Association between clinical respiratory signs, lung lesions detected by thoracic ultrasonography and growth performance in pre‐weaned dairy calves
Irish Veterinary Journal volume 74, Article number: 7 (2021)
Bovine respiratory disease (BRD) is the main cause of mortality among 1-to-5 month old calves in Ireland, accounting for approximately one-third of deaths. Despite widespread use of clinical respiratory signs for diagnosing BRD, lung lesions are detected, using thoracic ultrasonography (TUS) or following post-mortem, in calves showing no clinical signs. This highlights the limitation of clinical respiratory signs as a method of detecting sub-clinical BRD. Using 53 purchased artificially-reared male dairy calves, the objectives of this study were to: (i) characterise the BRD incidence detected by clinical respiratory signs and/or TUS, (ii) investigate the association between clinical respiratory signs and lung lesions detected by TUS, and (iii) assess the effect of BRD on pre-weaning growth.
Clinical BRD (based on Wisconsin clinical respiratory score and/or rectal temperature > 39.6 ºC) was detected in 43 % and sonographic changes (lung lesions) were detected in 64 % of calves from purchase (23 (SD; 6.2) days of age) until weaning, 53 days post-arrival. Calves with clinical BRD were treated. Sixty-one per cent calves affected with clinical BRD had lung lesions 10.5 days (median) before detection of clinical signs. Moderate correlations (rsp 0.70; P < 0.05) were found between cough and severe lung lesions on arrival day, and between rectal temperature > 39.6 ºC and lung lesions ≥ 2 cm2 on day 7 (rsp 0.40; P < 0.05) post-arrival. Mean average daily live weight gain (ADG) of calves from purchase to weaning was 0.75 (SD; 0.10) kg; calves with or without clinical BRD did not differ in ADG (P > 0.05), whereas ADG of those with severe lung lesions (lung lobe completely consolidated or pulmonary emphysema) was 0.12 kg/d less (P < 0.05) than calves without lung lesions.
Thoracic ultrasonography detected lung consolidation in calves that did not show signs of respiratory disease. The presence of severe lung lesions was associated with reduced pre-weaning growth. These findings emphasise the importance of using TUS in addition to clinical respiratory scoring of calves for an early and accurate detection of clinical and sub-clinical BRD.
Bovine respiratory disease (BRD) is a major health challenge for the cattle industry, and particularly young calves [1, 2]. It is a significant cause of morbidity and mortality in pre-weaned and weaned calves [1, 2], accounting for 34.3 per cent of deaths in calves between 1 and 5 months-old in Ireland . Bovine respiratory disease, including both clinical and sub-clinical, in calves causes substantial economic losses evidently associated with veterinary costs and mortality , but also less apparent costs associated with reduced average daily live weight gain (ADG), carcass weight [5, 6] and reduced milk production in female dairy heifers .
The evaluation of clinical respiratory signs, whether through clinical respiratory score (CRS) charts, auscultation [8, 9] or subjective criteria (e.g. depressive attitude, appearance) , is the main approach used for diagnosing BRD and establishing criteria for treatment. However, these methods are limited since they fail to detect calves with lung lesions but not showing clinical respiratory signs (sub-clinical BRD) [10, 11]. In North America, ultrasonographic examinations of calves revealed a high prevalence of lung lesions (64 %) compared to calves diagnosed with BRD using CRS (26 %) . Therefore, in order to detect these sub-clinical BRD cases, evaluation of lung appearance on the live animal is required, and this is performed using thoracic ultrasonography (TUS). The TUS instrument enables a rapid (1 min/calf), non-invasive and on-site detection of lung lesions in the live animal . Despite the fact that neither CRS or TUS are gold standard methods to asses BRD status of calves, previous authors reported a greater sensitivity (62 % vs. 79 %) and specificity (74 % vs. 94 %) of TUS compared with CRS to diagnose BRD in pre-weaned dairy calves . There are a limited number of studies evaluating the association between growth performance and TUS findings, in pre-weaned calves [11, 14].
