Epidemiological significance of home environment for cystic fibrosis patients with Pseudomonas aeruginosa lung infections
https://doi.org/10.66825/2949-4664-apps-3-3-26-37
Abstract
Background. For patients with cystic fibrosis (CF), respiratory tract infections caused by Pseudomonas aeruginosa, S. aureus, B. cepacia complex, and other non-fermenting bacteria (NGOs) are significant risk factors. Insufficient disinfection of environmental objects and care items used by children suffering from cystic fibrosis, as well as the circulation of pathogens in the home environment, can lead to reinfection and superinfection.
Objective. To determine the epidemiological significance of the home environment in the transmission of P. aeruginosa bacteria to children with CF and to evaluate the effectiveness of preventive measures at home.
Materials and methods. The living conditions of 27 children with CF with a chronic lung infection caused by P. aeruginosa and their families were assessed. A total of 265 samples collected from home environmental objects were analyzed. Surface samples were collected using swabs. The study was conducted using bacteriological and molecular genetic methods.
Results. An analysis of questionnaires revealed that 26% of families of children with CF did not use detergents or disinfectants to care for their inhalers. 41% of families did not adhere to the specified time (schedule) for sink disinfection. 83% of bathroom sinks were contaminated with microorganisms. Among the isolated microorganisms, the rate of P. aeruginosa isolation was 20%. Monitoring of the home environment revealed that sink drains were the main reservoirs of P. aeruginosa. Pseudomonas aeruginosa contamination of nebulizer masks and toothbrushes was also detected. PCR data obtained from studying P. aeruginosa isolates from different objects indicate the possibility of the circulation of a single genotype in the home environment. The effectiveness of preventive measures for disinfecting nebulizers and sinks was established to be insufficient. After disinfection, opportunistic pathogens were isolated from 22% of nebulizer surfaces. A. lwoffii, Aspergillus niger, Candida albicans, and S. aureus were isolated from nebulizer compressor filters and toothbrushes. These bacteria can infect the lungs of patients with CF, including in association with P. aeruginosa.
Conclusion. Control over microbiological risks in the home environment, including regular monitoring and strict protocols for the treatment of key objects, should be mandatory for patients with CF to achieve eradication of lung pathogens.
About the Authors
E. A. SiyanovRussian Federation
Ekaterina A. Siyanova, Cand. Sci. (Biol.), Researcher, Laboratory of Molecular Epidemiology of Nosocomial Infections
18 Gamaleya str., Moscow, 123098
Competing Interests:
The authors declare no conflict of interest
M. Yu. Chernukha
Russian Federation
Marina Yu. Chernukha, Dr. Sci. (Med.), Head of Laboratory of Molecular Epidemiology of Nosocomial Infections; Senior Researchers, Scientific Research Clinical Institute of Childhood
18 Gamaleya str., Moscow, 123098; 62 Bolshaya Serpukhovskaya str., Moscow, 115093
Competing Interests:
The authors declare no conflict of interest
L. R. Avetisyan
Russian Federation
Lusine R. Avetisyan, Dr. Sci. (Med.), Leading Researcher, Laboratory of Molecular Epidemiology of Nosocomial Infections
18 Gamaleya str., Moscow, 12309
Competing Interests:
The authors declare no conflict of interest
O. S. Medvedeva
Russian Federation
Olga S. Medvedeva, Junior Researcher, Laboratory of Molecular Epidemiology of Nosocomial Infections
18 Gamaleya str., Moscow, 123098
Competing Interests:
The authors declare no conflict of interest
A. Yu. Voronkova
Russian Federation
