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[Detection of rhodococcus equi by microbiological culture and by polymerase chain reaction in samples of tracheobronchial secretions of foals].

Abstract: The goal of the present study was to investigate whether new PCR-methods would improve diagnostic of R. equi. In a first step, sensitivity and specificity of the PCR-methods in respect to the"gold standard" microbiological culture were determined. Secondly, sensitivity and specificity of both microbiological methods were evaluated in respect to the clinical diagnosis. The tracheobronchial secretions of 48 foals with pulmonary abscesses and of 37 healthy foals were evaluated by bacteriological culture as well as by four PCR-methods: aceA-, ideR-, vapA- and VP-PCR. In respect to the"gold standard" microbiological culture, the sensitivity of most PCR methods lay between 63.9 and 69.4 % except the vapA-PCR (27.8 %). The specificity of all PCR methods in this comparison was between 98 to 100 %. In this analysis, clinical diagnosis had a low sensitivity (66.7 %) and a low specificity (51.0 %). In respect to the clinical diagnosis, microbiological culture sensitivity was 50.0 % and specificity 67.7 9%. In this analysis, sensitivity rates of aceA-, ideR and VP-PCR methods lay between 33.3 and 37.5 %, sensitivity of the vapA-PCR was lower (10.4 %). The specificity of all PCR methods ranged from 78.4 to 86.5 %. In conclusion, these results show that the diagnostic potential of the microbiological methods"Culture" and "PCR" is different and that for the diagnosis of R. equi-pneumonia in foals the combination of microbiological culture with PCR should be used for examination of samples of the airways of foals.
Publication Date: 2007-04-10 PubMed ID: 17416135
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  • Comparative Study
  • English Abstract
  • Journal Article

Summary

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The research investigates if newer PCR-methods enhance the diagnosis of Rhodococcus equi, a bacterium causing pneumonia in foals. The methods were compared with standard microbiological culture in terms of sensitivity and specificity. The results suggested the combination of both methods for comprehensive diagnosis.

Objective of the Study

  • The study aimed at assessing if the novel PCR (polymerase chain reaction) techniques improve the diagnostic accuracy of Rhodococcus equi infections, which cause pneumonia in foals.

Methodology

  • Researchers carried out a two-step process. Initially, they determined the sensitivity and specificity of the PCR methods with respect to microbiological culture methods, often referred to as the “gold standard”.
  • Next, they examined the sensitivity and specificity of both microbiological and PCR methods with respect to clinical diagnosis.
  • The sample comprised tracheobronchial secretions of 48 foals with pulmonary abscesses and 37 healthy foals. The evaluations were performed by bacteriological culture as well as four PCR methods: aceA-, ideR-, vapA- and VP-PCR.

Results

  • In terms of sensitivity, most PCR methods ranged between 63.9 to 69.4% except for vapA-PCR with 27.8%.
  • The specificity of all PCR methods ranged between 98 to 100%, suggesting these methods have a high probability of correctly identifying healthy foals.
  • In comparison, the clinical diagnosis showed a low sensitivity (66.7%) and low specificity (51.0%).
  • When analysed against the clinical diagnosis, the microbiological culture method demonstrated a sensitivity of 50.0% and specificity of 67.7%.
  • The sensitivity of aceA-, ideR-, and VP-PCR methods was between 33.3 and 37.5%, with vapA-PCR showing lower sensitivity (10.4%).
  • However, specificity of all PCR methods ranged from 78.4 to 86.5%.

Conclusion

  • The research concluded that the “Culture” and “PCR” techniques offer different diagnostic potentials in terms of detecting Rhodococcus equi infections.
  • Therefore, a combination of microbiological culture and PCR methods should be employed when examining tracheobronchial secretion samples from foals for a more accurate diagnosis of R. equi pneumonia.

Cite This Article

APA
Venner M, Heyers P, Strutzberg-Minder K, Lorenz N, Verspohl J, Klug E. (2007). [Detection of rhodococcus equi by microbiological culture and by polymerase chain reaction in samples of tracheobronchial secretions of foals]. Berl Munch Tierarztl Wochenschr, 120(3-4), 126-133.

Publication

ISSN: 0005-9366
NlmUniqueID: 0003163
Country: Germany
Language: ger
Volume: 120
Issue: 3-4
Pages: 126-133

Researcher Affiliations

Venner, Monica
  • Klinik für Pferde, Stiftung Tierärztliche Hochschule Hannover. monica.venner@tiho-hannover.de
Heyers, Paul
    Strutzberg-Minder, Katrin
      Lorenz, Nicole
        Verspohl, Jutta
          Klug, Erich

            MeSH Terms

            • Actinomycetales Infections / diagnosis
            • Actinomycetales Infections / veterinary
            • Animals
            • Animals, Newborn
            • Base Sequence
            • Colony Count, Microbial / methods
            • Colony Count, Microbial / veterinary
            • Female
            • Horse Diseases / diagnosis
            • Horses
            • Lung / microbiology
            • Lung Abscess / microbiology
            • Male
            • Polymerase Chain Reaction / methods
            • Polymerase Chain Reaction / veterinary
            • Rhodococcus equi / isolation & purification
            • Sensitivity and Specificity
            • Trachea / microbiology

            Citations

            This article has been cited 3 times.
            1. Majidzadeh M, Fatahi-Bafghi M. Current taxonomy of Rhodococcus species and their role in infections.. Eur J Clin Microbiol Infect Dis 2018 Nov;37(11):2045-2062.
              doi: 10.1007/s10096-018-3364-xpubmed: 30159693google scholar: lookup
            2. Rutenberg D, Venner M, Giguère S. Efficacy of Tulathromycin for the Treatment of Foals with Mild to Moderate Bronchopneumonia.. J Vet Intern Med 2017 May;31(3):901-906.
              doi: 10.1111/jvim.14717pubmed: 28421633google scholar: lookup
            3. Hildebrand F, Venner M, Giguère S. Efficacy of gamithromycin for the treatment of foals with mild to moderate bronchopneumonia.. J Vet Intern Med 2015 Jan;29(1):333-8.
              doi: 10.1111/jvim.12504pubmed: 25619521google scholar: lookup