Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Early detection of bovine respiratory disease (BRD) in feedlot cattle: why and how? Dr. E. Timsit DVM, PhD, Dip. ECBHM Dr. S. Assié, DVM, PhD, Dip. ECBHM Introduction • Heifer, 28 days after arrival (i.e. days on feed) • Found dead in pen, treated once the day before Introduction • Fatal fibrinous pneumonia (M. haemolytica) Detected and treated too late! Outline 1. Why is an early detection of BRD crucial? 2. How to early detect BRD? Why early detect BRD? Early BRD detection Early antibiotic treatment in the disease process • Avoid irreversible pulmonary lesions • Prevent emergence of antibiotic resistances • Maximize antibiotic action - Maximize clinical and bacterial cure - Limit BRD impact on performances Why early detect BRD? Mannheimia haemolytica Pasteurella multocida Mycoplasma Bovis Histophilus somni (Griffin et al.,2010) M. haemolytica Commensal organisms Why early detect BRD? Viral infection, stress and/or suboptimal environment Proliferation of bacteria in the nasopharynx Bacteria gain access to the lung via aerosolized droplets Adherence, colonization and replication in the lung Tissue destruction and inflammation Bacterial pleuro/broncho-pneumonia Why early detect BRD? Evolution of the disease process When bacteria colonize and replicate: 1) Secretion of enzymes and toxins Lipopolysaccharide (LPS), Leukotoxins (LKT), Lipoolysaccharide (LOS), etc. Lung damage Inflammation Inflammation can lead to tissue damage (Panciera et al., 2010) Why early detect BRD? When bacteria replicate: 2) Emergence of bacterial resistances Antibiotic-resistant bacteria Antibiotic-sensitive bacteria Time-lag before treatment (Lipsitch & Levin, 1997; Ferran et al., 2011) Total bacterial population > mutational frequency to resistance (10-6 to 10-8) => Presence of resistant population very likely (before any treatment) Why early detect BRD? When bacteria replicate: 2) Larger bacterial inoculum Time-lag before treatment (Ferran et al., 2011) Higher dose of antibiotic required to eradicate the bacterial inoculum Early treatment = lower dose of antibiotic needed Why early detect BRD? When pulmonary lesions and atelectasia => reduced antibiotic distribution Normal blood flow alveolar hypoxia Hypoxic pulmonary vasoconstriction reduced blood flow Reduced antibiotic distribution Obstruction Normal blood flow Early treatment = few (or no) obstructions Increased antibiotic action Why early detect BRD? Study of Ferran et al. (2011) Experimental lung infection (P. multocida) Control group Euthanasia (48 h) Early treatment group Late treatment group Antibiotic treatment 10 h post-infection Euthanasia (48 h) Antibiotic treatment 32 h post-infection Euthanasia (70 h) Why early detect BRD? Study of Ferran et al. (2011) Control group Late treatment group Early treatment group % of mice with P. multocida 93% (26/28) 36% (5/14) 0% (0/14) % of surviving mice 64% (18/28) 71% (10/14) 100% (14/14) % of lungs with resistant bacteria 33% (6/18) 10% (1/10) 0% (0/13) Early antibiotic treatment: Better bacterial and clinical outcomes Less frequent selection of resistant bacteria Why early detect BRD? Study of Assié et al. (unpublished data) “Early” BRD treatment Study design 30 young bulls BRD detection: Use of rumen temperature boluses Cefquinom 2.5 mg/kg once “Late” BRD treatment 30 young bulls BRD detection: Distant examination if BRD signs: rectal temperature Cefquinom 2.5 mg/kg twice Preliminary results (30 YB in each group) Treated animals: 22 Relapse: 6 (27%) Global antibiotic consumption: 22*2.5 mg/Kg = 55 mg/Kg Treated animals: 13 Relapse: 4 (30%) Global antibiotic consumption: 26*2.5 mg/Kg = 65 mg/Kg Why early detect BRD? In summary: • To avoid irreversible pulmonary lesions • To prevent emergence of antibiotic resistances • To maximize antibiotic action - Maximize clinical and bacterial cure - Limit BRD impact on performances Outline 1. Why is an early detection of BRD crucial? 