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Mastitis risk effect on the economic consequences of paratuberculosis control in dairy cattle: A stochastic modeling study


Authors: Leslie J. Verteramo Chiu aff001;  Loren W. Tauer aff002;  Yrjo T. Gröhn aff001;  Rebecca L. Smith aff003
Authors place of work: Department of Population Medicine and Diagnostic Sciences, Cornell University College of Veterinary Medicine, Ithaca, New York, United States of America aff001;  Charles H. Dyson School of Applied Economics and Management, Cornell SC Johnson Business College, Cornell University, Ithaca, New York, United States of America aff002;  Department of Pathobiology, University of Illinois, College of Veterinary Medicine, Urbana, Illinois, United States of America aff003
Published in the journal: PLoS ONE 14(9)
Category: Research Article
doi: https://doi.org/10.1371/journal.pone.0217888

Summary

The benefits and efficacy of control programs for herds infected with Mycobacterium avium subsp. paratuberculosis (MAP) have been investigated under various contexts. However, most previous research investigated paratuberculosis control programs in isolation, without modeling the potential association with other dairy diseases. This paper evaluated the benefits of MAP control programs when the herd is also affected by mastitis, a common disease causing the largest losses in dairy production. The effect of typically suggested MAP controls were estimated under the assumption that MAP infection increased the rate of clinical mastitis. We evaluated one hundred twenty three control strategies comprising various combinations of testing, culling, and hygiene, and found that the association of paratuberculosis with mastitis alters the ranking of specific MAP control programs, but only slightly alters the cost-benefit difference of particular MAP control components, as measured by the distribution of net present value of a representative U.S. dairy operation. In particular, although testing and culling for MAP resulted in a reduction in MAP incidence, that control led to lower net present value (NPV) per cow. When testing was used, ELISA was more economically beneficial than alternative testing regimes, especially if mastitis was explicitly modeled as more likely in MAP-infected animals, but ELISA testing was only significantly associated with higher NPV if mastitis was not included in the model at all. Additional hygiene was associated with a lower NPV per cow, although it lowered MAP prevalence. Overall, the addition of an increased risk of mastitis in MAP-infected animals did not change model recommendations as much as failing to consider.

Keywords:

Death rates – Milk – Enzyme-linked immunoassays – Hygiene – Mastitis – Paratuberculosis – Bovine mastitis – Molting

Introduction

Paratuberculosis, or Johne’s Disease, is a chronic intestinal disease of ruminants caused by infection with Mycobacterium avium subsp. paratuberculosis (MAP). Animals are usually infected at a young age, with a variable and often extended latent period [1]. Infected animals have lower milk production [29], decreased reproductive performance in later stages of disease [6,1012], and are often culled early [5,13]. It is difficult to control MAP in dairy herds; many tests have poor diagnostic sensitivity [14], MAP persists in the environment for long periods of time [15], paratuberculosis symptoms are slow to develop [16], and the available vaccines are limited in distribution due to their cross-reaction with tuberculosis diagnostics [17].

The debate over the economically optimal control method for MAP results from a wide range of models and assumptions. Some studies have found test and culling to be consistently economically beneficial [18,19], while others have found that cost-efficacy of test and cull required subsidized testing costs [20] or only culling of animals with decreased milk production during MAP latency [21]. Simulation models have identified economically beneficial programs, such as quarterly serum enzyme-linked immunosorbent assay (ELISA) testing [22], quarterly milk ELISA testing [23], risk-based testing accompanied by infection control [24], vaccination or infection control [25], testing in series with ELISA and quantitative polymerase chain reaction (qPCR) [26], and annual fecal culture accompanied by infection control [27]. Massaro et al. [28] found that a more sensitive ELISA test could be economically beneficial in US dairy herds. Others have found that hygiene improvement was effective in decreasing transmission rate [25,29], especially in combination with testing and culling [1,30]. Our previous work found that some MAP control programs were not significantly better than no control, and that some managerial practices can produce better results than some testing and culling controls [31].

One factor that none of these studies addressed is the role of MAP infection in susceptibility to other infections. For example, higher mastitis incidence has been found in MAP positive farms in two different studies [32,33], and Rossi et al. [34] found that MAP-infected animals had significantly higher rates of clinical mastitis. As clinical mastitis is one of the most economically important diseases of dairy herds, a positive association between MAP infection and mastitis could greatly alter the cost-benefit estimate of MAP and mastitis control. Even with no association, controlling for either disease may have spillover effects on the other disease.

The goal of this research is to examine the economic consequences of paratuberculosis in US dairy herds and the benefits of 123 specific control strategies involving various combinations of hygiene levels, types of testing, and decisions on culling, while accounting for the rise in mastitis cases associated with paratuberculosis infection.

Materials and methods

The infection and testing model (Fig 1) has been previously described [35], and used for an economic analysis of MAP [31]. This is a continuous-time model, simulated over 5 years after a burn-in of 50 years using values representative of US dairy herds. Details are available in the supplemental material (S1 Table). Briefly, calves may be born susceptible or infected via vertical transmission. Susceptible calves may be infected by contact with transiently-shedding infected calves or with shedding adults. All calves age into heifers; susceptible heifers may be infected by contact with shedding adults, while infected heifers are assumed to be latently infected. All heifers age into adults. Adults infected as calves or heifers may have progressing infections, resulting in fast transition from latency, through a low-shedding phase, to high shedding and clinical disease. However, some adults infected as calves or heifers and all adults infected by contact with shedding adults experience non-progressing infections, which remain in latency for a longer period of time and only enter the low-shedding phase. All animals may be culled or die, based on an age-appropriate mortality/culling rate.

