Distribution of secretory inhibitor of platelet microbicidal protein among urethral isolates with its correlation with prostatitis

• Published in: Asian journal of andrology Vol. 10; no. 2; pp. 189 - 192
• Main Authors: Ivanov, Iuri B., Gritsenko, Viktor A., Kuzmin, Michael D.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.03.2008; Medknow Publications & Media Pvt. Ltd
• Subjects: Bacillus subtilis; bacteriology; beta-Thromboglobulin - antagonists & inhibitors; Blood Bactericidal Activity - physiology; Blood Platelets - metabolism; Chronic Disease; Enterobacteriaceae; Enterococcus faecalis; Humans; In Vitro Techniques; Male; Phenotype; platelet microbicidal protein; prostatitis; Prostatitis - metabolism; Prostatitis - microbiology; Staphylococcus; Urethra - microbiology; 前列腺炎; 细菌学; 血小板
• ISSN: 1008-682X; 1745-7262
• DOI: 10.1111/j.1745-7262.2008.00344.x

Aim： To report the detection in vitro of secretory inhibitor of platelet microbicidal protein （SIPMP） phenotypes of urethral isolates along with a comparisonwith isolates from patients with or without chronic bacterial prostatitis （CBP）. Methods： Urethral isolates of Staphylococcus spp. （n = 64）, diphtheroids （n = 28）, micrococci （n = 15）, streptococci （n = 21）, Enterobacteriaceae （n = 9） and Enterococcusfaecalis （n = 19） from patients with or without CBP were tested. SIPMP production was tested by inhibition of platelet microbicidal protein （PMP） bioactivity against Bacillus subtilis and was expressed as percentage of inhibition of PMP bactericidal activity. Results： A significantly higher proportion of CBP-strains （57.78% vs. 16.67%） reduced PMP-induced killing of Bacillus subtilis than non- CBP strains did （P 〈 0.01）. SIPMP levels of staphylococci and Enterococcusfaecalis from the CBP group were significantly higher than those of the control group. Conclusion： These results suggest that SIPMP production is associated with the CBP source. Data from the present study might have significant implications for the understanding of the pathogenesis of CBP. （Asian J Androl 2008 Mar; 10： 189-192）.