Abstracts
Risk factors for anthelmintic resistance (AR) on bovine ranches were studied. Data were derived from a survey made to 50 ranch owners, who had conducted a faecal egg-count-reduction test. The questionnaire contained descriptors of bovine ranch management and nematode control. A case-control design study was undertaken and AR cases were present in 26 herds. Associations between the binary outcome variable (AR versus not AR) and risk factors recorded in the questionnaire were evaluated. Variables associated with the presence of AR at P< 0.15 and/or odds ratio (OR) > 2 were subjected to a multivariable logistic regression model. The main effects contributing to general AR (avermectin AVM and/or benzimidazole) in the final model were total number of annual treatments (OR 7.68; 95% CI 2.4 to 28.3) and use of more than 75% of AVM in the past (OR= 18.6; 95% CI 1.3 to 97.3), whereas for AVM resistance alone were total number of AVM annual treatments (OR= 11.5; 95% CI 2.9 to 45.5) and number of AVM Nov-Jan treatments (OR= 5.8; 95% CI 1.71 to 47.9). The results showed that treatment frequency, date of treatment and frequency of treatment in the past with a single drug were the main risk factors involved in AR development.
Nematode; cattle; anthelmintic resistance; risk factor
Fatores de risco para resistência anti-helmíntica (AR) em fazendas de criação de bovinos foram estudados de dados obtidos de um levantamento em 50 propriedades. Em todas foram conduzidos testes de redução de contagem de ovos (opg) e um questionário preenchido pelos proprietários sobre o manejo e o controle de verminose nessas fazendas. Um estudo com desenho de caso controlado foi realizado e casos de AR estavam presentes em 26 rebanhos. Associações foram avaliadas entre a variável binária produzida (AR versus sem AR) e fatores de risco registrados nos questionários. Variáveis associadas com o resultado de interesse a P<0.15 e/ou razão de prevalência (OR) > 2 foram usados num modelo de regressão logística multivariável. Os principais efeitos contribuintes para AR geral (avermectina AVM e/ou benzimidazole), no modelo final, foram número total de tratamentos anuais (OR 7,68; 95% IC 2,4 a 28,3) e uso no passado mais que 75% de AVM (OR= 18,6; 95% IC 1,3 a 97,3), e para resistência à AVM foram número total de tratamentos anuais (OR=11,5; 95% IC 2,9 a 45,5), número de tratamentos com AVM de novembro a janeiro (OR= 5,8; 95% IC 1,71 a 47,9). Estes resultados mostraram que a frequência dos tratamentos, a época do ano em que foram feitos os tratamentos e a frequência dos tratamentos no passado com uma única droga foram os principais fatores de risco implicado no desenvolvimento de AR.
Nematóide; gado; resistência anti-helmíntica; fator de risco
Introduction
Anthelmintic resistance (AR) in gastro-intestinal nematodes of cattle has become a problem in many countries, where several survey reports indicate widespread AR (KAPLAN, 2004Kaplan RM. Drug resistance in nematodes of Veterinary importance: a status report. Trends Parasitol 2004; 20(10): 477-81. PMid:15363441. http://dx.doi.org/10.1016/j.pt.2004.08.001
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). Moreover, the number of reports in the literature published over the past five years suggests that the problem is rapidly increasing (SUTHERLAND; LEATHWICK; 2011Sutherland IA, Leathwick DM. Anthelmintic resistant in nematode parasites of cattle: a global issue? Trends Parasitol 2011; 27(4): 176-81. PMid:21168366. http://dx.doi.org/10.1016/j.pt.2010.11.008
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). Numerous studies about bovine nematode AR have been reported worldwide, mostly in regions where production systems are based on grazing management, such as New Zealand, Brazil, Colombia, UK and the United States. AR has been reported for all the broad-spectrum anthelmintics (levamisole, benzimidazoles and macrocyclic lactones) used for cattle (PAIVA et al., 2001Paiva F, Sato MO, Acuña AH, Jensen JR, Bressan MCRV. Resistência a ivermectina constatadas em Haemonchus placei e Cooperia punctata em bovinos. Hora Vet 2001; 120: 29-34.; FAMILTON et al., 2001Familton AS, Mason P, Coles GC. Anthelmintic-resistant Cooperia species in cattle. Vet Rec 2001; 149(23): 719-20. PMid:11787788.; COLES, 2002Coles GC. Cattle nematodes resistant to anthelmintics: why so few cases? Vet Res 2002; 33(5): 481-9. PMid:12387485. http://dx.doi.org/10.1051/vetres:2002034
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; WAGHORN et al., 2006Waghorn TS, Leathwick DM, Rhodes AP, Jackson R, Pomroy WE, West DM, et al. Prevalence of anthelmintic resistance on 62 beef cattle farms in the North Island of New Zealand. N Z Vet J 2006; 54(6): 278-82. PMid:17151725. http://dx.doi.org/10.1080/00480169.2006.36711
http://dx.doi.org/10.1080/00480169.2006....