Anna Yu. Voronkova, Cand. Sci. (Med.), Leading Researcher, Scientific and Clinical Department of Cystic Fibrosis; Pediatrician, Cystic Fibrosis Department
1 Moskvorechye str., Moscow, 115522; 62 Bolshaya Serpukhovskaya str., Moscow, 115093
Competing Interests:
The authors declare no conflict of interest
E. I. Kondratieva
Russian Federation
Elena I. Kondrateva, Dr. Sci. (Med.), Prof., Head of Scientific Department of Cystic Fibrosis; Vice-Director for Research, Head of the Center for Hereditary Lung Diseases
1 Moskvorechye str., Moscow, 115522; 62 Bolshaya Serpukhovskaya str., Moscow, 115093
Competing Interests:
The authors declare no conflict of interest
E. M. Burmistrov
Russian Federation
Egor M. Burmistrov, Research Scientist, Laboratory of Molecular Epidemiology of Nosocomial Infections
18 Gamaleya str., Moscow, 123098
Competing Interests:
The authors declare no conflict of interest
N. B. Polyakov
Russian Federation
Nikita B. Polyakov, Researcher, Laboratory of Indication and Ultrastructural Analysis of Microorganisms
18 Gamaleya str., Moscow, 123098
Competing Interests:
The authors declare no conflict of interest
A. I. Solovyev
Russian Federation
Andrey I. Solovyev, Dr. Sci. (Biol.), Researcher, Laboratory of Indication and Ultrastructural Analysis of Microorganisms
18 Gamaleya str., Moscow, 123098
Competing Interests:
The authors declare no conflict of interest
V. G. Zhukhovitsky
Russian Federation
Vladimir G. Zhukhovitsky, Cand. Sci. (Med.), Head of Laboratory of Indication and ltrastructural Analysis of Microorganisms; Assoc. Prof., Department of Biochemistry and Immunopathology
18 Gamaleya str., Moscow, 123098
2/1, 1 Barrikadnaya str., Moscow, 125993
Competing Interests:
The authors declare no conflict of interest
E. K. Zhekayte
Russian Federation
Elena K. Zhekayte, Cand. Sci. (Med.), Senior Researcher, Department of Cystic Fibrosis, Scientific and Clinical Department of Cystic Fibrosis; Department of Cystic Fibrosis, Scientific
1 Moskvorechye str., Moscow, 11552; 62 Bolshaya Serpukhovskaya str., Moscow, 115093
Competing Interests:
The authors declare no conflict of interest
References
1. Cystic Fibrosis. 2nd edition, revised and supplemented (edited by N. Yu. Kashirskaya, N.I. Kapranov, and E.I. Kondratyeva). Moscow: MEDPRAKTIKA-M Publishing House, 2021, 680 p. (In Russ.). https://www.medpractika.ru/books/new/?id=316
2. Avetisyan L.R., Chernukha M. Yu., Burmistrov E.M., Siyanova E.A., et al. Adaptation of Staphylococcus aureus, Pseudomonas aeruginosa, Burkholderia cepacia complex, and Achromobacter spp. bacteria during chronic lung infection in patients with cystic fibrosis. Bulletin of the Orenburg Scientific Center. 2023(2). (In Russ.). doi: 10.24411/2304-9081-2023-12002.
3. Shaginyan I.A., Avetisyan L.R., Chernukha M. Yu., Siyanova E.A., et al. Epidemiological significance of genome variations in Pseudomonas aeruginosa causing chronic lung infection in patients with cystic fibrosis. CMAC. 21(4):340–351. (In Russ.). doi: 10.36488/cmac.2019.4.340-351.
4. Siyanova E.A., Chernuha M. Yu., Avetisyan L.R, et al. Monitoring of chronic lung infection in patients with cystic fibrosis caused by Pseudomonas аeruginosa. Pediatria n. a. G.N. Speransky. 2018;97(2):77–86. (In Russ.). https://cyberleninka.ru/article/n/monitoring-hronicheskoy-infektsii-legkihu-bolnyh-mukovistsidozom-vyzvannoy-bakteriyamipseudomonas-aeruginosa
5. Medical microbiology / Pokrovsky V.I. 4th ed., stereot. M.: GEOTAR Media, 2010. 768 р. (In Russ.).
6. Bergan T. Pathogenetic factors of Pseudomonas aeruginosa. Scandinavian journal of infectious diseases.1981;29:7–12. https://pubmed.ncbi.nlm.nih.gov/6797059/
7. Silva M.E., Filho I.C., Endo E.H., et аl. Characterisation of potential virulence markers in Pseudomonas aeruginosa isolated from drinking water. Antonie Van Leeuwenhoek. 2008;93(4):323–334. doi: 10.1007/s10482-007-9209-8.
