INTRODUCTION
Bovine tuberculosis (bTB) is an economically important chronic infectious disease that typically affects cattle, but that may also infect many other species, including humans.
Abattoir monitoring for bTB is a key surveillance component in countries with endemic infection, as well as in officially tuberculosis (TB)-free countries where meat inspection is the cornerstone for granting and maintaining official TB-free (OTF) status [Reference Whipple, Bolin and Miller1–Reference Domingo, Vidal and Marco5].
In Northern Ireland (NI), bTB is endemic in cattle, with significant economic and social consequences for the country and the farming community. Compulsory eradication of bTB began in 1959 and after initial rapid progress (reaching levels of <1% herd incidence during the 1960s), increasing herd incidence was observed during the late 1980s reaching a peak annual herd incidence in February 2003 (10·2%). A declining herd incidence followed but this levelled off (2007–2010; 5–6% bTB herd incidence) with a 2010 annual bTB herd incidence of 5·12%; its lowest level since 1998. A sharp rise took place in 2011 and this continued in 2012 when annual herd incidence was 7·34%. However, over 2013 herd incidence fell to 6·44%. The annual animal incidence has followed similar trends and it was 0·51% in 2013. In 2013, the confirmed bTB herd prevalence was 7·17% [6] and the cost of the eradication programme undertaken by the Department of Agriculture, Environment and Rural Affairs (DAERA) (formerly Department of Agriculture and Rural Development; DARD) was £27 million [7]. The programme consists of two surveillance components: live-animal surveillance and slaughterhouse surveillance [Reference Abernethy8]. The former is based on the single comparative intradermal tuberculin test (SCITT) and supplemented under specific circumstances with a gamma-interferon test. The sensitivity of the SCITT test has been estimated to be 56% [95% confidence interval (CI) 52·9–60·8] in the Republic of Ireland (ROI) [Reference Clegg9], whereas previous studies in other countries suggest that SICCT test sensitivity lies between 52% and 100%, with median values of 80% and 93·5% for standard and severe interpretations, respectively [Reference De la Rua-Domenech10]. Animals that react positively to the SCITT and high-risk in-contact animals are slaughtered, their herd of origin is placed under movement restrictions, and one clear whole-herd test 60 days after the removal of positive animals (among other measures) is needed for the herd to regain trading status (two clear tests 60 days apart if bTB infection is confirmed).
Animals with negative results to the live-animal surveillance tests are subjected to post-mortem examination (PME) when routinely slaughtered in accordance with EC directive 854/2004 [11]. All carcasses are examined for, among other things, visible signs of bTB infection.
When visible lesions suspicious of bTB infection are detected in animals that are not compulsorily slaughtered under the bTB programme, the animal is described as having a ‘lesion at routine slaughter’ (LRS) and a disease control response is automatically initiated by DAERA. The herd from which the slaughtered animal originated is subject to movement restrictions until confirmation or otherwise of Mycobacterium bovis as the cause of the lesion. Confirmation is established by follow-up testing by histological and bacteriological examination of the bTB-like lesions [12] at the Agri-Food and Biosciences Institute (AFBI) laboratory.
Costello et al. found that 10% of animals in bTB-infected herds that had visible bTB lesions did not react to the SCITT [Reference Costello13]. Moreover, an unpublished report from the Veterinary Epidemiology Unit (DAERA) (A. V. Pascual-Linaza, unpublished report) estimated that in NI between 5·2% and 6·4% of all disclosed bTB-infected animals were detected at PME during the years 2011–2013. Despite annual herd testing in NI, 18%−28% of the newly confirmed bTB breakdowns were first detected through slaughterhouse surveillance. The number and distribution of LRS animals is thus a useful ancillary measure of the underlying disease levels and trends within the national herd because it represents a sampling system that is independent of live-animal surveillance.
Thus, PME forms an effective surveillance method for detecting residual bTB infection as well as for monitoring infection trends in the population, and there is a need to regularly assess its efficacy and efficiency. However, the sensitivity of the PME is likely to be low and dependent upon different host, agent, and environmental factors [Reference Corner14].
