BMC Veterinary Research | |
Changes in the equine fecal microbiota associated with the use of systemic antimicrobial drugs | |
J Scott Weese4  Roberta G Gomes1  Emma Allen-Vercoe3  Luis G Arroyo2  Henry R Stämpfli2  Marcio C Costa4  | |
[1] Department of Clinical Studies, “Universidade Estadual de Londrina”, Londrina, Brazil;Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, Canada;Department of Molecular and Cellular Biology, College of Biological Sciences, University of Guelph, Guelph, Canada;Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Canada | |
关键词: Antimicrobial associated diarrhea; Microbiome; Intestinal bacteria; Intestinal microbiota; Antibiotics; Horses; | |
Others : 1131428 DOI : 10.1186/s12917-015-0335-7 |
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received in 2014-04-29, accepted in 2015-01-22, 发布年份 2015 | |
【 摘 要 】
Background
The intestinal tract is a rich and complex environment and its microbiota has been shown to have an important role in health and disease in the host. Several factors can cause disruption of the normal intestinal microbiota, including antimicrobial therapy, which is an important cause of diarrhea in horses. This study aimed to characterize changes in the fecal bacterial populations of healthy horses associated with the administration of frequently used antimicrobial drugs.
Results
Twenty-four adult mares were assigned to receive procaine penicillin intramuscularly (IM), ceftiofur sodium IM, trimethoprim sulfadiazine (TMS) orally or to a control group. Treatment was given for 5 consecutive days and fecal samples were collected before drug administration (Day 1), at the end of treatment (Days 5), and on Days 14 and 30 of the trial. High throughput sequencing of the V4 region of the 16S rRNA gene was performed using an Illumina MiSeq sequencer. Significant changes of population structure and community membership were observed after the use of all drugs. TMS caused the most marked changes on fecal microbiota even at higher taxonomic levels including a significant decrease of richness and diversity. Those changes were mainly due to a drastic decrease of Verrucomicrobia, specifically the “5 genus incertae sedis”. Changes in structure and membership caused by antimicrobial administration were specific for each drug and may be predictable. Twenty-five days after the end of treatment, bacterial profiles were more similar to pre-treatment patterns indicating a recovery from changes caused by antimicrobial administration, but differences were still evident, especially regarding community membership.
Conclusions
The use of systemic antimicrobials leads to changes in the intestinal microbiota, with different and specific responses to different antimicrobials. All antimicrobials tested here had some impact on the microbiota, but TMS significantly reduced bacterial species richness and diversity and had the greatest apparent impact on population structure, specifically targeting members of the Verrucomicrobia phylum.
【 授权许可】
2015 Costa et al.; licensee BioMed Central.
【 预 览 】
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Figure 1. | 53KB | Image | download |
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【 参考文献 】
- [1]Blaser MJ, Falkow S: What are the consequences of the disappearing human microbiota? Nat Publishing Group 2009, 7:887-94.
- [2]Glinsky MJ, Smith RM, Spires HR, Davis CL: Measurement of volatile fatty acid production rates in the cecum of the pony. J Anim Sci 1976, 42:1465-70.
- [3]Jassim Al RAM, Andrews FM: The bacterial community of the horse gastrointestinal tract and its relation to fermentative acidosis, laminitis, colic, and stomach ulcers. Vet Clin North Am Equine Pract 2009, 25:199-215.
- [4]Bordin AI, Suchodolski JS, Markel ME, Weaver KB, Steiner JM, Dowd SE, et al.: Effects of administration of live or inactivated virulent Rhodococccus equi and Age on the fecal microbiome of neonatal foals. PLoS One 2013, 8:e66640.
- [5]Costa MC, Arroyo LG, Allen-Vercoe E, Stampfli HR, Kim PT, Sturgeon A, et al.: Comparison of the fecal microbiota of healthy horses and horses with colitis by high throughput sequencing of the V3-V5 region of the 16S rRNA gene. PLoS One 2012, 7:e41484.
- [6]Dougal K, la Fuente de G, Harris PA, Girdwood SE, Pinloche E, Newbold CJ. Identification of a core bacterial community within the large intestine of the horse. PLoS ONE. 2013; 8:e77660.
