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Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases
BACKGROUND: Equine Granulocytic Anaplasmosis (EGA) is caused by Anaplasma phagocytophilum, a tick-transmitted, obligate intracellular bacterium. In Europe, it is transmitted by Ixodes ricinus. A large number of genetic variants of A. phagocytophilum circulate in nature and have been found in ticks a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170280/ https://www.ncbi.nlm.nih.gov/pubmed/21843364 http://dx.doi.org/10.1186/1756-3305-4-161 |
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author | Silaghi, Cornelia Liebisch, Gabriele Pfister, Kurt |
author_facet | Silaghi, Cornelia Liebisch, Gabriele Pfister, Kurt |
author_sort | Silaghi, Cornelia |
collection | PubMed |
description | BACKGROUND: Equine Granulocytic Anaplasmosis (EGA) is caused by Anaplasma phagocytophilum, a tick-transmitted, obligate intracellular bacterium. In Europe, it is transmitted by Ixodes ricinus. A large number of genetic variants of A. phagocytophilum circulate in nature and have been found in ticks and different animals. Attempts have been made to assign certain genetic variants to certain host species or pathologies, but have not been successful so far. The purpose of this study was to investigate the causing agent A. phagocytophilum of 14 cases of EGA in naturally infected horses with molecular methods on the basis of 4 partial genes (16S rRNA, groEL, msp2, and msp4). RESULTS: All DNA extracts of EDTA-blood samples of the horses gave bands of the correct nucleotide size in all four genotyping PCRs. Sequence analysis revealed 4 different variants in the partial 16S rRNA, groEL gene and msp2 genes, and 3 in the msp4 gene. One 16S rRNA gene variant involved in 11 of the 14 cases was identical to the "prototype" variant causing disease in humans in the amplified part [GenBank: U02521]. Phylogenetic analysis revealed as expected for the groEL gene that sequences from horses clustered separately from roe deer. Sequences of the partial msp2 gene from this study formed a separate cluster from ruminant variants in Europe and from all US variants. CONCLUSIONS: The results show that more than one variant of A. phagocytophilum seems to be involved in EGA in Germany. The comparative genetic analysis of the variants involved points towards different natural cycles in the epidemiology of A. phagocytophilum, possibly involving different reservoir hosts or host adaptation, rather than a strict species separation. |
format | Online Article Text |
id | pubmed-3170280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31702802011-09-10 Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases Silaghi, Cornelia Liebisch, Gabriele Pfister, Kurt Parasit Vectors Research BACKGROUND: Equine Granulocytic Anaplasmosis (EGA) is caused by Anaplasma phagocytophilum, a tick-transmitted, obligate intracellular bacterium. In Europe, it is transmitted by Ixodes ricinus. A large number of genetic variants of A. phagocytophilum circulate in nature and have been found in ticks and different animals. Attempts have been made to assign certain genetic variants to certain host species or pathologies, but have not been successful so far. The purpose of this study was to investigate the causing agent A. phagocytophilum of 14 cases of EGA in naturally infected horses with molecular methods on the basis of 4 partial genes (16S rRNA, groEL, msp2, and msp4). RESULTS: All DNA extracts of EDTA-blood samples of the horses gave bands of the correct nucleotide size in all four genotyping PCRs. Sequence analysis revealed 4 different variants in the partial 16S rRNA, groEL gene and msp2 genes, and 3 in the msp4 gene. One 16S rRNA gene variant involved in 11 of the 14 cases was identical to the "prototype" variant causing disease in humans in the amplified part [GenBank: U02521]. Phylogenetic analysis revealed as expected for the groEL gene that sequences from horses clustered separately from roe deer. Sequences of the partial msp2 gene from this study formed a separate cluster from ruminant variants in Europe and from all US variants. CONCLUSIONS: The results show that more than one variant of A. phagocytophilum seems to be involved in EGA in Germany. The comparative genetic analysis of the variants involved points towards different natural cycles in the epidemiology of A. phagocytophilum, possibly involving different reservoir hosts or host adaptation, rather than a strict species separation. BioMed Central 2011-08-16 /pmc/articles/PMC3170280/ /pubmed/21843364 http://dx.doi.org/10.1186/1756-3305-4-161 Text en Copyright ©2011 Silaghi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Silaghi, Cornelia Liebisch, Gabriele Pfister, Kurt Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title | Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title_full | Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title_fullStr | Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title_full_unstemmed | Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title_short | Genetic variants of Anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
title_sort | genetic variants of anaplasma phagocytophilum from 14 equine granulocytic anaplasmosis cases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170280/ https://www.ncbi.nlm.nih.gov/pubmed/21843364 http://dx.doi.org/10.1186/1756-3305-4-161 |
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