The aim of this study was to assess the variation in LRS detection risks between different NI slaughterhouses. The results from the study provide evidence for bTB policy makers on the current performance of slaughterhouse surveillance for bTB in NI, so they can target possible enhancements of the current bTB eradication programme.
MATERIALS AND METHODS
NI has 10 bovine slaughterhouses spread throughout the country (Fig. 1). Detailed information on all animals slaughtered in NI from 2011 to 2013 inclusive was extracted from the Animal and Public Health Information System (APHIS), which is a database used in NI since 1988 to record the details of all individual cattle, cattle holdings, cattle movements and tests [Reference Houston15].
Case definitions
Disclosure of an LRS was defined as the submission of lymph node/tissue sample(s) from an animal with suspected visible lesions of bTB infection identified at routine slaughter to the AFBI laboratory. Routine PMEs include visual examination of the carcass; palpation of the lungs, liver and tongue; incision of the lungs, heart and liver; as well as incision of head (submaxillar, parotid and retropharyngeal) and chest (apical, bronchial, mediastinal) lymph nodes. When bTB lesions are identified in one tissue, a more detailed examination of the rest of the carcass is carried out.
LRS confirmation was defined as the presence of histopathological features consistent with bTB and/or bacteriological culture of Mycobacterium bovis following examination at AFBI on suspect lesions. All disclosed LRS undergo a histopathological examination and a bacteriological culture. Of the 2210 confirmed LRS in this study, M. bovis was recovered from 78% (1741).
Data collation and analysis
Data on cattle slaughtered in NI between 2011 and 2013 inclusive were collated, including those on animal- and herd-level factors, movements and TB history of the herd of origin of the animals.
Selected potential risk factors included in the statistical analysis were: sex and age of the animal; whether the animal was purchased or homebred; the season when the animal was slaughtered; the years that the herd of origen was free of bTB, the patch bTB incidence for each year under study and the slaughterhouse. These factors were categorized as indicated in Table 1.
LRS, Lesion at routine slaughter; OTF, officially tuberculosis free; Q1, first quartile; Med, median; Q3, third quartile.
Data on the herd of origin of the animal were taken either from the presenting herd (H0), if the animal had spent ⩾75 days in this herd, or from the previous herd from which the animal was purchased (H1), if it had spent <75 days in H0. This decision was taken based on peer-reviewed articles in which a minimum period of 2–3 months was reported as the time needed for an infected animal to develop visible lesions [Reference Neill16, Reference Martin17].
During the descriptive analysis, it was observed that there was a possible linear effect of age on the disclosure of LRS. A better fit of the model was achieved including this variable as continuous in the multilevel statistical analysis.
There are 10 Divisional Veterinary Offices (DVOs) that are managed separately although following the same staff instructions. These DVOs are divided in a total of 124 patches, 6–16 patches per DVO. A patch was defined as an administrative area within each of the DVO areas in NI (Fig. 2).
Animals with missing data (i.e. age, DVO/patch or herd information), which constituted 8·5% of the original dataset, were excluded from the study. The majority of these missing data (95%) was due to imported animals going directly to slaughter.
Microsoft Access™ and MS Excel™ (Microsoft Corporation, USA) were used for data manipulation. ArcMap (Esri® ArcMap™ v. 10.1) was used to create the geographical representation of patch incidences and the location of the slaughterhouses.
For the estimation of the selected risk factors associated with LRS disclosure and confirmation (Table 1), a univariable, followed by a multivariable, generalized linear mixed model using a binomial distribution and a logit link function was generated in GenStat (GenStat for Windows 16th edn, VSN International Ltd, UK) and slaughterhouse was fitted as a random effect in order to account for within slaughterhouse variance. Collinearity between the various explanatory variables was assessed using the variance inflation factor [Reference Cook and Weisberg18]. All values were <10 thus collinearity was not considered an issue. The method used to assess the linearity of the explanatory variables was the method of design variables [Reference Hosmer, Lemeshow and Sturdivant19]. It was decided that in the interests of parsimony that any variable that was not linear was categorized using biologically appropriate cut-offs.