- [7]O’ Donnell MM, Harris HMB, Jeffery IB, Claesson MJ, Younge B, O’ Toole PW, Ross RP. The core faecal bacterial microbiome of Irish Thoroughbred racehorses. Lett Appl Microbiol. 2013; 57:492–501.
- [8]Shepherd ML, Swecker WSJ, Jensen RV, Ponder MA: Characterization of the fecal bacteria communities of forage-fed horses by pyrosequencing of 16S rRNA V4 gene amplicons. FEMS Microbiol Lett 2012, 326:62-8.
- [9]Steelman SM, Chowdhary BP, Dowd S, Suchodolski J, Janecka JE: Pyrosequencing of 16S rRNA genes in fecal samples reveals high diversity of hindgut microflora in horses and potential links to chronic laminitis. BMC Vet Res 2012, 8:1-1. BioMed Central Full Text
- [10]Willing BP, Voros A, Roos S, Jones C, Jansson A, Lindberg JE: Changes in faecal bacteria associated with concentrate and forage-only diets fed to horses in training. Equine Vet J 2009, 41:908-14.
- [11]Daly K, Proudman CJ, Duncan SH, Flint HJ, Dyer J, Shirazi-Beechey SP: Alterations in microbiota and fermentation products in equine large intestine in response to dietary variation and intestinal disease. Br J Nutr 2012, 107:989-95.
- [12]Kuhn M, Guschlbauer M, Feige K, Schluesener M, Bester K, Beyerbach M, et al.: Feed restriction enhances the depressive effects of erythromycin on equine hindgut microbial metabolism in vitro. Berl Munch Tierarztl Wochenschr 2012, 125:351-8.
- [13]Perkins GA, den Bakker HC, Burton AJ, Erb HN, McDonough SP, McDonough PL, et al.: Equine stomachs harbor an abundant and diverse mucosal microbiota. Appl Environ Microbiol 2012, 78:2522-32.
- [14]Faubladier C, Chaucheyras-Durand F, da Veiga L, Julliand V: Effect of transportation on fecal bacterial communities and fermentative activities in horses: Impact of Saccharomyces cerevisiae CNCM I-1077 supplementation. J Anim Sci 2013, 91:1736-44.
- [15]Harlow BE, Lawrence LM, Flythe MD: Diarrhea-associated pathogens, lactobacilli and cellulolytic bacteria in equine feces: Responses to antibiotic challenge. Vet Microbiol 2013, 166:225-32.
- [16]Chapman AM: Acute diarrhea in hospitalized horses. Vet Clin North Am Equine Pract 2009, 25:363-80.
- [17]Barr BS, Waldridge BM, Morresey PR, Reed SM, Clark C, Belgrave R, et al.: Antimicrobial-associated diarrhoea in three equine referral practices. Equine Vet J 2013, 45:154-8.
- [18]Cohen ND, Woods AM: Characteristics and risk factors for failure of horses with acute diarrhea to survive: 122 cases (1990–1996). J Am Vet Med Assoc 1999, 214:382-90.
- [19]Cochetière MF, Durand T, Lalande V, Petit JC, Potel G, Beaugerie L: Effect of antibiotic therapy on human fecal microbiota and the relation to the development of Clostridium difficile. Microb Ecol 2008, 56:395-402.
- [20]Dethlefsen L, Relman DA: Incomplete recovery and individualized responses of the human distal gut microbiota to repeated antibiotic perturbation. Proc Natl Acad Sci U S A 2011, 108(Suppl 1):4554-61.
- [21]Janczyk P, Pieper R, Souffrant WB, Bimczok D, Rothkötter H-J, Smidt H: Parenteral long-acting amoxicillin reduces intestinal bacterial community diversity in piglets even 5 weeks after the administration. ISME J 2007, 1:180-3.
- [22]Perez-Cobas AE, Gosalbes MJ, Friedrichs A, Knecht H, Artacho A, Eismann K, et al.: Gut microbiota disturbance during antibiotic therapy: a multi-omic approach. Gut 2013, 62:1591-601.
