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Background <p>Enzootic pneumonia in calves is associated with pathogens such as <i>Pasteurellaceae</i> bacteria and <i>Mycoplasmopsis bovis</i>. Some of these bacteria are commensals in healthy calves, complicating culture interpretation, discouraging laboratory diagnostic use, and limiting knowledge of their impact. This study aimed to investigate the occurrence and antimicrobial resistance pattern of respiratory pathogens in calves from dairy herds with enzootic pneumonia. Culture results between upper and lower airway sites in healthy and diseased calves were also compared to evaluate their diagnostic value. A cross-sectional study was conducted on 131 calves (72 healthy and 59 diseased) from nine Norwegian dairy herds. Nasal swabs (NS), nasopharyngeal swabs (NPS), and serum were obtained from each calf, and bronchoalveolar lavage (BAL) from 113 calves.</p> Results <p>At the calf level, <i>Pasteurella multocida</i> was present in 60%, <i>Mannheimia haemolytica</i> in 55%, and <i>Histophilus somni</i> in 3%. At the sampling site level, from NS, NPS, and BAL, <i>P. multocida</i> was detected in 47%, 45%, and 27%, and <i>M. haemolytica</i> in 46%, 37%, and 8%, respectively. <i>H. somni</i> was detected in ≤ 2% per site. <i>P. multocida</i> appeared as pure culture in 73% (22/30) of positive BAL cultures. Serum antibodies to <i>M. bovis</i> were not detected. Most <i>Pasteurellaceae</i> isolates were susceptible to penicillin and other common pneumonia antimicrobials (disc diffusion). The exceptions were penicillin-resistant <i>M. haemolytica</i> isolates in two calves. Logistic regression identified an association between dominant, abundant cultures of <i>P. multocida</i> from BAL and clinical disease. Agreement for <i>P. multocida</i> detection between NS and NPS cultures and BAL was fair (kappa). Positive predictive values of <i>P. multocida</i> culture results at different abundance levels in NS and NPS, relative to BAL, were at most 49%.</p> Conclusion <p><i>P. multocida</i> was the predominant bacterium in lungs of calves from Norwegian dairy herds with enzootic pneumonia, and its abundance in the lungs may help differentiate infection from colonization in clinically diseased calves. <i>M. haemolytica</i> and <i>H. somni</i> appeared to have less clinical impact. Antimicrobial resistance appeared to be low. Upper airway cultures were inaccurate predictors of bacterial presence and abundance in the lungs and must be interpreted carefully alongside other diagnostic tools.</p>

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Cross-sectional study of calves from Norwegian dairy herds with enzootic pneumonia: pathogen occurrence, antimicrobial resistance, culture result interpretation, and sampling site agreement

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  • 发表日期：

    2026年5月18日

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  • Lise M. Ånestad,
  • Silje E. Falkeid,
  • Veslemøy S. Oma,
  • Randi T. Garmo,
  • Ane M. Bjelland,
  • Amelia R. Woolums,
  • Maria Stokstad,
  • Thea B. Klem

摘要

Background

Enzootic pneumonia in calves is associated with pathogens such as Pasteurellaceae bacteria and Mycoplasmopsis bovis. Some of these bacteria are commensals in healthy calves, complicating culture interpretation, discouraging laboratory diagnostic use, and limiting knowledge of their impact. This study aimed to investigate the occurrence and antimicrobial resistance pattern of respiratory pathogens in calves from dairy herds with enzootic pneumonia. Culture results between upper and lower airway sites in healthy and diseased calves were also compared to evaluate their diagnostic value. A cross-sectional study was conducted on 131 calves (72 healthy and 59 diseased) from nine Norwegian dairy herds. Nasal swabs (NS), nasopharyngeal swabs (NPS), and serum were obtained from each calf, and bronchoalveolar lavage (BAL) from 113 calves.

Results

At the calf level, Pasteurella multocida was present in 60%, Mannheimia haemolytica in 55%, and Histophilus somni in 3%. At the sampling site level, from NS, NPS, and BAL, P. multocida was detected in 47%, 45%, and 27%, and M. haemolytica in 46%, 37%, and 8%, respectively. H. somni was detected in ≤ 2% per site. P. multocida appeared as pure culture in 73% (22/30) of positive BAL cultures. Serum antibodies to M. bovis were not detected. Most Pasteurellaceae isolates were susceptible to penicillin and other common pneumonia antimicrobials (disc diffusion). The exceptions were penicillin-resistant M. haemolytica isolates in two calves. Logistic regression identified an association between dominant, abundant cultures of P. multocida from BAL and clinical disease. Agreement for P. multocida detection between NS and NPS cultures and BAL was fair (kappa). Positive predictive values of P. multocida culture results at different abundance levels in NS and NPS, relative to BAL, were at most 49%.

Conclusion

P. multocida was the predominant bacterium in lungs of calves from Norwegian dairy herds with enzootic pneumonia, and its abundance in the lungs may help differentiate infection from colonization in clinically diseased calves. M. haemolytica and H. somni appeared to have less clinical impact. Antimicrobial resistance appeared to be low. Upper airway cultures were inaccurate predictors of bacterial presence and abundance in the lungs and must be interpreted carefully alongside other diagnostic tools.