Dogs infected with a human granulocytotropic Ehrlichia spp. (Rickettsiales: Ehrlichieae)

Dogs were found to be susceptible to human granulocytotropic Ehrlichia spp. Infection was produced through the bite of Ixodes scapularis Say (=dammini Spielman, Clifford, Piesman and Corwin) nymphs and adults that acquired infection while feeding as larvae on experimentally infected mice. Dogs were...

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Veröffentlicht in:Journal of medical entomology 1997-11, Vol.34 (6), p.710-718
Hauptverfasser: Ewing, S.A. (Oklahoma State University, Stillwater.), Dawson, J.E, Panciera, R.J, Mathew, J.S, Pratt, K.W, Katavolos, P, Telford, S.R. III
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container_end_page 718
container_issue 6
container_start_page 710
container_title Journal of medical entomology
container_volume 34
creator Ewing, S.A. (Oklahoma State University, Stillwater.)
Dawson, J.E
Panciera, R.J
Mathew, J.S
Pratt, K.W
Katavolos, P
Telford, S.R. III
description Dogs were found to be susceptible to human granulocytotropic Ehrlichia spp. Infection was produced through the bite of Ixodes scapularis Say (=dammini Spielman, Clifford, Piesman and Corwin) nymphs and adults that acquired infection while feeding as larvae on experimentally infected mice. Dogs were also infected by intravenous injection of mouse blood or dog blood from parasitemic donors. Parasites were demonstrable in neutrophils within 8 or 9 d after nymphs began feeding; prepatent periods were longer when infection was induced by adult tick feeding (18 d) or by transfusion of mouse blood (12 d). The shortest prepatent period observed was 5 d in a dog infected by transfusion of blood from a parasitemic dog. Infections in dogs were mild and apparently transient. Mild thrombocytopenia was the most commonly observed abnormality. Parasites could be detected by light microscopy during the acute phase of infection (4 or 5 d) and parasite DNA by polymerase chain reaction as early as 5 d after exposure but not at 6-9 d after morulae were first observed in neutrophils. Likewise, dog blood was infectious for mice at 2 d but not at 25 d, and for dogs at 3 d but not at 13 d after morulae were first observed in neutrophils. Seroconversion occurred as early as 11 d after onset of tick feeding and persisted until dogs were euthanatized. Gross and histopathologic lesions were similar to those observed in dogs with E. canis (Donatien and Lestoquard), E. chaffeensis Anderson, Dawson and Wilson, and E. ewingii Anderson, Greene, Jones and Dawson infections but were generally milder than any of these. The moderate enlargement of lymphoid organs observed grossly was reflected histologically as mild to moderate reactive hyperplasia, which was largely follicular (B cell)
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(Oklahoma State University, Stillwater.) ; Dawson, J.E ; Panciera, R.J ; Mathew, J.S ; Pratt, K.W ; Katavolos, P ; Telford, S.R. III</creator><creatorcontrib>Ewing, S.A. (Oklahoma State University, Stillwater.) ; Dawson, J.E ; Panciera, R.J ; Mathew, J.S ; Pratt, K.W ; Katavolos, P ; Telford, S.R. III</creatorcontrib><description>Dogs were found to be susceptible to human granulocytotropic Ehrlichia spp. Infection was produced through the bite of Ixodes scapularis Say (=dammini Spielman, Clifford, Piesman and Corwin) nymphs and adults that acquired infection while feeding as larvae on experimentally infected mice. Dogs were also