Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/128710
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Type: Journal article
Title: Innate immune response to bacterial urinary tract infection sensitises high-threshold bladder afferents and recruits silent nociceptors
Author: Brierley, S.M.
Goh, K.G.K.
Sullivan, M.J.
Moore, K.H.
Ulett, G.C.
Grundy, L.
Citation: Pain, 2020; 161(1):202-210
Publisher: International Association for the Study of Pain
Issue Date: 2020
ISSN: 0304-3959
1872-6623
Statement of
Responsibility: 
Stuart M. Brierley, Kelvin G.K. Goh, Matthew J. Sullivan, Kate H. Moore, Glen C. Ulett, Luke Grundy
Abstract: The bladder is innervated by primary afferent nerve fibres that detect bladder distension and, via projections into the spinal cord, provide sensory input to the central nervous system circuits regulating bladder sensation and function. Uropathogenic E. coli (UPEC) are the primary cause of urinary tract infection (UTI) in adults, inducing clinical symptoms characterised by exaggerated bladder sensation, including urgency, frequency, and pelvic pain. However, the mechanisms underlying UTI-induced modulation of bladder afferent function have yet to be explored. Here we isolated supernatants from the bladders of female mice acutely infected with UPEC (strain CFT073), or those sham-treated with phosphate buffered saline. Supernatants were then applied into the bladder lumen of healthy donor mice, and multiunit bladder afferent nerve responses to distension measured ex-vivo. Supernatant constituents from UPEC or sham-treated mice were analysed using a mouse cytokine multiplex assay. Supernatants from UPEC infected mice significantly enhanced bladder afferent firing to distension in the absence of changes in muscle compliance. Further evaluation revealed that UPEC supernatants exclusively sensitised high-threshold bladder mechanoreceptors to graded bladder distension and also recruited a population of 'silent nociceptors' to become mechanosensitive, thereby amplifying bladder afferent responses to physiological stimuli. UPEC supernatants contained significantly elevated concentrations of a range of cytokines released from innate immune cells, including, but not limited to TNFα, IL-1β, IL-6, IL-17, IFN-gamma, and MCP-1. These data provide novel mechanistic insight into how UPEC mediated UTI induces bladder hypersensitivity and the symptoms of frequency, urgency, and pelvic pain.
Keywords: Bladder; urinary tract infection; escherichia coli; hypersensitivity; mechanosensation; innate immune response
Rights: © 2019 by the International Association for the Study of Pain. Unauthorized reproduction of this article is prohibited.
RMID: 0030135033
DOI: 10.1097/j.pain.0000000000001692
Grant ID: http://purl.org/au-research/grants/nhmrc/1126378
http://purl.org/au-research/grants/nhmrc/1140297
http://purl.org/au-research/grants/nhmrc/1139366
Appears in Collections:Medicine publications

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