Fig. 1. Schematic of model for Mycobacterium avium subsp. paratuberculosis in a commercial dairy herd.
Schematic of model for <i>Mycobacterium avium</i> subsp. <i>paratuberculosis</i> in a commercial dairy herd.

The economic model tracks the daily milk production of all animals in the herd and calculates the net value of the herd as the value of the milk produced plus the value of any culled animals sold, minus the cost of producing milk, the cost of raising calves and heifers, and the cost of MAP testing. Milk production values used are based on previous analysis [9] of three commercial dairy herds in the Northeast US, chosen to be representative of the region. All herds used indoor freestall housing with typical diets and on-farm computerized record systems.[36]

Mastitis risk and milk production

The risk of first clinical mastitis (CM) case, and the incidence of CM, has been found to be associated with MAP infection status in cows [34], possibly due to the immune system being affected by MAP. Clinical mastitis risk was assumed to be constant for all cows; although clinical mastitis risk is known to increase with parity, this model was not age-stratified, thereby averaging out clinical mastitis risk among all animals. Annualized risk of CM by all causes was calculated from Bar et al. [37] by averaging the monthly risk over a 10 month lactation and across the first 4 lactations, then adding the total monthly risk, annualrisk=10*∑p=14∑m=110riskp,m104. The range of possible values was identified by adding up the monthly risk for each lactation individually (∑m=110riskp,m). Due to the lack of data to support modeling of secondary CM cases or subclinical mastitis, these events were not modeled.

In order to determine if the effect of CM on milk production would be exacerbated by MAP status, we statistically analyzed milk production in animals with well-defined MAP infection status as described previously [9]. Briefly, we conducted a linear regression analysis to assess the effect of MAP progression (defined as progressing, non-progressing, or test-negative, where progressing animals had at least one high-positive test result) and current MAP status (defined as test-negative, latent, low-shedding, or high-shedding). In this analysis, a dichotomous term was added to indicate whether an animal had experienced a CM event in the previous 30 days. In the previous study, the linear score (log10 of the somatic cell count) was included to control for subclinical and clinical mastitis; in this analysis, that variable was not included to avoid collinearity with the CM variable.

Model simulation

The model was simulated under 3 different assumptions: CM association with MAP (MA), no CM association with MAP (NMA), and no CM at all (NM). In the MA scenario, the rate of CM cases was assumed to be related to MAP status. The hazard ratios from the Cox proportional hazards model for MAP positive vs. negative animals [34], controlling for parity, were used to inflate the CM risk for MAP positive animals. In the NMA scenario, the rate of CM cases was assumed to be unchanged by MAP status. In the NM scenario, it was assumed that CM cases were excluded in the model. In the MA and NMA scenarios, CM occurred in susceptible adults at rate ψ, the annualized risk, and in MAP infected adults at rate ξIψ, where ξI is the hazard ratio 1.89 [34].

Upon the occurrence of a CM case, the following actions occurred: 1) remove the milk lost due to CM, qmast, from the period’s milk production; 2) add the cost of treating CM, tmast, to the period’s cost; 3) determine if the CM case resulted in mortality. Clinical mastitis mortality was assumed to be μm. It was assumed that no voluntary culling occurred due to a first case of CM.

The net present value (NPV) of each scenario was calculated as

where, t is time in years, κ(t) is the value of the herd in year t, r is the discount rate, and T is the final time period. The second term represents a terminal wealth term, the NPV of the last year cash flow continuing into perpetuity, to account for the value of the herd going forward past the terminal year of T. Herds were simulated for 5 years, which is considered a realistic planning window for commercial dairy herds.

Determining stochastic dominance

Ranking of control programs by the distribution of NPV from 100 iterations of a five year period was performed using first and second-order dominance [38]. First-order and second-order stochastic dominance (FOSD and SOSD, respectively) are methods of determining preference for an activity with variable (stochastic) results; a dominant strategy by either method is to be preferred to its comparator. First-order stochastic dominance is relevant for decision makers who prefer more wealth to less wealth (increasing utility function), and second-order stochastic dominance is relevant for decision makers who in addition to preferring more to less wealth are also risk averse (increasing and concave utility function). These are defined and interpreted by Levy [38].

Briefly, if NPVA is the cumulative distribution function of the NPV of control strategy A and NPVB is the cumulative distribution function of the NPV of control strategy B, first-order dominance of strategy A states that

for all possible values of x (the range of simulated NPV values for a farm in a given scenario) and with a strict inequality for at least one value of x.

Likewise, second-order dominance of strategy A states that

for all possible values of x (as in Eq 3), where AUC(i)[0:x] is the area under the curve of the cumulative distribution function of distribution i from 0 to x. For this analysis, we will focus on SOSD, as it covers FOSD and includes a measure of risk aversion. Examples of the use of SOSD can be found in Harris and Mapp.[39]

Analyzing dominance results

Each of the 123 control strategies comprises four components: hygiene level, test used, test frequency, and which animals are culled (Table 1). To estimate the effect of each of these components on dominance, we estimated a linear regression of the proportion of dominated strategies under SOSD on each of the strategies’ components, measured by dummy variables. The econometric model has the following form,

Where Y is the proportion that strategy i SOSD the other strategies, where the value of Y ranges from 0 to 1. H is an n x 2 matrix of hygiene level indicators (standard and high hygiene), T is an n x 4 matrix of test indicator (FC, ELISA, PCR, and hypothetical testing of calves with FC), C is an n x 2 matrix of culling policy (cull all test positive, and cull all high shedders), F is an n x 4 matrix of frequency of testing (annual, biannual, continuous annual, continuous biannual). Parameter α is the intercept term, which includes the effects of moderate hygiene, and culling after 2 positive tests. Parameters βH, βT, βC, βF are vectors to be estimated for each of the components of the strategies. This regression is conducted separately for each of the three mastitis assumptions and assumes additive linear effects only. To determine which factors are most associated with changes in the NPV, this analysis was repeated using the difference between the NPV of a particular iteration and the NPV of no control from the same starting condition, expressed as an amount per cow, as the Y. Each of these analyses was repeated for each of the mastitis assumptions (NM, NMA, and MA) and the fitted coefficients were compared. The analysis was repeated at two different herd sizes (100 and 1000) and two different initial MAP prevalence levels (7% and 20%), but results will focus on the 1000-head herd with 20% initial prevalence.

