Analyze Diet
BMC microbiology2017; 17(1); 184; doi: 10.1186/s12866-017-1092-5

Upper and lower respiratory tract microbiota in horses: bacterial communities associated with health and mild asthma (inflammatory airway disease) and effects of dexamethasone.

Abstract: The microbial composition of the equine respiratory tract, and differences due to mild equine asthma (also called Inflammatory Airway Disease (IAD)) have not been reported. The primary treatment for control of IAD in horses are corticosteroids. The objectives were to characterize the upper and lower respiratory tract microbiota associated with respiratory health and IAD, and to investigate the effects of dexamethasone on these bacterial communities using high throughput sequencing. Results: The respiratory microbiota of horses was dominated by four major phyla, Proteobacteria (43.85%), Actinobacteria (21.63%), Firmicutes (16.82%), and Bacteroidetes (13.24%). Fifty genera had a relative abundance > 0.1%, with Sphingomonas and Pantoea being the most abundant. The upper and lower respiratory tract microbiota differed in healthy horses, with a decrease in richness in the lower airways, and 2 OTUs that differed in abundance. There was a separation between bacterial communities in the lower respiratory tract of healthy and IAD horses; 6 OTUs in the tracheal community had different abundance with disease status, with Streptococcus being increased in IAD horses. Treatment with dexamethasone had an effect on the lower respiratory tract microbiota of both heathy and IAD horses, with 8 OTUs increasing in abundance (including Streptococcus) and 1 OTU decreasing. Conclusions: The lower respiratory tract microbiota differed between healthy and IAD horses. Further research on the role of Streptococcus in IAD is warranted. Dexamethasone treatment affected the lower respiratory tract microbiota, which suggests that control of bacterial overgrowth in IAD horses treated with dexamethasone could be part of the treatment strategy.
Publication Date: 2017-08-23 PubMed ID: 28835202PubMed Central: PMC5569571DOI: 10.1186/s12866-017-1092-5Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research investigates the bacteria present in the respiratory tract of horses, noting the differences in healthy horses and those with mild asthma, and explores how treatment with the drug dexamethasone alters these bacterial communities.

Overview of the Research

  • The study was designed to understand the composition of bacteria, or microbiota, in the upper and lower respiratory tracts of horses and how these are influenced by health status and treatment with dexamethasone, a corticosteroid commonly used to treat Inflammatory Airway Disease (IAD), which is a form of mild equine asthma.

Key Findings of the Research

  • Four major bacterial phyla were found dominant in the horse respiratory microbiota: Proteobacteria, Actinobacteria, Firmicutes, and Bacteroidetes, with fifty genera having a relative abundance of over 0.1%. The two most abundant were Sphingomonas and Pantoea.
  • The bacterial composition was found to vary between the upper and lower respiratory tracts in healthy horses, with lower richness observed in the lower airways, and difference in abundance of 2 operational taxonomic units (OTUs).
  • When considering horses with IAD, a clear distinction was observed in the bacterial communities in the lower respiratory tract when compared to healthy horses. Specifically, 6 OTUs in the tracheal community varied in abundance, and Streptococcus was found to increase in IAD horses.
  • The use of dexamethasone impacted the lower respiratory tract microbiota in both healthy and IAD horses, resulting in an increase in abundance of 8 OTUs (including Streptococcus) and a decrease of 1 OTU.

Implications of the Research

  • The study identifies notable differences in the lower respiratory tract microbiota between healthy horses and those with IAD, suggesting that certain bacteria may play a role in the disease. In particular, the research highlights the need for further investigation into the role of Streptococcus, which was found in greater abundance in IAD horses.
  • The findings also demonstrate that dexamethasone treatment affects the bacterial communities in the lower respiratory tract, which suggests that controlling bacterial overgrowth in IAD horses treated with dexamethasone may be a useful part of treatment strategies.

Cite This Article

APA
Bond SL, Timsit E, Workentine M, Alexander T, Léguillette R. (2017). Upper and lower respiratory tract microbiota in horses: bacterial communities associated with health and mild asthma (inflammatory airway disease) and effects of dexamethasone. BMC Microbiol, 17(1), 184. https://doi.org/10.1186/s12866-017-1092-5

Publication

ISSN: 1471-2180
NlmUniqueID: 100966981
Country: England
Language: English
Volume: 17
Issue: 1
Pages: 184
PII: 184

Researcher Affiliations

Bond, Stephanie L
  • Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
Timsit, Edouard
  • Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada. eftimsit@ucalgary.ca.
Workentine, Matthew
  • Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada.
Alexander, Trevor
  • Lethbridge Research Centre, Agriculture and Agri-Food Canada, Lethbridge, AB, Canada.
Léguillette, Renaud
  • Faculty of Veterinary Medicine, University of Calgary, Calgary, AB, Canada. rleguill@ucalgary.ca.