Consequently, the objectives of the present study were to, (i) characterise the BRD incidence detected by clinical respiratory signs and/or TUS, (ii) investigate the association between clinical respiratory signs and lung lesions detected by TUS, and (iii) assess the effect of BRD on pre-weaning growth performance of purchased artificially-reared male dairy calves.
Incidence of BRD and disease evolution
The classification of calves with clinical BRD (cBRD) and TUS score (TUSS) 1 to 4 from day (d) 0 to d 14 (TUS14) and d 30 (TUS30) post-arrival is represented in Table 1.
According to the cBRD classification, (23/53) 43 % of calves were categorised as cBRD + and (30/53) 57 % as cBRD- from arrival until weaning. From d 0 to d 14 post-arrival, 47 % of calves were detected to have lung lesions (TUSS2, 3 or 4). From d 0 until d 30 post-arrival, (34/53) 64 % of calves had lung lesions, of which (17/34) 50 % were classified as TUSS2, (9/34) 26 % as TUSS3 and (8/34) 24 % as TUSS4. Of the 34 calves with lung lesions, 19 were clinically detected and thereby treated, whereas 15 were not detected using clinical respiratory signs. Of the 23 cBRD + calves, 14 had lung lesions present a median of 10.5 days (range from 3 to 29) before detection of clinical signs. The cumulative percentage of diagnosed cBRD + calves and those TUSS > 1 during 30 d after arrival is represented in Fig. 1. By d 14, 79 % of the calves (30/38) with clinical or sub-clinical BRD had been detected. No calves developed cBRD after d 30 until weaning.
Descriptive statistics for clinical respiratory signs and presence of lung lesions on d 0, 7 and 14 are shown in Table 2.
No clinical signs were detected in calves on d 0 except for (2/53) 3.8 % and (1/53) 1.9 % of calves that showed rectal temperature > 39.6 ºC and cough, respectively; however, (11/53) 20.8 % of calves showed sonographic changes on d 0. On d 7 and 14 post-arrival, the most frequent clinical sign was nasal discharge ((16/53 calves) 30.2 % and (20/53 calves) 37.7 %, respectively), whereas there was a relatively low frequency (from (1/53 calves) 1.9 % to (8/53 calves) 15.1 %) for the remaining clinical signs. Lung lesions were detected in (14/53) 26.4 % and (20/53) 37.7 % of calves on d 7 and 14, respectively.
Association between clinical respiratory signs and lung lesions
The association between clinical respiratory signs and TUSS is presented in Table 3. A moderate positive correlation (rsp 0.70; P < 0.05) was found between presence of cough and TUSS4 on d 0. Moreover, there was a moderate positive correlation (rsp 0.43; P < 0.05) between rectal temperature > 39.6 ºC and TUSS3 on d 7.
Pre‐weaning growth performance
Mean ADG of calves during the pre-weaning period was 0.75 (SD; 0.1) kg. No differences (P > 0.05) in ADG were observed between calves classified as cBRD + and cBRD- (Table 4). In contrast, calves classified as TUSS4 had 0.12 kg reduced ADG (P = 0.05) compared to calves classified as TUSS1.
Clinical respiratory signs are widely used to diagnose BRD in dairy calves as it can be performed on-farm by personnel other than a veterinarian [1, 8]. In this study, clinical respiratory signs were only weak-to-moderately correlated with the simultaneous presence of lung lesions, thereby failing to detect sub-clinical BRD. Moreover, calves with severe (lung lobe completely consolidated or pulmonary emphysema) lung lesions grew 0.12 kg/d less than those without lung lesions, highlighting the importance of evaluating lung appearance through thoracic ultrasonography.
The incidence of cBRD from arrival until weaning reported in this study (43 %) is intermediate to values previously reported in Irish research herds for pre-weaned dairy calves where Wisconsin CRS evaluation, or a modification of it, was used (33 % , 40 %  and 50 % ) A lower incidence of clinical BRD using Wisconsin CRS evaluation (13–26 %) has been reported in pre-weaned dairy calves in North America [11, 18, 19]. Variances between these studies may be explained by differences in management systems. The male calves in this study faced a number of coinciding challenges (transport, co-mingling with other animals, placement in a new housing environment and adaptation to a new diet) that may have resulted in stress, and a greater predisposition to BRD ; these challenges are not as common in dairy heifer rearing systems where the calves are born and remain on the birth farm as replacement heifers.
