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In vitro susceptibility of ceftiofur against Streptococcus equi subsp zooepidemicus and subsp equi isolated from horses with lower respiratory disease in Europe since 2002.

Abstract: In vitro activity of ceftiofur and six other antimicrobial agents was evaluated against 79 Streptococcus equi subsp zooepidemicus isolates collected from horses with respiratory disease in Europe during 2007 and 2008. In addition, the in vitro activity of ceftiofur and other antimicrobial drugs was assessed against 59 S. equi subsp zooepidemicus and 49 S. equi subsp equi isolates collected by veterinary diagnostic laboratories in Europe from 2002 to 2006. The lowest concentration of ceftiofur that inhibited the growth of 90% of the isolates (MIC90) was 0.12 microg/ml, with the Clinical Laboratory Standards Institute-approved susceptible breakpoint set at ≤ 0.25 microg/ml for ceftiofur against S. equi subsp zooepidemicus. The MIC90 values remained consistent when comparing the isolates collected from diagnostic laboratories or from the field study.
Publication Date: 2009-01-01 PubMed ID: 20425729
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  • Journal Article

Summary

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The research examined the effectiveness of an antibiotic, ceftiofur, and other antimicrobial agents against two sub-types of Streptococcus equi, a bacteria infecting horses’ respiratory systems. The study found ceftiofur to be quite effective, with a low concentration needed to inhibit 90% of the bacterial growth.

Research Methodology

  • The researchers investigated in vitro (in a controlled lab environment) the performance of ceftiofur and six other antimicrobial agents against 79 isolates of Streptococcus equi subsp zooepidemicus. This bacterium was collected from horses experiencing respiratory issues in Europe during 2007 to 2008.
  • The same in vitro testing of the drugs was applied against two distinct sub-groups of Streptococcus equi collected between 2002 to 2006. These included 59 samples of S. equi subsp zooepidemicus and 49 samples of S. equi subsp equi. The isolates were provided by veterinary diagnostic laboratories from across Europe.

Results

  • The results showed a low concentration of ceftiofur (0.12 microg/ml) was sufficient to arrest the growth of 90% of the bacterial isolates. This measurement, known as the MIC90 (Minimum Inhibitory Concentration), reflects the lowest concentration at which a drug is able to inhibit bacterial growth.
  • This concentration is well within the ‘susceptible’ breakpoint defined by the Clinical Laboratory Standards Institute (≤ 0.25 microg/ml) for ceftiofur against S. equi subsp zooepidemicus. In other words, the bacterium is very susceptible to the administered ceftiofur within this concentration range.
  • The MIC90 values were consistent, holding true for samples collected from different sources, i.e., the diagnostic laboratories as well as the field study.

Conclusion

  • The study’s findings demonstrated the effectiveness of ceftiofur in combating two sub-types of Streptococcus equi bacteria that contribute to respiratory diseases in horses.
  • This kind of research contributes to the broader understanding of equine health and informs veterinarian practices when treating these types of infections.

Cite This Article

APA
Bade D, Portis E, Keane C, Hallberg J, Bryson L, Sweeney M, Boner P. (2009). In vitro susceptibility of ceftiofur against Streptococcus equi subsp zooepidemicus and subsp equi isolated from horses with lower respiratory disease in Europe since 2002. Vet Ther, 10(4), E1-E10.

Publication

ISSN: 1528-3593
NlmUniqueID: 100936368
Country: United States
Language: English
Volume: 10
Issue: 4
Pages: E1-E10

Researcher Affiliations

Bade, Donald
  • Microbial Research Inc., Fort Collins, CO 80524, USA.
Portis, Ellen
    Keane, Caroline
      Hallberg, John
        Bryson, Lawrence
          Sweeney, Mike
            Boner, Pamela

              MeSH Terms

              • Animals
              • Anti-Bacterial Agents / pharmacology
              • Cephalosporins / pharmacology
              • Drug Resistance, Bacterial
              • Europe / epidemiology
              • Horse Diseases / microbiology
              • Horses
              • Microbial Sensitivity Tests
              • Respiratory Tract Infections / epidemiology
              • Respiratory Tract Infections / microbiology
              • Respiratory Tract Infections / veterinary
              • Streptococcal Infections / epidemiology
              • Streptococcal Infections / microbiology
              • Streptococcal Infections / veterinary
              • Streptococcus equi / drug effects
              • Streptococcus equi / isolation & purification
              • Time Factors

              Citations

              This article has been cited 4 times.
              1. Cao D, Ammad M, Subhadra B, Panda MK, Inzana TJ, Cunha F, Casaro S, Jones KL, Ramirez-Hernandez R, Bromfield JJ, Galvão KNA, Jeon SJ. The interactive relationship between Fusobacterium necrophorum, Bacteroides pyogenes, and Porphyromonas levii in driving inflammatory uterine disease. Microbiome 2026 Jan 24;14(1):69.
                doi: 10.1186/s40168-025-02320-6pubmed: 41580838google scholar: lookup
              2. Rotinsulu DA, Ewers C, Kerner K, Amrozi A, Soejoedono RD, Semmler T, Bauerfeind R. Molecular Features and Antimicrobial Susceptibilities of Streptococcus equi ssp. equi Isolates from Strangles Cases in Indonesia. Vet Sci 2023 Jan 10;10(1).
                doi: 10.3390/vetsci10010049pubmed: 36669050google scholar: lookup
              3. Nocera FP, D'Eletto E, Ambrosio M, Fiorito F, Pagnini U, De Martino L. Occurrence and Antimicrobial Susceptibility Profiles of Streptococcus equi subsp. zooepidemicus Strains Isolated from Mares with Fertility Problems. Antibiotics (Basel) 2021 Dec 27;11(1).
                doi: 10.3390/antibiotics11010025pubmed: 35052902google scholar: lookup
              4. Boyle AG, Timoney JF, Newton JR, Hines MT, Waller AS, Buchanan BR. Streptococcus equi Infections in Horses: Guidelines for Treatment, Control, and Prevention of Strangles-Revised Consensus Statement. J Vet Intern Med 2018 Mar;32(2):633-647.
                doi: 10.1111/jvim.15043pubmed: 29424487google scholar: lookup