; MÁRQUEZ et al., 2008Márquez D, Jiménez G, García F, Garzón C. Resistencia a los antihelmínticos en nematodos gastrointestinales de bovinos en municipios de Cundinamarca y Boyacá. Rev Corpoica: Cienc Tecnol Agropec 2008; 9(1): 113-23.; GASBARRE et al., 2009Gasbarre LC, Smith LL, Lichtenfels JR, Pilitt PA. The identification of cattle nematode parasites resistant to multiple classes of anthelmintics in a commercial cattle population in the US. Vet Parasitol 2009; 166(3-4): 281-5. PMid:19900760. http://dx.doi.org/10.1016/j.vetpar.2009.08.018
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). In Argentina, the first cases of macrocyclic lactone and benzimidazoles resistance in cattle were reported by Anziani et al. (2001)Anziani OS, Zimmermann G, Guglielmone AA, Vázquez R, Suarez VH. Avermectin resistance in Cooperia pectinata in cattle in Argentina. Vet Rec 2001; 149(2): 58-9. PMid:11488345. http://dx.doi.org/10.1136/vr.149.2.58
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and Fiel et al. (2001)Fiel CA, Saumell CA, Steffan PE, Rodriguez EM. Resistance of Cooperia to ivermectin treatments in grazing cattle of the Humid Pampa, Argentina. Vet Parasitol 2001; 97(3): 211-7. http://dx.doi.org/10.1016/S0304-4017(01)00407-1
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. Cases of multiple anthelmintic and nematode species resistance were detected later (MEJÍA et al., 2003Mejía ME, Fernández Igártua B, Schmidt EE, Cabaret J. Multispecies and multiple anthelmintic resistance on cattle nematodes in a farm in Argentina: the beginning of high resistance? Vet Res 2003; 34(4): 1-7. PMid:12911862. http://dx.doi.org/10.1051/vetres:2003018
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; ANZIANI et al., 2004Anziani OS, Suarez VH, Guglielmone AA, Warnke O, Grande H, Coles GC. Resistance to benzimidazole and macrocyclic lactone anthelmintics in cattle nematodes in Argentina. Vet Parasitol 2004; 122(4): 303-6. PMid:15262008. http://dx.doi.org/10.1016/j.vetpar.2004.05.018
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). Some recent surveys made in Argentina have attempted to quantify regional AR occurrence in cattle ranches (CARACOSTANTOGOLO et al., 2005Caracostantogolo J, Castaño R, Cutullé C, Cetrá B, Lamberti R, Olaechea F, et al. Evaluación de la resistencia a los antihelmínticos en rumiantes en Argentina. In: Eddi C, Vargas Terán M, editors. Resistencia a los antiparasitarios internos en Argentina. Roma: FAO; 2005.; SUAREZ; CRISTEL, 2007Suarez VH, Cristel SL. Anthelmintic resistance in cattle nematode in the western Pampeana Region of Argentina. Vet Parasitol 2007; 144(1-2): 111-7. PMid:17049746. http://dx.doi.org/10.1016/j.vetpar.2006.09.016
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).