All explanatory variables were fitted in the first instance with the intention to use backward elimination; each explanatory variable in turn was then assessed by comparing the significance of its Wald statistic against all other terms using an appropriate χ 2 distribution. Any terms with P < 0·05 were included in the final model. Because all selected variables were significant (for submission model) backward elimination was not necessary. Some of the variables were not significant for the confirmation model, but were maintained for consistency between the two multivariable models.
A generalized linear model was ran in GenStat to rank the slaughterhouses on LRS disclosure and LRS confirmation. We first calculated the crude risk for each of the slaughterhouses reporting animals with LRS and then, using the results of the logistic regression model, we calculated the risk for each slaughterhouse disclosing an LRS, adjusted for confounders. The Pearson correlation coefficient between LRS submissions and bTB confirmation was derived. Interactions between variables were also investigated in both models. Statistical significance was set at the 5% level. The adequacy of the models was assessed by the Hosmer–Lemeshow test and by visual inspection of the appropiate residual plots.
RESULTS
Descriptive results
There were 1341886 cattle slaughtered in the 10 approved bovine slaughter establishments in NI between 2011 and 2013 (ranging from 6065 to 206281 by slaughterhouse). After exclusion of animals with missing data, analysis was carried out on 1227294 cattle from 22878 herds, of which 3558 (0·29%) animals had bTB-like lesions and 2210 (0·18%) were confirmed as bTB positive (Table 1).
More than half (55·4%) of the total animals slaughtered in NI between 2011 and 2013 were aged between 2 and 3 years. However, the highest risk of disclosure was found in animals aged 1–2 years (1·7%), although the risk of a disclosed lesion being confirmed as bTB was the lowest (6·7%). Animals slaughtered at age >5 years accounted for 17·9% of the total slaughtered animals, and lesions detected in these animals had the highest risk of confirmation (64·6–70·2%). Although the risk of disclosure was similar for all four slaughterhouse seasons (0·3%), a higher risk of confirmation was found in animals in which LRS were disclosed between July and September (67·3%, cf. 58·7% between April and June). Animals that originated in bTB-restricted herds accounted for 76·5% of the total animals slaughtered. However, a higher risk of LRS disclosure was found in animals that were presented for slaughter from herds that had a bTB breakdown in the previous 2–3 years prior to their slaughter date (0·7%, cf. 0·3% in animals from restricted herds). These animals also had the highest risk of confirmation (75%, cf. 57·1% in lesions from animals originating in herds with a bTB breakdown in the previous 1–2 years). Patch incidence maps for each of the 3 years under study (Fig. 2) were developed to evaluate the spatial distribution of bTB incidence, which ranged from 23·33% in 2012 to 0·83% in 2013. Animals from herds located in high-incidence patches (above the third quartile of each of the years: 9·48, 10·41 and 9·57% from 2011 to 2013, respectively; Fig. 2) accounted for 33·7% (n = 1200) of the LRS total, had a higher risk of disclosure than animals originated in lower incidence patches (0·4% vs. 0·3% in other patches), and lesions detected had a higher risk of confirmation (65·3% vs. 58·7% in animals from patches with incidence lower than first quartile).
Statistical analysis: univariable and multivariable analysis
LRS disclosure
For each year increase in age at slaughter the odds of that animal to be disclosed as an LRS increased by 1·06 (95% CI 1·04–1·07) (Table 2).
OR, Odds ratio; CI, confidence interval; OTF, officially tuberculosis free; Q1, first quartile; Med, median; Q3, third quartile; σ 2, variance; s.e., standard error of the random effect slaughterhouse (Slh).
In the univariable analysis, females had 1·31 times the odds of LRS disclosure than males (95% CI 1·23–1·4). These odds remained higher in females than in males in the multivariable analysis, although the value was slightly lower [odds ratio (OR) 1·20, 95% CI 1·11–1·30]. There was no difference on the odds of being a LRS disclosure between bulls and males in either the univariable or multivariable analysis.
Animals slaughtered from April to September were statistically less likely to be disclosed as LRS (OR 0·9, 95% CI 0·82–0·99) in univariable analysis, although only animals slaughtered during the summer (July–September) had lower odds of having an LRS disclosed (OR 0·89, 95% CI 0·80–0·96) than those slaughtered during winter (January–March) in multivariable analysis.
