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1.
J Med Entomol ; 45(2): 289-97, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18402145

ABSTRACT

In total, 394 questing adult blacklegged ticks, Ixodes scapularis Say (Acari: Ixodidae), collected at four sites were analyzed by polymerase chain reaction (PCR) for five microbial species: Anaplasma phagocytophilum, Babesia microti, Babesia odocoilei, Borrelia burgdorferi, and the rickettsial I. scapularis endosymbiont. Identities of genetic variants of A. phagocytophilum were determined by sequencing a portion of the 16S DNA. In 55% of infected ticks (193/351), a single agent was detected. In 45% (158/351), two or more agents were detected; 37% harbored two agents and 8% harbored three agents. One male tick, collected from Ft. McCoy, WI, harbored all four microbial genera The highest rates of co-infection were by the Ixodes endosymbiont and B. burgdorferi (95/351). Two species of Babesia co-occurred within a single tick population in Wells National Estuarine Research Reserve, Wells, ME, whereas only B. odocoilei was found in other tick populations. Only A. phagocytophilum human anaplasmosis variant was detected in questing ticks from Tippecanoe River State Park, IN; from Wells; and Ft. McCoy, whereas a single infected tick from Presque Isle, PA, was infected by AP-Variant 1. Partially engorged ticks from deer in Tippecanoe River State Park were all infected with AP-Variant 1. Frequency of infections with each agent varied among populations. Rates and types of co-infections were not significantly different from random except for the Ixodes endosymbiont and B. burgdorferi in male ticks, which co-occurred less frequently than expected. Thus, I. scapularis hosts an array of pathogenic and symbiotic agents and potential evidence of interactions among microbial species was observed.


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Babesia/isolation & purification , Borrelia burgdorferi/isolation & purification , Ixodes/microbiology , Rickettsia/isolation & purification , Anaplasma phagocytophilum/classification , Anaplasma phagocytophilum/genetics , Animals , Babesia/genetics , Borrelia burgdorferi/genetics , Female , Great Lakes Region , Maine , Male , Polymerase Chain Reaction , Rickettsia/genetics , Symbiosis/physiology , Tick-Borne Diseases/transmission
2.
J Med Entomol ; 43(2): 437-42, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16619631

ABSTRACT

The blacklegged tick, Ixodes scapularis Say, first reported in Indiana in 1987, has now been detected in more than half of Indiana's counties. The first case of human granulocytic ehrlichiosis (human anaplasmosis) in Indiana was reported in 2002. We now report the detection of Anaplasma phagocytophilum and Babesia odocoilei (Emerson and Wright 1968) in I. scapularis ticks collected in northern Indiana. Using polymerase chain reaction analysis, 41 of 193 adult ticks (21.2%) collected from deer were positive for A. phagocytophylum, and 22 (11.4%) were positive for Babesia sp. Restriction fragment analysis of 12, and sequencing of another five of the amplified products identified these parasites as B. odocoilei. Five ticks (2.6%) were coinfected. Eight of 68 questing adult ticks (11.8%) were positive for A. phagocytophilum; seven (10.3%) were positive for Babesia sp. Six of the latter seven positive samples were determined to be B. odocoilei by restriction fragment analysis and sequencing of two samples. None of 39 pools of nymphs was positive for Babesia sp. Three of 15 ticks (20%) collected from a dog were positive for A. phagocytophilum and three ticks (20%) were positive for Babesia sp. One was confirmed as B. odocoilei. One tick was coinfected. This is the first report of the presence of these two agents in ticks in Indiana.


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Arachnid Vectors/microbiology , Arachnid Vectors/parasitology , Babesia/isolation & purification , Ixodes/microbiology , Ixodes/parasitology , Anaplasma phagocytophilum/genetics , Animals , Babesia/genetics , DNA Restriction Enzymes/metabolism , DNA, Bacterial/analysis , DNA, Protozoan/analysis , Deer/parasitology , Dogs , Female , Indiana , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , RNA, Ribosomal, 18S/genetics
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