Detection of Borrelia burgdorferi in laboratory-reared Ixodes dammini (Acari: Ixodidae) fed on experimentally inoculated white-tailed deer

Larvae and nymphs of Ixodes dammini Spielman, Piesman, Clifford and Corwin from a laboratory colony were fed on two white-tailed deer, Odocoileus virginianus (Zimmermann) inoculated with either the SH2-82 or JD-1 strains of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt and Brenner. Ticks w...

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Veröffentlicht in:Journal of medical entomology 1992-11, Vol.29 (6), p.980-984
Hauptverfasser: Oliver, J.H. Jr. (Georgia Southern University, Statesboro, GA), Stallknecht, D, Chandler, F.W, James, A.M, McGuire, B.S, Howerth, E
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container_issue 6
container_start_page 980
container_title Journal of medical entomology
container_volume 29
creator Oliver, J.H. Jr. (Georgia Southern University, Statesboro, GA)
Stallknecht, D
Chandler, F.W
James, A.M
McGuire, B.S
Howerth, E
description Larvae and nymphs of Ixodes dammini Spielman, Piesman, Clifford and Corwin from a laboratory colony were fed on two white-tailed deer, Odocoileus virginianus (Zimmermann) inoculated with either the SH2-82 or JD-1 strains of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt and Brenner. Ticks were exposed to one deer 43 and 69 d after inoculation of the spirochete and to a second deer 35 and 61 d after inoculation. Polymerase chain reaction assays amplified the 158 bp OspA DNA target sequence in 11.1% (n = 9) of fed larvae and 3.3% (n = 30) of nymphs from the deer inoculated with the SH2-82 strain, and 22.7% (n = 22) of larvae and 0% (n = 21) of nymphs from a second deer inoculated with the JD-1 strain of B. burgdorferi. One of three females derived from nymphs fed on one of the inoculated deer showed presence of B. burgdorferi DNA, but none of four males was positive. Experimentally inoculated deer can serve as a source of at least two geographic strains of B. burgdorferi to I. dammini larvae and nymphs for at least several weeks
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Jr. (Georgia Southern University, Statesboro, GA) ; Stallknecht, D ; Chandler, F.W ; James, A.M ; McGuire, B.S ; Howerth, E</creator><creatorcontrib>Oliver, J.H. Jr. (Georgia Southern University, Statesboro, GA) ; Stallknecht, D ; Chandler, F.W ; James, A.M ; McGuire, B.S ; Howerth, E</creatorcontrib><description>Larvae and nymphs of Ixodes dammini Spielman, Piesman, Clifford and Corwin from a laboratory colony were fed on two white-tailed deer, Odocoileus virginianus (Zimmermann) inoculated with either the SH2-82 or JD-1 strains of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt and Brenner. Ticks were exposed to one deer 43 and 69 d after inoculation of the spirochete and to a second deer 35 and 61 d after inoculation. Polymerase chain reaction assays amplified the 158 bp OspA DNA target sequence in 11.1% (n = 9) of fed larvae and 3.3% (n = 30) of nymphs from the deer inoculated with the SH2-82 strain, and 22.7% (n = 22) of larvae and 0% (n = 21) of nymphs from a second deer inoculated with the JD-1 strain of B. burgdorferi. One of three females derived from nymphs fed on one of the inoculated deer showed presence of B. burgdorferi DNA, but none of four males was positive. 