IDENTIFICATION MARKERS OF INFECTION DUE TO C. TRACHOMATIS AND C. PNEUMONIAE, IN PATIENTS WITH DISEASES OF THE GASTROINTESTINAL TRACT

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Abstract

 To date, clinical data have convincingly shown that C. trachomatis and C. pneumoniae infectious can cause serious diseases with severe complications and consequences. There are assumptions that the developed chronic chlamydial infection can become an important factor in the pathogenesis of the gastrointestinal tract diseases, which are manifested in the so-called post-infectious period. It is commonly known that chlamydial infection has a tropism to the cylindrical epithelium, which covers the human mucous membrane of the urethra, cervix, rectum, conjunctiva of the eyes and the throat. However, the role of the causative agents of chlamydial infections, such as C. trachomatis and C. pneumoniae, in the occurrence of the gastrointestinal tract diseases has not been studied. In order to study the possible relationship between the gastrointestinal diseases and the presence of chlamydial infection markers, we have selected a group of patients with the gastrointestinal diseases and detected antibodies to C. trachomatis and C. pneumoniae and DNA of these pathogens in blood serum, liver biopsy and bile ducts. As a result, C. trachomatis DNA in blood serum was detected in 50% of cases, and in liver biopsies — in 59.3%. A new approach has been developed in the serological diagnosis of chlamydial infection caused by C. trachomatis, which allowed for revealing diagnostic antibody titers in 51.9% of cases in this group of patients, and in the comparison group — in 11.6% of cases. Among 50% of patients, in whom DNA was revealed in blood serum, it was also revealed in 64.3% of cases in biopsy samples of gastrointestinal organs. Upon detection of C. trachomatis DNA in blood serum, antibodies to the “cultural” antigen were detected in 60.1% of cases, and with the simultaneous detection of C. trachomatis DNA in blood serum and gastrointestinal organs, they were found in 72.2% of cases. Simultaneous detection of C. trachomatis, both in blood serum and in the gastrointestinal tract, may indicate the ability of C. trachomatis to spread hematogenously and infect organs away from the primary focus of infection. The obtained data absolutely require further study in light of the identification of the relationship between the detection of the pathogen and the development of the gastrointestinal pathology. But in general, the results are not yet studied evidence of the possible gastrointestinal organs infection by C. trachomatis.

About the authors

N. E. Bondareva

Gamaleya Research Center of Epidemiology and Microbiology.

Author for correspondence.
Email: nataliia.d@mail.ru

Researcher, Laboratory of Chlamydiosis, Department of Medical Microbiology.

123098, Russian Federation, Moscow, Gamaleya str., 18.

Phone: +7 962 985-07-55 (mobile).

Россия

E. Yu. Morgunova

Gamaleya Research Center of Epidemiology and Microbiology.

Email: fake@neicon.ru

Researcher, Laboratory of Chlamydiosis, Department of Medical Microbiology.

Moscow. Россия

N. A. Zigangirova

Gamaleya Research Center of Epidemiology and Microbiology.

Email: fake@neicon.ru

PhD, MD (Biology), Professor, Head of the Department of Medical Microbiology.

Moscow. Россия

Yu. G. Shapkin

Saratov State Medical University named after V.I. Razumovsky.

Email: fake@neicon.ru

PhD, MD (Medicine), Professor, Honored Physician of the Russian Federation, Head of the Department of General Surgery.

Saratov. Россия

Yu. V. Chalyk

Saratov State Medical University named after V.I. Razumovsky.

Email: fake@neicon.ru

PhD, MD (Medicine), Professor, Professor of the Department of General Surgery.

Saratov. Россия

R. Yu. Chalyk

Saratov City Clinical Hospital No. 6 named after academician V.N. Kosheleva.

Email: fake@neicon.ru

PhD (Medicine), Physician.

Saratov.

