Submitted:
03 December 2025
Posted:
05 December 2025
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Abstract
Bovine Respiratory Disease (BRD) remains one of the most consequential health and economic challenges in U.S. beef production, particularly within integrated systems where microbial, environmental, and management factors intersect. This review synthesizes contemporary epidemiological insights, emphasizing BRD’s multifactorial pathogenesis driven by dynamic host-pathogen-environment interactions involving agents such as Mannheimia haemolytica, Pasteurella multocida, and Mycoplasma bovis, alongside stressors from transportation, weaning, and commingling. BRD imposes annual losses exceeding two billion dollars through diminished feed efficiency, reduced carcass yield, increased treatment costs, and mortality. Despite progress in vaccination, biosecurity, and therapeutic interventions, BRD persists due to diagnostic subjectivity and limitations of traditional control measures. The review underscores emerging innovations, including precision livestock technologies, AI-enabled surveillance, and metabolomic biomarkers as transformative tools for early detection and targeted mitigation, while noting barriers related to cost, data harmonization, and scalability. The rising threat of antimicrobial resistance further highlights the need for stewardship frameworks that balance therapeutic effectiveness and public health priorities. Additionally, the paper analyzes policy and economic considerations, arguing for coordinated efforts among producers, veterinarians, researchers, and regulators. BRD is reframed as a systems-level challenge requiring integrated scientific, operational, and regulatory strategies to enhance resilience and sustainability across U.S. beef production.

Keywords:
1. Introduction
2. Epidemiology of BRD
2.1. Etiology, Pathogens, and Risk Factors
2.2. Pathogenesis of BRD
2.3. Clinical Symptoms and Diagnosis
2.4. Herd-Level Dynamics of BRD
2.5. Current BRD Prevention and Management Strategies
2.5.1. Vaccination Programs
2.5.2. Preconditioning
2.5.3. Metaphylaxis
2.5.4. Comparative Risk Profiling & Segregation of Risk Factors
2.5.5. Nutritional Management
2.5.6. General Management Practices
3. Epidemiological Studies on BRD
3.1. BRD Incidence, Prevalence, and Epidemiological Patterns
| BRD Morbidity, % | BRD Mortality, % | Year | Author |
|---|---|---|---|
| 75 | 50 | 1996 | [61] |
| 75* | 45* | 1998 | [60] |
| 20.60 | 5.90 | 2000 | [66] |
| 10.52* | 13.1#* | 2005 | [64] |
| 75* | 30* | 2008 | [62] |
| 14.70 | 0.70 | 2009 | [67] |
| 39 | 15.15* | 2010 | [68] |
| 100** | 31.9** | 2013 | [54] |
| 21 | 46.4# | 2013 | [69] |
| 75* | 45* | 2014 | [4] |
| 11.43* | 3 | 2014 | [70] |
| 22 | 3.50 | 2014 | [71] |
| 35* | 9* | 2015 | [72] |
| 87 | 33 | 2017 | [73] |
| 61.90 | 12.90 | 2018 | [13] |
| 33.90 | 5 | 2018 | [74] |
| 18 | 2.10 | 2020 | [21] |
| 12 | 5.60 | 2021 | [75] |
| 67.2** | 4.83** | 2021 | [63] |
| 75 | 60* | 2021 | [65] |
| 14.15* | 2.73* | 2022 | [40] |
| 44.50 | 3.30 | 2022 | [76] |
3.2. Selected Studies and Contributions to the Understanding of BRD Epidemiology
3.2.1. Temporal Disease Patterns and Treatment Outcomes in Feedlot Cattle (Case Study I)
3.2.2. Predictive Modeling for BRD Outcomes in Commercial Feedyards (Case Study II)
3.2.4. Economic Impacts and Performance Consequences of BRD (Case Study III)
4. Economic Impact of BRD
4.1. Financial Burden and Animal Performance Consequences
4.2. Economic Ramifications of Antimicrobial Usage and Stewardship in Managing BRD
4.3. Practical Implications for Farmers, Veterinarians, and Policymakers
5. Recommendations
5.1. Areas Requiring Further Exploration and In-Depth Studies
5.2. Suggestions for Refining Preventive Measures and Management Strategies
6. Conclusion
Author Contributions
Funding
Institutional Review Board Statement
Data Availability Statement
Conflicts of Interest
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| Method | Principle/Target | Advantages | Limitations | Key References |
| DART Scoring | Subjective clinical signs: depression, appetite, respiration, temperature | Low-cost; easy to implement quickly in the field | Low sensitivity/specificity (<70%); high inter-observer variability. | [19,20,22] |
| Thoracic Auscultation | Detects abnormal lung sounds via a stethoscope | Simple, immediate insights | Requires expertise; limited sensitivity, especially for lower lung lesions | [20] |
| Thoracic Ultrasound (TUS) | Visualizes lung consolidations and pleural lesions | High sensitivity (~85%); early lesion detection | Equipment cost, operator dependency, and animal handling are needed | [23] |
| Thoracic Radiography | X-ray imaging of lung structures | Can detect deep parenchymal lesions | Superimposition issues require anesthesia or restraint | [24] |
| Bacterial Culture & Serology | Identification of pathogen presence and immune response | Gold standard for pathogen ID; supports antimicrobial sensitivity testing | Takes days; may miss fastidious pathogens; serology may lack specificity | [25] |
| Multiplex PCR and qPCR | Detects DNA/RNA of multiple pathogens (viral & bacterial) | High sensitivity/specificity; can detect co-infections; quantitative | Infrastructure and cost barriers; positives may reflect colonization, not disease | [26] |
| Isothermal Amplification (LAMP, RPA) | Rapid on-site detection of specific pathogens | Field-friendly; colorimetric readout; ~1 hr results | Requires primer design; possible false positives; early-stage tool | [27] |
| ¹H NMR Metabolomics | Identifies systemic metabolic biomarkers in blood | High accuracy (~85%); reveals host response patterns | High cost; requires lab and ML models; less field-ready | [21] |
| Blood Transcriptomics (DEGs) | Uses gene-expression profiling to detect immune response | Early detection potential; highly specific insights | Requires RNA sequencing; high cost; technical demands | [28] |
| Near-Infrared Spectroscopy (NIRS) | Measures biochemical fingerprint in fluids/tissues | Non-invasive; potential rapid testing without a blood draw | Early research stage; needs standardization | [29] |
| Infrared Thermography | Measures surface temperature (eye/orbit) | Non-contact; early fever detection | Variable with ambient conditions; needs calibration | [30] |
| Accelerometers and Behavior Sensors | Detect changes in activity and rumination | Can detect illness ~3 days before clinical signs | Initial cost, data noise; requires algorithms | [31] |
| Acoustic Monitoring (Cough sensors) | Detects cough frequency in pens | Automated, non-invasive; early outbreak detection | Background noise interference | [32] |
| Breath Analysis (e.g., NO, VOCs) | Measures volatile biomarkers linked to inflammation | Non-invasive; rapid results | Technical complexity; needs calibration | [33] |
| Metagenomic Sequencing & AI-based Pathogen Profiling | Deep sequencing with ML models for pathogen signature | Potential for high-throughput, sensitive detection | High cost; bioinformatics demands; emerging technology | [34] |
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