In the current study, 28 % of calves had sub-clinical BRD that were undetected using clinical respiratory signs alone. Previous authors have described variable percentages (from 23 to 67 %) of dairy calves with sub-clinical BRD in facilities in North America [11, 12]. Furthermore, in the present study, the appearance of lung lesions was detected prior to the appearance of clinical respiratory signs in (14/23) 61 % of cBRD + calves, of which 6 were TUSS2, 6 TUSS3 and 2 TUSS4. Moreover (14/34) 41 % of calves identified with lung lesions developed cBRD afterwards. Similarly, it has been reported that 64 % of calves developed clinical pneumonia subsequent to the detection of lung lesions . These results suggest that TUS can detect sub-clinical BRD before the detection of clinical respiratory signs, implying that TUS should be used in addition to CRS for an early and accurate diagnosis of the different BRD forms. Antibiotic treatment should be considered only in inappetent and febrile calves.
The severity of lung lesions was reduced in 32% of cases after antibiotic treatment in the present study. Lung tissue has the capacity to repair and regenerate damaged cells after disease in humans and mice [21, 22], though there is no information in cattle. It is likely that animals with mild lung lesions in this study responded well to treatment. However, the evolution of lung lesions after therapy was not part of this study and further research is warranted to address this.
In the present study the majority (79 %) of clinical and sub-clinical cases were detected by d 14 post-arrival with all cases detected by d 30. The temporal proximity between diverse stressors such as transport, housing and dietary changes predispose calves to the development of BRD soon after these stressors . In feedlots, where similar stressors to those in this study (transport, new environment and diet) affect calves, BRD incidence density was greater during the first week after arrival and subsequently decreased . Similarly, in a study performed in recently-weaned 7 month old beef calves in Ireland, 50 % of BRD cases were detected by d 7 after arrival to the facilities and 80 % by d 14, with no more BRD cases detected after d 28 . Therefore, intensifying the monitoring of calves through CRS and TUS during the first weeks post-arrival may facilitate the detection of the majority of BRD-affected calves.
Only two moderate correlations were found between clinical respiratory signs and TUSS3 and 4 in our study. Likewise, Leruste et al.  reported weak correlations (rsp from 0.16 to 0.40) between clinical respiratory signs and moderate-to-severe lung lesions at slaughter, and no correlation with mild lung lesions. Intranasal vaccination of calves at arrival in the present study could have affected the correlations between lung lesions and clinical signs as previous authors reported a reduction of lung lesions in animals that received intranasal vaccination while the clinical signs remained unaffected . Clinical signs are generally used at farm level to diagnose BRD ante-mortem and as a criteria for treatment [1, 8]; however, this methodology fails to detect calves with lung lesions that may either develop into clinical BRD or go undetected as sub-clinical cases of BRD, causing important economic losses . Taking into consideration the development of resistance to antimicrobials, a recent study by our group highlighted the importance of the prudent use of antibiotics at farm level . In agreement with the present study, we reported that the highest risk period for disease in artificially reared calves was between birth and 30 days of age, with approximately two-thirds of all disease events occurring during this time period .
It is acknowledged that employment of TUS is limited as a routine diagnostic tool, particularly in large high-throughput facilities, where a rapid, repeatable, cost-effective method for prediction of risk to develop clinical BRD or lung lesions would be necessary in order to permit early intervention strategies. Additionally, further research is also warranted on antibiotic treatments based on sensitivity testing and the identification of resistant microbiomes which would inform their prudent use.
Interestingly, calves classified as TUSS4 in the pre-weaning period had a 13.8 % lower ADG compared with those classified as TUSS1. Similarly, a previous study performed with dairy heifer calves reported a 14 % poorer ADG (0.73 vs. 0.85 kg/d, respectively) in calves with lung lesions ≥ 1 cm2 compared with those without lung lesions . In contrast, based on the presence of clinical respiratory signs in the current study there was no difference in ADG between cBRD + and cBRD – calves. However, this lack of difference could be due to the daily examinations performed by the technical farm staff that led to detection of visual clinical signs and subsequent treatment. TUS provides an objective evaluation of the classification of lung lesions in calves with BRD, which could not be detected using CRS alone, and the severity of which will impact negatively on growth performance. Therefore, although more time is required, veterinarians should consider the combined use of CRS with TUS for a more accurate diagnosis of all forms of BRD in unweaned calves.
