Role of gram‐positive bacteria in chronic pelvic pain syndrome (CPPS)

INTRODUCTION Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non‐infectious with no well‐defined etiol...

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Published inThe Prostate Vol. 79; no. 2; pp. 160 - 167
Main Authors Murphy, Stephen F., Anker, Jonathan F., Mazur, Daniel J., Hall, Christel, Schaeffer, Anthony J., Thumbikat, Praveen
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.02.2019
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Abstract INTRODUCTION Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non‐infectious with no well‐defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram‐negative bacterial isolate can induce CPPS‐like symptoms in mice. Here we aimed to expand on these findings examining the role of gram‐positive patient‐derived bacteria in CPPS. METHODS A retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram‐positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS‐patients (pain inducers, PI) and one from a healthy volunteer (non‐pain inducer, NPI). These bacteria were inoculated intra‐urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry. RESULTS PI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra‐urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient‐isolates induced prostate inflammation specifically involving T‐cells and monocytes. CONCLUSIONS Gram‐positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram‐positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.
AbstractList INTRODUCTION Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non‐infectious with no well‐defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram‐negative bacterial isolate can induce CPPS‐like symptoms in mice. Here we aimed to expand on these findings examining the role of gram‐positive patient‐derived bacteria in CPPS. METHODS A retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram‐positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS‐patients (pain inducers, PI) and one from a healthy volunteer (non‐pain inducer, NPI). These bacteria were inoculated intra‐urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry. RESULTS PI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra‐urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient‐isolates induced prostate inflammation specifically involving T‐cells and monocytes. CONCLUSIONS Gram‐positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram‐positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.
Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non-infectious with no well-defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram-negative bacterial isolate can induce CPPS-like symptoms in mice. Here we aimed to expand on these findings examining the role of gram-positive patient-derived bacteria in CPPS.INTRODUCTIONChronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non-infectious with no well-defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram-negative bacterial isolate can induce CPPS-like symptoms in mice. Here we aimed to expand on these findings examining the role of gram-positive patient-derived bacteria in CPPS.A retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram-positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS-patients (pain inducers, PI) and one from a healthy volunteer (non-pain inducer, NPI). These bacteria were inoculated intra-urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry.METHODSA retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram-positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS-patients (pain inducers, PI) and one from a healthy volunteer (non-pain inducer, NPI). These bacteria were inoculated intra-urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry.PI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra-urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient-isolates induced prostate inflammation specifically involving T-cells and monocytes.RESULTSPI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra-urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient-isolates induced prostate inflammation specifically involving T-cells and monocytes.Gram-positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram-positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.CONCLUSIONSGram-positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram-positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.
Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non-infectious with no well-defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram-negative bacterial isolate can induce CPPS-like symptoms in mice. Here we aimed to expand on these findings examining the role of gram-positive patient-derived bacteria in CPPS. A retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram-positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS-patients (pain inducers, PI) and one from a healthy volunteer (non-pain inducer, NPI). These bacteria were inoculated intra-urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry. PI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra-urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient-isolates induced prostate inflammation specifically involving T-cells and monocytes. Gram-positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram-positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.
INTRODUCTIONChronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis is reflected by the absence of effective therapies. Although CPPS is deemed clinically non‐infectious with no well‐defined etiological role for microbes, bacteria is readily isolated from both healthy and patient prostate secretion and urine samples. Our laboratory has previously demonstrated that a specific gram‐negative bacterial isolate can induce CPPS‐like symptoms in mice. Here we aimed to expand on these findings examining the role of gram‐positive patient‐derived bacteria in CPPS.METHODSA retrospective analysis of bacterial cultures from CPPS patients from a single center was performed. Gram‐positive bacteria were isolated from the expressed prostatic secretion (EPS) of three CPPS‐patients (pain inducers, PI) and one from a healthy volunteer (non‐pain inducer, NPI). These bacteria were inoculated intra‐urethrally in two mouse backgrounds and analyzed for their ability to induce tactile allodynia, voiding dysfunction, and colonize the murine prostate. Host immune responses to bacterial instillation were analyzed by flow cytometry.RESULTSPI strains (Staphylococcus haemolyticus 2551, Enterococcus faecalis 427, and Staphylococcus epidermidis 7244) induced and maintained tactile allodynia responses (200% increase above baseline) for 28 days in NOD/ShiLtJ mice. Conversely the healthy subject derived strain (Staphylococcus epidermidis NPI) demonstrated no significant pelvic allodynia induction. Intra‐urethral inoculation of the four bacterial strains into C57BL/6 mice did not induce significant increases in pain responses. Infected NOD/ShiLtJ displayed significant voiding dysfunction compared to their control counterparts. Colony counts of prostate tissues from both NOD/ShiLtJ and C57BL/6 mice at day 28 demonstrated that bacterial strains colonized equally well, including NPI. We also determined that mechanistically, the patient‐isolates induced prostate inflammation specifically involving T‐cells and monocytes.CONCLUSIONSGram‐positive isolates from CPPS patients showed enhanced ability to induce tactile allodynia compared to a single taxonomically similar gram‐positive strain isolated from a healthy control. Responses were shown to be dependent on host genetic background and not on colonization differences between strains.
Author Schaeffer, Anthony J.
Mazur, Daniel J.
Thumbikat, Praveen
Hall, Christel
Murphy, Stephen F.
Anker, Jonathan F.
AuthorAffiliation 1 Dept. of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA
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Keywords infection
pain
prostatitis
gram-positive
CPPS
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Author contributions: SFM and JFA designed and executed in vivo and in vitro experiments. JFA and DM performed retrospective analysis. CH provided technical support and blinded all in vivo experiments. SFM and JFA wrote and edited the manuscript with AS and PT providing editorial oversight and clinical input.
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Snippet INTRODUCTION Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and...
Chronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and pathogenesis...
INTRODUCTIONChronic pelvic pain syndrome (CPPS) is a complex disorder that affects a large proportion of all men. A limited understanding of its etiology and...
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SubjectTerms Animals
Bacteria
Chronic Pain - immunology
Chronic Pain - microbiology
Colonization
CPPS
Etiology
Flow cytometry
Gram-negative bacteria
Gram-Positive Bacteria - isolation & purification
Gram-Positive Bacterial Infections - immunology
Gram-Positive Bacterial Infections - microbiology
gram‐positive
Humans
Hyperalgesia - microbiology
Immune response
infection
Inoculation
Lymph Nodes - immunology
Lymph Nodes - microbiology
Male
Mice
Mice, Inbred C57BL
Mice, Inbred NOD
Monocytes
Pain
Pain perception
Patients
Pelvic Pain - immunology
Pelvic Pain - microbiology
Prostate
Prostate - immunology
Prostate - microbiology
prostatitis
Prostatitis - microbiology
Random Allocation
Retrospective Studies
Staphylococcus epidermidis
Strains (organisms)
T-Lymphocytes - immunology
Tactile stimuli
Urethral Diseases - immunology
Urethral Diseases - microbiology
Urine
Title Role of gram‐positive bacteria in chronic pelvic pain syndrome (CPPS)
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpros.23721
https://www.ncbi.nlm.nih.gov/pubmed/30242864
https://www.proquest.com/docview/2157278250
https://www.proquest.com/docview/2111142929
https://pubmed.ncbi.nlm.nih.gov/PMC6623965
Volume 79
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