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Jr. (Georgia Southern University, Statesboro, GA)</creatorcontrib><creatorcontrib>Stallknecht, D</creatorcontrib><creatorcontrib>Chandler, F.W</creatorcontrib><creatorcontrib>James, A.M</creatorcontrib><creatorcontrib>McGuire, B.S</creatorcontrib><creatorcontrib>Howerth, E</creatorcontrib><title>Detection of Borrelia burgdorferi in laboratory-reared Ixodes dammini (Acari: Ixodidae) fed on experimentally inoculated white-tailed deer</title><title>Journal of medical entomology</title><addtitle>J Med Entomol</addtitle><description>Larvae and nymphs of Ixodes dammini Spielman, Piesman, Clifford and Corwin from a laboratory colony were fed on two white-tailed deer, Odocoileus virginianus (Zimmermann) inoculated with either the SH2-82 or JD-1 strains of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt and Brenner. Ticks were exposed to one deer 43 and 69 d after inoculation of the spirochete and to a second deer 35 and 61 d after inoculation. Polymerase chain reaction assays amplified the 158 bp OspA DNA target sequence in 11.1% (n = 9) of fed larvae and 3.3% (n = 30) of nymphs from the deer inoculated with the SH2-82 strain, and 22.7% (n = 22) of larvae and 0% (n = 21) of nymphs from a second deer inoculated with the JD-1 strain of B. burgdorferi. One of three females derived from nymphs fed on one of the inoculated deer showed presence of B. burgdorferi DNA, but none of four males was positive. Experimentally inoculated deer can serve as a source of at least two geographic strains of B. burgdorferi to I. dammini larvae and nymphs for at least several weeks</description><subject>Animals</subject><subject>BACTERIOSE</subject><subject>BACTERIOSIS</subject><subject>Biological and medical sciences</subject><subject>BORRELIA</subject><subject>Borrelia burgdorferi Group - genetics</subject><subject>Borrelia burgdorferi Group - isolation &amp; purification</subject><subject>Deer - microbiology</subject><subject>Disease Reservoirs</subject><subject>EXPERIMENTATION EN LABORATOIRE</subject><subject>EXPERIMENTOS EN LABORATORIO</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Invertebrates</subject><subject>IXODES DAMMINI</subject><subject>Larva - microbiology</subject><subject>Lyme Disease - microbiology</subject><subject>Lyme Disease - transmission</subject><subject>Male</subject><subject>Medically important nuisances and vectors, pests of stored products and materials: population survey and control</subject><subject>ODOCOILEUS VIRGINIANUS</subject><subject>Polymerase Chain Reaction</subject><subject>TECHNIQUE D'ELEVAGE</subject><subject>TECNICAS DE CRIANZA</subject><subject>Ticks - microbiology</subject><subject>Tropical medicine</subject><subject>VECTEUR DE MALADIE</subject><subject>VECTORES</subject><subject>Vectors. Intermediate hosts</subject><issn>0022-2585</issn><issn>1938-2928</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkM1u1DAUhS0EKkNhj5CQskAIFpn6L47NrpS_SpVYQNfWjXNdXDnxYCei8wo8NS4zgpVln-9-tg8hzxndMmrE2e2EI87LGTdbtTWaPiAbZoRuueH6IdlQynnLO909Jk9KuaWUaibNCTlhUlElzIb8_oALuiWkuUm-eZ9yxhigGdZ8M6bsMYcmzE2EIWVYUt63GSHj2FzepRFLM8I0hTk0b84d5PDu73EYAd82vkJVine76pjqGyHGfXUlt0ZYavjrR1iwXSDEuhkR81PyyEMs-Oy4npLrTx-_X3xpr75-vrw4v2qdkHxpFethkE5zbQYlWS8dU10vDdO0AzMCgHZMO-NHz0Qn-KCZAKVlJ7VSfqDilLw-eHc5_VyxLHYKxWGMMGNai-2FMFIKXkF6AF1OpWT0dle_AnlvGbX39dtj_ZYbq2ytv468PLrXoWb_Bw591_zVMYfiIPoMswvlHyY71nN9f_OLA-YhWbjJFbn-ZgTTQmjxB0JFmMw</recordid><startdate>19921101</startdate><enddate>19921101</enddate><creator>Oliver, J.H. 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Jr. (Georgia Southern University, Statesboro, GA) ; Stallknecht, D ; Chandler, F.W ; James, A.M ; McGuire, B.S ; Howerth, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-617ab4c8289b64174c1657491805a9daaa8c18c9fdf13532b813a68454866fb03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>BACTERIOSE</topic><topic>BACTERIOSIS</topic><topic>Biological and medical sciences</topic><topic>BORRELIA</topic><topic>Borrelia burgdorferi Group - genetics</topic><topic>Borrelia burgdorferi Group - isolation &amp; purification</topic><topic>Deer - microbiology</topic><topic>Disease Reservoirs</topic><topic>EXPERIMENTATION EN LABORATOIRE</topic><topic>EXPERIMENTOS EN LABORATORIO</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Invertebrates</topic><topic>IXODES DAMMINI</topic><topic>Larva - microbiology</topic><topic>Lyme Disease - microbiology</topic><topic>Lyme Disease - transmission</topic><topic>Male</topic><topic>Medically important nuisances and vectors, pests of stored products and materials: population survey and control</topic><topic>ODOCOILEUS VIRGINIANUS</topic><topic>Polymerase Chain Reaction</topic><topic>TECHNIQUE D'ELEVAGE</topic><topic>TECNICAS DE CRIANZA</topic><topic>Ticks - microbiology</topic><topic>Tropical medicine</topic><topic>VECTEUR DE MALADIE</topic><topic>VECTORES</topic><topic>Vectors. Intermediate hosts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oliver, J.H. Jr. (Georgia Southern University, Statesboro, GA)</creatorcontrib><creatorcontrib>Stallknecht, D</creatorcontrib><creatorcontrib>Chandler, F.W</creatorcontrib><creatorcontrib>James, A.M</creatorcontrib><creatorcontrib>McGuire, B.S</creatorcontrib><creatorcontrib>Howerth, E</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical entomology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oliver, J.H. Jr. (Georgia Southern University, Statesboro, GA)</au><au>Stallknecht, D</au><au>Chandler, F.W</au><au>James, A.M</au><au>McGuire, B.S</au><au>Howerth, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Borrelia burgdorferi in laboratory-reared Ixodes dammini (Acari: Ixodidae) fed on experimentally inoculated white-tailed deer</atitle><jtitle>Journal of medical entomology</jtitle><addtitle>J Med Entomol</addtitle><date>1992-11-01</date><risdate>1992</risdate><volume>29</volume><issue>6</issue><spage>980</spage><epage>984</epage><pages>980-984</pages><issn>0022-2585</issn><eissn>1938-2928</eissn><coden>JMENA6</coden><abstract>Larvae and nymphs of Ixodes dammini Spielman, Piesman, Clifford and Corwin from a laboratory colony were fed on two white-tailed deer, Odocoileus virginianus (Zimmermann) inoculated with either the SH2-82 or JD-1 strains of Borrelia burgdorferi Johnson, Schmid, Hyde, Steigerwalt and Brenner. Ticks were exposed to one deer 43 and 69 d after inoculation of the spirochete and to a second deer 35 and 61 d after inoculation. Polymerase chain reaction assays amplified the 158 bp OspA DNA target sequence in 11.1% (n = 9) of fed larvae and 3.3% (n = 30) of nymphs from the deer inoculated with the SH2-82 strain, and 22.7% (n = 22) of larvae and 0% (n = 21) of nymphs from a second deer inoculated with the JD-1 strain of B. burgdorferi. One of three females derived from nymphs fed on one of the inoculated deer showed presence of B. burgdorferi DNA, but none of four males was positive. Experimentally inoculated deer can serve as a source of at least two geographic strains of B. burgdorferi to I. dammini larvae and nymphs for at least several weeks</abstract><cop>Lanham, MD</cop><pub>Entomological Society of America</pub><pmid>1460639</pmid><doi>10.1093/jmedent/29.6.980</doi><tpages>5</tpages></addata></record>
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subjects Animals
BACTERIOSE
BACTERIOSIS
Biological and medical sciences
BORRELIA
Borrelia burgdorferi Group - genetics
Borrelia burgdorferi Group - isolation & purification
Deer - microbiology
Disease Reservoirs
EXPERIMENTATION EN LABORATOIRE
EXPERIMENTOS EN LABORATORIO
Fundamental and applied biological sciences. Psychology
Humans
Invertebrates
IXODES DAMMINI
Larva - microbiology
Lyme Disease - microbiology
Lyme Disease - transmission
Male
Medically important nuisances and vectors, pests of stored products and materials: population survey and control
ODOCOILEUS VIRGINIANUS
Polymerase Chain Reaction
TECHNIQUE D'ELEVAGE
TECNICAS DE CRIANZA
Ticks - microbiology
Tropical medicine
VECTEUR DE MALADIE
VECTORES
Vectors. Intermediate hosts
title Detection of Borrelia burgdorferi in laboratory-reared Ixodes dammini (Acari: Ixodidae) fed on experimentally inoculated white-tailed deer
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