Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity

Abstract Background Only a few studies have examined the presence of Anaplasma marginale and Anaplasma centrale in South Africa, and no studies have comprehensively examined these species across the whole country. To undertake this country-wide study we adapted a duplex quantitative real-time PCR (q...

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Main Authors: Paidashe Hove, Mamohale E. Chaisi, Kelly A. Brayton, Hamilton Ganesan, Helen N. Catanese, Moses S. Mtshali, Awelani M. Mutshembele, Marinda C. Oosthuizen, Nicola E. Collins
Format: Article
Language:English
Published: BMC 2018-01-01
Series:Parasites & Vectors
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13071-017-2595-5
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spelling doaj-a4eaef3ba4044572b9b1c477583b48422020-11-25T01:25:00ZengBMCParasites & Vectors1756-33052018-01-0111111310.1186/s13071-017-2595-5Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversityPaidashe Hove0Mamohale E. Chaisi1Kelly A. Brayton2Hamilton Ganesan3Helen N. Catanese4Moses S. Mtshali5Awelani M. Mutshembele6Marinda C. Oosthuizen7Nicola E. Collins8Vectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of PretoriaVectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of PretoriaVectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of PretoriaInqaba Biotechnical IndustriesSchool of Electrical Engineering and Computer Science, Washington State UniversityResearch and Scientific Services Department, National Zoological Gardens of South AfricaResearch and Scientific Services Department, National Zoological Gardens of South AfricaVectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of PretoriaVectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of PretoriaAbstract Background Only a few studies have examined the presence of Anaplasma marginale and Anaplasma centrale in South Africa, and no studies have comprehensively examined these species across the whole country. To undertake this country-wide study we adapted a duplex quantitative real-time PCR (qPCR) assay for use in South Africa but found that one of the genes on which the assay was based was variable. Therefore, we sequenced a variety of field samples and tested the assay on the variants detected. We used the assay to screen 517 cattle samples sourced from all nine provinces of South Africa, and subsequently examined A. marginale positive samples for msp1α genotype to gauge strain diversity. Results Although the A. marginale msp1β gene is variable, the qPCR functions at an acceptable efficiency. The A. centrale groEL gene was not variable within the qPCR assay region. Of the cattle samples screened using the assay, 57% and 17% were found to be positive for A. marginale and A. centrale, respectively. Approximately 15% of the cattle were co-infected. Msp1α genotyping revealed 36 novel repeat sequences. Together with data from previous studies, we analysed the Msp1a repeats from South Africa where a total of 99 repeats have been described that can be attributed to 190 msp1α genotypes. While 22% of these repeats are also found in other countries, only two South African genotypes are also found in other countries; otherwise, the genotypes are unique to South Africa. Conclusions Anaplasma marginale was prevalent in the Western Cape, KwaZulu-Natal and Mpumalanga and absent in the Northern Cape. Anaplasma centrale was prevalent in the Western Cape and KwaZulu-Natal and absent in the Northern Cape and Eastern Cape. None of the cattle in the study were known to be vaccinated with A. centrale, so finding positive cattle indicates that this organism appears to be naturally circulating in cattle. A diverse population of A. marginale strains are found in South Africa, with some msp1α genotypes widely distributed across the country, and others appearing only once in one province. This diversity should be taken into account in future vaccine development studies.http://link.springer.com/article/10.1186/s13071-017-2595-5msp1αmsp1βgroELqPCRNext-generation amplicon sequencing
collection DOAJ
language English
format Article
sources DOAJ
author Paidashe Hove
Mamohale E. Chaisi
Kelly A. Brayton
Hamilton Ganesan
Helen N. Catanese
Moses S. Mtshali
Awelani M. Mutshembele
Marinda C. Oosthuizen
Nicola E. Collins
spellingShingle Paidashe Hove
Mamohale E. Chaisi
Kelly A. Brayton
Hamilton Ganesan
Helen N. Catanese
Moses S. Mtshali
Awelani M. Mutshembele
Marinda C. Oosthuizen
Nicola E. Collins
Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
Parasites & Vectors
msp1α
msp1β
groEL
qPCR
Next-generation amplicon sequencing
author_facet Paidashe Hove
Mamohale E. Chaisi
Kelly A. Brayton
Hamilton Ganesan
Helen N. Catanese
Moses S. Mtshali
Awelani M. Mutshembele
Marinda C. Oosthuizen
Nicola E. Collins
author_sort Paidashe Hove
title Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
title_short Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
title_full Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
title_fullStr Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
title_full_unstemmed Co-infections with multiple genotypes of Anaplasma marginale in cattle indicate pathogen diversity
title_sort co-infections with multiple genotypes of anaplasma marginale in cattle indicate pathogen diversity
publisher BMC
series Parasites & Vectors
issn 1756-3305
publishDate 2018-01-01
description Abstract Background Only a few studies have examined the presence of Anaplasma marginale and Anaplasma centrale in South Africa, and no studies have comprehensively examined these species across the whole country. To undertake this country-wide study we adapted a duplex quantitative real-time PCR (qPCR) assay for use in South Africa but found that one of the genes on which the assay was based was variable. Therefore, we sequenced a variety of field samples and tested the assay on the variants detected. We used the assay to screen 517 cattle samples sourced from all nine provinces of South Africa, and subsequently examined A. marginale positive samples for msp1α genotype to gauge strain diversity. Results Although the A. marginale msp1β gene is variable, the qPCR functions at an acceptable efficiency. The A. centrale groEL gene was not variable within the qPCR assay region. Of the cattle samples screened using the assay, 57% and 17% were found to be positive for A. marginale and A. centrale, respectively. Approximately 15% of the cattle were co-infected. Msp1α genotyping revealed 36 novel repeat sequences. Together with data from previous studies, we analysed the Msp1a repeats from South Africa where a total of 99 repeats have been described that can be attributed to 190 msp1α genotypes. While 22% of these repeats are also found in other countries, only two South African genotypes are also found in other countries; otherwise, the genotypes are unique to South Africa. Conclusions Anaplasma marginale was prevalent in the Western Cape, KwaZulu-Natal and Mpumalanga and absent in the Northern Cape. Anaplasma centrale was prevalent in the Western Cape and KwaZulu-Natal and absent in the Northern Cape and Eastern Cape. None of the cattle in the study were known to be vaccinated with A. centrale, so finding positive cattle indicates that this organism appears to be naturally circulating in cattle. A diverse population of A. marginale strains are found in South Africa, with some msp1α genotypes widely distributed across the country, and others appearing only once in one province. This diversity should be taken into account in future vaccine development studies.
topic msp1α
msp1β
groEL
qPCR
Next-generation amplicon sequencing
url http://link.springer.com/article/10.1186/s13071-017-2595-5
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