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Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa

Cryptosporidium infection is one of the most common causes of parasitic diarrhoea worldwide in cattle and humans. In developing countries, human cryptosporidiosis is most prevalent during early childhood and links between zoonotic infection and animal related activities have been demonstrated. This...

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Autores principales: Abu Samra, Nada, Jori, Ferran, Cacciò, Simone M., Frean, John, Poonsamy, Bhavani, Thompson, Peter N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238718/
https://www.ncbi.nlm.nih.gov/pubmed/27247067
http://dx.doi.org/10.4102/ojvr.v83i1.1024
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author Abu Samra, Nada
Jori, Ferran
Cacciò, Simone M.
Frean, John
Poonsamy, Bhavani
Thompson, Peter N.
author_facet Abu Samra, Nada
Jori, Ferran
Cacciò, Simone M.
Frean, John
Poonsamy, Bhavani
Thompson, Peter N.
author_sort Abu Samra, Nada
collection PubMed
description Cryptosporidium infection is one of the most common causes of parasitic diarrhoea worldwide in cattle and humans. In developing countries, human cryptosporidiosis is most prevalent during early childhood and links between zoonotic infection and animal related activities have been demonstrated. This study investigated the prevalence and species/genotype distribution of Cryptosporidium among children (< 5 years) and calves (< 6 months) living in a rural farming area adjacent to the Kruger National Park in South Africa, where interactions between humans and wild and domestic animals are known to occur. Cryptosporidium oocysts were detected in 8/143 stool samples of children recruited within the hospital system (5.6%; 95% CI 2.4%, 10.7%) and in 2/352 faecal samples of calves (0.6%; 95% CI 0.1%, 2.0%) using the modified Ziehl–Neelsen (MZN) staining technique. Microscopy positive samples from children were further analysed by PCR targeting the 18S rRNA gene and identified as Cryptosporidium hominis (3/4) and Cryptosporidium meleagridis (1/4). Regardless of the microscopy outcome, randomly selected samples (n = 36) from calves 0–4 months of age were amplified and sequenced at the 18S rRNA gene using nested PCR. Two calves tested positive (5.6%; 95% CI 1.7%, 18.7%), and revealed the presence of Cryptosporidium parvum and Cryptosporidium bovis. The detection of only two zoonotic species (C. parvum in one calf and C. meleagridis in one child) suggests that zoonotic cryptosporidiosis is not currently widespread in our study area; however, the potential exists for amplification of transmission in an immunocompromised population.
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spelling pubmed-62387182018-11-26 Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa Abu Samra, Nada Jori, Ferran Cacciò, Simone M. Frean, John Poonsamy, Bhavani Thompson, Peter N. Onderstepoort J Vet Res Original Research Cryptosporidium infection is one of the most common causes of parasitic diarrhoea worldwide in cattle and humans. In developing countries, human cryptosporidiosis is most prevalent during early childhood and links between zoonotic infection and animal related activities have been demonstrated. This study investigated the prevalence and species/genotype distribution of Cryptosporidium among children (< 5 years) and calves (< 6 months) living in a rural farming area adjacent to the Kruger National Park in South Africa, where interactions between humans and wild and domestic animals are known to occur. Cryptosporidium oocysts were detected in 8/143 stool samples of children recruited within the hospital system (5.6%; 95% CI 2.4%, 10.7%) and in 2/352 faecal samples of calves (0.6%; 95% CI 0.1%, 2.0%) using the modified Ziehl–Neelsen (MZN) staining technique. Microscopy positive samples from children were further analysed by PCR targeting the 18S rRNA gene and identified as Cryptosporidium hominis (3/4) and Cryptosporidium meleagridis (1/4). Regardless of the microscopy outcome, randomly selected samples (n = 36) from calves 0–4 months of age were amplified and sequenced at the 18S rRNA gene using nested PCR. Two calves tested positive (5.6%; 95% CI 1.7%, 18.7%), and revealed the presence of Cryptosporidium parvum and Cryptosporidium bovis. The detection of only two zoonotic species (C. parvum in one calf and C. meleagridis in one child) suggests that zoonotic cryptosporidiosis is not currently widespread in our study area; however, the potential exists for amplification of transmission in an immunocompromised population. AOSIS 2016-05-20 /pmc/articles/PMC6238718/ /pubmed/27247067 http://dx.doi.org/10.4102/ojvr.v83i1.1024 Text en © 2016. The Authors http://creativecommons.org/licenses/by/2.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Abu Samra, Nada
Jori, Ferran
Cacciò, Simone M.
Frean, John
Poonsamy, Bhavani
Thompson, Peter N.
Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title_full Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title_fullStr Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title_full_unstemmed Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title_short Cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the Kruger National Park, South Africa
title_sort cryptosporidium genotypes in children and calves living at the wildlife or livestock interface of the kruger national park, south africa
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238718/
https://www.ncbi.nlm.nih.gov/pubmed/27247067
http://dx.doi.org/10.4102/ojvr.v83i1.1024
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