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Genotypic Diversity of Hepatitis C Virus in Tuberculosis Patients in the Tomsk Region

https://doi.org/10.31631/2073-3046-2025-24-1-42-49

Abstract

Relevance. People with tuberculosis (TB) are at an increased risk of spreading parenteral viral hepatitis, including hepatitis C virus (HCV). Hepatitis C in tuberculosis patients can often be detected only as a result of laboratory tests. Some of the anti-tuberculosis drugs have a pronounced hepatotoxic effect, which can lead to severe liver damage, especially in cases of combined TB and HCV infection.
Aim. Determination of genotypic diversity and molecular genetic characteristics of HCV isolates isolated from patients infected with tuberculosis in the Tomsk region.
Materials and methods. The study was conducted on 117 blood serum/plasma samples obtained from patients infected with tuberculosis. The identified HCV isolates were genotyped by amplifying a fragment of the core gene in two-round PCR followed by determination of the nucleotide sequences of the resulting amplicons. Viral load was determined by quantitative RT-PCR.
Results and discussion. The following distribution of subtypes in the studied sample was revealed: 1b (47.0%; 95% CI: 38.2–56.0), 3a (32.5%; 95% CI: 24.7–41.3), 1a (18.0%; 95% CI: 12.1–25.8) and recombinant 2k/1b (2.5%; 95% CI: 0.9–7.2). Among the variants of subtype 1b, polymorphisms in the core gene were identified, associated with resistance to interferon treatment: among 35 isolates, the L91M mutation was detected (63.6%; 95% CI: 31.4–56.7), substitutions at position R70Q were detected in 19 isolates /H (34.6%; 95% CI: 7.6–26.1). Both substitutions were found in 11 isolates (20.0%; 95% CI: 11.5–32.3). No differences were found in the distribution of subtypes between the four age groups (under 36, 36–40, 41–45, over 45). Significant differences were revealed (Pearson's χ² = 9.38; p = 0.025) in the distribution of subtypes between the examined men and women. In men, subtype 1b predominated, in women, subtype 3a predominated and there were practically no people infected with subtype 1a, unlike male patients.
Conclusion. HCV research among tuberculosis-infected people is important for choosing the most appropriate treatment tactics for patients, preventing complications of co-infection, as well as for planning and implementing preventive measures.

About the Authors

K. A. Svirin
State Research Center of Virology and Biotechnology VECTOR
Russian Federation

Kirill A. Svirin

Koltsovo

+7 (960) 977-98-06



O. G. Polovkova
Tomsk Phthisiopulmonological Medical Center
Russian Federation

Oksana G. Polovkova

Tomsk

+7 (960) 977-98-06



E. S. Fedorova
Tomsk Phthisiopulmonological Medical Center
Russian Federation

Elena S. Fedorova

Tomsk

+7 (913) 770-73-20



M. N. Kamalov
Tomsk Phthisiopulmonological Medical Center
Russian Federation

Mikhail N. Kamalov

Tomsk

+7 (923) 409-10-00



A. S. Zheleznova
State Research Center of Virology and Biotechnology VECTOR
Russian Federation

Alina S. Zheleznova

Koltsovo

+7 (953) 878-14-66



M. Yu. Kartashov
State Research Center of Virology and Biotechnology VECTOR
Russian Federation

Mikhail Yu. Kartashov

Koltsovo

+7 (923) 419-31-92



References

1. Ballester-Ferré M.P., Martínez F., Garcia-Gimeno N., et al. Miliary tuberculosis infection during hepatitis C treatment with sofosbuvir and ledipasvir plus ribavirin. World Journal of Hepatology. 2017;9(3):161–166. doi: 10.4254/wjh.v9.i3.161

2. Tuberculosis in Russian Federation [Internet]. World Health Organization. Available at: https://worldhealthorg.shinyapps.io/TBrief/?_inputs_&entity_type=%22country%22&iso2=%22RU%22&sidebarCollapsed=true&sidebarItemExpanded=null. Accessed: 24 June 2024.

3. Hepatitis C [Internet]. World Health Organization. Available at: https://www.who.int/news-room/fact-sheets/detail/hepatitis-c. Accessed: 24 June 2024.

4. Ivashkin V.T., Chulanov V.P., Mamonova N.A., et al. Klinicheskie rekomendatsii Rossiiskogo obshchestva po izucheniyu pecheni, Rossiiskoi gastroenterologicheskoi assotsiatsii, Natsionalnogo nauchnogo obshchestva infektsionistov po diagnostike i lecheniyu khronicheskogo virusnogo gepatita C. Rossijskij žurnal gastroènterologii, gepatologii, koloproktologii. 2023;33(1):84–124 (In Russ). doi: 10.22416/1382-4376-2023-33-1-84-124

5. Solovev D.V. Epidemiologicheskie osobennosti virusnykh gepatitov B i C u bolnykh tuberkulezom legkikh m i taktika ikh profilaktiki [dissertation]. Moscow; 2012. (In Russ).

