Developing a model for predicting the dynamics of cattle infestation by gastrointestinal nematodes in Aceh Province, Indonesia
Main Article Content
Abstract
High cases of gastrointestinal nematode (GIN) parasitism in cattle lead to substantial economic loss in grazing cattle in developing countries, including Indonesia, resulting from climatic change and poor sanitation. This research aimed to collect data from the field and subsequently develop a model to predict the dynamic of the infestation of cattle by GIN at various places (highlands and lowlands) in Aceh Province, Indonesia in February-August 2017 employing two approaches: a laboratory approach which collected and analysed cattle faeces and a survey approach. Simulation, Analysis, and Modeling Software II (SAAM II) was employed to conduct data analysis and develop a model for nematode infestation in cattle. This modeling software represented eggs per gram (EPG) of faeces influenced by rainfall. The results confirmed that rainfall inhibited larvae development in 91 days and reduced the number of eggs secreted by cattle in 20 days. Changes in the environment are believed to be an approach that can support avoiding an increase in EPG. The development of this basic model is expected to be the initial stage for a further and more advanced model to comprehensively enhance strategies to control GIN in cattle.
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
References
Fadli M, Oka IBM, Suratma NA. Prevalence of gastrointestinal nematodes in Bali cattle raised by breeders in Sobangan village, Mengwi, Badung. Indones Med Veterinus. 2014;3(5):411-422.
Bhermana A, Haryanto B, Adrial A, Munier FF. Spatial identification of worm parasite attacks on cattle in Central Kalimantan. In: Puastuti W, Muharsini S, Inounu I, Tiesnamurti B, Kusumaningtyas E, Wina E, editors. National Seminar on Animal Husbandry and Veterinary Technology; 2017 Aug 8-9; Bogor, Indonesia. Jakarta: IAARD Press; 2017. p. 173-183.
Purwaningsih P, Noviyanti N, Sembodo P. Investment of digestive tract worms in ettawa breeding bean goats in amban kelurahan, Manokwari Barat District, Manokwari Regency, West Papua province. JIPT. 2017;5(1):8-12.
Zulfikar Z, Hambal H, Razali R. Prevalence of gastrointestinal nematode in cattle in Pintu Rime Gayo Highland of Bener Meriah Regency. IJTVBR. 2017;2(1):34-37.
Gasbarre LC, Leighton EA, Sonstergard T. Role of the bovine immune system and genome in resistance to gastrointestinal nematodes. Vet Parasitol. 2001;98(1-3):51-64.
Bain RK, Urquhart GM. The significance and control of stomach worms in British cattle. J Outlook Agric. 1986;15(1):10-14.
Charlier J, Höglund J, Himmelstjerna SG, Dorny P, VercruysseJ. Gastrointestinal nematode infections in adult dairy cattle: impact on production, diagnosis and control. Vet Parasitol. 2009;164(1):70-79.
Fox NJ, Marion G, Davidson, RS, White PCL, Hutchings MR. Modelling parasite transmissions in grazing system: the importance of host behavior and immunity. PloS One. 2013;8(11):1-11.
Pfukenyi DM, Mukaratirwa S. A review of the epidemiology and control of gastrointestinal nematode infections in cattle in Zimbabwe: review article. OJVR. 2013; 80(1):1-12.
Rivera B, Parra D, Garcia O, Aycardi E. Gastro-intestinal parasites in calves in Colombia. Trop Anim Health Prod. 1983;15(2):107-114.
Heckler RP, Borges FDA. Climate variations and the environmental populations of gastrointestinal nematodes of ruminants. Nematoda. 2016;3(1):e012016.
Mackinnon MJ, Meyer K, Hetzel DJ. Genetic variation and covariation for growth, parasite resistance and heat tolerance in tropical cattle. Livest Prod Sci. 1991;27(2-3):105-122.
Berk Z, Bishop SC, Forbes AB, Kyriazakis I. A simulation model to investigate interactions between first season grazing calves and Ostertagia ostertagi. Vet Parasitol. 2016;226:198-209.
Skuce PJ, Morgan ER, VanDijk J, Mitchell M. Animal health aspects of adaptation to climate change: beating the heat and parasites in a warming Europe. 2013;7(s2):333-345.