During the last 20 years, in central Argentina technologies for nematode infection control in bovines have been based on the over-use of broad anti-parasitic drugs. Endectocides and benzimidazoles were the most frequently used anthelmintics (SUAREZ, 2002Suarez VH. Helminthic control of grazing ruminants and environmental risks in South America. Vet Res 2002; 33(5): 563-73. PMid:12387490. http://dx.doi.org/10.1051/vetres:2002039
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). In this region, anthelmintic treatments were frequently applied from autumn (weaning) to mid winter, with an additional drench in late winter or late spring during the fattening period of cattle. This practice is supported by the hypothesis that AR was caused by frequent anthelmintic treatments (PRICHARD et al., 1980Prichard RK, Hall CA, Kelly JD, Martin IC, Donald AD. The problem of anthelmintic resistance in nematodes. Aust Vet J 1980; 56(5): 239-51. PMid:7002142. http://dx.doi.org/10.1111/j.1751-0813.1980.tb15983.x
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). Many ranch advisors on nematode control recommended adopting suppressive drenches, such as monthly treatments. In other cases, they recommended strategic management practices, such as treatment and move to a clean annual crop (oat or rye) when the number of larvae in pastures is low (SUAREZ; LORENZO, 2000Suarez VH, Lorenzo RM. Ecology of the free living stages of cattle nematodes during summer contamination in Argentina western pampas. Parasite 2000; 7(4): 255-61. PMid:11147033.) or treatment during late spring or summer when weather conditions are deleterious to larval survival. Veterinarians also frequently proposed rotating between anthelmintic drugs to avoid AR.
In the last years, information has been generated about which practices are highly selective for AR in sheep nematodes (LEATHWICK et al., 2009Leathwick DM, Hosking BC, Bisset SA, McKay CH. Managing anthelmintic resistance: Is it feasible in New Zealand to delay the emergence of resistance to a new anthelmintic class? N Z Vet J 2009; 57(4): 181-92. PMid:19649011. http://dx.doi.org/10.1080/00480169.2009.36900
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). It has been postulated that in many situations all these recommendations, such as suppressive or strategic treatments, have accelerated the selection for AR by permitting only the survival of resistant larvae at the moment when there are no nonresistant larvae in refugia (VAN WYK, 2001; VAN WYK et al., 2006). However, very little is known about selection for AR in cattle nematodes (STAFFORD; COLES, 1999Stafford K, Coles GC. Nematode control practices and anthelmintic resistance in dairy calves in the south west of England. Vet Record 1999; 144(24):659-61. http://dx.doi.org/10.1136/vr.144.24.659
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) despite the urgent need for studies exploring factors associated with AR development.
The objective of this study was to examine the association between the development of AR and farm practices for the control of cattle gastrointestinal nematodes and other farm management activities.
Materials and Methods
Farm selection
A case-control study was undertaken with data obtained from interview surveys (either by telephone or face to face) made to 50 cattle ranch owners who had conducted a faecal egg-count-reduction test (FECRT) on their herds no more than three years before. The sampled farms were selected based on the AR status (half of them had AR and the other half did not). The cattle ranches were located mostly in central Argentina, in the following regions: Humid Pampas (n=15), Subhumid Pampas (n=24) and Semiarid Pampas and North Patagonian region (n=11). AR was present in 26 of the ranches. Avermectin (AVM) resistance was present in 25 herds, benzimidazole (BZD) resistance in 11 herds and AR to both drugs in 10 herds. The surveyed farms were mainly mixed cow-calf and finishing or only finishing operations.
Data of 23 FECRTs were obtained from Suarez and Cristel (2007)Suarez VH, Cristel SL. Anthelmintic resistance in cattle nematode in the western Pampeana Region of Argentina. Vet Parasitol 2007; 144(1-2): 111-7. PMid:17049746. http://dx.doi.org/10.1016/j.vetpar.2006.09.016
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and data of 27 FECRTs were kindly provided by the following colleague parasitologists: O. Anziani, C. Descarga, C. Rossanigo, M. Buffarini, R. Sanabria, J. Romero, F. Olaechea, C. Entrocasso, C. Fiel. In all cases, FECRTs and resistance were confirmed by a mean egg count reduction percentage of less than 95% (100(1-[T2/C2])) and the 95% confidence level of less than 90%, according to the protocol of the WAAVP (COLES et al., 1992Coles GC, Bauer C, Borgsteede FH, Geerts S, Klei TR, Taylor MA, et al. World Association for the Advancement of Veterinary Parasitology (WAAVP) methods for the detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol 1992; 44(1-2): 35-44. http://dx.doi.org/10.1016/0304-4017(92)90141-U
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). Ivermectin (IVM), fenbendazole or albendazole (BZD) and levamisole (LVM) were tested. Ranches were defined as either AR (IVM, BZD or IVM and BZD resistant) or not AR for the case-control analysis.