MeSH Terms

  • Animals
  • Asthma / drug therapy
  • Asthma / microbiology
  • Asthma / veterinary
  • Bacteria / classification
  • Bacteria / drug effects
  • Bacteria / isolation & purification
  • Bacteria / pathogenicity
  • Biodiversity
  • Bronchoalveolar Lavage Fluid / immunology
  • Bronchoalveolar Lavage Fluid / microbiology
  • DNA, Bacterial
  • Dexamethasone / pharmacology
  • Horse Diseases / drug therapy
  • Horse Diseases / immunology
  • Horse Diseases / microbiology
  • Horses / microbiology
  • Inflammation / drug therapy
  • Inflammation / microbiology
  • Metagenomics
  • Microbial Consortia / drug effects
  • Microbiota / drug effects
  • Respiratory System / immunology
  • Respiratory System / microbiology

Conflict of Interest Statement

ETHICS APPROVAL AND CONSENT TO PARTICIPATE: This study was conducted in strict accordance with the recommendations of the Canadian Council of Animal Care. This research protocol was reviewed and approved by the University of Calgary Veterinary Sciences Animal Care Committee (ACC17-0036) and a consent form was signed by the owner of the horses. CONSENT FOR PUBLICATION: Not applicable. COMPETING INTERESTS: The authors declare they have no competing interests. PUBLISHER’S NOTE: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