Animals coming from patches where bTB incidence was above the third quartile (9·48, 10·41 and 9·47% in 2011, 2012 and 2013, respectively; Fig. 2) were more likely to be LRS disclosed (univariable analysis: OR 1·28, 95% CI 1·16–1·4; multivariable analysis: OR 1·19, 95% CI 1·08–1·31) than animals coming from patches where bTB incidence was below the first quartile in each year (4·03, 5·32 and 5·14% in 2011, 2012 and 2013, respectively; Fig. 2).
Regarding the bTB status of the attributed herd of origin of the LRS (either H0 or H1), it was found that, relative to bTB-restricted herds, there was a higher chance of disclosing LRS in cattle originating from herds that had been clear of bTB for 2–3 years (OR 2·01, 95% CI 1·14–3·56). There was no statistical difference between bTB-restricted herds and herds that were clear of bTB for >3 years, either in the univariable or multivariable analysis.
Suspect LRS were more likely to be identified in purchased animals than from homebred animals in multivariable analysis (OR 1·22,95% CI 1·12–1·32).
LRS confirmation
For every year increase in age of the animal in which an LRS was disclosed, there were higher odds of confirmation of bTB infection (OR 1·05 95% CI 1·03–1·08) (Table 3).
OR, Odds ratio; CI, confidence interval; OTF, officially tuberculosis free; Q1, first quartile; Med, Median; Q3, third quartile; σ 2, variance; s.e., standard error of the random effect slaughterhouse (Slh).
Given that an LRS was detected, there was no statistical difference between males and females or between bulls and males in the odds of confirmation of the disease (OR 0·95, 95% CI 0·81–1·12 for females and OR 0·89, 95% CI 0·58–136 for bulls).
LRSs found in summer (July–September) had a higher chance of being confirmed (univariable analysis: OR 1·26, 95% CI 1·06–1·53; multivariable analysis: OR 1·25, 95% CI 1·03–1·53) than those found from January to March.
The LRSs disclosed in animals that originated in patches with a high incidence (above third quartile) had a higher chance of being confirmed as bTB (univariable analysis: OR 1·33; 95% CI 1·1–1·61; multivariable analysis: OR 1·35, 95% CI 1·11–1·64) than LRS disclosed in animals originated in low incidence patches (below the first quartile)
bTB status of the attributed herd of origin of the LRS was not statistical associated with confirmation of infection in either the univariable or the multivariable analysis.
LRSs disclosed in purchased animals were less likely to be confirmed as bTB by multivariable analysis (OR 0·83; 95% CI 0·70–0·98) than those in homebred animals.
Ranking of slaughterhouses
There was a wide range of crude LRS disclosure risks between some of the slaughterhouses (Table 4), from 0·08 to 0·54 (>6 times the risk in slaughterhouse no. 8 than in slaughterhouse no. 3), with an average LRS disclosure risk of 0·3 across all slaughterhouses. The adjusted risk of LRS disclosure ranged from 0·08 (slaughterhouse no. 3) to 0·60 (slaughterhouse no. 8). The ranking of slaughterhouses by LRS disclosure risk did not change when adjusted for potential confounders.
LRS, Lesion at routine slaughter; OTF, officially tuberculosis free.
The average crude risk for LRS confirmation was 64·2% (Table 5) ranging from 57·9% and 72·4% and the average adjusted risk for LRS confirmation was 65·1% (range 56·1–73·2%). The ranking of the slaughterhouses regarding confirmation rates changed slightly when considering adjusted risk rather than crude. The crude LRS confirmation risk from slaughterhouse no. 8 was the most affected by adjusting for confounders (crude risk 60·6%, adjusted risk 64·7%).
LRS, Lesion at routine slaughter; OTF, officially tuberculosis free.
Comparing the ranking for LRS disclosure (Table 4) to the ranking for LRS confirmation (Table 5), there appeared to be an inverse relationship (e.g. slaughterhouse nos. 8 and 3) although the risks were not significantly well correlated (crude risk: r = −0·6004, P = 0·066; adjusted risk: r = −0·4709, P = 0·169).
