Prevalence of Parasitic Intestinal Infections in livestock in Kalat, Iran

Main Article Content

Mir Asadollah Amiri
Nona Moradpour
Hassan Borji

Abstract

Introduction: Rodents are the largest group of mammals and act as a reservoir for many common human diseases, leading to societal health and economic problems. Due to the different prevalence rates of rodent-borne parasitic infections in various regions, this study was conducted to determine the prevalence of intestinal parasites in wild and domestic rodents in Kalat County, located in the north of Khorasan Razavi Province, Iran, in 2016.


Materials and methods: The study was performed using a descriptive method on 86 mountainous and domestic rodents randomly caught using live traps. After anesthesia and species identification, the gastrointestinal tract was dissected, and the digestive system worms were separated and preserved in 10% formalin until identification. The nematodes were clarified with lactophenol and stained with carmine acid. All worms were identified using diagnostic keys, and the results were presented using descriptive statistics.


Results: The prevalence of gastrointestinal worm infections in rodents in the study area was 75.5%. The captured rodents in this area included Microtus 46 (53.4%), Mus musculus 15 (17.4%), Pikas 13 (15.1%), Apodemus agrarius 11 (12.7%), and Allactaga elater 1 (1.1%). Six species of nematodes and one cestode species were identified in this study. The prevalence of parasitic infections shared between humans and rodents included Syphacia obvelata (83%), Aspicularis tetraptera (18.5%), Trichuris fossor (16.9%), Hymenolepis nana (6.1%), Heligmosomoides polygyrus (10.7%), and Nipostrongylus braziliensis (1.5%). Capillaria spp were found in 1.5% of rodents.


Conclusion: The results revealed a high prevalence of gastrointestinal worm infections in rodents, with an overall prevalence rate of 75.5% in Kalat, Iran. These findings highlight the potential health risks associated with rodent-borne parasitic infections in the study area and emphasize the importance of implementing effective control and prevention measures to mitigate the impact on human health and the local economy.

Article Details

How to Cite
Asadollah Amiri, M., Moradpour, N., & Borji, H. (2023). Prevalence of Parasitic Intestinal Infections in livestock in Kalat, Iran. Journal of Lab Animal Research, 2(3), 11–15. https://doi.org/10.58803/jlar.v2i3.18
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References

Dammhahn M, Mazza V, Schirmer A, Göttsche C, and Eccard JA. Of city and village mice: Behavioural adjustments of striped field mice to urban environments. Sci Rep. 2020; 10(1): 13056. DOI: https://doi.org/10.1038/s41598-020-69998-6

D'Elía G, Fabre PH, and Lessa EP. Rodent systematics in an age of discovery: Recent advances and prospects. J Mammalo. 2019; 100(3): 852-871. DOI: https://doi.org/10.1093/jmammal/gyy179

Guo X, Himsworth CG, Lee MJ, and Byers KA. A systematic review of rat ecology in urban sewer systems. Urban Ecosyst. 2022; 26: 223-232. DOI: https://doi.org/10.1007/s11252-022-01292-x

Chellappan M. Rodents. Polyphagous Pests of Crops. 2021: 457-532. DOI: https://doi.org/10.1007/978-981-15-8075-8_11

ShahrokhiA, MoradpourN, SiahsarvieR, and BorjiH. An investigation of potentially zoonotic helminth parasites of allactaga elaterin

Sarakhs, Iran. J Lab Anim Res. 2022; 1(1): 8-13. Available at: https://jlar.rovedar.com/index.php/JLAR/article/view/7/14

Strand TM, and Lundkvist Å. Rat-borne diseases at the horizon. A systematic review on infectious agents carried by rats in Europe 1995-2016. Infect Ecol Epidemiol. 2019; 9(1): 1553461. DOI: https://doi.org/10.1080/20008686.2018.1553461

Zhang K, Fu Y, Li J, and Zhang L. Public health and ecological significance of rodents in Cryptosporidium infections. One Health. 2022; 14: 100364. DOI: https://doi.org/10.1016/j.onehlt.2021.100364

Rahman MT, Sobur MA, Islam MS, Ievy S, Hossain MJ, El Zowalaty ME, et al. Zoonotic diseases: Etiology, impact, and control. Microorganisms. 2020; 8(9): 1405. DOI: https://doi.org/10.3390/microorganisms8091405

Wu G. Important roles of dietary taurine, creatine, carnosine, anserine and 4-hydroxyproline in human nutrition and health. Amino Acids. 2020; 52(3): 329-360. DOI: https://doi.org/10.1007/s00726-020-02823-6

Lotfalizadeh N, Sadr S, Moghaddam S, NajjarMS, Khakshoor A, Simab PA, et al. The innate immunity defense against gastrointestinal nematodes: Vaccine development. Farm Anim Health Nutr. 2022; 1(2): 31-38. DOI: https://doi.org/10.58803/fahn.v1i2.10

Sadr S, Yousefsani Z, Ahmadi Simab P, Alizadeh AJR, Lotfalizadeh N, and Borji H. Trichinella spiralis as a potential antitumor agent: An Update. World Vet J. 2023; 13(1): 65-74. DOI: https://doi.org/10.54203/scil.2023.wvj7

Sadr S, Charbgoo A, Borji H, and Hajjafari A. Interactions between innate immunity system and Echinococcus granulosus: Permission for vaccine development. Series Med Sci. 2022; 3(1): 1-18. Available at: https://seriesscience.com/wp-content/uploads/2023/01/Interactions-between-Innate-Immunity.pdf