The use of clinical respiratory signs alone failed to detect sub-clinical BRD, whereas TUS is an effective tool for that purpose. The use of TUS in addition to CRS improved diagnosis and provided early and accurate detection of different forms of BRD. Calves with severe lung lesions (lung lobe consolidation or pulmonary emphysema) had reduced growth performance compared with calves without lung lesions. It is also important to note that finding calves with lung lesions does not mean that lung consolidation should be used as a tool for treatment purpose. Therefore, TUS could be implemented for calf health monitoring to provide an accurate description of BRD. More research is warranted concerning the antibiotic treatment of the different BRD forms, within the scope of responsible use of antibiotics.
A total of 53 male dairy-bred calves, comprising of 28 HF × AA (24 (SD; 7.1) days old; 53.5 (SD; 8.8) kg) and 25 HF (21 (SD; 4.6) days old; 51.7 (SD; 5.4) kg), were purchased from 13 different commercial farms during February and March 2020 and transported by road to Teagasc, Grange Research Centre (transport duration ranged from 30 min to 240 min). Following arrival (d 0), calves were randomly accommodated indoors in straw-bedded individual pens, in a naturally ventilated area (n = 32) or in a fan ventilated area (n = 21), until weaning at 75 (SD; 8.8) days of age (d 53). Each calf was then administered a sub-cutaneous dose of 1.5 mg meloxicam (Metacam, Boehringer Ingelheim) and 24 h later was vaccinated through single intranasal doses against bovine respiratory syncytial virus, parainfluenza-3-virus (Rispoval RS + PI3, Zoetis) and bovine alphaherpesvirus-1 (Rispoval IBR-Marker inactivated, Zoetis). Immediately following arrival calves received 2 L of oral electrolytes (Lectade Plus, Elanco). From d 1, calves were offered 2 L of milk replacer (23 % crude protein - Golden Maverick A, Volac, Co. Cavan, Ireland) at 12.5 % a concentration of 12.5 % solids, twice-daily by bucket and had ad-libitum access to calf starter pencils (crude protein 18 %; crude oil and fat 4.0 %; crude ash 7.5 % - Lakeland Dairies, Monaghan, Ireland) and fresh clean water. Calves were weaned when they had achieved at least 85 kg individual bodyweight. The mean indoor temperature during the study period was 7 °C (range from 2 to 16 °C).
This study was a retrospective cohort study, and the experimental design is detailed in Fig. 2. The power analysis calculation was made based on analysis of data collected as part of a microbiome study, in which 20 BRD cases were necessary to detect differences compared with healthy cases. Calves were weighed using a calf weighing platform scales with Dini Argeo display (Gravitation Ltd, Ireland) at d 0 and every two weeks until weaning, d 53. All calves were observed twice daily, from arrival until weaning, for clinical signs of BRD by the same farm technician with expertise in calf health management. Recording of clinical respiratory signs (rectal temperature, cough, ear position, nasal and eye discharge) included in the scoring system of University of Wisconsin , and of TUS evaluations were performed by the same trained research veterinarian on d 0, 7 and 14. Thirty-three of the 53 calves, as part of calf health management, were subjected to an additional TUS evaluation between 14 and 30 d post-arrival. Rectal temperature was measured in calves showing depression, anorexia and/or dyspnoea and those with rectal temperature > 39.6 °C and/or with CRS ≥ 5 from arrival until weaning received BRD treatment consisting of a sub-cutaneous dose containing 40 mg/kg florfenicol and 2.2 mg/kg flunixin meglumine (Resflor, MSD Animal Health). Calves were classified as either cBRD+ (BRD treatment) or cBRD- (no BRD treatment) from arrival until weaning.