Rose H, Rinaldi L, Bosco A, Mavrot F, Waal T, Skuce P, et al. Widespread anthelmintic resistance in European farmed ruminants: a systematic review. Vet Rec. 2015;176(21):546.
Liang S, Spear RC, Seto E, Hubbard A, Qiu DA. Multi-group model of Schistosoma j aponicum transmission dynamics and control: model calibration and control prediction. Trop Med Int Health. 2005;10(3):263-278.
Höglund J, Dahlström F, Sollenberg S, Hessle A. Weight gain-based targeted selective treatments (TST) of gastrointestinal nematodes in first-season grazing cattle. Vet Parasitol. 2013;196(3-4):358-365.
Smith G, Greenfell BT, Anderson RM, Beddington J. Population biology of Ostertagia ostertagi and anthelmintic strategies against ostertagiasis in calves. Parasitology. 1987;95(2):407-420.
Ward CJ. Mathematical models to assess strategies for the control of gastrointestinal roundworms in cattle: construction. Vet Parasitol. 2006;138(3-4):247-267.
Barrett PHR, Bell BM, Cobelli C, Golde H, Schumitzky A, Vicini P, et al. SAAM II: simulation, analysis and modeling software for tracer and pharmacokinetic studies. Metab. 1998;47(4):484-492.
Ferasyi TR, Koets AP, Stegeman JA, Kruitwagen CL. The dynamics of antigen specific of proliferative responses of lymphocytes at early stages of bovine paratuberculosis infection. JITV. 2008;2(1):103-110.
Elsheika H. Endoparasites in cattle: studies and diagnostics. Vet Times. 2017;47(31):8-10.
Berk Z, Laurenson YC, Forbes AB, Kyriazakis I. A stochastic model to investigate the effects of control strategies on calves exposed to Ostertagia ostertagi. Parasitology. 2016;143(13):1755-1772.
Roberts MG, Greenfell BT. The population dynamics of nematode infections of ruminants: periodic perturbations as a model for management. Math Med Biol. 1991;8(2):83-93.
Roberts MG, Heesterbeek JAP. The dynamics of nematode infections of farmed ruminants. Parasitology. 1995;110(4):493-502.
Roeber F, Jex AR, Gasse RB. Impact of gastrointestinal parasitic nematodes of sheep, and the role of advanced molecular tools for exploring epidemiology and drug resistance-an Australian perspective. Parasit Vectors. 2013;6(1):1-3.
Laha R, Bhattacharya D, Ramakhrisna C, Sikdar A. In vitro egg laying capacity, percent hatchability and thereby recovery of infective larvae of Haemonchuscontortus of goats. J Parasit Appl Anim. Biol. 2000;9(2):97-100.
Ashad FA, Annisuzzaman M, Begum N, Dey AR, Mondal MM. Factors affecting the development and hatching of eggs and the survival of infective larvae of Haemonchus contortus in laboratory conditions. Progress Agric. 2011;22(1-2):75-83.
Dimander SO. Epidemiology and control of gastrointestinal nematodes in first season-grazing cattle in Sweden [thesis]. Uppsala: Swedish University of Agricultural Sciences; 2003.
Rose H, Hoar B, Kutz SJ, Morgan ER. Exploiting parallels between livestock and wildlife: predicting the impact of climate change on gastrointestinal nematodes in ruminants. Int J Parasitol Parasites Wildl. 2014;3(2):209-219.
Acosta TJ, Hoste H. Alternative of improved methods to limit gastro-intestinal parasitism in grazing sheep and goats. Small Rumin Res. 2008;77(2-3):159-173.
Alexandre G, Garcia GE, Lallo CH, Jimenez OE, Pariacote F, Archimede H, et al. Goat management and systems of production: global framework and study cases in the Carribean. Small Rumin Res. 2010;89(2-3):193-206.
Dijk VJ, Sargison ND, Kenyon F, Skuce PJ. Climate change and infectious disease: helminthological challenges to farmed ruminants in temperate regions. Animal. 2010;4(3):377-392.
Altizer S, Ostfeld RS, Johnson PT, Kutz S, Harvell CD. Climate change and infectious diseases: from evidence to a predictive framework. Science. 2013;341(6145):514-519.
Molnár PK, Kutz SJ, Hoar BM, Dobson AP. Metabolic approaches to understanding climate change impacts on seasonal host macroparasite dynamics. Ecol Lett. 2013;16(1):9-21.