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Equine veterinary journal2026; doi: 10.1002/evj.70207

Bacteremia in horses undergoing routine dental prophylaxis: Before, during, and after the procedure.

Abstract: Transient bacteremia after dental procedures is well-documented in the literature, but the prevalence and clinical significance in horses remains largely unexplored. Objective: To assess whether routine dental prophylaxis in clinically healthy horses is associated with detection of bacteria in blood, using culture and 16S rDNA sequencing. Our central hypothesis is that a percentage of horses would demonstrate detectable but transient bacteremia in the immediate post-procedural period following dental prophylaxis. Methods: Prospective, observational study. Methods: Venous blood samples from 20 horses without evidence of significant dental disease were collected before, immediately after, 30 min, 60 min, and 24 h post-procedure and submitted for routine aerobic and anaerobic bacterial culture and 16S rDNA sequencing. Results: Data were analysed for normality by Shapiro-Wilk and Kruskal-Wallis analysis of variance (ANOVA) on ranks was performed on non-normally distributed data. Sixteen of twenty horses had positive blood cultures at one or more time points with no significant difference in the proportion of positive blood cultures among time points but differential abundance analysis identified eight bacterial families with increased and three with decreased relative abundance at one or more post-procedural time points compared to baseline. Several of these families have been associated with the equine oral or gastrointestinal microbiota, whereas others are commonly reported in plant soil and reagent-associated communities. Conclusions: Small sample size, lack of age-matched controls, absence of technical negative controls, and low-biomass nature of blood samples limit interpretation. Conclusions: Culturable bacteria and bacterial DNA were detected from blood samples of clinically healthy horses before and after routine dental prophylaxis, though overall culture positivity and community diversity remained stable. Differential abundance analyses identified subtle post-procedural changes in low-abundance taxa; however, without negative controls, these findings may reflect biological variation or contamination and should be interpreted cautiously.
Publication Date: 2026-07-26 PubMed ID: 42503025DOI: 10.1002/evj.70207Google Scholar: Lookup
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  • Journal Article

Summary

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Research Overview

  • This study investigated whether routine dental cleaning in healthy horses leads to bacteria entering the bloodstream (bacteremia).
  • Researchers collected and analyzed blood samples before and after dental prophylaxis using bacterial culture and genetic sequencing to check for bacteria presence and changes.

Background and Objective

  • Transient bacteremia—temporary presence of bacteria in the blood—is known after dental procedures in humans and some animals.
  • However, for horses undergoing routine dental care, the frequency and clinical importance of bacteremia had not been clearly studied.
  • The objective was to determine if routine dental prophylaxis in healthy horses leads to detectable bacteria in blood samples immediately after and at various times post-procedure.
  • The central hypothesis was that some horses would show short-lived bacteremia after receiving dental cleaning.

Methods

  • Study design: A prospective, observational study was conducted.
  • Subjects: 20 clinically healthy horses without significant dental disease were included.
  • Sampling: Venous blood samples were taken at five time points:
    • Before the procedure (baseline)
    • Immediately after the dental cleaning
    • 30 minutes post-procedure
    • 60 minutes post-procedure
    • 24 hours post-procedure
  • Analytical techniques:
    • Bacterial cultures were performed under both aerobic and anaerobic conditions to identify live, culturable bacteria.
    • 16S rDNA sequencing was used to detect and identify bacterial DNA, allowing detection of a broader range of bacteria including those not easily cultured.
  • Statistical analysis:
    • Shapiro-Wilk test was used to assess normality of data.
    • Kruskal-Wallis ANOVA on ranks was applied to non-normally distributed data.
    • Differential abundance analyses compared bacterial community profiles at post-procedure time points versus baseline.

Results

  • Culture positivity: 16 out of 20 horses had positive blood cultures at one or more time points.
  • Time point comparison: There was no statistically significant difference in the proportion of positive cultures between pre- and post-procedure time points.
  • Bacterial community changes: Differential abundance analysis revealed:
    • Eight bacterial families increased in relative abundance at one or more post-procedure time points compared to baseline.
    • Three bacterial families decreased in relative abundance after the procedure.
  • Origin of bacteria:
    • Some bacterial families detected are common in equine oral or gastrointestinal microbiota, possibly reflecting transient bacteremia or normal biology.
    • Other families are typically found in soil or are known contaminants from reagents used in laboratory processes, raising concerns about contamination.

Conclusions and Limitations

  • Bacteria and bacterial DNA could be detected in the blood of clinically healthy horses both before and after routine dental cleaning, indicating that the presence of bacteria in blood is not uncommon even without active dental disease or recent procedures.
  • Overall, the rates of culture positivity and the diversity of bacterial communities remained stable across time points, suggesting no major increase in bacteremia due to the dental procedures.
  • Subtle changes in low-abundance bacterial taxa were observed post-procedure, but interpreting these changes is complicated due to:
    • Small sample size limiting statistical power and generalizability.
    • Lack of age-matched controls to rule out confounding variables.
    • Absence of technical negative controls in sequencing, making it difficult to distinguish genuine biological signals from contamination, especially given that blood is a low-biomass sample prone to contamination artifacts.
  • Therefore, while transient bacteremia may occur in some horses after dental cleaning, these findings should be interpreted cautiously, and future studies with better controls and larger cohorts are needed to clarify the clinical relevance.