Россия

References

  1. Абакарова П.Р. Урогенитальный хламидиоз: принципы диагностики и лечения // Гинекология. 2006. Т. 8, № 2. С. 21–23.
  2. Мавров Г.И. Хламидийные инфекции: биология возбудителей, патогенез, клиника, диагностика, лечение, профилактика. Киев, 2005. 524 с.
  3. Султанахмедов Э.С., Утц С.Р., Салтыков Ю.В., Мотин В.Л., Федорова В.А. Детекция Chlamydia trachomatis в образцах крови как метод диагностики осложненных и персистирующих форм урогенитальной хламидийной инфекции // Саратовский научно-медицинский журнал. 2015. Т. 11, № 3. С. 381–385.
  4. Al-Aydie S.N., Obeidat N.M., Al-Younes H.M. Role of Chlamydia pneumoniae in community-acquired pneumonia in hospitalized Jordanian adults // J. Infect. Dev. Ctries, 2016, vol. 10, no. 3, pp. 227–236. doi: 10.3855/jidc.6590
  5. Bartlett J.G., Breiman R.F., Mandell L.A., Fine T.M. Jr. Community-acquired pneumonia in adults: guidelines for management. Clin. Infect. Dis., 1998, vol. 26, no. 4, pp. 811–838. doi: 10.1086/513953
  6. Beatty W.L., Morrison R.P., Byrne G.I. Persistent chlamydiae: from cell culture to a paradigm for chlamydial pathogenesis. Microbiol. Rev., 1994, vol. 58, no. 4, pp. 686–699.
  7. Blasi F., Damato S., Cosentini R., Tarsia P., Raccanelli R., Centanni S., Allegra L.; Chlamydia InterAction with COPD (CIAC) Study Group. Chlamydia pneumoniae and chronic bronchitis: association with severity and bacterial clearance following treatment. Thorax, 2002, vol. 57, no. 8, pp. 672–676. doi: 10.1136/thorax.57.8.672
  8. Caldwell H.D., Wood H., Crane D., Bailey R., Jones R.B., Mabey D., Maclean I., Mohammed Z., Peeling R., Roshick C., Schachter J., Solomon A.W., Stamm W.E., Suchland R.J., Taylor L., West S.K., Quinn T.C., Belland R.J., McClarty G. Polymorphisms in Chlamydia trachomatis tryptophan synthase genes differentiate between genital and ocular isolates. J. Clin. Invest., 2003, vol. 111, no. 11, pp. 1757–1769. doi: 10.1172/JCI17993
  9. Carter J.D., Inman R.D. Chlamydia-induced reactive arthritis: hidden in plain sight? Best Pract. Res. Clin. Rheumatol., 2011, vol. 25, no. 3, pp. 359–374. doi: 10.1016/j.berh.2011.05.001
  10. Choroszy-Król I., Frej-Mądrzak M., Hober M., Sarowska J., Jama-Kmiecik A. Infections caused by Chlamydophila pneumoniae. Adv. Clin. Exp. Med., 2014, vol. 23, no. 1, pp. 123–126
  11. Dlugosz A., Törnblom H., Mohammadian G., Morgan G., Veress B., Edvinsson B., Sandström G., Lindberg G. Chlamydia trachomatis antigens in enteroendocrine cells and macrophages of the small bowel in patients with severe irritable bowel syndrome. BMC Gastroenterol., 2010, vol. 10: 19. doi: 10.1186/1471-230X-10-19
  12. Francis C., Prior A., Whorwell P.J., Morris J. Chlamydia trachomatis infection: is it relevant in irritable bowel syndrome? Digestion, 1998, vol. 59, no. 2, pp. 157–159. doi: 10.1159/000007481
  13. Haggerty C.L., Gottlieb S.L., Taylor B.D., Low N., Xu F., Ness R.B. Risk of sequelae after Chlamydia trachomatis genital infection in women. J. Infect. Dis., 2010, vol. 201, no. 2, pp. 134–155. doi: 10.1086/652395
  14. Jakus S., Neuer A., Dieterle S., Bongiovanni A.M., Witkin S.S. Antibody to the Chlamydia trachomatis 60 kDa heat shock protein in follicular fluid and in vitro fertilization outcome. Am. J. Reprod. Immunol., 2008, vol. 59, no. 2, pp. 85–89. doi: 10.1111/j.1600- 0897.2007.00539.x
  15. Linhares I.M., Witki S.S. Immunopathogenic consequences of Chlamydia trachomatis 60 kDa heat shock protein expression in the female reproductive tract. Cell. Stress Chaperones, 2010, vol. 15, no. 5, pp. 467–473. doi: 10.1007/s12192-010-0171-4
  16. Mascellino M.T., Ciardi M.R., Oliva A., Cecinato F., Hassemer M.P., Borgese L. Chlamydia trachomatis detection in a population of asymptomatic and symptomatic women: correlation with the presence of serological markers for this infection. New Microbiol., 2008, no. 31, pp. 249–256.
