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 in | The Prostate Vol. 79; no. 2; pp. 160 - 167 |
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Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: 1 Dept. of Urology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA |
Author_xml | – sequence: 1 givenname: Stephen F. surname: Murphy fullname: Murphy, Stephen F. organization: Northwestern University – sequence: 2 givenname: Jonathan F. surname: Anker fullname: Anker, Jonathan F. organization: Northwestern University – sequence: 3 givenname: Daniel J. surname: Mazur fullname: Mazur, Daniel J. organization: Northwestern University – sequence: 4 givenname: Christel surname: Hall fullname: Hall, Christel organization: Northwestern University – sequence: 5 givenname: Anthony J. surname: Schaeffer fullname: Schaeffer, Anthony J. organization: Northwestern University – sequence: 6 givenname: Praveen surname: Thumbikat fullname: Thumbikat, Praveen email: thumbikat@northwestern.edu organization: Northwestern University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30242864$$D View this record in MEDLINE/PubMed |
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Keywords | infection pain prostatitis gram-positive CPPS |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 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. Co-first authors |
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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) |
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