Questionnaire
The survey questionnaire comprised 29 questions, including descriptors of the ranch management and gastrointestinal nematode control and other questions addressing the principal AR development hypotheses. The questionnaire was pilot-tested by 10 owners and the final questionnaire took approximately 20 minutes for completion. Some variables, such as AVM use as external parasiticide, drench gun calibration or cropping practices in the ranch, were not incorporated to the analysis because most participants had responded similarly.
Several hypotheses, such as herd annual treatment frequency, under-dosing, treatment recommended by veterinarians by monitoring diagnoses from egg counts or live weight gain were tested in the questionnaire. The refugia hypothesis (VAN WYK, 2001) was analysed through questions on the percentage of annual or safe pastures used, treatment and movement to safe pastures or enclosure feed system for weaning calves during a short period (less than 3 months), treatment of bovines older than two years, and drenching during November-January. Likewise, a refugia index (0 to 1) was developed using the following variables: more than 25% of annual crops (0.25), treatment of two-year-old or adult bovines (0.25), treatment and move to clean pastures (0.25), treatment before move to temporary enclosure feedlot system (0.25); and the indicative level was more than the average farm level (≥0.36).
Statistical methods
Associations between the binary outcome variable (AR versus not AR) and ranch-level risk factors were analyzed. A screening test was carried out using either the Chi-square test for independence for categorical variables or univariable logistic-regression analysis for continuous independent variables. Likewise, a simple linear regression was used to test dependent variables as percentage of anthelmintic drug efficacy and continuous independent variables. Variables associated with the outcome at P<0.15 or odds ratio (OR) > 2 were evaluated using multivariable logistic-regression model. The ORs calculated from the estimated coefficients in the final models were used to measure the strength of the association.
The relative contribution of each factor to the probability of AR presence or absence was determined by applying the multivariable logistic regression model (DI RIENZO et al., 2008). Backward elimination was used to determine which factors could be excluded from the model based on a likelihood ratio Chi-square statistic corresponding to P = 10% at each step.
Results
Mean FECRT efficacies for IVM in ranches with (n= 25) and without (n= 25) resistance were 69.66 ± 23.3 % and 97.57 ± 2.3 %, respectively, and for BZD with (n= 11) and without (n= 39) resistance were 78.91 ± 22.9 % and 98.58 ± 1.7 %, respectively. Figure 1 shows the level of FECRT in each ranch with and without AR. LVM resistance was not present. The responses of the surveyed owners about the categorical or continuous variables evaluated that were not associated with ranch AR status by univariable analysis are the following: type of cattle system, cattle breed, region, partial feedlot practices, treatment of calves before move to feedlot, treatment according to the live weight gain of the growing lot, anthelmintic dose estimation, stocking rate (heads per ha), proportion of ranch annual crops, proportion of ranch perennial and natural pastures, and number of annual BZD treatments in the past.
Regarding the owners' responses about ranch herd ivermectin (IVM) or benzimidazole (BZD) resistant status, the variables more than 75% of IVM was used in the past (OR= 3.2; P< 0.05) or more than 75% of BZD was used in the past (OR= 0.8; P< 0.30) were tested.
Finally, 13 variables were included in the multivariable model (Tables 1 and 2); these variables reflected the frequency of treatments hypothesis (n= 3), the annual period of the treatments (n= 4), the type of control plan or methods included (n= 2), refugia hypothesis (this aspect is partially included in the other variables, n= 2), ranch practices (n=2) and use of egg counts and veterinarian advice (n= 1).
The results of linear regression between continuous variables and the percentage of efficacies obtained from ivermectin and benzimidazole FECRTs are presented in Table 3. These results show that there is a significant correlation between the number of annual total anthelmintic drenches and the average IVM and BZD efficacy of the ranch and between the number of annual avermectin drenches and IVM efficacy. These results are presented in Figure 2, which shows a significant decrease in drug efficacy with increasing annual herd anthelmintic drenches.
Correlation between number of drug annual treatments and the percentage of ivermectin (IVM) efficacy (y= 100.5+-7.59x; p<0,031) and the average of ivermectin and benzimidazole (BZD) efficacy (y= 101.7+-3.51x ; p<0,0004).
Correlation (c. cor.) and lineal regression between continuous variables and the percentage of anthelmintic efficacies. The ranch herd efficacy of avermectin (AVM) and benzimidazole (BZD) was calculated by means of the average of the result of FECRT with both drugs.