Tab. 1. Paratuberculosis control strategies and ID numbers.
Paratuberculosis control strategies and ID numbers.

Sensitivity analysis

Global sensitivity analysis was performed using optimized Latin Hypercube sampling via the lhs package [40] with 500 parameter sets. For each parameter set, a 1000 head herd was simulated 100 times from the same randomly drawn initial population values under three generalized culling strategies (none, cull all positive adults, and cull all positive calves) with and without improved hygiene. Impact of parameters on NPV was determined using the Pearson’s rank correlation coefficient. All parameters used are shown in Tables 24. Where variability in parameters was not provided by the source, parameters were varied by ± 10% for the sensitivity analysis. Where variability in parameters was available, parameters were varied over their interquartile ranges. Testing parameters were varied over the range of the interquartile ranges of all tests, and hygiene parameters were varied over the range of the possible additional hygiene levels. Parameters were considered significantly related to NPV at the level of α = 0.05 with Bonferroni’s correction.

Tab. 2. Biological parameters and interquartile ranges (IQR) used in a model of Mycobacterium avium subsp. paratuberculosis and clinical mastitis co-infection in a dairy herd.
Biological parameters and interquartile ranges (IQR) used in a model of <i>Mycobacterium avium</i> subsp. <i>paratuberculosis</i> and clinical mastitis co-infection in a dairy herd.
Tab. 3. Testing parameters and interquartile ranges (IQR) used in a model of Mycobacterium avium subsp. paratuberculosis infection in a dairy herd.
Testing parameters and interquartile ranges (IQR) used in a model of <i>Mycobacterium avium</i> subsp. <i>paratuberculosis</i> infection in a dairy herd.
Tab. 4. Economic parameters and inter-quartile ranges (IQR) used in a model of Mycobacterium avium subsp. paratuberculosis and mastitis co-infection in dairy herds.
Economic parameters and inter-quartile ranges (IQR) used in a model of <i>Mycobacterium avium</i> subsp. <i>paratuberculosis</i> and mastitis co-infection in dairy herds.

Results

Milk production results

There were 31,583 monthly milk observations available for analysis, of which 537 occurred within a month of a CM event. Of those, 424 were in test-negative individuals, 97 were in non-progressing animals (85 latent, 12 low-shedding), and 16 were in progressing animals (14 latent, 2 low-shedding). Adding a variable indicating a recent CM did not improve the fit of the model including an interaction between MAP progression and status (BIC = 216,536 with the term and BIC = 216,527 without the term), so milk loss in animals with both MAP infection and CM was simulated to be additive.

Model results

For simplicity, we will present rankings of only 13 potential control options, and the results of SOSD only, as SOSD implies FOSD. These 13 control options were chosen as they were the highest-ranked options, by SOSD, when compared to all possible control options. The base for comparison is no MAP control. If testing is used, we assume that it will be based on the serum enzyme-linked immunosorbent assay (ELISA) test, administered to all animals either annually or biannually. Animals may be culled after any positive test, only after a test result indicating a high-positive response, or only after the second positive test result. Additionally, the farm may choose to continue ELISA testing after 5 negative whole-herd tests, or to discontinue testing after the 5th negative whole-herd test.

Model results for this subset of control options are shown in Table 5 for a 1,000 head herd with 20% initial shedding prevalence under CM association with MAP (MA), no CM association with MAP (NMA), and no CM at all (NM); results for other initial herd sizes and initial shedding prevalence are generally similar, and are shown in S2 Table. The model predicted that all control programs would decrease the median true infection prevalence of paratuberculosis over 5 years, and most would decrease the median shedding prevalence (Fig 2).

Tab. 5. ELISA-based testing strategies and their NPV distribution and number of second-order dominated strategies for each mastitis scenario.
ELISA-based testing strategies and their NPV distribution and number of second-order dominated strategies for each mastitis scenario.
Results are for a 20% initial MAP prevalence in a 1,000 head herd.
Fig. 2. Predicted change in shedding prevalence of paratuberculosis infection after 5 years of control in a 1,000 cow herd with a median initial prevalence of 20%.
Predicted change in shedding prevalence of paratuberculosis infection after 5 years of control in a 1,000 cow herd with a median initial prevalence of 20%.

Stochastic dominance results

Regression results for the econometric model of SOSD rank for each of the CM scenarios and MAP prevalence are shown in Fig 3 and Table 6, using results of all 123 control combinations (Table 1). All six regressions have a similar set of significant variables, but their effects can be different across herd scenarios. Not testing was consistently significantly worse than annual testing, with the exception being in a herd with low initial prevalence and assuming NMA. Biannual testing was not significantly different from annual testing in most scenarios. Continuing to test after 5 negative whole-herd tests was significantly better than discontinuing testing. ELISA testing was significantly better than FC or testing calves in the MA and NM scenarios, but not in the NMA scenario. However, in the NMA scenario with high initial prevalence, FC and PCR were significantly worse than testing calves. High levels of hygiene were significantly worse than standard in all cases, and moderate levels of hygiene were significantly worse than standard in most cases.

