Abstract

BackgroundActinobacillus (A.) pleuropneumoniae is the causative agent of porcine pleuropneumonia. For control of the disease the detection of sub-clinically infected pigs is of major importance to avoid transmitting of subclinical infections. One method recommended is the testing of tonsillar samples for the presence of A. pleuropneumoniae. This is routinely done by PCR techniques. However, based upon PCR susceptibility testing and monitoring of resistance development is impossible. Therefore, in this study the informative values of bacteriological culture of tonsilar samples for the colonisation status of pigs were tested. In total, 163 German Landrace nursery pigs were experimentally exposed to A. pleuropneumoniae serotype 7 by aerosol and the rate of isolation from lung tissue and tonsils and the corresponding degree of lung lesions were investigated.ResultsOverall a significant correlation (p < 0.001) between degree of clinical disease, degree of lung alterations and degree of A. pleuropneumoniae isolation from tonsillar and lung tissue after exposure was detected. Of these animals tested, 74.8% were tested positive in tonsillar and lung samples, 7.4% remained completely negative and in 4.3% the tonsils were tested positive despite negative isolation results from lung tissue. In 13.5% of the pigs A. pleuropneumoniae could be isolated in lung tissue but not in tonsillar samples. In 36.4% of these animals a heavy colonization of the lungs and in 40.9% moderate to severe lung alterations were proven. Hence, the diagnostic sensitivity for the detection of a positive colonization status of the pigs by bacterial culture examination of tonsillar samples was 84.7%, the diagnostic specificity was 66.7% and the predictive values were 94.6% (positive) and 35.3% (negative). The overall sensitivity for A. pleuropneumoniae exposure was 78.2% (tonsils) and 88.0% (lung tissue).ConclusionsIn conclusion, tonsil examination alone for the detection of a positive colonization status of pigs performed might lead to false negative results as lungs might be heavily colonized despite negative tonsillar isolation results. Therefore culture of tonsillar samples should not be the sole test for the confirmation of a pigs’ status but used in combination with methods also evaluating the colonization status of the lower respiratory tract.

Highlights

  • Actinobacillus (A.) pleuropneumoniae is the causative agent of porcine pleuropneumonia

  • Regarding the isolation of A. pleuropneumoniae it could be isolated from the tonsils of 129 pigs and from the lungs, it was isolated of 144 pigs

  • As the evaluation of all cultures from tonsillar samples was possible and no sample had to be excluded due to overgrowth by accompanying microflora this study shows that in contrast to the results of other studies [11, 13] the bacteriological culture using selective media [18] can be utilized for the detection of A

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Summary

Introduction

Actinobacillus (A.) pleuropneumoniae is the causative agent of porcine pleuropneumonia. One method recommended is the testing of tonsillar samples for the presence of A. pleuropneumoniae. This is routinely done by PCR techniques. Actinobacillus (A.) pleuropneumoniae is the causative agent of porcine pleuropneumia, a respiratory disease of pigs causing severe economic losses in pork production worldwide. Even antibiotic treatment is not able to clear A. pleuropneumoniae completely from these localizations [3]. These subclinically infected pigs are the major sources for spreading of the disease, either by transmission of the pathogen from the sows to their offspring or by pig-to-pig contact during trading of living animals [4]. Studies show that more than 30% of piglets from infected sows are positive for A. pleuropneumoniae at the time of weaning, increasing to 50% or more at the age of 10 weeks [5, 6]

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