The final logistic regression model of risk factors for general AR is presented in Table 4. This model explains that the variables such as frequency of annual treatments (OR 7.68; p<0.002) and recurrent use of practically one anthelmintic drug in the past (OR 18.62; p<0-028) were significantly associated with risk of AR development. Likewise, the main effects contributing to IVM resistance (Table 5) were total number of AVM annual treatments (OR=11.50; p<0.0005), number of AVM Nov.-Jan. treatments (OR= 5.83; p<0.10) and the use of AVM in the past as minor effect (OR= 4.45; p<0.19).
Discussion
This study has the advantage that all the herds have been tested and their AR status obtained in parasitological laboratories. However, using this methodology it is difficult to ensure the representativeness of the process of ranch herd sample selection. The selection of the owners of cattle ranches that had made a FECRT during the last 3 years is quite biased, because in Argentina it is not easy to locate those farmers or their advisors. Adoption of the FECRT by cattle owners was very low and we used FECRT information from the literature and from research trials kindly provided by several colleagues. Therefore, our effort was focused on the quality and confidence of AR diagnosis to have a reliable farm sample; thus, we obtained a reliable but limited small sample size. An additional limitation is the field method used for AR diagnosis. FECRT is widely adopted because all family of drugs can be evaluated, no sophisticated laboratory equipment is required and its cost is relatively low. However, it is well known that this test has low sensitivity for incipient AR in a nematode population; FECRT is only capable of detecting AR at an advanced stage, when at least 25% of the nematode population has the resistant phenotype (MARTIN et al., 1989Martin PJ, Anderson N, Jarrett RG. Detecting benzimidazole resistance with faecal egg counts reduction tests and in vitro assay. Aust Vet J 1989; 66(8): 236-40. PMid:2590136. http://dx.doi.org/10.1111/j.1751-0813.1989.tb13578.x
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), but in practical terms this is the test that we can use under field conditions. Currently, there are more sensitive genetic tests, but only to evaluate BZD resistance and it is too expensive to be used in routine field diagnosis (HUMBERT et al., 2001Humbert JF, Cabaret J, Elard L, Leignel V, Silvestre A. Molecular approaches to studying benzimidazole resistance in trichostrongylid nematode parasites of small ruminants. Vet Parasitol 2001; 101(3-4): 405-14. http://dx.doi.org/10.1016/S0304-4017(01)00565-9
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).
Even though the logistic regression method overestimates odds ratios in studies with small to moderate sample size (NEMES et al., 2009Nemes S, Jonasson JM, Anna Genell A, Steineck G. Bias in odds ratios by logistic regression modelling and sample size. BMC Med Res Methodol 2009; 9: 56. PMid:19635144 PMCid:PMC2724427. http://dx.doi.org/10.1186/1471-2288-9-56
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), these present results support the frequency of treatment hypothesis and the frequency of use the same drug in the past on the development of AR (PRICHARD et al., 1980Prichard RK, Hall CA, Kelly JD, Martin IC, Donald AD. The problem of anthelmintic resistance in nematodes. Aust Vet J 1980; 56(5): 239-51. PMid:7002142. http://dx.doi.org/10.1111/j.1751-0813.1980.tb15983.x
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). The use of more than 75% of AVM in the previous survey years mostly implies the use of the same type of drug and is directly correlated with AVM resistance. Likewise, the use of only AVM during the last years refers also to the lack of annual rotation of drug classes.
Previous studies in the Pampas region demonstrate that late spring and summer conditions were associated with rapid development and migration of third-stage larvae (L3) to herbage, but also with high mortality rate and low L3 detection after initial recoveries (SUAREZ; LORENZO, 2000Suarez VH, Lorenzo RM. Ecology of the free living stages of cattle nematodes during summer contamination in Argentina western pampas. Parasite 2000; 7(4): 255-61. PMid:11147033.). In addition, larva availability for tracer calves on naturally infected pastures during this period was generally very small (SUAREZ, 1990Suarez VH. Inhibition patterns and seasonal availability of nematodes for beef cattle grazing on Argentina's Western Pampas. Int J Parasitol 1990; 20(8): 1031-6. http://dx.doi.org/10.1016/0020-7519(90)90046-P
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; SUAREZ; LORENZO, 2000Suarez VH, Lorenzo RM. Ecology of the free living stages of cattle nematodes during summer contamination in Argentina western pampas. Parasite 2000; 7(4): 255-61. PMid:11147033.). Then, under the refugia hypotheses Nov-Jan period can be considered the time when more resistant selection pressure is exerted on the nematode populations in the Pampas region.
