Gut microbiota composition in recurrent acute otitis media: a cross-sectional observational study
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, pozorovací studie
Grantová podpora
ARIS SF Infrastructure core activity
Javna Agencija za Raziskovalno Dejavnost RS
PubMed
38837014
PubMed Central
PMC11485140
DOI
10.1007/s12223-024-01174-z
PII: 10.1007/s12223-024-01174-z
Knihovny.cz E-zdroje
- Klíčová slova
- Turicibacter, Gut microbiota, Metagenomics, Nasopharynx, Recurrent acute otitis media,
- MeSH
- akutní nemoc MeSH
- Bacteria * klasifikace genetika izolace a purifikace MeSH
- dítě MeSH
- feces mikrobiologie MeSH
- kojenec MeSH
- lidé MeSH
- nazofarynx mikrobiologie MeSH
- otitis media * mikrobiologie MeSH
- předškolní dítě MeSH
- prospektivní studie MeSH
- průřezové studie MeSH
- recidiva MeSH
- RNA ribozomální 16S * genetika MeSH
- střevní mikroflóra * MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mužské pohlaví MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- Názvy látek
- RNA ribozomální 16S * MeSH
Recurrent acute otitis media (rAOM) poses a significant challenge in children aged 1 to 6 years, characterized by frequent and treatment-resistant ear infections. While existing studies predominantly focus on alterations in the nasopharyngeal microbiome associated with rAOM, our research explores the understudied association with the gut microbiome. In this cross-sectional observational prospective study, we enrolled 35 children aged 1 to 6 years during the 2021/2022 cold season. The test group comprised children with rAOM (n = 16), and the control group consisted of generally healthy children (n = 19). Samples (stool and nasopharyngeal swabs) were collected in late spring to ensure an antibiotic-free period. Detailed metadata was gathered through a questionnaire examining factors potentially influencing microbiota. Microbiota composition was assessed through amplicon sequencing of the V3-V4 region of the 16S rRNA gene. Our findings revealed limited alterations in gut microbiota composition among children with rAOM compared to healthy controls. Six bacterial taxa (Veillonella, Lachnospiraceae, Ruminococcaceae, Lachnospiraceae, Bacteroides and Blautia) were differentially represented with weak statistical significance. However, several bacterial taxa displayed correlations with multiple consecutive infections, with Turicibacter showing the most significant association. Additionally, day care centre attendance emerged as a potent gut microbiota modifier, independent of rAOM. Although our study identified limited differences in gut microbiota composition between children with rAOM and healthy controls, the observed correlations between the number of infections and specific bacterial taxa suggest a potential link between rAOM and the gut microbiota, warranting further investigation.
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Amir A, Erez-Granat O, Braun T, Sosnovski K, Hadar R, BenShoshan M, Heiman S, Abbas-Egbariya H, Glick Saar E, Efroni G, Haberman Y (2022) Gut microbiome development in early childhood is affected by day care attendance. NPJ Biofilms Microbiomes 8:2. 10.1038/s41522-021-00265-w PubMed PMC
Assiri K, Hudise J, Obeid A (2023) Risk factors for chronic and recurrent otitis media in children: a review article. Indian J Otolaryngol Head Neck Surg. 10.1007/s12070-023-04256-5 PubMed PMC
Bosshard PP, Zbinden R, Altwegg M (2002) Turicibacter sanguinis gen. nov., sp. nov., a novel anaerobic, Gram-positive bacterium. Int J Syst Evol Microbiol 52:1263–1266. 10.1099/00207713-52-4-1263 PubMed
Brouwer CNM, Rovers MM, Maillé AR, Veenhoven RH, Grobbee DE, Sanders EAM, Schilder AGM (2005) The impact of recurrent acute otitis media on the quality of life of children and their caregivers. Clin Otolaryngol 30:258–265. 10.1111/j.1365-2273.2005.00995.x PubMed
Chen J, Wright K, Davis JM, Jeraldo P, Marietta EV, Murray J, Nelson H, Matteson EL, Taneja V (2016) An expansion of rare lineage intestinal microbes characterizes rheumatoid arthritis. Genome Medicine 8:43. 10.1186/s13073-016-0299-7 PubMed PMC
Dagan R, Pelton S, Bakaletz L, Cohen R (2016) Prevention of early episodes of otitis media by pneumococcal vaccines might reduce progression to complex disease. Lancet Infect Dis 16:480–492. 10.1016/S1473-3099(15)00549-6 PubMed
Edgar RC (2010) Search and clustering orders of magnitude faster than BLAST. Bioinformatics 26:2460–2461. 10.1093/bioinformatics/btq461 PubMed
Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R (2011) UCHIME improves sensitivity and speed of chimera detection. Bioinformatics 27:2194–2200. 10.1093/bioinformatics/btr381 PubMed PMC