Clinical respiratory score and thoracic ultrasonography
The Wisconsin CRS classifies rectal temperature, presence of cough, appearance of eye and nasal discharges, and ear position with scores ranging from 0 to 3 (from normal to very abnormal) and the sum of all scores of each clinical sign define the CRS. Calves with CRS ≥ 5 are considered as having BRD.
Thoracic ultrasonography was performed as described by Ollivett et al. . Briefly, an 8 MHz Wi-Fi linear transducer (Tecnoscan SR-1 C, Imporvet, Spain) was used at a maximal depth of 8 cm, and gain of 60 dB. The thorax of calves was clipped using electrical clippers and isopropyl alcohol (70 %) was used as transducing agent. Thoracic ultrasonography was performed on each side of the thorax. Systematic scanning was performed starting in the 10th intercostal space (ICS) and moving cranially until the 1st ICS to the right and the 2nd ICS to the left, sliding the transducer along the grain of the hair within each ICS. When normal lungs or presence of comet-tailing artefacts were visualised, data were annotated on-site and later transcribed to a database. In the case of lung alterations, a 10-second loop of ultrasound footage was stored to measure its size off-line after the study period was complete. For measuring consolidation size, squares in the screen representing 1 cm2 each, were used. Based on TUS evaluations, an adaptation of Cramer and Ollivett  ultrasonography score was performed to classify calves into four TUSS categories from normal lung to lung with severe lesions: TUSS1 designated those calves with normal lungs or presence of comet tails on all days when ultrasound evaluations were performed. The ultrasonogram of a normal aerated lung was characterized by the visualization of a bright hyperechoic line representing the pleura with several reverberation artefacts below it (Fig. 3, TUSS1). An ultrasonogram with one or more hyperechoic lines, also called comet tails, which perpendicularly arise from the visceral pleura indicate pleural roughening (Fig. 3, TUSS1). Calves with lung lesions < 2 cm2 in, at least, one assessment were considered TUSS2. Calves with lung lesions ≥ 2 cm2 in, at least, one evaluation were classified as TUSS3. Lung lesions (also referred to as consolidations) appear in the ultrasonogram as a hypoechoic area of varying size that disrupts the reverberation artefacts (Fig. 3, TUSS2-3). Finally, TUSS4 designated those calves with, at least, one complete consolidated lobe and/or pulmonary emphysema. A complete consolidated lobe was observed in the ultrasonogram as a wide hypoechoic area with a sonogram similar to that of the liver parenchyma. Ramifications of the fluid bronchogram were observed within the consolidated area (Fig. 3, TUSS4). The presence of emphysema was visualised in the ultrasonogram as multiple hyperechoic bands that originate from the pleura which did not permit visualisation of the lung tissue below the pleura  (Fig. 3, TUSS4).
Data management and statistical analyses
Statistical analyses were performed using SAS v.9.4 software (SAS Institute Inc. Cary, NC, USA). Animal was the experimental unit. Farm of origin was included as random.
Data were checked for normality and homogeneity of variance by histograms, q–q plots, and formal statistical tests as part of the UNIVARIATE procedure of SAS. Clinical respiratory signs at d 0, 7, 14 were expressed as percentages (PROC FREQ) of observed calves that showed clinical signs (rectal temperature > 39.6 ºC, cough, nasal discharge, eye discharge and ear abnormal position) and percentage of calves with presence of lung lesions detected though TUS classified in each category. Association between presence of clinical respiratory signs and presence of lung lesions (TUSS2, TUSS3 and TUSS4) on d 0, 7 and 14 were evaluated by calculating correlation coefficients between variables using Spearman rank correlation (rsp, PROC CORR). A post-hoc Bonferroni correction was applied on the P values obtained from the multiple Spearman correlation. Univariable associations between development of cBRD or lung lesions and calf-level covariate variables (age at arrival, breed and house (natural or fan ventilated)) were tested via a X2 test and logistic regression analysis. Variables with a value of P ≤ 0.20 were included in the multivariable analyses. Calf ADG was calculated for the period from arrival until weaning. To evaluate the effect of cBRD and lung lesions had on ADG, a multivariable linear regression model (PROC GLM with MANOVA) was conducted including cBRD, TUS classification, breed and house. The Wilks’ lambda post-hoc test, multivariate version of the F-test statistic in one-way ANOVA, was applied to assesses the differences between two or more groups on multiple variables at once.