In New Zealand, an analysis of sheep AR through a field survey indicated refugia as an important risk factor (HUGHES et al. 2007Hughes PL, Dowling AF, Callinan APL. Resistance to macrocyclic lactone anthelmintics and associated risk factors on sheep farms in the lower North Island of New Zealand. N Z Vet J 2007; 55(4): 177-83. PMid:17676082. http://dx.doi.org/10.1080/00480169.2007.36764
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). Their results showed that the prevalence of AR was higher on farms on which more than 50% of lambs were weaned onto paddocks not grazed for a long period by lambing ewes and where lambs were not always returned to the same paddock after drenching. Other surveys conducted with small ruminants showed that underdosing, repeated use of one class of drug and refugia size at treatment time can be associated with AR (SILVESTRE et al., 2002Silvestre A, Leignel V, Berrag B, Gasnier N, Humbert JF, Chartier C, et al. Sheep and goat nematode resistance to anthelmintics: pro and cons among breeding management factors. Vet Res 2002; 33(5): 465-80. PMid:12387484. http://dx.doi.org/10.1051/vetres:2002033
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).
Our results also indicate that the number of autumn-winter drenches alone contributed to the development of AR (X2 7.83; p<0006). The average number of autumn-winter herd drenches given in the last 3-5 years was 2.91 and the odds ratio of AR of herds exposed to more than three treatments was 24 times higher than not exposed herds (Table 2). This contribution of autumn-winter treatments to the development of AR is not so clear, because this period is the most favourable for the survival of infective larvae in pastures (SUAREZ; LORENZO, 2000Suarez VH, Lorenzo RM. Ecology of the free living stages of cattle nematodes during summer contamination in Argentina western pampas. Parasite 2000; 7(4): 255-61. PMid:11147033.; SUAREZ, 2001Suarez VH. Ecología de los estadios de vida libre de los nematodes bovinos durante la contaminación otoño-invernal en la región semiarida pampeana. Rev Med Vet 2001; 82(6): 316-23.) and minimum resistant selection could be exerted. However, most of these grazing systems use annual crop pastures (oats and ryegrass) during the winter and when animals are first introduced to these pastures, larva availability for grazing animals is negligible (SUAREZ, 1990Suarez VH. Inhibition patterns and seasonal availability of nematodes for beef cattle grazing on Argentina's Western Pampas. Int J Parasitol 1990; 20(8): 1031-6. http://dx.doi.org/10.1016/0020-7519(90)90046-P
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). A strategy involving treatment and then moving stock to clean crops without refugia may be a suitable method for AR selection. Similarly, selection can be produced with another herd management strategy: owners during the fattening period standardized the live weight of acquired or weaning calves by drenching and move to feedlots; then after a short period, the animals are moved again to pastures. Treatment and move to feedlot yards with negligible nematode presence should also select for AR.
These results reinforce the hypothesis of increased frequency of anthelmintic application as the principal risk factor; however, it is difficult to separate this hypothesis from that of refugia, because it is associated with the factor that autumn-winter drenching is frequently used along with Nov-Jan drenching and the approach involving treatment before move to annual crops. The latter two factors reduce the number of larvae in refugia.