Goycoolea MV, Hueb MM, Ruah C (1991) Otitis media: the pathogenesis approach. Definitions and terminology. Otolaryngol Clin North Am 24:757–761 PubMed
Greenberg D, Bilenko N, Liss Z, Shagan T, Zamir O, Dagan R (2003) The burden of acute otitis media on the patient and the family. Eur J Pediatr 162:576–581. 10.1007/s00431-003-1260-5 PubMed
Hermes GDA, Eckermann HA, de Vos WM, de Weerth C (2020) Does entry to center-based childcare affect gut microbial colonization in young infants? Sci Rep 10:10235. 10.1038/s41598-020-66404-z PubMed PMC
Ihekweazu FD, Versalovic J (2018) Development of the pediatric gut microbiome: impact on health and disease. Am J Med Sci 356:413–423. 10.1016/j.amjms.2018.08.005 PubMed PMC
Kienesberger S, Cox LM, Livanos A, Zhang X-S, Chung J, Perez-Perez GI, Gorkiewicz G, Zechner EL, Blaser MJ (2016) Gastric Helicobacter pylori infection affects local and distant microbial populations and host responses. Cell Rep 14:1395–1407. 10.1016/j.celrep.2016.01.017 PubMed PMC
Kitamoto S, Nagao-Kitamoto H, Hein R, Schmidt TM, Kamada N (2020) The bacterial connection between the oral cavity and the gut diseases. J Dent Res 99:1021–1029. 10.1177/0022034520924633 PubMed PMC
Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C, Horn M, Glockner FO (2013) Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res 41:e1. 10.1093/nar/gks808 PubMed PMC
Kujala T, Alho O-P, Kristo A, Uhari M, Renko M, Pokka T, Koivunen P (2017) Recurrent acute otitis media detracts from health-related quality of life. J Laryngol Otol 131:128–137. 10.1017/S0022215116009944 PubMed
Mancabelli L, Taurino G, Ticinesi A, Ciociola T, Vacondio F, Milani C, Fontana F, Lugli GA, Tarracchini C, Alessandri G, Viappiani A, Bianchi M, Nouvenne A, Chetta AA, Turroni F, Meschi T, Mor M, Bussolati O, Ventura M (2023) Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection. Microbiology Spectrum 11:e02194-e2223. 10.1128/spectrum.02194-23 PubMed PMC
Ngo CC, Massa HM, Thornton RB, Cripps AW (2016) Predominant bacteria detected from the middle ear fluid of children experiencing otitis media: a systematic review. PLoS ONE 11:e0150949. 10.1371/journal.pone.0150949 PubMed PMC
Nogues JC, Pérez-Losada M, Preciado D (2020) Review of otitis media microbiome studies: what do they tell us? Laryngoscope Investig Otolaryngol 5:936–940. 10.1002/lio2.460 PubMed PMC
Presley LL, Wei B, Braun J, Borneman J (2010) Bacteria associated with immunoregulatory cells in mice. Appl Environ Microbiol 76:936–941. 10.1128/AEM.01561-09 PubMed PMC
Schmidt TS, Hayward MR, Coelho LP, Li SS, Costea PI, Voigt AY, Wirbel J, Maistrenko OM, Alves RJ, Bergsten E, de Beaufort C, Sobhani I, Heintz-Buschart A, Sunagawa S, Zeller G, Wilmes P, Bork P (2019) Extensive transmission of microbes along the gastrointestinal tract. eLife 8:e42693. 10.7554/eLife.42693 PubMed PMC
Scott AM, Clark J, Julien B, Islam F, Roos K, Grimwood K, Little P, Del Mar CB (2019) Probiotics for preventing acute otitis media in children. Cochrane Database Syst Rev 6:CD012941. 10.1002/14651858.CD012941.pub2 PubMed PMC
Tan X, Wang Y, Gong T (2023) The interplay between oral microbiota, gut microbiota and systematic diseases. J Oral Microbiol 15:2213112. 10.1080/20002297.2023.2213112 PubMed PMC
Thapa S, Runge JK, Venkatachalam A, Denne C, Luna RA, Anon JB (2020) The nasopharyngeal and gut microbiota in children in a pediatric otolaryngology practice. Pediatr Infect Dis J 39:e226. 10.1097/INF.0000000000002703 PubMed
Vacca M, Celano G, Calabrese FM, Portincasa P, Gobbetti M, De Angelis M (2020) The controversial role of human gut lachnospiraceae. Microorganisms 8:573. 10.3390/microorganisms8040573 PubMed PMC
Wang Q, He L, Tan H, Huang G, Liu J (2023) Causal relationship between gut microbiota and otitis media: a two-sample Mendelian randomized study. Eur Arch Otorhinolaryngol. 10.1007/s00405-023-08102-w PubMed
Willers M, Viemann D (2021) Role of the gut microbiota in airway immunity and host defense against respiratory infections. Biol Chem 402:1481–1491. 10.1515/hsz-2021-0281 PubMed
Xu R, Lu R, Zhang T, Wu Q, Cai W, Han X, Wan Z, Jin X, Zhang Z, Zhang C (2021) Temporal association between human upper respiratory and gut bacterial microbiomes during the course of COVID-19 in adults. Commun Biol 4:1–11. 10.1038/s42003-021-01796-w PubMed PMC
Zama D, Totaro C, Biscardi L, Rocca A, Turroni S, Brigidi P, Lanari M (2022) The relationship between gut microbiota and respiratory tract infections in childhood: a narrative review. Nutrients 14:2992. 10.3390/nu14142992 PubMed PMC