Fig. 3. Coefficients from multivariable linear regressions for the overall second-order stochastic dominance rank (1 = best, 123 = worst) of MAP control programs, separated by herd size, initial shedding prevalence, and assumption about relationship between MAP and clinical mastitis (MA: Mastitis association; NMA: No mastitis association; NM: No mastitis).
Coefficients from multivariable linear regressions for the overall second-order stochastic dominance rank (1 = best, 123 = worst) of MAP control programs, separated by herd size, initial shedding prevalence, and assumption about relationship between MAP and clinical mastitis (MA: Mastitis association; NMA: No mastitis association; NM: No mastitis).
Central bar is estimate, box shows 95% confidence interval around estimate.
Tab. 6. Linear regression results of the proportion of dominated strategies under SOSD on strategy characteristics on all initial herds.
Linear regression results of the proportion of dominated strategies under SOSD on strategy characteristics on all initial herds.
Constant term includes the effects of annual continuous testing of calves, culling animals after one positive test, and standard hygiene. Model assumes additive linear effects.

Regression results for the econometric model of NPV for each of the CM scenarios and herds are shown in Fig 4. Biannual testing was significantly associated with a lower NPV compared to not testing, as was annual testing in almost all cases. Use of an ELISA test was significantly associated with a higher NPV than other test choices. Moderate or high hygiene levels were significantly associated with a lower NPV than standard hygiene. In a large herd, culling only high positive cows or after the second positive test was significantly associated with a slightly higher NPV; this relationship was not seen in small herds. There were few differences in coefficient values across CM scenarios.

Fig. 4. Coefficients from multivariable linear regressions for change in NPV per cow by adding MAP control programs, separated by herd size, initial shedding prevalence, and assumption about relationship between MAP and clinical mastitis (MA: Mastitis association; NMA: No mastitis association; NM: No mastitis).
Coefficients from multivariable linear regressions for change in NPV per cow by adding MAP control programs, separated by herd size, initial shedding prevalence, and assumption about relationship between MAP and clinical mastitis (MA: Mastitis association; NMA: No mastitis association; NM: No mastitis).
Central bar is estimate, box shows 95% confidence interval around estimate.

Sensitivity analysis results

The partial rank correlation coefficients of all significantly correlated parameters from the global sensitivity analysis are shown in Fig 5. Most scenarios had the same parameters consistently related with NPV, primarily economic and production-related parameters. The risk of clinical mastitis was significantly related to NPV in all scenarios.

Fig. 5. Partial rank correlation coefficients (PRCC) from a global sensitivity analysis on net present value over 5 years of paratuberculosis control, assuming an association between mastitis incidence and MAP infection.
Partial rank correlation coefficients (PRCC) from a global sensitivity analysis on net present value over 5 years of paratuberculosis control, assuming an association between mastitis incidence and MAP infection.

Discussion

This research shows that, in the case of MAP and clinical mastitis, consideration of interacting disease systems did not importantly change the results of this economic analysis of disease control. Adding an increased rate of CM among infected animals to an economic model of paratuberculosis control only slightly changed the ranking of control programs. Specifically, failing to include CM in the model resulted in a weaker preference for standard hygiene alone. Including CM but not its association with paratuberculosis resulted in a stronger preference for standard hygiene alone, biannual ELISA testing and culling adults after 2 positive tests, and continuous ELISA with the same culling policy. Culling for paratuberculosis should in theory have the side benefit of partially controlling for CM. However, the inclusion of an association between CM and paratuberculosis did not change the overall conclusions of this economic model. This is likely due to two factors: the high cost of MAP control and the relatively small size of the impact of MAP on mastitis.

We believe that the high cost of MAP control is the reason that few control strategies have been shown to economically dominate no control. If the cost of implementing testing or hygiene, not including costs related to culling of animals, were removed from the NPV, the distributions are somewhat similar for many control programs (S1 Fig). However, the cost of these programs is high (S3 Table): over a 5 year period, in a 1,000-head herd, the discounted cost of testing all adults annually via ELISA was calculated at $16,148. Testing all adult cows biannually using fecal culture or PCR was more than an order of magnitude higher. These numbers do not include the costs of culling test-positive animals, or the lower income due to smaller milking herd sizes after test-based culling in closed herds, each of which would raise the cost of control even more.

Previous studies have disagreed as to the cost-benefit of testing for MAP. While some models suggest that test and cull programs are effective at reducing the prevalence of MAP [30], others suggest that they are not sufficient to control MAP by themselves [23,67]. Our work here has shown that they are capable of decreasing the shedding prevalence of MAP, but are unlikely to be economically beneficial. The exception would be ELISA testing, which others have also found to be potentially economically beneficial [28]. This is likely due to the low cost and fast turn-around time for ELISA results.

We found here that hygiene was not economically beneficial by any measure, and that this was unrelated to the relationship between MAP and mastitis. We had hypothesized that expensive control programs such as hygiene improvement (estimated here to cost a 1,000-head herd between $95,652 and $133,600 over a five year period) would become economically beneficial as their effect on other pathogens was considered. The hygiene changes made to improve MAP control, however, are unlikely to directly impact CM incidence. While other models have suggested that hygiene changes are indeed economically beneficial [29], these may be assuming a lower base hygiene level than our simulated herds. There also may be more benefits from hygiene improvement over a longer time frame than the 5 years used here.