infected by intravenous injection of mouse blood or dog blood from parasitemic donors. Parasites were demonstrable in neutrophils within 8 or 9 d after nymphs began feeding; prepatent periods were longer when infection was induced by adult tick feeding (18 d) or by transfusion of mouse blood (12 d). The shortest prepatent period observed was 5 d in a dog infected by transfusion of blood from a parasitemic dog. Infections in dogs were mild and apparently transient. Mild thrombocytopenia was the most commonly observed abnormality. Parasites could be detected by light microscopy during the acute phase of infection (4 or 5 d) and parasite DNA by polymerase chain reaction as early as 5 d after exposure but not at 6-9 d after morulae were first observed in neutrophils. Likewise, dog blood was infectious for mice at 2 d but not at 25 d, and for dogs at 3 d but not at 13 d after morulae were first observed in neutrophils. Seroconversion occurred as early as 11 d after onset of tick feeding and persisted until dogs were euthanatized. Gross and histopathologic lesions were similar to those observed in dogs with E. canis (Donatien and Lestoquard), E. chaffeensis Anderson, Dawson and Wilson, and E. ewingii Anderson, Greene, Jones and Dawson infections but were generally milder than any of these. 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(Oklahoma State University, Stillwater.)</creatorcontrib><creatorcontrib>Dawson, J.E</creatorcontrib><creatorcontrib>Panciera, R.J</creatorcontrib><creatorcontrib>Mathew, J.S</creatorcontrib><creatorcontrib>Pratt, K.W</creatorcontrib><creatorcontrib>Katavolos, P</creatorcontrib><creatorcontrib>Telford, S.R. III</creatorcontrib><title>Dogs infected with a human granulocytotropic Ehrlichia spp. (Rickettsiales: Ehrlichieae)</title><title>Journal of medical entomology</title><addtitle>J Med Entomol</addtitle><description>Dogs were found to be susceptible to human granulocytotropic Ehrlichia spp. Infection was produced through the bite of Ixodes scapularis Say (=dammini Spielman, Clifford, Piesman and Corwin) nymphs and adults that acquired infection while feeding as larvae on experimentally infected mice. Dogs were also infected by intravenous injection of mouse blood or dog blood from parasitemic donors. Parasites were demonstrable in neutrophils within 8 or 9 d after nymphs began feeding; prepatent periods were longer when infection was induced by adult tick feeding (18 d) or by transfusion of mouse blood (12 d). The shortest prepatent period observed was 5 d in a dog infected by transfusion of blood from a parasitemic dog. Infections in dogs were mild and apparently transient. Mild thrombocytopenia was the most commonly observed abnormality. Parasites could be detected by light microscopy during the acute phase of infection (4 or 5 d) and parasite DNA by polymerase chain reaction as early as 5 d after exposure but not at 6-9 d after morulae were first observed in neutrophils. Likewise, dog blood was infectious for mice at 2 d but not at 25 d, and for dogs at 3 d but not at 13 d after morulae were first observed in neutrophils. Seroconversion occurred as early as 11 d after onset of tick feeding and persisted until dogs were euthanatized. Gross and histopathologic lesions were similar to those observed in dogs with E. canis (Donatien and Lestoquard), E. chaffeensis Anderson, Dawson and Wilson, and E. ewingii Anderson, Greene, Jones and Dawson infections but were generally milder than any of