8. Crone S., Vives-Florez M., Kvich L., et al. The environmental occurrence of Pseudomonas aeruginosa. APMIS.2020;128(3):220–231. doi: 10.1111/apm.13010.
9. Vorobyev A.A. Microbiology / Vorobyov A.A., Bykov A.S., Pashkov E.P., Rybakova A.M. 2nd ed. M.: Medicine 2003. 335 р. (In Russ.).
10. Nesse L.L., Simm R. Biofilm: A hotspot for emerging bacterial genotypes. Adv. Appl. Microbiol. 2018;103:223– 246. doi: 10.1016/bs.aambs.2018.01.003.
11. Moradali M.F., Ghods S., Rehm B.H. Pseudomonas aeruginosa Lifestyle: A Paradigm for Adaptation, Survival, and Persistence. Front Cell Infect Microbiol. 2017;7:39. Published 2017 Feb 15. doi: 10.3389/fcimb.2017.00039.
12. Boyle M., Ford T., Maki J.S., et al. Biofilms and the survival of opportunistic pathogens in recycled water. Waste Manag Res. 1991;9(5):465–470. doi: 10.1177/0734242X9100900165.
13. Schelstraete P., Van Daele S., De Boeck K., et al. Pseudomonas aeruginosa in the home environment of newly infected cystic fibrosis patients. Eur Respir J. 2008;31(4):822–829. doi: 10.1183/09031936.00088907.
14. Regnath T., Kreutzberger M., Illing S., et аl. Prevalence of Pseudomonas aeruginosa in households of patients with cystic fibrosis. Int J Hyg Environ Health. 2004;207(6):585–588. doi: 10.1078/1438-4639-00331.
15. Purdy-Gibson M.E., France M., Hundley T.C., et аl. Pseudomonas aeruginosa in CF and non-CF homes is found predominantly in drains. J Cyst Fibros. 2015;14(3):341–346. doi: 10.1016/j.jcf.2014.10.008
16. Kondratenko O.V. Impact of microflora of environmental medium on ambulatory airway colonization in patients with cystic fibrosis. Ulyanovsk Medico-¬biological Journal. 2018;4:156–164. (In Russ.). https://cyberleninka.ru/article/n/otsenka-vliyaniyamikroflory-obektov-okruzhayuschey-sredy-na-vozmozhnost-vnestatsionarnoy-kolonizatsii-dyhatelnyh-putey-patsientov-s (available at: 16.01.2026).
17. Guidelines. MUK 4.2.2942–11 Methods of Sanitary and Bacteriological Studies of Environmental Objects, Air, and Sterility Control in Healthcare Facilities. (In Russ.).
18. Chernukha M. Yu., Avetisyan L.R., Shaginyan I.A., et al. Microbiological diagnosis algorithm for chronic lung infection in Patients with Cystic Fibrosis. Clinical Microbiology and Antimicrobial Chemotherapy. 2014;16(4):312–324. (In Russ.). https://cyberleninka.ru/article/n/algoritm-mikrobiologicheskoy-diagnostikihronicheskoy-infektsii-lyogkih-u-bolnyh-mukovistsidozom
19. Curran B., Jonas D., Grundmann H., et al. Development of a multilocus sequence typing scheme for the opportunistic pathogen Pseudomonas aeruginosa. J Clin Microbiol. 2004;42(12):5644–5649. doi: 10.1128/JCM.42.12.5644-5649.2004.