Our model did not show a strong effect of paratuberculosis association with CM on economically optimal control. The global sensitivity analysis also showed that the hazard ratio for CM incidence in MAP-infected animals was not significantly associated with NPV. Likely, this is because the association between paratuberculosis and CM is so small in a practical sense. The hazard ratio for first CM cases among MAP-infected animals is 1.89 (IQR: 1.53–2.33). However, with an annualized rate of 0.27 CM cases/animal/year, this translates into an annual average of 27 extra cases of CM in a 1,000 head herd with 20% MAP infection prevalence. Given a cost per case of CM of $90, not counting mortality, the additional cost to the herd is approximately $2,500. Discounted over a 5 year simulation period, that results in a total cost of $11,655 due to additional CM cases. This is less than the cost of the least expensive MAP control program (annual ELISA testing), and, as no program can immediately eliminate MAP in the herd, not all of the potential cost from the increased CM cases would be avoided by implementing control.

One large limitation of this model was the lack of age stratification, resulting in the necessary simplification of constant clinical mastitis risk. It is known that clinical mastitis risk increases with parity [68] and changes throughout the lactation [37]. However, accounting for age and lactation stage in a compartmental model would cause the model to become intractable. We were also limited by other assumptions inherent in this modeling structure, such as homogeneous infection risk and progression pathways and the necessity of using average milk production values for all animals. For more realistic modeling frameworks, it becomes necessary to transition to a more computationally demanding modeling system, such as the agent-based model presented in Verteramo Chiu et al. [69].

Regardless of the effects of MAP associations with CM, some overall preferences were determined. On average, continuing to test and cull after 5 negative whole-herd tests was always preferred. ELISA was the best-ranked test, followed by no testing. Standard hygiene was always preferred, with increasing hygiene levels associated with economically worse-ranked programs.

Conclusion

We have found that, in the setting of a typical commercial US dairy, the addition of clinical mastitis to a model for MAP control only slightly changed the ranking of individual control programs, but did not greatly change the overall cost-benefit difference of components of MAP control. These suggest that only testing by ELISA may be economically beneficial.

Supporting information

S1 Fig [tiff]
Net present value and discounted cost of control for each paratuberculosis control strategy over 5 years in a 1,000-head dairy herd with 7% initial paratuberculosis prevalence and increased mastitis in paratuberculosis-infected cows.

S1 Table [docx]
Events, changes, and rates used for simulation via Gillespie’s direct algorithm.

S2 Table [docx]
ELISA-based strategies and their NPV distribution and number of dominated strategies for each mastitis scenario and herd type.

S3 Table [docx]
Discounted cost of implementing different possible paratuberculosis controls, not including culling and replacement costs, over a 5 year period in a 1,000-head dairy herd.


Zdroje

1. Marcé C, Ezanno P, Weber MF, Seegers H, Pfeiffer DU, Fourichon C. Modeling within-herd transmission of Mycobacterium avium subspecies paratuberculosis in dairy cattle: a review. J Dairy Sci. 2010;93: 4455–70. doi: 10.3168/jds.2010-3139 20854979

2. Kudahl AB, Nielsen SS, Sørensen JT. Relationship between antibodies against Mycobacterium avium subsp. paratuberculosi s in milk and shape of lactation curves. Prev Vet Med. 2004;62: 119–134. doi: 10.1016/j.prevetmed.2003.11.008 15156998

3. Aly SS, Anderson RJ, Adaska JM, Jiang J, Gardner IA. Association between Mycobacterium avium subspecies paratuberculosis infection and milk production in two California dairies. J Dairy Sci. 2010;93: 1030–40. doi: 10.3168/jds.2009-2611 20172223

4. Nielsen SS, Krogh MA, Enevoldsen C. Time to the occurrence of a decline in milk production in cows with various paratuberculosis antibody profiles. J Dairy Sci. 2009;92: 149–55. doi: 10.3168/jds.2008-1488 19109273

5. Lombard JE, Garry FB, McCluskey BJ, Wagner BA. Risk of removal and effects on milk production associated with paratuberculosis status in dairy cows. J Am Vet Med Assoc. 2005;227: 1975–1981. doi: 10.2460/javma.2005.227.1975 16379637

6. Raizman EA, Fetrow JP, Wells SJ, Godden SM, Oakes MJ, Vazquez G. The association between Mycobacterium avium subsp. paratuberculosis fecal shedding or clinical Johne’s disease and lactation performance on two Minnesota, USA dairy farms. Prev Vet Med. 2007;78: 179–195. doi: 10.1016/j.prevetmed.2006.10.006 17118473

7. Gonda MG, Chang YM, Shook GE, Collins MT, Kirkpatrick BW. Effect of Mycobacterium paratuberculosis infection on production, reproduction, and health traits in US Holsteins. Prev Vet Med. 2007;80: 103–119. doi: 10.1016/j.prevetmed.2007.01.011 17350703

8. Sorge US, Lissemore KD, Godkin A, Hendrick SH, Wells SJ, Kelton DF. Associations between paratuberculosis milk ELISA result, milk production, and breed in Canadian dairy cows. J Dairy Sci. 2011;94: 754–761. doi: 10.3168/jds.2010-3404 21257043

9. Smith RL, Gröhn YT, Pradhan AK, Whitlock RH, Van Kessel JS, Smith JM, et al. The effects of progressing and nonprogressing Mycobacterium avium ssp. paratuberculosis infection on milk production in dairy cows. J Dairy Sci. 2016;99: 1383–1390. doi: 10.3168/jds.2015-9822 26686721