Availability of data and materials
All data supporting these research findings are included within the manuscript. The databases (without personally identifiable information) are available from the corresponding author upon request.
Average daily gain
Bovine respiratory disease
Clinical respiratory score
Thoracic ultrasonography score
McGuirk SM. Disease management of dairy calves and heifers. Vet Clin North Am Food Anim Pract. 2008;24(1):139.
Todd CG, McGee M, Tiernan K, Crosson P, O’Riordan E, McClure J, et al. An observational study on passive immunity in Irish suckler beef and dairy calves: Tests for failure of passive transfer of immunity and associations with health and performance. Prev Vet Med. 2018;159:182–95.
All-Island Animal Disease Surveillance Report. Dept. of Agriculture, Food and the Marine. 2019.
Dubrovsky SA, Van Eenennaam AL, Aly SS, Karle BM, Rossitto PV, Overton MW, et al. Preweaning cost of bovine respiratory disease (BRD) and cost-benefit of implementation of preventative measures in calves on California dairies: The BRD 10K study. J Dairy Sci. 2020;103(2):1583–97.
Delabouglise A, James A, Valarcher JF, Hagglünd S, Raboisson D, Rushton J. Linking disease epidemiology and livestock productivity: The case of bovine respiratory disease in France. PLoS One. 2017;12(12):e0189090.
Pardon B, Hostens M, Duchateau L, Dewulf J, De Bleecker K, Deprez P. Impact of respiratory disease, diarrhea, otitis and arthritis on mortality and carcass traits in white veal calves. BMC Vet Res. 2013;9:79.
Dunn TR, Ollivett TL, Renaud DL, Leslie KE, LeBlanc SJ, Duffield TF, et al. The effect of lung consolidation, as determined by ultrasonography, on first-lactation milk production in Holstein dairy calves. J Dairy Sci. 2018;101(6):5404–10.
Love WJ, Lehenbauer TW, Kass PH, Van Eenennaam AL, Aly SS. Development of a novel clinical scoring system for on-farm diagnosis of bovine respiratory disease in pre-weaned dairy calves. PeerJ. 2014;2:e238.
McGuirk SM, Peek SF. Timely diagnosis of dairy calf respiratory disease using a standardized scoring system. Anim Health Res Rev. 2014;15(2):145–7.
Leruste H, Brscic M, Heutinck LF, Visser EK, Wolthuis-Fillerup M, Bokkers EA, et al. The relationship between clinical signs of respiratory system disorders and lung lesions at slaughter in veal calves. Prev Vet Med. 2012;105(1–2):93–100.
Cramer MC, Ollivett TL. Growth of preweaned, group-housed dairy calves diagnosed with respiratory disease using clinical respiratory scoring and thoracic ultrasound-A cohort study. J Dairy Sci. 2019;102(5):4322–31.
Ollivett TL, Buczinski S. On-Farm Use of Ultrasonography for Bovine Respiratory Disease. Vet Clin North Am Food Anim Pract. 2016;32(1):19.
Buczinski S, L Ollivett T, Dendukuri N. Bayesian estimation of the accuracy of the calf respiratory scoring chart and ultrasonography for the diagnosis of bovine respiratory disease in pre-weaned dairy calves. Prev Vet Med. 2015;119(3–4):227–31.
Tejero C, Bach A. The hidden cost of a hidden disease: growth performance of calves as affected by bovine respiratory disease diagnosed using ultrasonography. J Anim Sci. 2016;94:48.
Conneely M, Berry DP, Murphy JP, Lorenz I, Doherty ML, Kennedy E. Effects of milk feeding volume and frequency on body weight and health of dairy heifers calves. Livestock Science. 2014;161:90–4.
Johnston D, Kenny DA, McGee M, Waters SM, Kelly AK, Earley B. Electronic feeding behavioural data as indicators of health status in dairy calves. Irish J Agr Food Res. 2016;55:159–68.
