Immun., 2010, 78, 1509–1519 Lyte M., Bailey M.T., Neuroendocrine-bacterial interactions in a neurotoxin-induced model of trauma, J. Surg. Res., 1997, 70, 195–201 Pullinger G.D., van Diemen P.M., Carnell S.C., Davies H., Lyte M., Stevens M.P., 6-hydroxydopaminemediated release of norepinephrine increases faecal excretion of Salmonella enterica serovar Typhimurium in pigs, Vet. Res., 2010, 41, 68 Kendall M., Rasko D., Sperandio V., Global effects of the cell-to-cell signalling molecules autoinducer-2, autoinducer-3, and epinephrine in a luxS mutant of enterohemorrhagic Escherichia coli, Infect. Immun., 2007, 75, 4875–4884 Peterson G., Kumar A., Gart E., Narayanan S., Catecholamines increase conjugative gene transfer between enteric bacteria, Microb Pathog., 2011, 51, 1–8 Woods D.E., Jones A.L., Hill P.J., Interaction of insulin with Pseudomonas pseudomallei, Infect. Immun., 1993, 61, 4045–4050 Weiss M., Ingbar S.H., Winblad S. Kasper D.L., Demonstration of a saturable binding site for thyrotropin in Yersinia enterocolitica, Science, 1983, 219, 1331–1333 Zaborina O., Lepine F., Xiao G., Valuckaite V., Chen Y., Li T., et al., Dynorphin activates quorum sensing quinolone signaling in Pseudomonas aeruginosa, PLoS Pathog., 2007, 3, e35. Das M., Datta A., Steroid binding protein(s) in yeasts, Biochem. Int., 1985, 11, 171–176 Sonnex C., Influence of ovarian hormones on urogenital infection, Sex. Transm. Infect., 1998, 74, 11–19 Madani N.D., Malloy P.J., Rodriguez-Pombo P., Krishnan A.V., Feldman, D., Candida albicans estrogen-binding protein gene encodes an oxidoreductase that is inhibited by estradiol, Proc. Natl. Acad. Sci. USA, 1994, 91, 922–926 Roshchina V,V., Neurotransmitters in plant life, Plymouth Science Publishers, 2001 Waalkes T.P., Sjoerdsma A., Creveling C.R., Weissbach H., Udenfriend S., Serotonin, norepinephrine, and related compounds in bananas, Science, 1958, 127, 648–650 Rabey J.M., Vered Y., Shabtai H, Graff E, Korczyn A.D., Improvement of parkinsonian features correlate with high plasma levodopa values after broad bean (Vicia faba) consumption, J. Neuro. Neurosurg Psych., 1992, 55, 725–727 Apaydin H., Broad bean (Vicia faba)—a natural source of L-DOPA—prolongs ‘on’ periods in patients with Parkinson’s disease who have ‘on-off’ fluctuations, Mov. Disord., 2000, 15, 164–166 Tsavkelova E.A., Klimova S.Y., Cherdyntseva T.A., Netrusov, A.I., Hormones and hormone-like substances of microorganisms: a review, Appl. Biochem. Microbiol. (Russia), 2006, 42, 229–235 Freestone P.P.E., Haigh R.D., Lyte, M., Blockade of catecholamine-induced growth by adrenergic and dopaminergic receptor antagonists in Escherichia coli O157: H7, Salmonella enterica and Yersinia enterocolitica, BMC Microbiology, 2007, 7, 8 (1–13). Clarke M.B., Hughes D.T., Zhu C., Boedeker E. C., Sperandio V., The QseC sensor kinase: a bacterial adrenergic receptor, Proc. Natl. Acad. Sci. USA., 2006, 103, 10420–10425 Pullinger G, Carnell SC, Farveen F, van Diemen P, Dziva F, Morgan E, Lyte, et al., Norepinephrine augments Salmonella-induced bovine enteritis in a manner associated with increased net replication but independent of the putative adrenergic sensor kinases QseC and QseE, Infect. Immun., 2010, 78, 372–380