these. The moderate enlargement of lymphoid organs observed grossly was reflected histologically as mild to moderate reactive hyperplasia, which was largely follicular (B cell)</description><subject>Animal bacterial diseases</subject><subject>Animals</subject><subject>Arachnid Vectors - microbiology</subject><subject>Bacterial diseases</subject><subject>BACTERIOSE</subject><subject>BACTERIOSES</subject><subject>BACTERIOSIS</subject><subject>Biological and medical sciences</subject><subject>BLOOD DISORDERS</subject><subject>CHIEN</subject><subject>Disease Reservoirs</subject><subject>Dog Diseases - microbiology</subject><subject>Dog Diseases - transmission</subject><subject>DOGS</subject><subject>EHRLICHIA</subject><subject>Ehrlichia - isolation &amp; purification</subject><subject>Ehrlichiosis - microbiology</subject><subject>Ehrlichiosis - transmission</subject><subject>Ehrlichiosis - veterinary</subject><subject>ENFERMEDADES TRANSM POR GARRAPATAS</subject><subject>EXPERIMENTACION IN VIVO</subject><subject>EXPERIMENTAL INFECTION</subject><subject>EXPERIMENTATION IN VIVO</subject><subject>GRANULOCITOS</subject><subject>GRANULOCYTE</subject><subject>GRANULOCYTES</subject><subject>Granulocytes - microbiology</subject><subject>HISTOPATHOLOGIE</subject><subject>HISTOPATHOLOGY</subject><subject>HISTOPATOLOGIA</subject><subject>HL-60 Cells</subject><subject>HOSTS</subject><subject>HOTE</subject><subject>HUESPEDES</subject><subject>HUMAN EHRLICHIOSIS</subject><subject>Humans</subject><subject>IMMUNE RESPONSE</subject><subject>IN VIVO EXPERIMENTATION</subject><subject>INFECCION EXPERIMENTAL</subject><subject>INFECTION EXPERIMENTALE</subject><subject>Infectious diseases</subject><subject>INFECTIVITY</subject><subject>IXODES</subject><subject>Ixodes - microbiology</subject><subject>IXODES SCAPULARIS</subject><subject>MALADIE TRANSMISSIBLE PAR TIQUES</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>PATHOGENESE</subject><subject>PATHOGENESIS</subject><subject>PATHOGENICITY</subject><subject>PATOGENESIS</subject><subject>PATOGENICIDAD</subject><subject>PERRO</subject><subject>PLATELETS</subject><subject>POUVOIR PATHOGENE</subject><subject>PREPATENT PERIOD</subject><subject>REPONSE IMMUNITAIRE</subject><subject>RESERVOIR COMPETENCE</subject><subject>RESERVOIR HOSTS</subject><subject>RESPUESTA INMUNOLOGICA</subject><subject>RICKETTSIALES</subject><subject>SEROCONVERSION</subject><subject>THROMBOCYTE</subject><subject>THROMBOCYTOPENIA</subject><subject>TICKBORNE DISEASES</subject><subject>TRASTORNOS SANGUINEOS</subject><subject>TROMBOCITOS</subject><subject>TROUBLE SANGUIN</subject><issn>0022-2585</issn><issn>1938-2928</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1P3DAQhq0KRBfaey-VckAVPWTxV_zBrQJakJCQCkjcLMc73jXNJsF2VPHvMSLaHnuaw_vMq5kHoS8ELwnW7PRpCyvo8ynjS7GUBH9AC6KZqqmmag8tMKa0po1qPqLDlJ4wxopwfYAONGeaULlAjxfDOlWh9-AyrKq_IW8qW22mre2rdbT91A3uJQ85DmNw1eUmdsFtgq3SOC6rk9_B_YGcU7AdpLNdDBa-f0L73nYJPs_zCD38vLw_v6pvbn9dn_-4qR0nKtdMCqGxbzj2rMXAqGSsEcx63VIGfiUA81Y5ANVKzhvZOuq41FJruXKKWHaEvr33jnF4niBlsw3JQdfZHoYpGakbSpRo_gsSQaXUTBcQv4MuDilF8GaMYWvjiyHYvFk3s3XDuBGmWC8rX-fuqS3ZbmHWXPLjObfJ2c4XsS6kHUYJVuXIfzXeDsauY0Ee7kh5FUvZEMFeAbMXlKA</recordid><startdate>19971101</startdate><enddate>19971101</enddate><creator>Ewing, S.A. (Oklahoma State University, Stillwater.)