2. How to early detect BRD? How to early detect BRD? • How are cattle with BRD detected? – Distant examination • Owner and/or staff • Once or twice daily – Detection of clinical signs • • • • Depression Anorexia/dysorexia Increased respiratory rate Lacrimal and nasal discharges, cough, etc. (Duff & Gaylean, 2006) How to early detect BRD? • Does distant examination enable an early BRD detection? Answer: No Study of Timsit et al. (2011a) Rumen temperature bolus How to early detect BRD? Solution: By using automatic health-monitoring systems Growsafe® Schaefer® B) Changes in feeding behavior => Growsafe system, ENGS system A) Changes in body temperature rumen T°C boluses, IRT, ear mounted thermometers C) Changes in physical activity => pedometers, accelerometers How to early detect BRD? A) Monitoring body temperature to early detect BRD Fever occurs very early in the disease process (within hours) BRD Treatment (0 h) (Fajt et al., 2004) Experimental infection of 3 heifers (181±19 kg) with M. haemolytica (-21 h) How to early detect BRD? A) Monitoring body temperature to early detect BRD Study of Timsit et al. (2011b) Drinking Treatment Fever episode Rumen temperature of a feeder bull BRD affected animals detected 12 to 177 h (mean = 51h) prior to BRD treatment How to early detect BRD? A) Monitoring body temperature to early detect BRD Study of Schafer et al. (2007 & 2012) BRD affected animals detected 4 to 6 days prior to the onset of clinical symptoms of BRD How to early detect BRD? A) Monitoring body temperature to early detect BRD Study of McCorkell et al., accepted Fever Tags® (old version) Promising tools Cheap <15€ But low sensitivity (21/46 = 46%) • Inadequate probe placement • Probe displacement • High threshold for activation New version with adjustable probe size and activation threshold “Fever Alert” distributed by Merck Animal Health (France) need to be evaluated How to early detect BRD? Solution: By using automatic health-monitoring systems Growsafe® Schaefer® B) Changes in feeding behavior => Growsafe system, ENGS system A) Changes in body temperature rumen T°C boluses, IRT, ear mounted thermometers Yes How to early detect BRD? B) Monitoring feeding behavior Study of Sowell et al. (1999) Growsafe® (Sowell et al., 1998) Diseased feedlot cattle spent on average 30% less time at the feed bunk than healthy cattle (46 min/day versus 60 min/day) How to early detect BRD? B) Monitoring feeding behavior Study of Quimby et al. (2001) Growsafe® Decreased frequency and duration of feed bunk visit Detected as sick by the Cusum test Diseased cattle detected on average 4.1 days earlier than pen checker How to early detect BRD? Solution: By using automatic health-monitoring systems Growsafe® Schaefer® B) Changes in feeding behavior => Growsafe system, ENGS system Yes A) Changes in body temperature rumen T°C boluses, IRT, ear mounted thermometers Yes C) Changes in physical activity => pedometers, accelerometers How to early detect BRD? C) Monitoring physical activity Study of Hanzlicek et al. (2010) M. Haemolytica infection Experimental infection of 14 steers (199 kg) with M. haemolytica How to early detect BRD? C) Monitoring physical activity Study of White et al. (2012) <10% consolidated lung tissue M. bovis infection >10% consolidated lung tissue Experimental infection of 20 Holstein calves (5-9 week old) with M. bovis How to early detect BRD? Solution: By using automatic health-monitoring systems Growsafe® Schaefer® B) Changes in feeding behavior => Growsafe system, ENGS system Yes A) Changes in body temperature rumen T°C boluses, IRT, ear mounted thermometers Yes C) Changes in physical activity => pedometers, accelerometers Yes How to early detect BRD? • Why are health-monitoring systems not currently used in feedlots? 1st explanation = costs $$$ • • • Rumen temperature bolus = $35-100 Infrared camera = $7000 Growsafe system = $25 per head Costs are decreasing rapidly! 2nd explanation = low specificity! • Numerous “false-positive” detection How to early detect BRD? • Lack of specificity of fever and abnormal feeding behavior: 1) Study of Timsit et al. (2011b) Up to 75% of the fever episode detected by rumen T°C bolus lasted less than 47 hours without any treatment => viral infection only? Successful immune response? Hyperthermia? Vaccination? 