- [23]Jakobsson HE, Jernberg C, Andersson AF, Sjölund-Karlsson M, Jansson JK, Engstrand L: Short-term antibiotic treatment has differing long-term impacts on the human throat and Gut microbiome. PLoS One 2010, 5:e9836.
- [24]White G, Prior SD: Comparative effects of oral administration of trimethoprim/sulphadiazine or oxytetracycline on the faecal flora of horses. Vet Rec 1982, 111:316-8.
- [25]Gustafsson A, Baverud V, Franklin A, Gunnarsson A, Ogren G, Ingvast-Larsson C: Repeated administration of trimethoprim/sulfadiazine in the horse–pharmacokinetics, plasma protein binding and influence on the intestinal microflora. J Vet Pharmacol Ther 1999, 22:20-6.
- [26]Grà nvold A-MR, L’Abà e-Lund TM, Sà rum H, Skancke E, Yannarell AC, Mackie RI. Changes in fecal microbiota of healthy dogs administered amoxicillin. FEMS Microbiol Ecol. 2010; 71:313–326.
- [27]La Cochetiere De MF, Durand T, Lepage P, Bourreille A, Galmiche JP, Doré J: Resilience of the dominant human fecal microbiota upon short-course antibiotic challenge. J Clin Microbiol 2005, 43:5588-92.
- [28]Blackmore TM, Dugdale A, Argo CM, Curtis G, Pinloche E, Harris PA, et al.: Strong stability and host specific bacterial community in faeces of ponies. PLoS One 2013, 8:e75079.
- [29]Ferran AA, Bibbal D, Pellet T, Laurentie M, Gicquel-Bruneau M, Sanders P, et al.: Pharmacokinetic/pharmacodynamic assessment of the effects of parenteral administration of a fluoroquinolone on the intestinal microbiota: comparison of bactericidal activity at the gut versus the systemic level in a pig model. Int J Antimicrob Agents 2013, 42:429-35.
- [30]Tanayama S, Yoshida K, Adachi K, Kondo T: Metabolic fate of SCE-1365, a new broad-spectrum cephalosporin, after parenteral administration to rats and dogs. Antimicrob Agents Chemother 1980, 18:511-8.
- [31]Peris-Bondia F, Latorre A, Artacho A, Moya A, D’Auria G: The active human Gut microbiota differs from the total microbiota. PLoS One 2011, 6:e22448.
- [32]Robinson CJ, Young VB: Antibiotic administration alters the community structure of the gastrointestinal micobiota. Gut Microbes 2010, 1:279-84.
- [33]Morotomi N, Fukuda K, Nakano M, Ichihara S, Oono T, Yamazaki T, et al.: Evaluation of intestinal microbiotas of healthy Japanese adults and effect of antibiotics using the 16S ribosomal RNA gene based clone library method. Biol Pharm Bull 2011, 34:1011-20.
- [34]Klindworth A, Pruesse E, Schweer T, Peplies J, Quast C, Horn M, et al.: Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res 2013, 41:e1.
- [35]Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, et al.: Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 2009, 75:7537-41.
- [36]Kozich JJ, Westcott SL, Baxter NT, Highlander SK, Schloss PD: Development of a dual-index sequencing strategy and curation pipeline for analyzing amplicon sequence data on the MiSeq illumina sequencing platform. Appl Environ Microbiol 2013, 79:5112-20.
- [37]Quast C, Pruesse E, Yilmaz P, Gerken J, Schweer T, Yarza P, et al.: The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Res 2013, 41:D590-6.
- [38]Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R: UCHIME improves sensitivity and speed of chimera detection. Bioinformatics 2011, 27:2194-200.
- [39]Cole JR, Wang Q, Fish JA, Chai B, McGarrell DM, Sun Y, et al.: Ribosomal database Project: data and tools for high throughput rRNA analysis. Nucleic Acids Res 2014, 42:D633-42.
- [40]Bunge J: Estimating the number of species with CatchAll. Pac Symp Biocomput 2011:121–130.