  17. Miyashita N., Fukano H., Yoshida K., Niki Y., Matsushima T. Chlamydia pneumoniae infection in adult patients with persistent cough. J. Med. Microbiol., 2003, no. 52, pp. 265–269.
  18. Neuer A., Lam K.N., Tiller F.W., Kiesel L., Witkin S.S. Humoral immune response to membrane components of Chlamydia trachomatis and expression of the human 60 kDa heat shock protein in follicular fluid of in-vitru fertilization patients. Hum. Reprod., 1997, vol. 12, no. 5, pp. 925–929.
  19. Ondondo B.O., Brunham R.C., Harrison W.G., Kinyari T., Sheth P.M., Mugo N.R., Cohen C.R. Frequency and magnitude of Chlamydia trachomatis elementary body- and heat shock protein 60-stimulated interferon γ responses in peripheral blood mononuclear cells and endometrial biopsy samples from women with high exposure to infection. J. Infect. Dis., 2009, vol. 199, no. 12, pp. 1771–1779. doi: 10.1086/599095
  20. Peeling R.W., Bailey R.L., Conway D.J., Holland M.J., Campbell A.E., Jallow O., Whittle H.C., Mabey C.W. Antibody response to the 60-kDa chlamydial heat-shock protein is associated with scarring trachoma. J. Infect. Dis., 1998, vol. 177, no. 1, pp. 256–259. doi: 10.1086/517367
  21. Peipert J.F. Clinical practice. Genital chlamydial infections. N. Engl. J. Med., 2003, vol. 349, no. 25, pp. 2424–2430. doi: 10.1056/ NEJMcp030542
  22. Persson К., Boman J. Comparison of five serologic tests for diagnosis of acute infections by Chlamydia pneumoniae. Clin. Diagn. Lab. Immunol., 2000, vol. 7, no. 5, pp. 739–740.
  23. Rank R.G., Yeruva L. Hidden in plain sight: chlamydial gastrointestinal infection and its relevance to persistence in human genital infection. Infect. Immun., 2014, vol. 82, no. 4, pp. 1362–1371. doi: 10.1128/IAI.01244-13
  24. Schachter J., Moncada J., Liska S., Shayevich C., Klausner J.D. Nucleic acid amplification tests in the diagnosis of chlamydial and gonococcal infections of the oropharynx and rectum in men who have sex with men. Sex. Transm. Dis., 2008, vol. 35, no. 7, pp. 637–642. doi: 10.1097/OLQ.0b013e31817bdd7e
  25. Seraceni S., De Seta F., Colli C., Del Savio R., Pesel G., Zanin V., D’Agaro P., Contini C., Comar M. High prevalence of HPV multiple genotypes in women with persistent chlamydia trachomatis infection. Infect. Agent. Cancer, 2014, vol. 9: 30. doi: 10.1186/1750- 9378-9-30
  26. Skilton R.J., Cutcliffen L.T., Barlow D., Wang Y., Salim O., Lambden P.R., Clarke I.N. Penicillin induced persistence in Chlamydia trachomatis: high quality time lapse video analysis of the developmental cycle. PLoS ONE, 2009, vol. 4, no. 11: e7723. doi: 10.1371/ journal.pone.0007723
  27. Smith-Norowitz T.A., Chotikanatis K., Erstein D.P., Perlman J., Norowitz Y.M., Joks R., Durkin H.G., Hammerschlag M.R., Kohlhoff S. Chlamydia pneumoniae enhances the Th2 profile of stimulated peripheral blood mononuclear cells from asthmatic patients. Hum. Immunol., 2016, vol. 77, no. 5, pp. 382–388. doi: 10.1016/j.humimm.2016.02.010
  28. Tiitinen A., Surcel H.M., Halttunen M., Birkelund S., Bloigu A., Christiansen G., Koskela P., Morrison S.G., Morrison R.P., Paavonen J. Chlamydia trachomatis and chlamydial heat shock protein 60-specific antibody and cell-mediated responses predict tubal factor infertility. Hum. Reprod., 2006, vol. 21, no. 6, pp. 1533–1538. doi: 10.1093/humrep/del014
  29. Zigangirova N.A., Rumyantseva Y.P., Morgunova E.Y., Kapotina L.N., Didenko L.V., Kost E.A., Koroleva E.A., Bashmakov Y.K., Petyaev I.M. Detection of C. trachomatis in the serum of the patients with urogenital chlamydiosis. Biomed. Res. Int., 2013, 7 p. doi: 10.1155/2013/489489

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Copyright (c) 2018 Bondareva N.E., Morgunova E.Y., Zigangirova N.A., Shapkin Y.G., Chalyk Y.V., Chalyk R.Y.

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