6. Asratyan A.A., Solovev D.V., Rusakova E.V. Sovremennaya epidemicheskaya situatsiya po zabolevaemosti virusnymi gepatitami i tuberkulezom v Moskve. Èpidemiologiâ i vakcinoprofilaktika. 2015;14(3):42–48 (In Russ). doi: 10.31631/2073-3046-2015-14-3-42-48

7. Manca C., Tsenova L., Bergtold A., et al. Virulence of a Mycobacterium tuberculosis clinical isolate in mice is determined by failure to induce Th1 type immunity and is associated with induction of IFN-alpha/beta. Proceedings of the National Academy of Science USA. 2001;98(10):5752–5757. doi: 10.1073/pnas.091096998

8. Kempker R.R., Alghamdi W.A., Al-Shaer M.H., et al. A Pharmacology Perspective on Simultaneous Tuberculosis and Hepatitis C Treatment. Antimicrobial Agents and Chemotherapt. 2019;63(12):e01215–e01219. doi: 10.1128/aac.01215-19

9. Olaru I.D., Beliz Meier M., Mirzayev F., et al. Global prevalence of hepatitis B or hepatitis C infection among patients with tuberculosis disease: systematic review and metaanalysis. ClinicalMedicine. 2023;58:101938. doi: 10.1016/j.eclinm.2023.101938

10. Kim W.S., Lee S.S., Lee C.M., et al. Hepatitis C and not Hepatitis B virus is a risk factor for anti-tuberculosis drug induced liver injury. BMC Infectious Diseases. 2016;16:50. doi: 10.1186/s12879-016-1344-2

11. Ungo J.R., Jones D., Ashkin D., et al. Antituberculosis drug-induced hepatotoxicity. The role of hepatitis C virus and the human immunodeficiency virus. American Journal of Respiratory and Critical Care Medicine. 1998;157(6 Pt 1):1871–1876. doi: 10.1164/ajrccm.157.6.9711039

12. Lin S.Y., Chen T.C., Lu P.L., et al. Incidence rates of tuberculosis in chronic hepatitis C infected patients with or without interferon based therapy: a population-based cohort study in Taiwan. BMC Infectious Diseases. 2014;14:705. doi: 10.1186/s12879-014-0705-y

13. Zein N.N. Clinical significance of hepatitis C virus genotypes. Clinical Microbiology Reviews. 2000;13(2):223–235. doi: 10.1128/CMR.13.2.223

14. Probst A., Dang T., Bochud M., et al. Role of Hepatitis C virus genotype 3 in liver fibrosis progression – a systematic review and meta-analysis. Journal of Viral Hepatitis. 2011;18(11):745–759. doi: 10.1111/j.1365-2893.2011.01481.x

15. Poynard T., Marcellin P., Lee S.S., et al. Randomised trial of interferon alpha2b plus ribavirin for 48 weeks or for 24 weeks versus interferon alpha2b plus placebo for 48 weeks for treatment of chronic infection with hepatitis C virus. International Hepatitis Interventional Therapy Group (IHIT). Lancet. 1998;352(9138):1426–1432. doi: 10.1016/s0140- 6736(98)07124-4

16. Srednevzveshennaya stoimost skhemy lecheniya gepatita S sostavlyaet 300—400 tys. rublei [Internet]. Farmatsevticheskii Vestnik. Available at: https://pharmvestnik.ru/content/news/Srednevzveshennaya-stoimost-shemy-lecheniya-gepatita-S-sostavlyaet-300-400-tys-rublei.html. Accessed: 24 June 2024.

17. Akimov I.A., Timofeev D.I., Mavzyutov A.R., et al. Vyyavlenie tsirkuliruyushchei rekombinantnoi formy RF1_2k/1b virusa gepatita C v syvorotke krovi patsientov metodom OT-PСR v rezhime realnogo vremeni. Klinicheskaya laboratornaya diagnostika. 2021;66(2):122–128. (In Russ). doi: 10.51620/0869-2084-2021-66-122-128

18. Esteban J.I., Sauleda S., Quer J. The changing epidemiology of hepatitis C virus infection in Europe. Journal of Hepatology. 2008;48(1):148–162. doi: 10.1016/j.jhep.2007.07.033

19. Pimenov N., Kostyushev D., Komarova S., et al. Epidemiology and Genotype Distribution of Hepatitis C Virus in Russia. Pathogens. 2022;11(12):1482. doi: 10.3390/pathogens11121482

20. Kichatova V.S., Kyuregyan K.K., Soboleva N.V., et al. Frequency of Interferon-Resistance Conferring Substitutions in Amino Acid Positions 70 and 91 of Core Protein of the Russian HCV 1b Isolates Analyzed in the T-Cell Epitopic Context. Journal of Immunology Research. 2018;2018:7685371. doi: 10.1155/2018/7685371

21. Chida T., Watanabe S., Ohta K., et al. Impact of amino acid substitutions in hepatitis C virus core region on the severe oxidative stress. Free Radical Biology and Medicine. 2024;212:199–206. doi: 10.1016/j.freeradbiomed.2023.12.014


Review

For citations:


Svirin K.A., Polovkova O.G., Fedorova E.S., Kamalov M.N., Zheleznova A.S., Kartashov M.Yu. Genotypic Diversity of Hepatitis C Virus in Tuberculosis Patients in the Tomsk Region. Epidemiology and Vaccinal Prevention. 2025;24(1):42-49. (In Russ.) https://doi.org/10.31631/2073-3046-2025-24-1-42-49

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ISSN 2073-3046 (Print)
ISSN 2619-0494 (Online)