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Seroprevalence Among Ugandan Slaughter Cattle: Comparison of Sero-Status With Renal Infection

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Journal Front Vet Sci
Date 2020 Mar 19
PMID 32185188
Citations 9
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Abstract

Despite evidence of both human and animal exposures in Uganda, the epidemiology of the disease is still not well-investigated. Contact with animals and their environments have been pointed out as potential source of infection with species in humans; and cattle may be an important reservoir in Uganda. In this cross-sectional study, we estimated the prevalence of anti- antibodies by the standard microscopic agglutination test (MAT); and associated risk factors among slaughtered cattle. We also compared the performance of the MAT used in this study against a based real time PCR (qPCR) assay previously conducted on the kidneys and urine of the same slaughter cattle as tested in this reported study. Of 500 cattle sampled, 27.8% (95% CI 23.9-32.0) tested positive (titer ≥ 100) to at least one serovar, with the majority of seropositive cattle reacting to serovars Tarassovi (sg Tarassovi) (11.6%), Sejroe (Sg Sejroe) (7.8%), and Australis (Sg Australis) (5.2%). Older animals had 2.8 times (95% CI 1.0-8.2, -value 0.055) greater odds of being seropositive than younger ones (<1.5 years). The sensitivity and specificity of the MAT over the qPCR were 65.9% (95% CI 50.1-79.5) and 75.9% (95% CI 71.7-79.7), respectively; with a negative predictive value of 95.8% and positive predictive value of 20.9%. In conclusion, slaughter cattle in this study were significantly exposed to pathogenic species of mainly the Tarassovi, Sejroe, and Australis serogroups, with seroprevalence being higher among older cattle. The high specificity and negative predictive value of MAT as used in this study when compared to the qPCR assay may imply a rather strong association between seronegativity and absence of renal infection. However, MAT predictability for renal infection may be interpreted cautiously since predictive values of diagnostic tests are dependent on prevalence.

Citing Articles

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Cross-sectional serosurvey of Leptospira species among slaughter pigs, goats, and sheep in Uganda.

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References
1.
Schoonman L, Swai E . Herd- and animal-level risk factors for bovine leptospirosis in Tanga region of Tanzania. Trop Anim Health Prod. 2010; 42(7):1565-72. DOI: 10.1007/s11250-010-9607-1. View

2.
Alinaitwe L, Kankya C, Allan K, Rodriguez-Campos S, Torgerson P, Dreyfus A . Bovine leptospirosis in abattoirs in Uganda: Molecular detection and risk of exposure among workers. Zoonoses Public Health. 2019; 66(6):636-646. DOI: 10.1111/zph.12616. View

3.
Bajani M, Ashford D, Bragg S, Woods C, Aye T, Spiegel R . Evaluation of four commercially available rapid serologic tests for diagnosis of leptospirosis. J Clin Microbiol. 2003; 41(2):803-9. PMC: 149700. DOI: 10.1128/JCM.41.2.803-809.2003. View

4.
Dreyfus A, Odoch T, Alinaitwe L, Rodriguez-Campos S, Tsegay A, Jaquier V . Cross-Sectional Serological Survey for Leptospira spp. in Beef and Dairy Cattle in Two Districts in Uganda. Int J Environ Res Public Health. 2017; 14(11). PMC: 5708060. DOI: 10.3390/ijerph14111421. View

5.
Kerfua S, Shirima G, Kusiluka L, Ayebazibwe C, Mwebe R, Cleaveland S . Spatial and temporal distribution of foot-and-mouth disease in four districts situated along the Uganda-Tanzania border: Implications for cross-border efforts in disease control. Onderstepoort J Vet Res. 2018; 85(1):e1-e8. PMC: 6238673. DOI: 10.4102/ojvr.v85i1.1528. View