AI Article Synopsis

  • This study examines the presence and genetic diversity of Anaplasma phagocytophilum strains in Ixodes ricinus ticks in Germany, as no human cases of acute granulocytic ehrlichiosis have been reported there.
  • Out of 1,022 ticks tested, 42 (4.1%) were found to be infected, with genetic sequencing revealing that most were closely related to strains found in human cases in Europe, suggesting potential for human disease.
  • The research identified some new ankA gene sequences that differ from known strains, highlighting a need for further studies on their biological significance and potential health risks.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC262509PMC
http://dx.doi.org/10.1128/JCM.41.11.5033-5040.2003DOI Listing

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