Inability of a Variant Strain ofAnaplasma phagocytophilumto Infect Mice
Author(s) -
Robert F. Massung,
Rachael A. Priestley,
Nathan J. Miller,
Thomas N. Mather,
Michael L. Levin
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/379725
Subject(s) - peromyscus , ixodes scapularis , anaplasma phagocytophilum , biology , anaplasma , virology , polymerase chain reaction , ixodes , xenodiagnosis , tick , ixodidae , gene , immunology , genetics , zoology , parasite hosting , borrelia burgdorferi , trypanosoma cruzi , world wide web , computer science , antibody
Nymphal Ixodes scapularis ticks were collected from several sites in Rhode Island. Polymerase chain reaction and DNA sequencing were used to determine the presence and prevalence of Anaplasma phagocytophilum human agent (AP-ha) and a genetic variant not associated with human disease (AP-variant 1). The remaining ticks from each cohort were allowed to feed to repletion on either white-footed (Peromyscus leucopus) or DBA/2 (Mus musculus) mice. The engorged ticks and murine blood samples were evaluated for the presence of AP-ha and AP-variant 1. Although a high percentage of the infecting ticks harbored AP-variant 1, only AP-ha was amplified from the murine blood samples. Additional ticks were fed on immunocompromised SCID mice, and, again, only AP-ha was capable of establishing an infection, and only AP-ha could be detected by xenodiagnosis. These data suggest that AP-variant 1 cannot establish an infection in mice, and we propose that AP-variant 1 has an alternative natural reservoir, possibly white-tailed deer.
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