20. The Main Site PubMLST at the Department of Biology, Oxford University, Great Britain Public databases for molecular typing and microbial genome diversity. https://www.pubmlst.org
21. Lee A.C., Jones A.L. Multi-resistant Pseudomonas aeruginosa ST235 in cystic fibrosis. Paediatr Respir Rev. 2018;27:18–20. doi: 10.1016/j.prrv.2018.05.009.
22. Treepong P., Kos V.N., Guyeux C., et al. Global emergence of the widespread Pseudomonas aeruginosa ST235 clone. Clin Microbiol Infect. 2018;24(3):258–266. doi: 10.1016/j.cmi.2017.06.018.
23. Chichon G., Lopez M., de Toro M., et al. Spread of Pseudomonas aeruginosa ST274 Clone in Different Niches: Resistome, Virulome, and Phylogenetic Relationship. Antibiotics (Basel, Switzerland). 2023;12(11):1561. doi: 10.3390/antibiotics12111561.
24. Ocampo-Sosa A.A., Fernandez-Martinez M., Cabot G., et al. Draft Genome Sequence of the Quorum-Sensing and Biofilm-Producing Pseudomonas aeruginosa Strain Pae221, Belonging to the Epidemic High-Risk Clone Sequence Type. Genome Announc. 2015;3: e01343–14. doi: 10.1128/genomeA.01343-14.
25. Nageeb W., Amin D.H., Mohammedsaleh Z.M., et al. Novel Molecular Markers Linked to Pseudomonas aeruginosa Epidemic High-Risk Clones. Antibiotics. 2021;10:35. doi: 10.3390/antibiotics10010035.
26. Ahmed M.A.S., Hadi H.A., Abu Jarir S., et al. Prevalence and microbiological and genetic characteristics of multidrug-resistant Pseudomonas aeruginosa over three years in Qatar. Antimicrob. Steward. Healthc. Epidemiol. 2022;2: e96. doi: 10.1017/ash.2022.226.
27. Cortes-Lara S., del Barrio-Tofino E., Lopez-Causape C., et al Predicting Pseudomonas aeruginosa susceptibility phenotypes from whole genome sequence resistome analysis. Clin. Microbiol. Infect. 2021;27:1631–1637. doi: 10.1016/j.cmi.2021.05.011.
28. Bocharova Y.A., Savinova T.A., Lyamin A.V., et al. Genome features and antibiotic resistance of Pseudomonas aeruginosa strains isolated in patients with cystic fibrosis in the Russian Federation. Russ. Clin. Lab. Diagn. 2021;66:629– 634. doi: 10.51620/0869-2084-2021-66-10-629-634.
29. Van Mansfeld R., Willems R., Brimicombe R., et al. Pseudomonas aeruginosa genotype prevalence in Dutch cystic fibrosis patients and age dependency of colonization by various P. aeruginosa sequence types. J. Clin. Microbiol. 2009;47:4096–4101. doi: 10.1128/JCM.01462-09.
30. Mitchelmore P.J., Randall J., Bull M.J., et al. Molecular epidemiology of Pseudomonas aeruginosa in an unsegregated bronchiectasis cohort sharing hospital facilities with a cystic fibrosis cohort.2017;73:677–679. doi: 10.1136/thoraxjnl-2016-209889.
Review
For citations:
Siyanov E.A., Chernukha M.Yu., Avetisyan L.R., Medvedeva O.S., Voronkova A.Yu., Kondratieva E.I., Burmistrov E.M., Polyakov N.B., Solovyev A.I., Zhukhovitsky V.G., Zhekayte E.K. Epidemiological significance of home environment for cystic fibrosis patients with Pseudomonas aeruginosa lung infections. Archives of Pediatrics and Pediatric Surgery. 2025;3(3):26-37. (In Russ.) https://doi.org/10.66825/2949-4664-apps-3-3-26-37
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