</creator><creator>Dawson, J.E</creator><creator>Panciera, R.J</creator><creator>Mathew, J.S</creator><creator>Pratt, K.W</creator><creator>Katavolos, P</creator><creator>Telford, S.R. III</creator><general>Entomological Society of America</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SS</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19971101</creationdate><title>Dogs infected with a human granulocytotropic Ehrlichia spp. (Rickettsiales: Ehrlichieae)</title><author>Ewing, S.A. (Oklahoma State University, Stillwater.) ; Dawson, J.E ; Panciera, R.J ; Mathew, J.S ; Pratt, K.W ; Katavolos, P ; Telford, S.R. III</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-376690f540f3b0e32733563af9b23efd6e04b8cee8b74457bc2c4797997dc81a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animal bacterial diseases</topic><topic>Animals</topic><topic>Arachnid Vectors - microbiology</topic><topic>Bacterial diseases</topic><topic>BACTERIOSE</topic><topic>BACTERIOSES</topic><topic>BACTERIOSIS</topic><topic>Biological and medical sciences</topic><topic>BLOOD DISORDERS</topic><topic>CHIEN</topic><topic>Disease Reservoirs</topic><topic>Dog Diseases - microbiology</topic><topic>Dog Diseases - transmission</topic><topic>DOGS</topic><topic>EHRLICHIA</topic><topic>Ehrlichia - isolation &amp; purification</topic><topic>Ehrlichiosis - microbiology</topic><topic>Ehrlichiosis - transmission</topic><topic>Ehrlichiosis - veterinary</topic><topic>ENFERMEDADES TRANSM POR GARRAPATAS</topic><topic>EXPERIMENTACION IN VIVO</topic><topic>EXPERIMENTAL INFECTION</topic><topic>EXPERIMENTATION IN VIVO</topic><topic>GRANULOCITOS</topic><topic>GRANULOCYTE</topic><topic>GRANULOCYTES</topic><topic>Granulocytes - microbiology</topic><topic>HISTOPATHOLOGIE</topic><topic>HISTOPATHOLOGY</topic><topic>HISTOPATOLOGIA</topic><topic>HL-60 Cells</topic><topic>HOSTS</topic><topic>HOTE</topic><topic>HUESPEDES</topic><topic>HUMAN EHRLICHIOSIS</topic><topic>Humans</topic><topic>IMMUNE RESPONSE</topic><topic>IN VIVO EXPERIMENTATION</topic><topic>INFECCION EXPERIMENTAL</topic><topic>INFECTION EXPERIMENTALE</topic><topic>Infectious diseases</topic><topic>INFECTIVITY</topic><topic>IXODES</topic><topic>Ixodes - microbiology</topic><topic>IXODES SCAPULARIS</topic><topic>MALADIE TRANSMISSIBLE PAR TIQUES</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>PATHOGENESE</topic><topic>PATHOGENESIS</topic><topic>PATHOGENICITY</topic><topic>PATOGENESIS</topic><topic>PATOGENICIDAD</topic><topic>PERRO</topic><topic>PLATELETS</topic><topic>POUVOIR PATHOGENE</topic><topic>PREPATENT PERIOD</topic><topic>REPONSE IMMUNITAIRE</topic><topic>RESERVOIR COMPETENCE</topic><topic>RESERVOIR HOSTS</topic><topic>RESPUESTA INMUNOLOGICA</topic><topic>RICKETTSIALES</topic><topic>SEROCONVERSION</topic><topic>THROMBOCYTE</topic><topic>THROMBOCYTOPENIA</topic><topic>TICKBORNE DISEASES</topic><topic>TRASTORNOS SANGUINEOS</topic><topic>TROMBOCITOS</topic><topic>TROUBLE SANGUIN</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ewing, S.A. (Oklahoma State University, Stillwater.)</creatorcontrib><creatorcontrib>Dawson, J.E</creatorcontrib><creatorcontrib>Panciera, R.J</creatorcontrib><creatorcontrib>Mathew, J.S</creatorcontrib><creatorcontrib>Pratt, K.W</creatorcontrib><creatorcontrib>Katavolos, P</creatorcontrib><creatorcontrib>Telford, S.R. 