For the Hosmer–Lemeshow test, we obtained P values >0·05 (P = 0·538 for the LRS disclosure model and P = 0·522 for the LRS confirmation model), which indicated that the model was a good fit.
DISCUSSION
This is the first study to assess the performance of different slaughterhouses in NI for the detection of bTB lesions in routinely slaughtered animals. It will enable DAERA policy makers to target improvements in slaughterhouse surveillance to enhance the bTB eradication programme.
PME in cattle is an important component of the bTB surveillance programme in NI; not only for the early detection of infected herds not yet disclosed by field surveillance (SCITT surveillance) or for detecting cattle that, for different reasons, were not disclosed as positives in the SCITT (e.g. anergic animals), but also to provide a supplementary means of monitoring the efficiency of field surveillance.
The LRS disclosure rate between 2011 and 2013 was 3 cattle/1000 slaughtered. Between 5·2% and 6·4% of all confirmed bTB-infected animals in those three years were detected at PME (unpublished results). The proportion of new bTB breakdowns first detected through slaughterhouse surveillance ranged from 18% in 2012 to 28% in 2013 (unpublished results), which is similar to that reported previously for NI [Reference Krebs20]. These figures give us an indication of the importance of slaughterhouse surveillance within the bTB eradication policy in NI. Similar figures were estimated in Great Britain (GB), where approximately 17% of all new OTF-status-withdrawn incidents detected in cattle herds every year (ranging from 16% in endemic TB annual testing areas to 31% in four-yearly testing areas) were first disclosed by slaughterhouse surveillance [21]. In the ROI, 27–46% of new bTB breakdowns between 2003 and 2004 were initially detected at slaughter [Reference Frankena22].
Our analysis standardized all slaughterhouses by considering differences in classes of cattle (age, whether they were purchased or not, and sex), time that the presenting herd had been free of bTB, incidence in the area of origin, and season of slaughter; this allowed a meaningful comparison of the risk of LRS disclosure and confirmation between different slaughterhouses.
There were substantial variations with regard to both LRS disclosure and bTB confirmation risks between the 10 approved bovine slaughter establishments in the country.
Ranking of the slaughterhouses by disclosure risk did not change between crude and adjusted analysis, which suggested that differences in the risk of disclosure and confirmation between slaughterhouses might be due to internal factors specific to slaughterhouses, such as line speed, light, and meat inspector performances [Reference Corner14, Reference Frankena22–Reference Olea-Popelka24]. There is scope for improvement, specifically in those slaughterhouses where the risk of disclosure is low and that of confirmation is high. It would be of benefit to the bTB control programme to increase sensitivity at the cost of lowering the specificity of slaughterhouse surveillance for bTB. An investigation should be carried out in those slaughterhouses with lower LRS disclosure risk to identify and address those characteristics that might lower their ability to identify bTB.
This study did not consider production type which has been described in the literature as a risk factor for bTB. However, in our data, 82·2% of the animals originated in beef production herds of which 76·7% were purchased. Beef cattle are very likely to be purchased instead of homebred and therefore we think that production type would have added similar information. Furthermore, purchase information was likely to have more biological meaning given that purchased animal would have more opportunities of becoming infected.
Factors such as age, slaughter season, patch incidence, time with OTF status, and whether the animal was purchased or homebred affected both the risk of LRS disclosure and LRS confirmation. The correlation between submission and confirmation was low and not statistically significant when adjusting for confounders. Animals killed between July and September were less likely to be identified as LRS, but their risk of being confirmed was higher compared with animals slaughtered between January and March. This may be related to diferences in transmission rates and testing frequency during grazing/housing seasons. Increased opportunities for infection transmission during the housing season [Reference Menzies and Neill25], a decrease in SCITT surveillance during the grazing season and the time for lesions to develop after infection may lead to more likely LRS confirmation during July to September. The inverse relationship was also the case for purchased animals, which had more risk of having an LRS disclosed [Reference Skuce26], but which were less likely to have the sample confirmed than homebred animals. Older animals had more chance of LRS disclosure, with the odds increasing with age. Studies on the associations between bTB and other cattle diseases, as well as between bTB and the location of bTB-like lesions, are currently being carried out by the Veterinary Sciences Division at the AFBI and by the Veterinary Epidemiology Unit in DAERA. Animals from herds located in high-incidence patches (above the third quantile; 9·48, 10·41 and 9·47 in 2011, 2012 and 2013, respectively; Fig 2) were more likely to have an LRS disclosed and confirmed as bTB in the laboratory.