10. Vanleeuwen JA, Haddad JP, Dohoo IR, Keefe GP, Tiwari A, Tremblay R. Associations between reproductive performance and seropositivity for bovine leukemia virus, bovine viral-diarrhea virus, Mycobacterium avium subspecies paratuberculosis, and Neospora caninum in Canadian dairy cows. Prev Vet Med. 2010;94: 54–64. doi: 10.1016/j.prevetmed.2009.11.012 20015556

11. Smith RL, Strawderman RL, Schukken YH, Wells SJ, Pradhan AK, Espejo LA, et al. The effect of Johne’s disease status on reproduction and culling in dairy cattle. J Dairy Sci. 2010;93: 3513–3524. doi: 10.3168/jds.2009-2742 20655419

12. Marcé C, Beaudeau F, Bareille N, Seegers H, Fourichon C. Higher non-return rate associated with Mycobacterium avium subspecies paratuberculosis infection at early stage in Holstein dairy cows. Theriogenology. 2009;71: 807–16. doi: 10.1016/j.theriogenology.2008.10.017 19117602

13. Tiwari A, VanLeeuwen JA, Dohoo IR, Stryhn H, Keefe GP, Haddad JP. Effects of seropositivity for bovine leukemia virus, bovine viral diarrhoea virus, Mycobacterium avium subspecies paratuberculosis, and Neospora caninum on culling in dairy cattle in four Canadian provinces. Vet Microbiol. 2005;109: 147–158. doi: 10.1016/j.vetmic.2005.05.011 15970402

14. Barkema HW, Orsel K, Nielsen SS, Koets AP, Rutten VPMG, Bannantine JP, et al. Knowledge gaps that hamper prevention and control of Mycobacterium avium subspecies paratuberculosis infection. Transbound Emerg Dis. 2017;65: 125–148. doi: 10.1111/tbed.12723 28941207

15. Moravkova M, Babak V, Kralova a, Pavlik I, Slana I. Culture and quantitative IS900 Real-time PCR-based analysis of the persistence of Mycobacterium avium subsp. paratuberculosis in a controlled dairy cow farm environment. Appl Environ Microbiol. 2012;78: 6608. doi: 10.1128/AEM.01264-12 22773642

16. Ferrouillet C, Wells SJ, Hartmann WL, Godden SM, Carrier J. Decrease of Johne’s disease prevalence and incidence in six Minnesota, USA, dairy cattle herds on a long-term management program. PrevVetMed. 2009;88: 128–137.

17. Garcia AB, Shalloo L. Invited review : The economic impact and control of paratuberculosis in cattle. J Dairy Sci. 2015;98: 1–21.

18. Pillars RB, Grooms DL, Wolf CA, Kaneene JB. Economic evaluation of Johne’s disease control programs implemented in Michigan dairy farms. Prev Vet Med. 2009;90: 223–232. doi: 10.1016/j.prevetmed.2009.04.009 19464741

19. Radia D, Bond K, Limon G, van Winden S, Guitian J. Relationship between periparturient management, prevalence of MAP and preventable economic losses in UK dairy herds. Vet Rec. 2013;173: 343–+. doi: 10.1136/vr.101408 23897995

20. Groenendaal H, Wolf CA. Farm-level economic analysis of the US national Johne’s Disease Demonstration Herd Project. J Am Vet Med Assoc. 2008;233: 1852–1858. doi: 10.2460/javma.233.12.1852 19072597

21. Wolf R, Clement F, Barkema HW, Orsel K. Economic evaluation of participation in a voluntary Johne’s disease prevention and control program from a farmer’s perspective-The Alberta Johne’s Disease Initiative. J Dairy Sci. 2014;97: 2822–34. doi: 10.3168/jds.2013-7454 24582447

22. Robins J, Bogen S, Francis A, Westhoek A, Kanarek A, Lenhart S, et al. Agent-based model for Johne’s disease dynamics in a dairy herd. Vet Res. 2015;46: 68. doi: 10.1186/s13567-015-0195-y 26091904

23. Kudahl AB, Sørensen JT, Nielsen SS, Østergaard S. Simulated economic effects of improving the sensitivity of a diagnostic test in paratuberculosis control. Prev Vet Med. 2007;78: 118–29. doi: 10.1016/j.prevetmed.2006.10.004 17101188

24. Kudahl AB, Nielsen SS, Østergaard S. Economy, efficacy, and feasibility of a risk-based control program against paratuberculosis. J Dairy Sci. 2008;91: 4599–609. doi: 10.3168/jds.2008-1257 19038935

25. Groenendaal H, Galligan DT. Economic consequences of control programs for paratuberculosis in midsize dairy farms in the United States. J Am Vet Med Assoc. 2003;223: 1757–1763. doi: 10.2460/javma.2003.223.1757 14690205

26. Aly SS, Anderson RJ, Whitlock RH, Fyock TL, McAdams SC, Byrem TM, et al. Cost-effectiveness of diagnostic strategies to identify Mycobacterium avium subspecies paratuberculosis super-shedder cows in a large dairy herd using antibody enzyme-linked immunosorbent assays, quantitative real-time polymerase chain reaction, and bacte. J Vet Diagnostic Investig. 2012;24: 821–32. doi: 10.1177/1040638712452107 22807510

27. Cho J, Tauer LW, Schukken YH, Smith RL, Lu Z, Gröhn YT. Cost Effective Control Strategies for Johne’s Disease in Dairy Herds. Can J Agric Econ. 2013;61: 583–608. doi: 10.1111/j.1744-7976.2012.01270.x

28. Massaro T, Lenhart S, Spence M, Drakes C, Yang G, Agusto F, et al. Modeling For Cost Analysis Of Johne’s Disease Control Based On EVELISA Testing. J Biol Syst. 2013;21: 1340010. doi: 10.1142/S021833901340010X

29. Dorshorst NC, Collins MT, Lombard JE. Decision analysis model for paratuberculosis control in commercial dairy herds. Prev Vet Med. 2006;75: 92–122. Available: http://www.sciencedirect.com/science/article/pii/S0167587706000547 16564101

30. Konboon M, Bani-yaghoub M, Id POP, Rhee N, Id SA. A nested compartmental model to assess the efficacy of paratuberculosis control measures on U. S. dairy farms. 2018; 1–25.

