Anaplasma phagocytophilum evolves in geographical and biotic niches of vertebrates and ticks.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
28 Jun 2019
Historique:
received: 02 04 2019
accepted: 24 06 2019
entrez: 30 6 2019
pubmed: 30 6 2019
medline: 14 8 2019
Statut: epublish

Résumé

Anaplasma phagocytophilum is currently regarded as a single species. However, molecular studies indicate that it can be subdivided into ecotypes, each with distinct but overlapping transmission cycle. Here, we evaluate the interactions between and within clusters of haplotypes of the bacterium isolated from vertebrates and ticks, using phylogenetic and network-based methods. The presence of A. phagocytophilum DNA was determined in ticks and vertebrate tissue samples. A fragment of the groEl gene was amplified and sequenced from qPCR-positive lysates. Additional groEl sequences from ticks and vertebrate reservoirs were obtained from GenBank and through literature searches, resulting in a dataset consisting of 1623 A. phagocytophilum field isolates. Phylogenetic analyses were used to infer clusters of haplotypes and to assess phylogenetic clustering of A. phagocytophilum in vertebrates or ticks. Network-based methods were used to resolve host-vector interactions and their relative importance in the segregating communities of haplotypes. Phylogenetic analyses resulted in 199 haplotypes within eight network-derived clusters, which were allocated to four ecotypes. The interactions of haplotypes between ticks, vertebrates and geographical origin, were visualized and quantified from networks. A high number of haplotypes were recorded in the tick Ixodes ricinus. Communities of A. phagocytophilum recorded from Korea, Japan, Far Eastern Russia, as well as those associated with rodents had no links with the larger set of isolates associated with I. ricinus, suggesting different evolutionary pressures. Rodents appeared to have a range of haplotypes associated with either Ixodes trianguliceps or Ixodes persulcatus and Ixodes pavlovskyi. Haplotypes found in rodents in Russia had low similarities with those recorded in rodents in other regions and shaped separate communities. The groEl gene fragment of A. phagocytophilum provides information about spatial segregation and associations of haplotypes to particular vector-host interactions. Further research is needed to understand the circulation of this bacterium in the gap between Europe and Asia before the overview of the speciation features of this bacterium is complete. Environmental traits may also play a role in the evolution of A. phagocytophilum in ecotypes through yet unknown relationships.

Sections du résumé

BACKGROUND BACKGROUND
Anaplasma phagocytophilum is currently regarded as a single species. However, molecular studies indicate that it can be subdivided into ecotypes, each with distinct but overlapping transmission cycle. Here, we evaluate the interactions between and within clusters of haplotypes of the bacterium isolated from vertebrates and ticks, using phylogenetic and network-based methods.
METHODS METHODS
The presence of A. phagocytophilum DNA was determined in ticks and vertebrate tissue samples. A fragment of the groEl gene was amplified and sequenced from qPCR-positive lysates. Additional groEl sequences from ticks and vertebrate reservoirs were obtained from GenBank and through literature searches, resulting in a dataset consisting of 1623 A. phagocytophilum field isolates. Phylogenetic analyses were used to infer clusters of haplotypes and to assess phylogenetic clustering of A. phagocytophilum in vertebrates or ticks. Network-based methods were used to resolve host-vector interactions and their relative importance in the segregating communities of haplotypes.
RESULTS RESULTS
Phylogenetic analyses resulted in 199 haplotypes within eight network-derived clusters, which were allocated to four ecotypes. The interactions of haplotypes between ticks, vertebrates and geographical origin, were visualized and quantified from networks. A high number of haplotypes were recorded in the tick Ixodes ricinus. Communities of A. phagocytophilum recorded from Korea, Japan, Far Eastern Russia, as well as those associated with rodents had no links with the larger set of isolates associated with I. ricinus, suggesting different evolutionary pressures. Rodents appeared to have a range of haplotypes associated with either Ixodes trianguliceps or Ixodes persulcatus and Ixodes pavlovskyi. Haplotypes found in rodents in Russia had low similarities with those recorded in rodents in other regions and shaped separate communities.
CONCLUSIONS CONCLUSIONS
The groEl gene fragment of A. phagocytophilum provides information about spatial segregation and associations of haplotypes to particular vector-host interactions. Further research is needed to understand the circulation of this bacterium in the gap between Europe and Asia before the overview of the speciation features of this bacterium is complete. Environmental traits may also play a role in the evolution of A. phagocytophilum in ecotypes through yet unknown relationships.