Missing data for any of the variables used in the study accounted for 8·5% of the total slaughtered animals in NI, with 95% of these data being animals imported for direct slaughter. As part of an investigation of the proportionality of TB-positive animals imported from the ROI into NI from 2010 to 2012, it was reported that there was no statistical significance on the risk of LRS being detected and confirmed as bTB for cattle from NI compared with cattle imported from ROI for direct slaughter when adjusted for age, breed and sex (unpublished results). Therefore, we considered that these exclusions did not bias the study significantly.
It needs to be recognized that not all animals with bTB-like lesions would be found at PME, even if the examination technique were perfect and the conditions within the slaughterhouses were ideal for accurate examination. Some lesions are invisible to the naked eye. The primary complex is most frequently located in the lower parts of the respiratory tract and 70% of these lesions may only be found during careful examination and disection of the lungs into thin sections [Reference Domingo, Vidal and Marco5, Reference De Kantor27]. Also, it is important to highlight that not all infected animals have lesions at the time of slaughter. The existence of bTB lesions is directly related to the interplay between the host's defence mechanism and mycobacterial virulence factors [Reference Domingo, Vidal and Marco5]. A study in Australia comparing the sensitivity of routine slaughterhouse inspection procedures and detailed necropsy, estimated that slaughterhouse inspection failed to detect 47% of cattle with TB lesions [Reference Corner14]. This study concluded that the sensitivity of gross PME was affected by the method employed and the anatomical sites examined. Failure to detect visible lesions in TB skin reactors may be due to early infection and/or poor necropsy technique [Reference Corner28]. Indeed, McIlroy et al. found that 70% of lung lesions were <1 cm in diameter in a study of TB reactors [Reference McIlroy, Neill and McCracken23]. Experimental studies suggested that bTB lesions could be found in cattle as early as 14 days post-inoculation [Reference Cassidy29], whereas another study concluded that they could be found at 6–8 weeks post-infection [Reference Palmer30]. Garcia-Saenz et al. estimated that the individual slaughterhouse surveillance sensitivity for bTB in Catalonia (Spain) was 31% (95% CI 28·6–36·2 [Reference Garcia-Saenz31]. Therefore, the use of PME for the detection of bTB-infected animals is accepted as being poorly sensitive [Reference Whipple, Bolin and Miller1, Reference Corner14, Reference De Kantor27].
These results are in broad agreement with the results from several studies in ROI and GB [Reference Frankena22, Reference Olea-Popelka24, Reference Martin, O'Keeffe, White and Costello32–Reference Shittu34]. Especially in bTB endemic countries, an assessment of the efficiency of slaughterhouse surveillance to target improvements in inspection procedure is a useful tool to improve the country's eradication programme.
CONCLUSIONS
PME continues to play an important role in the bTB eradication programme in NI. The results of this study showed that there were differences in the risk of disclosure of bTB-like lesions in slaughtered cattle between slaughterhouses that could not be explained even when adjusted for selected variables related to animal and herd characteristics. Moreover, these differences might be explained by slaughterhouse-specific factors, such as inspection facilities or procedures. It is recommended that these slaughterhouses are assessed and areas that could be improved identified to increase detection of bTB, and therefore, improve the sensitivity of this surveillance component.
ACKNOWLEDGEMENTS
The authors thank Mark Woodside (DAERA) for extracting the data used in this study, and the Veterinary Officers (DAERA) and the Agri-Food and Biosciences Intitute for gathering part of the data used in this study.
This research received no specific grant from any funding agency, commercial or not-for-profit sectors.
DECLARATION OF INTEREST
None.