High diversity of ankA sequences of Anaplasma phagocytophilum among Ixodes ricinus ticks in Germany

J Clin Microbiol. 2003 Nov;41(11):5033-40. doi: 10.1128/JCM.41.11.5033-5040.2003.

Abstract

In Germany humans with acute granulocytic ehrlichiosis have not yet been described. Here, we characterized three different genes of Anaplasma phagocytophilum strains infecting German Ixodes ricinus ticks in order to test whether they differ from strains in other European countries and the United States. A total of 1,022 I. ricinus ticks were investigated for infection with A. phagocytophilum by nested PCR and sequence analysis. Forty-two (4.1%) ticks were infected. For all positive ticks, parts of the 16S rRNA and groESL genes were sequenced. The complete coding sequence of the ankA gene could be determined in 24 samples. The 16S rRNA and groESL gene sequences were as much as 100% identical to known sequences. Fifteen ankA sequences were >/=99.37% identical to sequences derived from humans with granulocytic ehrlichiosis in Europe and from a horse with granulocytic ehrlichiosis in Germany. Thus, German I. ricinus ticks most likely harbor A. phagocytophilum strains that can cause disease in humans. Nine additional sequences were clearly different from known ankA sequences. Because these newly described sequences have never been obtained from diseased humans or animals, their biological significance is currently unknown. Based on this unexpected sequence heterogeneity, we propose to use the ankA gene for further phylogenetic analyses of A. phagocytophilum and to investigate the biology and pathogenicity of strains that differ in the ankA gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaplasma phagocytophilum / classification
  • Anaplasma phagocytophilum / genetics*
  • Anaplasma phagocytophilum / isolation & purification
  • Animals
  • Bacterial Proteins / genetics*
  • Base Sequence
  • DNA Primers
  • Genetic Variation / genetics*
  • Germany
  • Ixodes / microbiology*
  • Phylogeny
  • Polymerase Chain Reaction

Substances

  • Bacterial Proteins
  • DNA Primers