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III</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dogs infected with a human granulocytotropic Ehrlichia spp. (Rickettsiales: Ehrlichieae)</atitle><jtitle>Journal of medical entomology</jtitle><addtitle>J Med Entomol</addtitle><date>1997-11-01</date><risdate>1997</risdate><volume>34</volume><issue>6</issue><spage>710</spage><epage>718</epage><pages>710-718</pages><issn>0022-2585</issn><eissn>1938-2928</eissn><coden>JMENA6</coden><abstract>Dogs were found to be susceptible to human granulocytotropic Ehrlichia spp. Infection was produced through the bite of Ixodes scapularis Say (=dammini Spielman, Clifford, Piesman and Corwin) nymphs and adults that acquired infection while feeding as larvae on experimentally infected mice. Dogs were also infected by intravenous injection of mouse blood or dog blood from parasitemic donors. Parasites were demonstrable in neutrophils within 8 or 9 d after nymphs began feeding; prepatent periods were longer when infection was induced by adult tick feeding (18 d) or by transfusion of mouse blood (12 d). The shortest prepatent period observed was 5 d in a dog infected by transfusion of blood from a parasitemic dog. Infections in dogs were mild and apparently transient. Mild thrombocytopenia was the most commonly observed abnormality. Parasites could be detected by light microscopy during the acute phase of infection (4 or 5 d) and parasite DNA by polymerase chain reaction as early as 5 d after exposure but not at 6-9 d after morulae were first observed in neutrophils. Likewise, dog blood was infectious for mice at 2 d but not at 25 d, and for dogs at 3 d but not at 13 d after morulae were first observed in neutrophils. Seroconversion occurred as early as 11 d after onset of tick feeding and persisted until dogs were euthanatized. Gross and histopathologic lesions were similar to those observed in dogs with E. canis (Donatien and Lestoquard), E. chaffeensis Anderson, Dawson and Wilson, and E. ewingii Anderson, Greene, Jones and Dawson infections but were generally milder than any of these. The moderate enlargement of lymphoid organs observed grossly was reflected histologically as mild to moderate reactive hyperplasia, which was largely follicular (B cell)</abstract><cop>Lanham, MD</cop><pub>Entomological Society of America</pub><pmid>9439127</pmid><doi>10.1093/jmedent/34.6.710</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Animal bacterial diseases
Animals
Arachnid Vectors - microbiology
Bacterial diseases
BACTERIOSE
BACTERIOSES
BACTERIOSIS
Biological and medical sciences
BLOOD DISORDERS
CHIEN
Disease Reservoirs
Dog Diseases - microbiology
Dog Diseases - transmission
DOGS
EHRLICHIA
Ehrlichia - isolation & purification
Ehrlichiosis - microbiology
Ehrlichiosis - transmission
Ehrlichiosis - veterinary
ENFERMEDADES TRANSM POR GARRAPATAS
EXPERIMENTACION IN VIVO
EXPERIMENTAL INFECTION
EXPERIMENTATION IN VIVO
GRANULOCITOS
GRANULOCYTE
GRANULOCYTES
Granulocytes - microbiology
HISTOPATHOLOGIE
HISTOPATHOLOGY
HISTOPATOLOGIA
HL-60 Cells
HOSTS
HOTE
HUESPEDES
HUMAN EHRLICHIOSIS
Humans
IMMUNE RESPONSE
IN VIVO EXPERIMENTATION
INFECCION EXPERIMENTAL
INFECTION EXPERIMENTALE
Infectious diseases
INFECTIVITY
IXODES
Ixodes - microbiology
IXODES SCAPULARIS
MALADIE TRANSMISSIBLE PAR TIQUES
Medical sciences
Mice
Mice, Inbred C3H
PATHOGENESE
PATHOGENESIS
PATHOGENICITY
PATOGENESIS
PATOGENICIDAD
PERRO
PLATELETS
POUVOIR PATHOGENE
PREPATENT PERIOD
REPONSE IMMUNITAIRE
RESERVOIR COMPETENCE
RESERVOIR HOSTS
RESPUESTA INMUNOLOGICA
RICKETTSIALES
SEROCONVERSION
THROMBOCYTE
THROMBOCYTOPENIA
TICKBORNE DISEASES
TRASTORNOS SANGUINEOS
TROMBOCITOS
TROUBLE SANGUIN
title Dogs infected with a human granulocytotropic Ehrlichia spp. (Rickettsiales: Ehrlichieae)
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