Cargando…
Variation in disease phenotype is marked in equine trypanosomiasis
BACKGROUND: Equine trypanosomiasis is a severe and prevalent disease that has the greatest impact globally upon working equids due to its distribution across lower income countries. Morbidity and mortality rates are high; disease management strategies in endemic regions are ineffective and cost proh...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085162/ https://www.ncbi.nlm.nih.gov/pubmed/32199454 http://dx.doi.org/10.1186/s13071-020-04020-6 |
_version_ | 1783508888694292480 |
---|---|
author | Raftery, Alexandra G. Jallow, Saloum Coultous, Robert M. Rodgers, Jean Sutton, David G. M. |
author_facet | Raftery, Alexandra G. Jallow, Saloum Coultous, Robert M. Rodgers, Jean Sutton, David G. M. |
author_sort | Raftery, Alexandra G. |
collection | PubMed |
description | BACKGROUND: Equine trypanosomiasis is a severe and prevalent disease that has the greatest impact globally upon working equids due to its distribution across lower income countries. Morbidity and mortality rates are high; disease management strategies in endemic regions are ineffective and cost prohibitive. Individual variation in disease phenotype in other species suggests host factors could reveal novel treatment and control targets but has not been investigated in equids. METHODS: A prospective clinical evaluation of equines presenting for a free veterinary examination was performed in hyperendemic villages in The Gambia. Age, body condition score and body weight were estimated by validated methods, and haematocrit and total protein concentration measured. Animals fulfilling 2 out of 5 clinical inclusion criteria (anaemia, poor body condition, pyrexia, history of abortion, oedema) for a diagnosis of trypanosomiasis received trypanocidal treatment with follow-up at 1 and 2 weeks. Blood samples underwent PCR analysis with specific Trypanosoma spp. primers and results were compared to the subject’s clinical and clinicopathological features. A mixed effects generalised linear model was generated to evaluate the association of infection status with degree of pyrexia and anaemia. RESULTS: Morbidity was high within examined (n = 641) and selected (n = 247) study populations. PCR status was not associated with a defined disease phenotype; there was intra- and inter-species variability. Donkeys were more frequently Trypanosoma spp.-positive (P < 0.001) and febrile (P < 0.001) than horses, but infected horses were more anaemic (P < 0.001), and in poorer body condition (P < 0.001) than donkeys. Sex was correlated to disease phenotype: males were more anaemic (P = 0.03) and febrile (P < 0.001). Haemoparasite co-infections were more common than a single infection. CONCLUSIONS: There was evidence of diversity in trypanosomiasis clinical signs plus variable disease phenotypes within equid subpopulations that warrant further investigation. The complex co-infection profile of field cases requires greater consideration to optimise disease management. [Image: see text] |
format | Online Article Text |
id | pubmed-7085162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70851622020-03-23 Variation in disease phenotype is marked in equine trypanosomiasis Raftery, Alexandra G. Jallow, Saloum Coultous, Robert M. Rodgers, Jean Sutton, David G. M. Parasit Vectors Research BACKGROUND: Equine trypanosomiasis is a severe and prevalent disease that has the greatest impact globally upon working equids due to its distribution across lower income countries. Morbidity and mortality rates are high; disease management strategies in endemic regions are ineffective and cost prohibitive. Individual variation in disease phenotype in other species suggests host factors could reveal novel treatment and control targets but has not been investigated in equids. METHODS: A prospective clinical evaluation of equines presenting for a free veterinary examination was performed in hyperendemic villages in The Gambia. Age, body condition score and body weight were estimated by validated methods, and haematocrit and total protein concentration measured. Animals fulfilling 2 out of 5 clinical inclusion criteria (anaemia, poor body condition, pyrexia, history of abortion, oedema) for a diagnosis of trypanosomiasis received trypanocidal treatment with follow-up at 1 and 2 weeks. Blood samples underwent PCR analysis with specific Trypanosoma spp. primers and results were compared to the subject’s clinical and clinicopathological features. A mixed effects generalised linear model was generated to evaluate the association of infection status with degree of pyrexia and anaemia. RESULTS: Morbidity was high within examined (n = 641) and selected (n = 247) study populations. PCR status was not associated with a defined disease phenotype; there was intra- and inter-species variability. Donkeys were more frequently Trypanosoma spp.-positive (P < 0.001) and febrile (P < 0.001) than horses, but infected horses were more anaemic (P < 0.001), and in poorer body condition (P < 0.001) than donkeys. Sex was correlated to disease phenotype: males were more anaemic (P = 0.03) and febrile (P < 0.001). Haemoparasite co-infections were more common than a single infection. CONCLUSIONS: There was evidence of diversity in trypanosomiasis clinical signs plus variable disease phenotypes within equid subpopulations that warrant further investigation. The complex co-infection profile of field cases requires greater consideration to optimise disease management. [Image: see text] BioMed Central 2020-03-21 /pmc/articles/PMC7085162/ /pubmed/32199454 http://dx.doi.org/10.1186/s13071-020-04020-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Raftery, Alexandra G. Jallow, Saloum Coultous, Robert M. Rodgers, Jean Sutton, David G. M. Variation in disease phenotype is marked in equine trypanosomiasis |
title | Variation in disease phenotype is marked in equine trypanosomiasis |
title_full | Variation in disease phenotype is marked in equine trypanosomiasis |
title_fullStr | Variation in disease phenotype is marked in equine trypanosomiasis |
title_full_unstemmed | Variation in disease phenotype is marked in equine trypanosomiasis |
title_short | Variation in disease phenotype is marked in equine trypanosomiasis |
title_sort | variation in disease phenotype is marked in equine trypanosomiasis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085162/ https://www.ncbi.nlm.nih.gov/pubmed/32199454 http://dx.doi.org/10.1186/s13071-020-04020-6 |
work_keys_str_mv | AT rafteryalexandrag variationindiseasephenotypeismarkedinequinetrypanosomiasis AT jallowsaloum variationindiseasephenotypeismarkedinequinetrypanosomiasis AT coultousrobertm variationindiseasephenotypeismarkedinequinetrypanosomiasis AT rodgersjean variationindiseasephenotypeismarkedinequinetrypanosomiasis AT suttondavidgm variationindiseasephenotypeismarkedinequinetrypanosomiasis |