31. Smith RL, Al-Mamun MA, Gröhn YT. Economic consequences of paratuberculosis control in dairy cattle: A stochastic modeling study. Prev Vet Med. 2017;138: 17–27. doi: 10.1016/j.prevetmed.2017.01.007 28237232

32. Diéguez FJ, Arnaiz I, Sanjuan ML, Vilar MJ, Yus E. Management practices associated with Mycobacterium avium subspecies paratuberculosis infection and the effects of the infection on dairy herds. Vet Rec. 2008;162: 614–617. doi: 10.1136/vr.162.19.614 18480020

33. Arrazuria R, Arnaiz I, Fouz R, Calvo C, Eiras C, Diaguez F. Association between Mycobacterium avium subsp. paratuberculosis infection and culling in dairy cattle herds Asociación entre la infección por Mycobacterium avium subsp. paratuberculosis y las causas de eliminación en rebaños de ganado lechero. Arch Med Vet. 2008;44: 39–44. doi: 10.4067/S0301-732X2014000100006

34. Rossi G, Gröhn YT, Schukken YHYHYH, Smith RL. The effect of Mycobacterium avium subspecies paratuberculosis infection on clinical mastitis occurrence in dairy cows. J Dairy Sci. 2017;100: 7446–7454. doi: 10.3168/jds.2017-12721 28711261

35. Smith RL, Schukken YH, Gröhn YT. A new compartmental model of Mycobacterium avium subsp paratuberculosis infection dynamics in cattle. Prev Vet Med. 2015;122: 298–305. doi: 10.1016/j.prevetmed.2015.10.008 26520176

36. Pradhan AK, Van Kessel JAS, Karns JS, Wolfgang DR, Hovingh E, Nelen KA, et al. Dynamics of endemic infectious diseases of animal and human importance on three dairy herds in the northeastern United States. J Dairy Sci. 2009;92: 1811–1825. doi: 10.3168/jds.2008-1486 19307664

37. Bar D, Tauer LW, Bennett GJ, González RN, Hertl JA, Schukken YH, et al. The cost of generic clinical mastitis in dairy cows as estimated by using dynamic programming. J Dairy Sci. 2008;91: 2205–14. doi: 10.3168/jds.2007-0573 18487643

38. Levy H. Stochastic Dominance and Expected Utility : Survey and Analysis. 1Management Sci. 1992;38: 555–593.

39. Harris TR, Mapp HP. A Stochastic Dominance Comparison of Water-Conserving Irrigation Strategies. Am J Agric Econ. 1986;68: 298. doi: 10.2307/1241431

40. Carnell R. lhs: Latin Hypercube Samples [Internet]. 2017. https://cran.r-project.org/package=lhs

41. Mitchell RM, Whitlock RH, Gröhn YT, Schukken YH. Back to the real world: Connecting models with data. Prev Vet Med. 2015;118: 215–225. doi: 10.1016/j.prevetmed.2014.12.009 25583453

42. Smith RL, Al-Mamun MA, Gröhn YT. Economic consequences of paratuberculosis control in dairy cattle: A stochastic modeling study. Prev Vet Med. 2017;138: 17–27. doi: 10.1016/j.prevetmed.2017.01.007 28237232

43. Collins MT, Eggleston V, Manning EJB. Successful control of Johne’s disease in nine dairy herds: results of a six-year field trial. J Dairy Sci. 2010;93: 1638–43. doi: 10.3168/jds.2009-2664 20338441

44. Benedictus A, Mitchell RM, Linde-Widmann M, Sweeney RW, Fyock TL, Schukken YH, et al. Transmission parameters of Mycobacterium avium subspecies paratuberculosis infections in a dairy herd going through a control program. Prev Vet Med. 2008;83: 215–227. doi: 10.1016/j.prevetmed.2007.07.008 17868937

45. Nielsen SS, Toft N. Effect of management practices on paratuberculosis prevalence in Danish dairy herds. J Dairy Sci. 2011;94: 1849–1857. doi: 10.3168/jds.2010-3817 21426974

46. Clark DL, Koziczkowski JJ, Radcliff RP, Carlson RA, Ellingson JLE. Detection of Mycobacterium avium subspecies paratuberculosis: comparing fecal culture versus serum enzyme-linked immunosorbent assay and direct fecal polymerase chain reaction. J Dairy Sci. 2008;91: 2620–7. doi: 10.3168/jds.2007-0902 18565921

47. Sweeney RW, Whitlock RH, McAdams SC, Fyock TL. Longitudinal Study of ELISA Seroreactivity to Mycobacterium Avium subsp. Paratuberculosis in Infected Cattle and Culture-Negative Herd Mates. J Vet Diagnostic Investig. 2006;18: 2–6. doi: 10.1177/104063870601800102 16566252

48. van Schaik G, Stehman SM, Jacobson RH, Schukken YH, Shin SJ, Lein DH. Cow-level evaluation of a kinetics ELISA with multiple cutoff values to detect fecal shedding of Mycobacterium avium subspecies paratuberculosis in New York State dairy cows. Prev Vet Med. 2005;72: 221–236. doi: 10.1016/j.prevetmed.2005.01.019 16169619