Murray GM, More SJ, Clegg TA, Earley B, O’Neill RG, Johnston D, et al. Risk factors associated with exposure to bovine respiratory disease pathogens during the peri-weaning period in dairy bull calves. BMC Vet Res. 2018;14(1):53.
Stanton AL, Kelton DF, LeBlanc SJ, Wormuth J, Leslie KE. The effect of respiratory disease and a preventative antibiotic treatment on growth, survival, age at first calving, and milk production of dairy heifers. J Dairy Sci. 2012;95(9):4950–60.
Quick AE, Ollivett TL, Kirkpatrick BW, Weigel KA. Genomic analysis of bovine respiratory disease and lung consolidation in preweaned Holstein calves using clinical scoring and lung ultrasound. J Dairy Sci. 2020;103(2):1632–41.
Earley B, Buckham Sporer K, Gupta S. Invited review: Relationship between cattle transport, immunity and respiratory disease. Animal. 2017;11(3):486–92.
Herriges M, Morrisey EE. Lung development: orchestrating the generation and regeneration of a complex organ. Development. 2014;141(3):502–13.
Zacharias WJ, Frank DB, Zepp JA, Morley MP, Alkhaleel FA, Kong J, et al. Regeneration of the lung alveolus by an evolutionarily conserved epithelial progenitor. Nature. 2018;555(7695):251–5.
Duff GC, Galyean ML. Board-invited review: recent advances in management of highly stressed, newly received feedlot cattle. J Anim Sci. 2007;85(3):823–40.
Sanderson MW, Dargatz DA, Wagner BA. Risk factors for initial respiratory disease in United States’ feedlots based on producer-collected daily morbidity counts. Can Vet J. 2008;49:373–8.
Cuevas-Gómez I, McGee M, McCabe M, Cormican P, O’Riordan E, McDaneld T, et al. Growth performance and haematological changes of weaned beef calves diagnosed with respiratory disease using respiratory scoring and thoracic ultrasonography. J Anim Sci. 2020;98(11).
Ollivett TL, Leslie KE, Duffield TF, Nydam DV, Hewson J, Caswell J, et al. Field trial to evaluate the effect of an intranasal respiratory vaccine protocol on calf health, ultrasonographic lung consolidation, and growth in Holstein dairy calves. J Dairy Sci. 2018;101(9):8159–68.
Blakebrough-Hall C, McMeniman JP, González LA. An evaluation of the economic effects of bovine respiratory disease on animal performance, carcass traits, and economic outcomes in feedlot cattle defined using four BRD diagnosis methods. J Anim Sci. 2020;98(2).
Earley B, Arguello A, O’Riordan E, Crosson P, McGee M. Quantifying antimicrobial drug usage from birth to 6 months of age in artificially reared dairy calves and in suckler beef calves. J Appl Anim Res. 2019;47:474–85.
Hussein HA, Binici C, Staufenbiel R. Comparative evaluation of ultrasonography with clinical respiratory score in diagnosis and prognosis of respiratory diseases in weaned dairy buffalo and cattle calves. J Anim Sci Technol. 2018;60:29.
The authors would like to extend their thanks to: the field research Technician, Donall Fahy, the farm staff and under-graduate students for the care and management of the animals at Teagasc AGRIC Grange.
This project is funded through the US-Ireland DAFM grant (Project number 2018US-IRL200).
All animals’ procedures performed in this study were reviewed and approved by the Teagasc Animal Ethics Committee (TAEC-221-2019) and were conducted under experimental license from the Health Products Regulatory Authority, Dublin, Ireland (AE19132-P101) in accordance with the protection of animals used for scientific purposes i.e. Directive 2010/63/EU and S.I. No. 543 of 2012, as amended by S.I. No. 434 of 2013 and S.I. No. 174 of 2014.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Cuevas-Gómez, I., McGee, M., Sánchez, J.M. et al. Association between clinical respiratory signs, lung lesions detected by thoracic ultrasonography and growth performance in pre‐weaned dairy calves. Ir Vet J 74, 7 (2021). https://doi.org/10.1186/s13620-021-00187-1