2) Study of Wolfger et al. (2012) Pulling cattle only based on abnormal feeding behavior during the first weeks on feed could lead to pull as much as 90% of the healthy animals => Adaptation to the bunk? How can the specificity of fever and anorexia/dysorexia be improved? How to early detect BRD? • How to improve specificity of fever? – by taking into consideration the duration of fever 75% of fever episodes lasting longer than 48 hrs led to clinical BRD 100% 90% 80% 48 hrs was also proposed by Radostits et al., 2010 70% 60% 50% 40% Recommendations: treat cattle with fever 48 hrs after onset (if no other signs) 30% 20% 10% 0% 0 to 24 h n=45 No BRD signs BRD signs and treatment 24 to 48 h n=29 >48h n=21 (Timsit and Assié, personal communication) How to early detect BRD? • How to improve specificity of fever and abnormal feeding behavior? – by combining this parameters (i.e. series testing) + Pull and treat only cattle having concomitantly fever and anorexia/dysorexia How to early detect BRD? On-going study (Timsit and Booker) Objective • To describe the changes in body temperature, feeding behavior and physical activity associated with BRD Materials and methods • 560 steers studied during first 50 DOF • Simultaneous monitoring of body temperature, feeding behavior and physical activity How to early detect BRD? On-going study (Timsit and Booker) Preliminary data (n = 12 sick animals) Treatment Treatment Steer n°9569 Steer n°9569 • Fever (n =12): onset = 2 to 9 d before detection/treatment; med = 4 d • Anorexia/dysorexia (n = 9): onset = 0 to 3 d after fever; med = 2 d • Decreased activity (n =8): onset = 0 to 3 d after fever; med = 2 d Take home message • Early BRD detection i) limits impact of BRD on performance, ii) maximizes clinical and bacterial cure and iii) reduces emergence of bacterial resistances • Distant examination alone cannot enable an early BRD detection • Health monitoring systems can enable an early BRD detection but further research is needed and is performed already! Thank you very much for your attention! Source: Dr. Eugene Janzen Literature cited • • • • • • • • • • • • • • • • Duff G et al.. 2007. Board-invited review: recent advances in management of highly stressed, newly received feedlot cattle. J Anim Sci. 85:823-40. Fajt V et al. 2004. Effect of danofloxacin and tilmicosin on body temperatures of beef calves with pneumonia experimentally induced by inoculation with Mannheimia haemolytica. Am J Vet Res. 65:610-615. Ferran A et al. 2011. Impact of early versus later fluoroquinolone treatment on the clinical: microbiological and resistance outcomes in a mouse-lung model of Pasteurella multocida infection. Vet Microbiol. 148: 292-297. Griffin D et al. 2010. Bacterial pathogens of the bovine respiratory disease complex. Vet Clin North Am Food Anim Pract. 26:381-394. Hanzlicek G et al. 2010. Serial evaluation of physiologic, pathological, and behavioral changes related to disease progression of experimentally induced Mannheimia haemolytica pneumonia in postweaned calves. Am J Vet Res. 71: 359-369. Lipsitch M et al. 1997. The population dynamics of antimicrobial chemotherapy. Antimicrob Agents Chemother. 41:363-73. McCorkell et al. 2014. Limited efficacy of Fever Tag® temperature sensing ear tags in calves with naturally occurring Bovine Respiratory Disease or induced Bovine Viral Diarrhea Virus infection. Can Vet J. Accepted. Panciera RJ et al. 2010. Pathogenesis and pathology of bovine pneumonia. Vet Clin North Am Food Anim Pract. 26:191-214. Quimby W et al. 2001. Application of feeding behaviour to predict morbidity of newly received calves in a commercial feedlot. Can J Anim Sci. 81: 315-320. Schaefer A et al. 2012. The non-invasive and automated detection of bovine respiratory disease onset in receiver calves using infrared thermography. Res Vet Sci. 93: 928-935. Schaefer A et al. 2007. The use of infrared thermography as an early indicator of bovine respiratory disease complex in calves. Res Vet Sci. 83: 376-384. Sowell BF et al. 1999. Feeding and watering behavior of healthy and morbid steers in a commercial feedlot. J Anim Sci. 77:1105-1112. Timsit E at al. 2011a: Early detection of bovine respiratory disease in young bulls using reticulo-rumen temperature boluses. Vet J. 190: 136-142. Timsit E at al. 2011b: Fever episodes without visually apparent clinical signs in newly-received beef bulls at fattening operation: occurrence, duration and impact on performance J Anim Sci. 89: 4272-4280. White BJ et al. 2012. Clinical, behavioral, and pulmonary changes in calves following inoculation with Mycoplasma bovis. Am J Vet Res. 73:490-497. Wolfger B et al. 2012. Pattern recognition of feeding and drinking behaviour as a tool in early identification of diseased feedlot animals. 13th ISVEE. Maastricht. Netherland.