Identifiants

pubmed: 31253201
doi: 10.1186/s13071-019-3583-8
pii: 10.1186/s13071-019-3583-8
pmc: PMC6599317
doi:

Substances chimiques

Chaperonin 60 0

Types de publication

Journal Article

Langues

eng

Pagination

328

Subventions

Organisme : Grantová Agentura České Republiky
ID : 17-16009S

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Auteurs

Ryanne I Jaarsma (RI)

Centre for Infectious Disease Control (CIb), National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.

Hein Sprong (H)

Centre for Infectious Disease Control (CIb), National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Laboratory of Entomology, Wageningen University, Wageningen, The Netherlands.

Katsuhisa Takumi (K)

Centre for Infectious Disease Control (CIb), National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.

Maria Kazimirova (M)

Institute of Zoology, Slovak Academy of Sciences, Bratislava, Slovakia.

Cornelia Silaghi (C)

Friedrich-Loeffler-Institut, Federal Research Institute for Animal Health, Greifswald-Insel Riems, Germany.

Atle Mysterud (A)

Centre for Ecological and Evolutionary Synthesis (CEES), Department of Biosciences, University of Oslo, P.O. Box 1066, Blindern, 0316, Oslo, Norway.

Ivo Rudolf (I)

Institute of Vertebrate Biology, v.v.i, Medical Zoology Laboratory, Academy of Sciences of the Czech Republic, Brno, Czech Republic.

Relja Beck (R)

Department for Bacteriology and Parasitology, Croatian Veterinary Institute, Savska Cesta 143, Zagreb, Croatia.

Gábor Földvári (G)

Department of Parasitology and Zoology, University of Veterinary Medicine Budapest, Budapest, Hungary.
Evolutionary Systems Research Group, Centre for Ecological Research, Hungarian Academy of Sciences, Tihany, Hungary.

Laura Tomassone (L)

Department of Veterinary Sciences, University of Turin, Via L. da Vinci 44, Grugliasco, 10095, Turin, Italy.

Margit Groenevelt (M)

Diergeneeskundig Centrum Zuid-Oost Drenthe, Coevorden, The Netherlands.

Reinard R Everts (RR)

Diergeneeskundig Centrum Zuid-Oost Drenthe, Coevorden, The Netherlands.

Jolianne M Rijks (JM)

Dutch Wildlife Health Centre, Utrecht University, Utrecht, The Netherlands.

Frauke Ecke (F)

Department of Wildlife, Fish, and Environmental Studies, Swedish University of Agricultural Sciences, Umeå, Sweden.

Birger Hörnfeldt (B)

Department of Wildlife, Fish, and Environmental Studies, Swedish University of Agricultural Sciences, Umeå, Sweden.

David Modrý (D)

Department of Pathology and Parasitology, Faculty of Veterinary Medicine, University of Veterinary and Pharmaceutical Sciences, Brno, Czech Republic.
Biology Centre, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic.

Karolina Majerová (K)

Biology Centre, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic.
Department of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.

Jan Votýpka (J)

Biology Centre, Institute of Parasitology, Czech Academy of Sciences, České Budějovice, Czech Republic.
Department of Parasitology, Faculty of Science, Charles University, Prague, Czech Republic.

Agustín Estrada-Peña (A)

Department of Parasitology, Faculty of Veterinary Medicine, University of Zaragoza, Zaragoza, Spain. aestrada@unizar.es.
Emerging Zoonoses Research Group, Instituto Agroalimentario de Aragón (IA2), Zaragoza, Spain. aestrada@unizar.es.

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