In Argentina, as in other countries (STAFFORD; COLES, 1999Stafford K, Coles GC. Nematode control practices and anthelmintic resistance in dairy calves in the south west of England. Vet Record 1999; 144(24):659-61. http://dx.doi.org/10.1136/vr.144.24.659
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; SOUTELLO et al., 2007Soutello RGV, Seno MCZ, Amarante AFT. Anthelmintic resistance in cattle nematodes in northwestern São Paulo State, Brazil. Vet Parasitol 2007; 148(3-4): 360-4. PMid:17656022. http://dx.doi.org/10.1016/j.vetpar.2007.06.023
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; SUAREZ et al., 2011Suarez VH, Miranda AO, Arenas SM, Schmidt EE, Lambert J, Schieda A, et al. Incidencia y control de los nematodes gastrointestinales bovinos en el este de la provincia de La Pampa, Argentina. RIA 2011; 37: 26-36.), there is evidence that cattle owners might be using more anthelmintics than required to prevent bovine meat and milk losses. This overuse of anthelmintics, especially injectable and persistent drugs (mainly avermectins) seems to decrease larvae in refugia, because when drug profiles decline over time there will be a period when resistant larvae are able to establish but susceptible genotypes are not. As resistance builds up in a population, this mechanism will become evident as a reduction in the period of protection against ingested larvae, as previously observed in sheep (SUTHERLAND et al., 1997Sutherland IA, Leathwick DM, Brown AE, Miller CM. Prophylactic efficacy of persistent anthelmintics against challenge with drug-resistant and susceptible Ostertagia circumcincta. Vet Rec 1997; 141(5): 120-3. PMid:9342086. http://dx.doi.org/10.1136/vr.141.5.120
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) and cattle (V.H. Suarez, unpublished data). Coles et al. (2006)Coles GC, Jackson F, Pomroy WE, Prichard RK, Von Samson-Himmelstjerna G, Silvestre A, et al. The detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol 2006; 136(3-4): 167-85. PMid:16427201. http://dx.doi.org/10.1016/j.vetpar.2005.11.019
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proposed that an AVM reduced period of protection of 50% could be considered a possible case of AR.
Another outcome factor that was associated with AR, but also strongly related to the number of annual drenches, was the type of anthelmintic control plan. One type was the strategic programmed nematode control, whereby owners programmed drug application at a fixed date regardless of the epidemiological knowledge that focused on the probable larval challenge or worm burden size. The other type was a control plan that generally involves a programmed treatment (at weaning and/or then a short period later) followed by tactic drenches based on different herd criteria (symptoms, body condition score, live weight gain or egg counts) and sometimes based on the epidemiological studies in our region (FIEL et al., 1994Fiel CA, Daffner A, Alvarez J. Epidemiología de los nematodes gastrointestinales en la región subtropical. In: Nari A, Fiel C. Enfermedades parasitarias de importancia económica en bovinos: bases epidemiológicas para su prevención y control en Argentina y Uruguay. Montevideo: Hemisferio Sur; 1994. p. 115-29.; SUAREZ et al., 1999Suarez VH, Lorenzo RM, Busetti MR, Santucho GM. Physiological and parasitological responses to nematode infections of fattening cattle in the western pampas of Argentina. Vet Parasitol 1999; 81(2): 137-48 http://dx.doi.org/10.1016/S0304-4017(98)00183-6
http://dx.doi.org/10.1016/S0304-4017(98)...
). This latter type of control reduced the number of drenches and was generally associated with the veterinarian advice, which used the egg counts and live weight gains of the herd to make drench decisions. The latter factor shows that veterinary advice could be profitable in reducing the number of treatments to those that the herd truly needs, therefore reducing the risk of AR development.
Likewise, some management strategies that employ refugia-based methods to prolong the efficacy of current cattle anthelmintics should be suggested to veterinarians and cattle owners. Nematode control methods, such as targeted timed whole herd drenches or targeted selective treatments (KENYON et al., 2009Kenyon F, Greer AW, Coles GC, Cringoli G, Papadopoulos E, Cabaret J, et al. The role of targeted selective treatments in the development of refugia-based approaches to the control of gastrointestinal nematodes of small ruminants. Vet Parasitol 2009; 164(1): 3-11. PMid:19450930. http://dx.doi.org/10.1016/j.vetpar.2009.04.015
http://dx.doi.org/10.1016/j.vetpar.2009....
) based, for example, on production data (herd live weight gain or body condition score) serve to reduce the number of drenches, minimising pasture contamination with resistant parasites and favouring dilution with susceptible genotypes.
In conclusion, these results show that treatment frequency, the period of the year for treatment and the past treatment frequency with a single drug were the main risk factors involved in AR development and mostly support the frequency of treatments hypothesis. These results also show a need for reducing the number of treatments by applying regional epidemiological knowledge, refugia criteria and control advice and herd monitoring by professionals.
The authors would like to thank O. Anziani, C. Descarga, C. Rossanigo, M. Buffarini, R. Sanabria, J. Romero, F. Olaechea, C. Entrocasso and C. Fiel, who kindly provided research information of FECRT.
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Publication Dates
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Publication in this collection
Apr-Jun 2014
History
-
Received
22 July 2013 -
Accepted
17 Feb 2014