Cite This Article

APA
Dockery A, Whitfield-Cargile C, Knopp V, Sinay T. (2026). Bacteremia in horses undergoing routine dental prophylaxis: Before, during, and after the procedure. Equine Vet J. https://doi.org/10.1002/evj.70207

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English

Researcher Affiliations

Dockery, Allison
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Whitfield-Cargile, Canaan
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Knopp, Vanessa
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.
Sinay, Taylor
  • Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens, Georgia, USA.

Grant Funding

  • The University of Georgia

References

This article includes 42 references
  1. Townsend KS, Johnson PJ, LaCarrubba AM, Martin LM, Ericsson AC. Exodontia associated bacteremia in horses characterized by next generation sequencing.. Sci Rep 2021;18(1):6314.
  2. Kennedy R, Lappin DF, Dixon PM, Buijs MJ, Zaura E, Crielaard W. The microbiome associated with equine periodontitis and oral health.. Vet Res 2016;47:49.
  3. Gao W, Chan Y, You M, Lacap‐Bugler DC, Leung WK, Watt RM. In‐depth snapshot of the equine subgingival microbiome.. Microb Pathog 2016;94:76–89.
  4. Sykora S, Pieber K, Simhofer H, Hackl V, Brodesser D, Brandt S. Isolation of treponema and Tannerella spp. from equine odontoclastic tooth resorption and hypercementosis related periodontal disease.. Equine Vet J 2014;46(3):358–363.
  5. Borkent D, Reardon RJM, McLachlan G, Glendinning L, Dixon PM. A microbiome analysis of equine peripheral dental caries using next generation sequencing.. Equine Vet J 2020;52:67–75.
  6. Kern I, Bartmann CP, Verspohl J, Rohde J, Bienert‐Zeit A. Bacteraemia before, during and after tooth extraction in horses in the absence of antimicrobial administration.. Equine Vet J 2017;49(2):178–182.
  7. Nieves MA, Hartwig P, Kinyon JM, Riedesel DH. Bacterial isolates from plaque and from blood during and after routine dental procedures in dogs.. Vet Surg 1997;26(1):26–32.
  8. Blazevich MI, Ericsson AC, McAdams ZL, Rindt H, Grobman ME, Graham A. The presence of bacteremia in 13 dogs undergoing oral surgery without the use of antibiotic therapy.. J Vet Dent 2024;41(4):312–323.
    doi: 10.1177/08987564231207208google scholar: lookup
  9. Martins CC, Lockhart PB, Firmino RT, Kilmartin C, Cahill TJ, Dayer M. Bacteremia following different oral procedures: a systematic review and meta‐analysis.. Oral Dis 2023.
    doi: 10.1111/odi.14531google scholar: lookup
  10. Harari J, Besser TE, Gustafson SB, Meinkoth K. Bacterial isolates from blood cultures of dogs undergoing dentistry.. Vet Surg 1993;22:27–30.
  11. Sreenivasan PK, Tischio‐Bereski D, Fine DH. Reduction in bacteremia after brushing with a triclosan/copolymerdentifrice—a randomized clinical study.. J Clin Periodontol 2017;44(10):1020–1028.
  12. Zhu Y, Jiang W, Holyoak R, Liu B, Li J. Investigation of oral microbiome in donkeys and the effect of dental care on oral microbial composition.. Animals (Basel) 2020;10:2245.
  13. Glickman LT, Glickman NW, Moore GE, Goldstein GS, Lewis HB. Evaluation of the risk of endocarditis and other cardiovascular events on the basis of the severity of periodontal disease in dogs.. J Am Vet Med Assoc 2009;234(4):486–494.
  14. Paju S, Scannapieco FA. Oral biofilms, periodontitis, and pulmonary infections.. Oral Dis 2007;13(6):508–512.
  15. Zetterström B, Ericsson AC, Franklin CL, Zeng J, McAdams ZL, Rindt H. Association between oral health status and systemic bacterial DNA in horses.. Sci Rep 2021;11:6314.
  16. Verdegaal EJM, de Heer N, Meertens NM, Maree JTM, Sloet van Oldruitenborgh‐Oosterbaan MM, van Weeren PR. A right‐sided bacterial endocarditis of dental origin in a horse.. Equine Vet Educ 2006;18(4):191–195.
  17. Arndt S, Kilcoyne I, Heney CM, Wong TS, Magdesian KG. Bacterial meningitis after dental extraction in a 17‐year‐old horse.. Can Vet J 2021;62(4):403–407.
  18. Simms N, Bertone JJ, Melgarejo T, O'Shea C, Linde A. Equine blood microbiome in a cohort of clinically healthy trail riding horses.. J Vet Intern Med 2025;39(3):e70082.
    doi: 10.1111/jvim.70082google scholar: lookup
