Changes in biochemical analytes in female dogs with subclinical Ancylostoma spp. infection

Schmidt, E. M.S., Tvarijonaviciute, A., Martinez-Subiela, S., Ceron, J. and Eckersall, P. D. (2016) Changes in biochemical analytes in female dogs with subclinical Ancylostoma spp. infection. BMC Veterinary Research, 12, 203. (doi: 10.1186/s12917-016-0833-2) (PMID:27623952) (PMCID:PMC5022191)

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Background: Ancylostoma spp. is one of the most prevalent canine intestinal nematode infections which usually causes subclinical disease in adult dogs and has zoonotic implications. Therefore, the aim of this study was to explore and evaluate the possible pathophysiological changes that Ancylostoma spp. could produce in female dogs naturally infected but without clinical signs of disease, by screening a wide variety of biochemical markers for potential changes. Samples of feces and blood of 45 dogs were collected and fecal flotation and zinc sulphate centrifugal flotation were performed. The biochemical analytes determined were: the acute-phase proteins C-reactive protein (CRP) and haptoglobin (Hp); the lipid profile (cholesterol, triglycerides, HDL, LDL); the serum iron profile: iron, unsaturated iron binding-capacity (UIBC), and ferritin; the enzyme butyrylcholinesterase (BChe); the pancreatic profile: amylase, lipase, and trypsin-like immunoreactivity (TLI); the oxidative stress markers: total antioxidant capacity (TAC) and paraoxonase −1 (PON-1), along with total protein, albumin, and insulin-like growth factor – 1 (IGF – 1). Ancylostoma spp. eggs were detected in 29/45 dogs (64.4 %). Dogs were divided into two groups according to the results of fecal flotation methods. Group 1: negative fecal floatation (n = 16), and Group 2: subclinical infection with the observation of Ancylostoma spp. type eggs/x 40 objective fields (n = 29). Results: Mann–Whitney U test was used to compare the biochemical analyte results between the two groups (P < 0.05). Significant increases in CRP (μg/mL) (median): non-infected dogs: 5.5; subclinically infected dogs 18.7; P = 0.03, Hp (g/L) (median): G1: 2.4; G2: 3.3; P = 0.03, and UIBC (μg/dL) (median): non-infected dogs: 139.4; subclinically infected dogs: 216; P = 0.0015, and significantly decreased iron (μg/dL) (median): non-infected dogs: 202.5; subclinically infected dogs: 125.7; P = 0.0041, IGF-1 (ng/mL) (median): non-infected dogs: 224; subclinically infected dogs: 123; P = 0.02, and albumin (g/dL) (median): non-infected dogs: 2.8; subclinically infected dogs: 2.5; P = 0.04 concentrations were observed in dogs with subclinical Ancylostoma spp. infection when compared to non-infected dogs. Conclusion: These findings provide an overview of the biochemical effects produced by patent Ancylostoma spp. in naturally infected dogs without any evident clinical signs of disease, which could be considered in differential diagnosis, especially in an endemic area for this parasite.

Item Type:Articles
Additional Information:Part of the present work was carried out at the Institute of Biodiversity, Animal Health and Comparative Medicine, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK and supported by Marie Curie (FP07 Nematode Health System) – ITN 2012 – 264639 (EMSS training fellow grant). Part of this work was carried out at the Interdisciplinary Laboratory of Clinical Pathology, Interlab-UMU, Campus of Excellence Mare Nostrum - University of Murcia, Spain and partially supported by CNPq – Brazil (PD 203241/2014-2) (EMSS PD grant). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Glasgow Author(s) Enlighten ID:Eckersall, Professor David and Schmidt, Ms Elizabeth
Authors: Schmidt, E. M.S., Tvarijonaviciute, A., Martinez-Subiela, S., Ceron, J., and Eckersall, P. D.
College/School:College of Medical Veterinary and Life Sciences > Institute of Biodiversity Animal Health and Comparative Medicine
College of Medical Veterinary and Life Sciences > School of Veterinary Medicine
Journal Name:BMC Veterinary Research
Publisher:BioMed Central Ltd
ISSN (Online):1746-6148
Copyright Holders:Copyright © 2016 The Authors
First Published:First published in BMC Veterinary Research 12:203
Publisher Policy:Reproduced under a Creative Commons License

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