Asouli A, Sadr S, Mohebalian H, and Borji H. Anti-tumor effect of protoscolex hydatid cyst somatic antigen on inhibition cell growth of K562. Acta Parasitol. 2023; 68(2): 385-392. DOI: https://doi.org/10.1007/s11686-023-00680-3

Bismarck N, Payne V, Cedric Y, and Nadia N. Gastro-intestinal helminth infections and associated risk factors amongst school aged children in kouoptamo noun division, West region, Cameroon. Int Arch Public Health Community Med. 2020; 4(2): 039. DOI: https://doi.org/10.23937/2643-4512/1710039

Gehlen H, Wulke N, Ertelt A, Nielsen MK, Morelli S, Traversa D, et al. Comparative analysis of intestinal helminth infections in colic and non-colic control equine patients. Animals. 2020; 10(10): 1916. DOI: https://doi.org/10.3390/ani10101916

Wolday D, Gebrecherkos T, Arefaine ZG, Kiros YK, Gebreegzabher A, Tasew G, et al. Effect of co-infection with intestinal parasites on COVID-19 severity: a prospective observational cohort study. Clin Med. 2021; 39: 101054. DOI: https://doi.org/10.1016/j.eclinm.2021.101054

Thompson R. Zoonotic helminths-why the challenge remains. J Helminthol. 2023; 97: e21. DOI: https://doi.org/10.1017/S0022149X23000020

Nath TC, Eom KS, Choe S, Islam S, Sabuj SS, Saha E, et al. Insights to helminth infections in food and companion animals in Bangladesh: Occurrence and risk profiling. Parasite Epidemiol Control. 2022; 17: e00245. DOI: https://doi.org/10.1016/j.parepi.2022.e00245

Islam MM, Farag E, Hassan MM, Jaffrey SS, Atta M, Al-Marri AM, et al. Rodent-borne zoonoses in Qatar: A possible one-health framework for the intervention of future epidemic. One Health. 2023; 16: 100517. DOI: https://doi.org/10.1016/j.onehlt.2023.100517

Shahabi S, Pouryousef A, Azizi K, and Sarkari B. Intestinal helminths infections of calomyscus cf. bailwardi (Rodentia: Calomyscidae) from Fars Province, Southern Iran. J Health Sci Surveill Syst. 2019; 7(3): 163-166. DOI: https://doi.org/10.30476/jhsss.2020.85071.1054

Kusumarini S, Danuarta MF, Karami F, Yesica R, Wisesa IBGR, Yudhana A, et al. Screening strongyloides spp. infection from wild rodents implications for public awareness and attitudes on zoonotic diseases in malang city, Indonesia. J Med Vet. 2022; 5(2): 196-206. DOI:10.20473/jmv.vol5.iss2.2022.196-206

Davis S, and Calvet E. Fluctuating rodent populations and risk to humans from rodent-borne zoonoses. J Vector Borne Dis. 2005; 5(4): 305-314. DOI: https://doi.org/10.1089/vbz.2005.5.305

Meerburg BG, Singleton GR, and Kijlstra A. Rodent-borne diseases and their risks for public health. Crit Rev Microbiol. 2009; 35(3): 221-270. DOI: https://doi.org/10.1080/10408410902989837

Rabiee MH, Mahmoudi A, Siahsarvie R, Kryštufek B, and Mostafavi E. Rodent-borne diseases and their public health importance in Iran. PLoS Negl Trop Dis. 2018; 12(4): e0006256. DOI: https://doi.org/10.1371/journal.pntd.0006256

Morand S, Bordes F, CHEN HW, Claude J, COSSON JF, Galan M, et al. Global parasite and Rattus rodent invasions: The consequences for rodent‐borne diseases. Integr Zool. 2015; 10(5): 409-423. DOI: https://doi.org/10.1111/1749-4877.12143

Goudarzi F, Mohtasebi S, Teimouri A, Yimam Y, Heydarian P, Sangani GS, et al. A systematic review and meta-analysis of Hymenolepis nana in human and rodent hosts in Iran: A remaining public health concern. Comp Immunol Microbiol Infect Dis. 2021; 74: 101580. DOI: https://doi.org/10.1016/j.cimid.2020.101580

Julius RS, Zengeya TA, Schwan EV, and Chimimba CT. Geospatial modelling and univariate analysis of commensal rodent-borne cestodoses: The case of invasive spp. of Rattus and indigenous Mastomys coucha

from South Africa. Front Vet Sci. 2021; 8: 678478. DOI: https://doi.org/10.3389/fvets.2021.678478

Kazemi-Moghaddam V, Dehghani R, Hadei M, Dehqan S, Sedaghat MM, Latifi M, et al. Rodent-borne and rodent-related diseases in Iran. Comp Clin Path. 2019; 28: 893-905. DOI: https://doi.org/10.1007/s00580-018-2690-9

Montaño KJ, Cuéllar C, and Sotillo J. Rodent models for the study of soil-transmitted helminths: A proteomics approach. Front cell infect. 2021; 11: 639573. DOI: https://doi.org/10.3389/fcimb.2021.639573

White RJ, and Razgour O. Emerging zoonotic diseases originating in mammals: A systematic review of effects of anthropogenic land‐use change. Mamm Rev. 2020; 50(4): 336-352. DOI: https://doi.org/10.1111/mam.12201

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