Preview

Astrakhan medical journal

Advanced search

Regional features of the circulation of micro-organisms of representatives of the order Enterobacterales in neonatology hospitals

https://doi.org/10.17021/1992-6499-2026-2-99-108

Abstract

Antibiotic resistance is one of the most serious threats to global health in the modern world. In the context of all these events, the growing number of infectious diseases caused by polyresistant strains of microorganisms in neonatology departments is of particular concern. Escherichia coli and Klebsiella pneumoniae belong to the “ESKAPE” group of pathogens. This group is included in the priority list in the fight against their growing resistance, since “ESKAPE” pathogens are most often found as the causative agent of healthcare-associated infections and in neonatal intensive care units. Goal. Assessment of antibiotic resistance of E. coli and K. pneumoniae microorganisms in neonatal intensive care units in Volgograd. Materials and methods. The work was carried out in the clinic of “Family Medicine” in Volgograd. The material for the study was smears from the pharynx, feces, blood, urine of newborns from 4 days to 4 months. Identification of microorganisms and determination of the sensitivity of bacteria to antimicrobial drugs were performed using a bacteriological automatic analyzer. Results. As a result of the study, it was found that K. pneumoniae exhibits absolute resistance (100 %) to most common classes of antibiotics, including beta-lactams (for example, cephalosporins of the first generation, cefepime, ceftriaxone), aminoglycosides (gentamicin, amikacin), fluoroquinolones (ciprofloxacin, levofloxacin) and even some carbapenems (ertapenem). E. coli showed complete resistance (100 %) to a number of important groups of antibiotics, including second-generation cephalosporins (cefazolin, cefuroxime), aminoglycosides (gentamicin, amikacin), fluoroquinolones (ciprofloxacin, levofloxacin) and carbapenems (ertapenem). Conclusion. The vast majority of K. pneumoniae strains are absolutely resistant to a number of broad-spectrum antibiotics, including penicillins, cephalosporins, aminoglycosides, and fluoroquinones. Moreover, despite the relatively lower excretion of E. coli, this microorganism is also characterized by a high level of resistance to key antibiotics.

About the Authors

V. A. Kosov
Volgograd State Medical University
Russian Federation

Vyacheslav A. Kosov - Assistant of the Department, Volgograd State Medical University.

Volgograd



I. S. Stepanenko
Volgograd State Medical University
Russian Federation

Irina S. Stepanenko - Dr. Sci. (Med.), Associate Professor, Head of the Department, Volgograd State Medical University.

Volgograd



M. R. Kitsenko
Volgograd State Medical University
Russian Federation

Mikhail R. Kitsenko - Assistant of the Department, Volgograd State Medical University.

Volgograd



R. A. Kuznetsov
Volgograd State Medical University
Russian Federation

Roman A. Kuznetsov - postgraduate student, Volgograd State Medical University.

Volgograd



References

1. World Health Organization. Global antimicrobial resistance and use surveillance system (GLASS) report 2022. World Health Organization, 2022.

2. Ivanova M. V. Optimizatsiya epidemiologicheskogo nadzora za vnutriutrobnymi infektsiyami i infektsiyami, svyazannymi s okazaniem meditsinskoy pomoshchi u novorozhdennykh = Optimization of epidemiological surveillance of intrauterine infections and infections related to the provision of medical care in newborns. Moscow; 2021. 24 p. (In Russ.).

3. Swartz E. P., Rohde P. A. Klebsiella (Friedländer’s Bacillus) infections in an army hospital. American Journal of Clinical Pathology. 1946; 16 (2): 88–97.

4. Mukherjee S., Mitra S., Dutta S., Basu S. Neonatal sepsis: the impact of carbapenem-resistant and hypervirulent Klebsiella pneumonia. Frontiers in Medicine. 2021; 8: 634349.

5. Mukherjee S., Bhadury P., Mitra S., Naha S., Saha B., Dutta S., Basu S. Hypervirulent Klebsiella pneumoniae causing neonatal bloodstream infections: emergence of NDM-1-producing hypervirulent ST11-K2 and ST15-K54 strains possessing pLVPK-associated markers. Microbiology Spectrum. 2023; 11 (2): e04121-22.

