Sequence Analysis of the msp4 Gene of Anaplasma phagocytophilum Strains

Author:

de la Fuente José12,Massung Robert F.3,Wong Susan J.4,Chu Frederick K.5,Lutz Hans6,Meli Marina6,von Loewenich Friederike D.7,Grzeszczuk Anna8,Torina Alessandra9,Caracappa Santo9,Mangold Atilio J.10,Naranjo Victoria2,Stuen Snorre11,Kocan Katherine M.1

Affiliation:

1. Department of Veterinary Pathobiology, College of Veterinary Medicine, Oklahoma State University, Stillwater, Oklahoma

2. Instituto de Investigación en Recursos Cinegéticos IREC (CSIC-UCLM-JCCM), Ciudad Real, Spain

3. Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia

4. Diagnostic Immunology Laboratory, Wadsworth Center

5. Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany, New York

6. Clinical Laboratory, Faculty of Veterinary Medicine, University of Zurich, Zurich, Switzerland

7. Institute of Medical Microbiology and Hygiene, Department of Medical Microbiology and Hygiene, University Clinic of Freiburg, Freiburg, Germany

8. Department of Infectious Diseases, Medical University of Bialystok, Bialystok, Poland

9. Istituto Zooprofilattico Sperimentale della Sicilia, Palermo, Italy

10. Instituto Nacional de Tecnología Agropecuaria, Estación Experimental Agropecuaria Rafaela, Rafaela, Santa Fe, Argentina

11. Department of Production Animal Clinical Sciences, Norwegian School of Veterinary Science, Sandnes, Norway

Abstract

ABSTRACT The causative agent of human granulocytic ehrlichiosis was recently reclassified as Anaplasma phagocytophilum , unifying previously described bacteria that cause disease in humans, horses, dogs, and ruminants. For the characterization of genetic heterogeneity in this species, the homologue of Anaplasma marginale major surface protein 4 gene ( msp4 ) was identified, and the coding region was PCR amplified and sequenced from a variety of sources, including 50 samples from the United States, Germany, Poland, Norway, Italy, and Switzerland and 4 samples of A. phagocytophilum -like organisms obtained from white-tailed deer in the United States. Sequence variation between strains of A. phagocytophilum (90 to 100% identity at the nucleotide level and 92 to 100% similarity at the protein level) was higher than in A. marginale . Phylogenetic analyses of msp4 sequences did not provide phylogeographic information but did differentiate strains of A. phagocytophilum obtained from ruminants from those obtained from humans, dogs, and horses. The sequence analysis of the recently discovered A. phagocytophilum msp2 gene corroborated these results. The results reported here suggest that although A. phagocytophilum -like organisms from white-tailed deer may be closely related to A. phagocytophilum , they could be more diverse. These results suggest that A. phagocytophilum strains from ruminants could share some common characteristics, including reservoirs and pathogenicity, which may be different from strains that infect humans.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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