  19. Kelley D, Maddux R, Houp A, Tanner RB. A retrospective study of dental floating on pregnancy outcomes in Thoroughbred broodmares.. Equine Vet Educ 2025;37:593–596.
    doi: 10.1111/eve.14130google scholar: lookup
  20. Vidović Juras D, Škrinjar I, Križnik T, Andabak Rogulj A, Lončar Brzak B, Gabrić D. Antibiotic prophylaxis prior to dental procedures.. Dent J (Basel) 2024;12(11):364.
  21. Nuttall HE, Ravenhill PJ. Prevalence and analysis of equine periodontal disease, diastemata and peripheral caries in a first‐opinion horse population in the UK.. Vet J 2019;246:98–102.
  22. Rodrigues JB, Dixon PM, Bastos E, San Roman F, Viegas C. A clinical survey on the prevalence and types of cheek teeth disorders present in 400 Zamorano‐Leonés and 400 Mirandês donkeys (Equus asinus).. Vet Rec 2013;173(23):581.
  23. Occhiogrosso L, Capozza P, Buonavoglia A, Decaro N, Trotta A, Marin C. Bacterial periodontitis in horses: an epidemiological study in southern Italy.. Animals (Basel) 2023;13(11):1814.
    doi: 10.3390/ani13111814google scholar: lookup
  24. Whitfield‐Cargile CM, Chung HC, Coleman MC, Cohen ND, Chamoun‐Emanuelli AM, Ivanov I. Integrated analysis of gut metabolome, microbiome, and exfoliome data in an equine model of intestinal injury.. Microbiome 2024;12(1):74.
  25. Bolyen E, Rideout JR, Dillon MR, Bokulich NA, Abnet CC, al‐Ghalith GA. Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2.. Nat Biotechnol 2019;37:852–857.
  26. Callahan BJ, McMurdie PJ, Rosen MJ. DADA2: high resolution sample inference from Illumina amplicon data.. Nat Methods 2016;13:581–583.
  27. Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability.. Mol Biol Evol 2013;30:772–780.
  28. Price MN, Dehal PS, Arkin AP. FastTree 2—approximately maximum‐likelihood trees for large alignments.. PLoS One 2010;5:e9490.
  29. McMurdie PJ, Holmes S. Phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data.. PLoS One 2013;8:e61217.
  30. Wickham H. ggplot2: elegant graphics for data analysis.. New York: Springer‐Verlag; 2016.
  31. Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA‐seq data with DESeq2. Genome Biol 2014;15:550.
    doi: 10.1186/s13059-014-0550-8google scholar: lookup
  32. Lundström 2020
  33. Klugh DO. Equine periodontal disease. Clin Tech Equine Pract 2005;4:135–147.
  34. Scarsella E, Sandri M, Monego SD, Licastro D, Stefanon B. Blood microbiome: a new marker of gut microbial population in dogs?. Vet Sci 2020;4:198.
  35. Scarsella E, Zecconi A, Clintio M, Stefanon B. Characterization of microbiome on feces, blood, and milk in dairy cows with different milk leucocyte pattern. Animals (Basel) 2021;5:1463.
  36. Vientós‐ Plotts AI, Ericsson AC, Rindt H, Grobman ME, Graham A, Bishop K. Dynamic changes of the respiratory microbiota and its relationship to fecal and blood microbiota in healthy young cats. PLoS One 2017;12(3):e0173818.
  37. Wittle E, Leonared MO, Harrison R, Gant TW, Tonge DP. Multi‐method characterization of the human circulating microbiome. Front Microbiol 2018;9:3266.
  38. Salter SJ, Cox MJ, Turek EM, Calus ST, Cookson WO, Moffatt MF. Reagent and laboratory contamination can critically impact sequence‐based microbiome analyses. BMC Biol 2014;12:87.
    doi: 10.1186/s12915-014-0087-zgoogle scholar: lookup
  39. Raspa F, Chessa S, Bergero D, Sacchi P, Ferrocino I, Cocolin L. Microbiota characterization throughout the digestive tract of horses fed a high‐fiber vs. a high‐starch diet. Front Vet Sci 2024;11:1386135.
  40. Ayoub C, Arroyo LG, MacNicol JL, Renaud D, Weese JS, Gomez DE. Fecal microbiota of horses with colitis and its association with laminitis and survival during hospitalization. J Vet Intern Med 2022;36(6):2213–2223.
    doi: 10.1111/jvim.16562google scholar: lookup
  41. Park T, Cheong H, Yoon J, Kim A, Yun Y, Unno T. Comparison of the fecal microbiota of horses with intestinal disease and their healthy counterparts. Vet Sci 2021;8(6):113.
    doi: 10.3390/vetsci8060113google scholar: lookup
  42. Weese JS, Holcombe SJ, Lavoie JP, Hauck S, Stevenson K, Roy MF. The fecal microbiota of horses with colic is distinct from that of healthy horses. PLoS One 2015;10(3):e0117748.

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