6. Merino S., Camprubí S., Albertí S., Benedí V. J., Tomas J. Mechanisms of Klebsiella pneumoniae resistance to complement-mediated killing. Infection and immunity. 1992; 60 (6): 2529–2535.

7. Chebotar I. V., Bocharova Yu. A., Podoprigora I. V., Shagin D. A. Why Klebsiella pneumoniae is becoming a leading opportunistic pathogen. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya = Clinical Microbiology and antimicrobial chemotherapypiya. 2020; 22 (1): 4–19 (In Russ.).

8. Nasrollahian S., Graham J. P., Halaji M. A review of the mechanisms that confer antibiotic resistance in pathotypes of E. coli. Frontiers in Cellular and Infection Microbiology. 2024; 14: 1387497.

9. Pakbin B., Brück W. M., Rossen J. W. A. Virulence factors of enteric pathogenic Escherichia coli: A review. International Journal of Molecular Sciences. 2021; 22 (18): 9922.

10. Jiménez-Rojas V., Villanueva-García D., Miranda-Vega A. L., Aldana-Vergara R., Aguilar-Rodea P., López-Marceliano B., Reyes-López A., Alcántar-Curiel M. D. Gut colonization and subsequent infection of neonates caused by extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumonia. Frontiers in Cellular and Infection Microbiology. 2024; 13: 1322874.

11. Roy S., Gaind R., Chellani H., Mohanty S., Datta S., Singh A. K., Basu S. Neonatal septicaemia caused by diverse clones of Klebsiella pneumoniae & Escherichia coli harbouring blaCTX-M-15. Indian Journal of Medical Research. 2013; 137 (4): 791–799.

12. Zarras C., Iosifidis E., Simitsopoulou M., Pappa S., Kontou A., Roilides E., Papa A. Neonatal Bloodstream Infection with Ceftazidime-Avibactam-Resistant bla KPC-2-Producing Klebsiella pneumoniae Carrying bla VEB-25. Antibiotics. 2023; 12 (8): 1290.

13. Carattoli A., Hasman H. PlasmidFinder and in silico pMLST: identification and typing of plasmid replicons in whole-genome sequencing (WGS). Horizontal gene transfer: methods and protocols. 2020: 285–294.

14. Kosov V.A., Stepanenko I.S., Timofeeva A.S., Mikhailova L.V., Solovyova A.A. Study of local features of antibiotic sensitivi ty of hospital strains of microorganisms. Problemy meditsinskoy mikologii = Problem in medical mycology. 2024; 26 (2): 147–148 (In Russ.).

15. Kozlov R. S., Palagin I. S., Ivanchik N. V., Trushin I. V., Dekhnich A. V., Edelstein M. V., Perepanova T. S. and «DARMIS – 2023» Study Group. National monitoring of antibiotic resistance of pathogens causing communityacquired urinary tract infections in Russia: results of the multicenter epidemiological study “DARMIS – 2023”. Klinicheskaya mikrobiologiya i antimikrobnaya khimioterapiya = Clinical Microbiology and antimicrobial chemotherapypiya. 2024; 26 (3): 328–337 (In Russ.).

16. Boronina L. G., Kochneva N. A., Samatova E. V., Asnovskaya A. G., Ustuygova S. S., Panova S. A., Stepanova A. Yu., Zakharchuk K. V. Comparative characteristics of bacterial pathogens isolated from patients in ICU reservation departments of children’s hospital. Klinicheskaya laboratornaya diagnostika = Clinical laboratory diagnostics. 2024; 69 (5): 215–221 (In Russ.).

17. Sherif M., Abera D., Desta K. Prevalence and antibiotic resistance pattern of bacteria from sepsis suspected neonates at St. Paul’s Hospital Millennium Medical College, Addis Ababa, Ethiopia. BMC pediatrics. 2023; 23 (1): 575.


Review

For citations:


Kosov V.A., Stepanenko I.S., Kitsenko M.R., Kuznetsov R.A. Regional features of the circulation of micro-organisms of representatives of the order Enterobacterales in neonatology hospitals. Astrakhan medical journal. 2026;21(2):99-108. (In Russ.) https://doi.org/10.17021/1992-6499-2026-2-99-108

Views: 174

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1992-6499 (Print)