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Volume 60, Issue 4, Pages 300-305 (April 2010)


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First detection of the Anaplasma phagocytophilum groEL-A genotype in man

Elisabeth Haschke-Bechera, Rainer Bernauerb, Anna-Maria Walleczeka, Petra Apfalterc, Shahrzad Afazel-Saeedia, Joerg Krausb, Gunther Ladurnerab, Peter StrasseraCorresponding Author Informationemail address

Accepted 17 December 2009. published online 11 January 2010.

Summary 

Objective

Human Granulocytic Anaplasmosis (HGA) is an emerging disease caused by the gram-negative bacterium Anaplasma phagocytophilum which is transmitted by ticks of the genus Ixodes ricinus. For molecular detection of the pathogen by PCR, a conserved portion of the groEL gene within the groESL operon is frequently used as a target. A single G/A polymorphism in this region allows to discriminate between two genotypes, groEL-G and groEL-A.

Methods

Total DNA from peripheral blood samples of two HGA patients was analysed by RealTime PCR, employing a protocol designed for genotyping groEL-G- and groEL-A variants of A. phagocytophilum.

Results

We confirmed two clinical cases of HGA by PCR; in one patient, and for the first time in a human host, the groEL-A variant was detected, in the other case the pathogen was recognised as the groEL-G variant, up to now representing the only genotype reported in man.

Conclusions

It is documented that HGA infections can be caused by two A. phagocytophilum groEL genotypes. At present, the preference of the A. phagocytophilum groEL-G genotype in humans remains unclear, as we describe the first patient with HGA caused by the groEL-A variant. For a conclusive interpretation, more data from HGA patients will be required.

a Central Laboratory, University Hospital of Neurology, Paracelsus Medical University of Salzburg (PMU), Ignaz-Harrer-Strasse 79, A-5020 Salzburg, Austria

b University Hospital of Neurology, Paracelsus Medical University of Salzburg (PMU), Ignaz-Harrer-Strasse 79, A-5020 Salzburg, Austria

c Department of Clinical Microbiology, Institute of Hygiene and Medical Microbiology, Medical University Vienna, Kinderspitalgasse 15, A-1095 Vienna, Austria

Corresponding Author InformationCorresponding author. Tel.: +43 662 4483 4367; fax: +43 662 4483 3314.

PII: S0163-4453(09)00394-6

doi:10.1016/j.jinf.2009.12.010


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