49. Collins MT, Gardner IA, Garry F, Roussel AJ, Wells SJ. Consensus recommendations on diagnostic testing for the detection of paratuberculosis in cattle in the United States. J Am Vet Med Assoc. 2006;229: 1912–1919. Available: http://avmajournals.avma.org/doi/abs/10.2460/javma.229.12.1912 17173528

50. Whitlock RH, Wells SJ, Sweeney RW, Van Tiem J. ELISA and fecal culture for paratuberculosis (Johne’s disease): sensitivity and specificity of each method. Vet Microbiol. 2000;77: 387–398. Available: http://www.sciencedirect.com/science/article/pii/S0378113500003242 11118724

51. Taddei S, Robbi C, Cesena C, Rossi I, Schiano E, Arrigoni N, et al. Detection of Mycobacterium Avium Subsp. Paratuberculosis in Bovine Fecal Samples: Comparison of Three Polymerase Chain Reaction—Based Diagnostic Tests with a Conventional Culture Method. J Vet Diagnostic Investig. 2004;16: 503–508. doi: 10.1177/104063870401600603 15586564

52. Leite FL, Stokes KD, Robbe-Austerman S, Stabel JR. Comparison of fecal DNA extraction kits for the detection of Mycobacterium avium subsp. paratuberculosis by polymerase chain reaction. J Vet Diagnostic Investig. 2013;25: 27–34. doi: 10.1177/1040638712466395 23166181

53. Meens E, Rambaud T, Arnaud D. Evaluation of diagnostic tests to classify cattle, in control plans, according to their levels of excretion of Mycobacterium avium Paratuberculosis. 12th International Colloquium on Paratuberculosis. Parma, Italy; 2014. p. P-03.13.

54. Vitale N, Possidente R, D’Errico V, Dondo A, Bergagna S, Barbero R, et al. Estimating diagnostic accuracy of paratuberculosis (PTB) diagnostic test with latent class models. 12th International Colloquium on Paratuberculosis. Parma, Italy; 2014. p. P-02.10.

55. Sweeney RW, Gardner IA, Hines MEI, Anderson R, Byrem TM, Collins MT, et al. Comparison of 3 fecal culture, 2 fecal PCR, 2 serum ELISA, and milk ELISA for diagnosis of paratuberculosis in US dairy cattle. 12th International Colloquium on Paratuberculosis. Parma, Italy; 2014. p. P-02.47.

56. Adaska JM, Anderson RJ. Seroprevalence of Johne’s-disease infection in dairy cattle in California, USA. Prev Vet Med. 2003;60: 255–261. 12900163

57. Cornell University Animal Health Diagnostic Center. Test and Fee Schedule [Internet]. 2015. https://ahdc.vet.cornell.edu/

58. Collins MT, Manning EJB. Testing Services. In: Johne’s Information Center [Internet]. 2015. http://www.johnes.org/testserv/index.html#tests

59. Besser T. New Strategies for Johne’s Disease Testing. In: Washington Animal Disease Diagnostic Lab [Internet]. 2015 [cited 10 Dec 2015]. http://waddl.vetmed.wsu.edu/animal-disease-faq/johne’s-testing

60. Tests and Fees. In: Iowa State Veterinary Diagnostic Laboratory [Internet]. 2015 [cited 10 Dec 2015]. http://vetmed.iastate.edu/veterinary-diagnostic-laboratory-vdl/tests-and-fees#j

61. Indiana Animal Disease Diagnostic Laboratory. Fee Schedule [Internet]. 2015 [cited 10 Dec 2015]. https://www.addl.purdue.edu/TestsFees/ByTest.aspx

62. USDA:ERS. National Milk Cost of Production. In: Milk Cost of Production Estimates [Internet]. 2010 [cited 9 Sep 2015]. http://www.ers.usda.gov/data-products/milk-cost-of-production-estimates.aspx

63. Karszes J. Dairy Replacement Programs : Costs & Analysis 3 rd Quarter 2012. 2014;

64. USDA:NASS. Quick Stats. In: Quick Stats. 2015.

65. USDA. Agricultural Prices Summary 2003–2007. In: Agricultural Prices [Internet]. 2008. http://usda.mannlib.cornell.edu/MannUsda/view-DocumentInfo.do?documentID=1003.

66. Bar D, Gröhn YT, Bennett GJ, González RN, Hertl JA, Schulte HF, et al. Effect of repeated episodes of generic clinical mastitis on milk yield in dairy cows. J Dairy Sci. 2007;90: 4643–53. doi: 10.3168/jds.2007-0145 17881685

67. Groenendaal H, Nielen M, Jalvingh AW, Horst SH, Galligan DT, Hesselink JW. A simulation of Johne’s disease control. Prev Vet Med. 2002;54: 225–245. Available: http://www.sciencedirect.com/science/article/B6TBK-45X2PMN-8/2/35a11301cbb515872fab227714a730ec 12114011

68. Breen JE, Green MJ, Bradley AJ. Quarter and cow risk factors associated with the occurrence of clinical mastitis in dairy cows in the United Kingdom. J Dairy Sci. 2009;92: 2551–61. doi: 10.3168/jds.2008-1369 19447987

69. Verteramo Chiu LJ, Tauer LW, Al-Mamun MA, Kaniyamattam K, Smith RL, Gröhn YT. An agent-based model evaluation of economic control strategies for paratuberculosis in a dairy herd. J Dairy Sci. 2018; doi: 10.3168/jds.2017-13175 29705432


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