Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis
Ehrlichia ruminantium, the agent of cowdriosis transmitted by Amblyomma ticks, presents an extensive genetic and antigenic diversity of key importance for vaccine formulation. Two means of nested polymerase chain reaction (PCR) targeting were developed to conduct molecular epidemiology studies in the Caribbean and Africa. The first used a conserved DNA fragment for detection of the pathogen in animals and vectors, and the second relied on the polymorphic map1 gene for genotyping. As compared to a PCR, the nested PCR showed a 2-Log10 improvement of sensitivity and allowed amplification from ticks, blood, brain, and lungs from infected animals, providing a more ac-curate picture of the tick infection rate. In Guadeloupe, this rate reached 36% (N = 212) instead of 1.7% (N = 224), as previously estimated. Genetic typing was done by restriction fragment length polymorphism or sequencing of map1 amplification products. Molecular epidemiology studies conducted in field sites selected for vaccination trials with inactivated vaccine, revealed the circulation of genetically divergent strains in limited geographical areas. It is known, then, that genetic clustering based on map1 has no predictive value regarding the protective value of a given strain against a new strain. However, tracing the strains by this technique revealed the extent of E. ruminantium diversity that one can expect in a given region, and the method allows differentiation between an inadequate immune response and the challenge by a breakthrough strain on animals dying despite vaccination. Up to now, genetic typing does not avoid cross-protection studies, which were conducted in parallel, although on a more limited scale. The importance of pathogen diversity studies for optimization of vaccine design is discussed as well as the research for new polymorphic genes. These genes may allow better predictions on cross-protection, given the recent completion of the sequence of the full genome of two E. ruminantium strains.
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Subjects: | L50 - Physiologie et biochimie animales, Ehrlichia, Amblyomma, vaccin, PCR, maladie bactérienne, biologie moléculaire, http://aims.fao.org/aos/agrovoc/c_2504, http://aims.fao.org/aos/agrovoc/c_333, http://aims.fao.org/aos/agrovoc/c_8130, http://aims.fao.org/aos/agrovoc/c_34079, http://aims.fao.org/aos/agrovoc/c_770, http://aims.fao.org/aos/agrovoc/c_4891, http://aims.fao.org/aos/agrovoc/c_3406, http://aims.fao.org/aos/agrovoc/c_8081, http://aims.fao.org/aos/agrovoc/c_3081, |
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dig-cirad-fr-5259442024-11-05T17:01:11Z http://agritrop.cirad.fr/525944/ http://agritrop.cirad.fr/525944/ Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis. Martinez Dominique, Vachiery Nathalie, Stachurski Frédéric, Kandassamy Yane, Raliniaina Modestine, Aprelon Rosalie, Gueye Arona. 2004. Annals of the New York Academy of Sciences, 1026 : 106-113. Biennial Conference of the Society for Tropical Veterinary Medicine. 7, Iguaçu Falls, Brésil, 22 Juin 2003/27 Juin 2003.https://doi.org/10.1196/annals.1307.014 <https://doi.org/10.1196/annals.1307.014> Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis Martinez, Dominique Vachiery, Nathalie Stachurski, Frédéric Kandassamy, Yane Raliniaina, Modestine Aprelon, Rosalie Gueye, Arona eng 2004 Annals of the New York Academy of Sciences L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 Guadeloupe Burkina Faso France http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 Ehrlichia ruminantium, the agent of cowdriosis transmitted by Amblyomma ticks, presents an extensive genetic and antigenic diversity of key importance for vaccine formulation. Two means of nested polymerase chain reaction (PCR) targeting were developed to conduct molecular epidemiology studies in the Caribbean and Africa. The first used a conserved DNA fragment for detection of the pathogen in animals and vectors, and the second relied on the polymorphic map1 gene for genotyping. As compared to a PCR, the nested PCR showed a 2-Log10 improvement of sensitivity and allowed amplification from ticks, blood, brain, and lungs from infected animals, providing a more ac-curate picture of the tick infection rate. In Guadeloupe, this rate reached 36% (N = 212) instead of 1.7% (N = 224), as previously estimated. Genetic typing was done by restriction fragment length polymorphism or sequencing of map1 amplification products. Molecular epidemiology studies conducted in field sites selected for vaccination trials with inactivated vaccine, revealed the circulation of genetically divergent strains in limited geographical areas. It is known, then, that genetic clustering based on map1 has no predictive value regarding the protective value of a given strain against a new strain. However, tracing the strains by this technique revealed the extent of E. ruminantium diversity that one can expect in a given region, and the method allows differentiation between an inadequate immune response and the challenge by a breakthrough strain on animals dying despite vaccination. Up to now, genetic typing does not avoid cross-protection studies, which were conducted in parallel, although on a more limited scale. The importance of pathogen diversity studies for optimization of vaccine design is discussed as well as the research for new polymorphic genes. These genes may allow better predictions on cross-protection, given the recent completion of the sequence of the full genome of two E. ruminantium strains. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/525944/1/525944.pdf text Cirad license info:eu-repo/semantics/restrictedAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1196/annals.1307.014 10.1196/annals.1307.014 info:eu-repo/semantics/altIdentifier/doi/10.1196/annals.1307.014 info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1196/annals.1307.014 |
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L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 |
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L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 Martinez, Dominique Vachiery, Nathalie Stachurski, Frédéric Kandassamy, Yane Raliniaina, Modestine Aprelon, Rosalie Gueye, Arona Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
description |
Ehrlichia ruminantium, the agent of cowdriosis transmitted by Amblyomma ticks, presents an extensive genetic and antigenic diversity of key importance for vaccine formulation. Two means of nested polymerase chain reaction (PCR) targeting were developed to conduct molecular epidemiology studies in the Caribbean and Africa. The first used a conserved DNA fragment for detection of the pathogen in animals and vectors, and the second relied on the polymorphic map1 gene for genotyping. As compared to a PCR, the nested PCR showed a 2-Log10 improvement of sensitivity and allowed amplification from ticks, blood, brain, and lungs from infected animals, providing a more ac-curate picture of the tick infection rate. In Guadeloupe, this rate reached 36% (N = 212) instead of 1.7% (N = 224), as previously estimated. Genetic typing was done by restriction fragment length polymorphism or sequencing of map1 amplification products. Molecular epidemiology studies conducted in field sites selected for vaccination trials with inactivated vaccine, revealed the circulation of genetically divergent strains in limited geographical areas. It is known, then, that genetic clustering based on map1 has no predictive value regarding the protective value of a given strain against a new strain. However, tracing the strains by this technique revealed the extent of E. ruminantium diversity that one can expect in a given region, and the method allows differentiation between an inadequate immune response and the challenge by a breakthrough strain on animals dying despite vaccination. Up to now, genetic typing does not avoid cross-protection studies, which were conducted in parallel, although on a more limited scale. The importance of pathogen diversity studies for optimization of vaccine design is discussed as well as the research for new polymorphic genes. These genes may allow better predictions on cross-protection, given the recent completion of the sequence of the full genome of two E. ruminantium strains. |
format |
article |
topic_facet |
L50 - Physiologie et biochimie animales Ehrlichia Amblyomma vaccin PCR maladie bactérienne biologie moléculaire http://aims.fao.org/aos/agrovoc/c_2504 http://aims.fao.org/aos/agrovoc/c_333 http://aims.fao.org/aos/agrovoc/c_8130 http://aims.fao.org/aos/agrovoc/c_34079 http://aims.fao.org/aos/agrovoc/c_770 http://aims.fao.org/aos/agrovoc/c_4891 http://aims.fao.org/aos/agrovoc/c_3406 http://aims.fao.org/aos/agrovoc/c_8081 http://aims.fao.org/aos/agrovoc/c_3081 |
author |
Martinez, Dominique Vachiery, Nathalie Stachurski, Frédéric Kandassamy, Yane Raliniaina, Modestine Aprelon, Rosalie Gueye, Arona |
author_facet |
Martinez, Dominique Vachiery, Nathalie Stachurski, Frédéric Kandassamy, Yane Raliniaina, Modestine Aprelon, Rosalie Gueye, Arona |
author_sort |
Martinez, Dominique |
title |
Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
title_short |
Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
title_full |
Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
title_fullStr |
Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
title_full_unstemmed |
Nested PCR for detection and genotyping of Ehrlichia ruminantium: Use in genetic diversity analysis |
title_sort |
nested pcr for detection and genotyping of ehrlichia ruminantium: use in genetic diversity analysis |
url |
http://agritrop.cirad.fr/525944/ http://agritrop.cirad.fr/525944/1/525944.pdf |
work_keys_str_mv |
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_version_ |
1816146837540700160 |