This article includes 43 references

Citations

This article has been cited 25 times.
  1. Pirolo M, Espinosa-Gongora C, Alberdi A, Eisenhofer R, Soverini M, Eriksen EØ, Pedersen KS, Guardabassi L. Bacterial topography of the upper and lower respiratory tract in pigs.. Anim Microbiome 2023 Jan 16;5(1):5.
    doi: 10.1186/s42523-023-00226-ypubmed: 36647171google scholar: lookup
  2. Bond S, McMullen C, Timsit E, Léguillette R. Topography of the respiratory, oral, and guttural pouch bacterial and fungal microbiotas in horses.. J Vet Intern Med 2023 Jan;37(1):349-360.
    doi: 10.1111/jvim.16612pubmed: 36607177google scholar: lookup
  3. Saint-Martin V, Quéré P, Trapp S, Guabiraba R. Uncovering the core principles of the gut-lung axis to enhance innate immunity in the chicken.. Front Immunol 2022;13:956670.
    doi: 10.3389/fimmu.2022.956670pubmed: 36268022google scholar: lookup
  4. Vientós-Plotts AI, Ericsson AC, McAdams ZL, Rindt H, Reinero CR. Respiratory dysbiosis in cats with spontaneous allergic asthma.. Front Vet Sci 2022;9:930385.
    doi: 10.3389/fvets.2022.930385pubmed: 36157187google scholar: lookup
  5. Brock AK, Chamoun-Emanuelli AM, Howard EA, Huntzinger KD, Lawhon SD, Bryan LK, Cosgriff-Hernandez EM, Cohen ND, Whitfield-Cargile CM. Wound swabs versus biopsies to detect methicillin resistant Staphylococcus aureus in experimental equine wounds.. Vet Surg 2022 Nov;51(8):1196-1205.
    doi: 10.1111/vsu.13872pubmed: 36102600google scholar: lookup
  6. Ma Y, Chen X, Zahoor Khan M, Xiao J, Liu S, Wang J, Alugongo GM, Cao Z. Biodegradation and hydrolysis of rice straw with corn steep liquor and urea-alkali pretreatment.. Front Nutr 2022;9:989239.
    doi: 10.3389/fnut.2022.989239pubmed: 35990351google scholar: lookup
  7. Simões J, Batista M, Tilley P. The Immune Mechanisms of Severe Equine Asthma-Current Understanding and What Is Missing.. Animals (Basel) 2022 Mar 16;12(6).
    doi: 10.3390/ani12060744pubmed: 35327141google scholar: lookup
  8. Rodríguez N, Whitfield-Cargile CM, Chamoun-Emanuelli AM, Hildreth E, Jordan W, Coleman MC. Nasopharyngeal bacterial and fungal microbiota in normal horses and horses with nasopharyngeal cicatrix syndrome.. J Vet Intern Med 2021 Nov;35(6):2897-2911.
    doi: 10.1111/jvim.16307pubmed: 34783081google scholar: lookup
  9. Akter R, El-Hage CM, Sansom FM, Carrick J, Devlin JM, Legione AR. Metagenomic investigation of potential abortigenic pathogens in foetal tissues from Australian horses.. BMC Genomics 2021 Oct 2;22(1):713.
    doi: 10.1186/s12864-021-08010-5pubmed: 34600470google scholar: lookup
  10. Guo MY, Chen HK, Ying HZ, Qiu FS, Wu JQ. The Role of Respiratory Flora in the Pathogenesis of Chronic Respiratory Diseases.. Biomed Res Int 2021;2021:6431862.
    doi: 10.1155/2021/6431862pubmed: 34435047google scholar: lookup
  11. Mainguy-Seers S, Lavoie JP. Glucocorticoid treatment in horses with asthma: A narrative review.. J Vet Intern Med 2021 Jul;35(4):2045-2057.
    doi: 10.1111/jvim.16189pubmed: 34085342google scholar: lookup
  12. Mach N, Baranowski E, Nouvel LX, Citti C. The Airway Pathobiome in Complex Respiratory Diseases: A Perspective in Domestic Animals.. Front Cell Infect Microbiol 2021;11:583600.
    doi: 10.3389/fcimb.2021.583600pubmed: 34055660google scholar: lookup
  13. Zhu Y, Chen S, Yi Z, Holyoak R, Wang T, Ding Z, Li J. Nasopharyngeal Microbiomes in Donkeys Shedding Streptococcus equi Subspecies equi in Comparison to Healthy Donkeys.. Front Vet Sci 2021;8:645627.
    doi: 10.3389/fvets.2021.645627pubmed: 33969039google scholar: lookup
  14. Payette F, Charlebois A, Fairbrother JH, Beauchamp G, Leclere M. Nicoletella semolina in the airways of healthy horses and horses with severe asthma.. J Vet Intern Med 2021 May;35(3):1612-1619.
    doi: 10.1111/jvim.16140pubmed: 33942932google scholar: lookup
  15. Mulholland KA, Robinson MG, Keeler SJ, Johnson TJ, Weber BW, Keeler CL Jr. Metagenomic Analysis of the Respiratory Microbiome of a Broiler Flock from Hatching to Processing.. Microorganisms 2021 Mar 31;9(4).
    doi: 10.3390/microorganisms9040721pubmed: 33807233google scholar: lookup
  16. Vientós-Plotts AI, Ericsson AC, Rindt H, Reinero CR. Blood cultures and blood microbiota analysis as surrogates for bronchoalveolar lavage fluid analysis in dogs with bacterial pneumonia.. BMC Vet Res 2021 Mar 23;17(1):129.
    doi: 10.1186/s12917-021-02841-wpubmed: 33757515google scholar: lookup
  17. Gomez DE, Arroyo LG, Lillie B, Weese JS. Nasal bacterial microbiota during an outbreak of equine herpesvirus 1 at a farm in southern Ontario.. Can J Vet Res 2021 Jan;85(1):3-11.
    pubmed: 33390647
  18. Zhao F, Jiang G, Ji C, Zhang Z, Gao W, Feng P, Li H, Li M, Liu H, Liu G, Magalhaes HB, Li J. Effects of long-distance transportation on blood constituents and composition of the nasal microbiota in healthy donkeys.. BMC Vet Res 2020 Sep 15;16(1):338.
    doi: 10.1186/s12917-020-02563-5pubmed: 32933535google scholar: lookup
  19. Couetil L, Cardwell JM, Leguillette R, Mazan M, Richard E, Bienzle D, Bullone M, Gerber V, Ivester K, Lavoie JP, Martin J, Moran G, Niedźwiedź A, Pusterla N, Swiderski C. Equine Asthma: Current Understanding and Future Directions.. Front Vet Sci 2020;7:450.
    doi: 10.3389/fvets.2020.00450pubmed: 32903600google scholar: lookup
  20. Vendl C, Slavich E, Wemheuer B, Nelson T, Ferrari B, Thomas T, Rogers T. Respiratory microbiota of humpback whales may be reduced in diversity and richness the longer they fast.. Sci Rep 2020 Jul 28;10(1):12645.
    doi: 10.1038/s41598-020-69602-xpubmed: 32724137google scholar: lookup
  21. Ericsson AC, Personett AR, Rindt H, Grobman ME, Reinero CR. Respiratory dysbiosis and population-wide temporal dynamics in canine chronic bronchitis and non-inflammatory respiratory disease.. PLoS One 2020;15(1):e0228085.
    doi: 10.1371/journal.pone.0228085pubmed: 31990924google scholar: lookup
  22. Manguin E, Pépin E, Boivin R, Leclere M. Tracheal microbial populations in horses with moderate asthma.. J Vet Intern Med 2020 Mar;34(2):986-995.
    doi: 10.1111/jvim.15707pubmed: 31985115google scholar: lookup
  23. Bond SL, Greco-Otto P, MacLeod J, Galezowski A, Bayly W, Léguillette R. Efficacy of dexamethasone, salbutamol, and reduced respirable particulate concentration on aerobic capacity in horses with smoke-induced mild asthma.. J Vet Intern Med 2020 Mar;34(2):979-985.
    doi: 10.1111/jvim.15696pubmed: 31953974google scholar: lookup
  24. Bond SL, Workentine M, Hundt J, Gilkerson JR, Léguillette R. Effects of nebulized dexamethasone on the respiratory microbiota and mycobiota and relative equine herpesvirus-1, 2, 4, 5 in an equine model of asthma.. J Vet Intern Med 2020 Jan;34(1):307-321.
    doi: 10.1111/jvim.15671pubmed: 31793692google scholar: lookup
  25. Bond SL, Hundt J, Léguillette R. Effect of injected dexamethasone on relative cytokine mRNA expression in bronchoalveolar lavage fluid in horses with mild asthma.. BMC Vet Res 2019 Nov 6;15(1):397.
    doi: 10.1186/s12917-019-2144-xpubmed: 31694631google scholar: lookup