Coxiella burnetii Infection in C.B-17 Scid-bg Mice Xenotransplanted with Fetal Bovine Tissue
Two from a group of approximately 50 C. B-17 scid-bg mice were examined because of lethargy, dehydration, and rough coat. Three months prior to development of clinical signs of disease, mice of this study had been surgically implanted with fetal bovine liver, thymus, and lymph node. At necropsy, mar...
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description | Two from a group of approximately 50 C. B-17 scid-bg mice were examined because of lethargy, dehydration, and rough coat. Three months prior to development of clinical signs of disease, mice of this study had been surgically implanted with fetal bovine liver, thymus, and lymph
node. At necropsy, marked splenomegaly and mild hepatomegaly were observed in both animals. Large areas of necrosis and inflammation, with associated intracytoplasmic granular basophilic inclusions, were observed in histologic sections of multiple organs. Aerobic and anaerobic culturing of
the liver yielded negative results. Six months after the initial case, four more reconstituted scid-bg mice from a different fetal donor had identical clinical, gross, and histologic signs of disease. To determine whether the basophilic inclusions represented an infective agent, 4-month-old
immune-naïve C. B-17 scid-bg mice were inoculated intraperitoneally with a liver and spleen homogenate from an affected mouse. Two weeks after inoculation, mice developed clinical signs of disease and lesions identical to those seen in the signal mice. On ultrastructural examination
of the liver, pleomorphic bacteria were found in large cytoplasmic vacuoles of hepatocytes. Bacterial DNA was amplified from the liver, using primers that amplify a segment of the16S rRNA gene from many bacterial species. Sequencing of the polymerase chain reaction (PCR) product revealed gene
sequence identical to that of Coxiella burnetii, the agent of Q-fever. These results highlight the need to consider infective agents of the donor species when working with xenografted animals. |
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node. At necropsy, marked splenomegaly and mild hepatomegaly were observed in both animals. Large areas of necrosis and inflammation, with associated intracytoplasmic granular basophilic inclusions, were observed in histologic sections of multiple organs. Aerobic and anaerobic culturing of
the liver yielded negative results. Six months after the initial case, four more reconstituted scid-bg mice from a different fetal donor had identical clinical, gross, and histologic signs of disease. To determine whether the basophilic inclusions represented an infective agent, 4-month-old
immune-naïve C. B-17 scid-bg mice were inoculated intraperitoneally with a liver and spleen homogenate from an affected mouse. Two weeks after inoculation, mice developed clinical signs of disease and lesions identical to those seen in the signal mice. On ultrastructural examination
of the liver, pleomorphic bacteria were found in large cytoplasmic vacuoles of hepatocytes. Bacterial DNA was amplified from the liver, using primers that amplify a segment of the16S rRNA gene from many bacterial species. Sequencing of the polymerase chain reaction (PCR) product revealed gene
sequence identical to that of Coxiella burnetii, the agent of Q-fever. These results highlight the need to consider infective agents of the donor species when working with xenografted animals.</description><identifier>ISSN: 1532-0820</identifier><identifier>PMID: 11924795</identifier><language>eng</language><publisher>United States: American Association for Laboratory Animal Science</publisher><subject>Abdomen ; Animals ; Cattle ; Cattle Diseases - microbiology ; Coxiella burnetii - genetics ; Coxiella burnetii - isolation & purification ; DNA, Bacterial - analysis ; Environmental Microbiology ; Equipment Contamination ; Female ; Fetal Tissue Transplantation ; Hepatitis, Chronic - etiology ; Hepatitis, Chronic - microbiology ; Hepatitis, Chronic - pathology ; Immunocompromised Host ; Liver - embryology ; Liver - microbiology ; Liver Transplantation ; Lymph Nodes - embryology ; Lymph Nodes - microbiology ; Lymph Nodes - transplantation ; Mice ; Mice, SCID - microbiology ; Mice, SCID - surgery ; Polymerase Chain Reaction ; Postoperative Complications - microbiology ; Postoperative Complications - pathology ; Q Fever - microbiology ; Q Fever - pathology ; Q Fever - transmission ; Thymus Gland - embryology ; Thymus Gland - microbiology ; Thymus Gland - transplantation ; Transplantation Chimera - microbiology ; Transplantation, Heterologous ; Transplantation, Heterotopic</subject><ispartof>Comparative medicine, 2001-08, Vol.51 (4), p.357-360</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>288,289,314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11924795$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Criley, Jennifer M.</creatorcontrib><creatorcontrib>Carty, Anthony J.</creatorcontrib><creatorcontrib>Besch-Williford, Cynthia L.</creatorcontrib><creatorcontrib>Franklin, Craig L.</creatorcontrib><title>Coxiella burnetii Infection in C.B-17 Scid-bg Mice Xenotransplanted with Fetal Bovine Tissue</title><title>Comparative medicine</title><addtitle>Comp Med</addtitle><addtitle>Comp Med</addtitle><description>Two from a group of approximately 50 C. B-17 scid-bg mice were examined because of lethargy, dehydration, and rough coat. Three months prior to development of clinical signs of disease, mice of this study had been surgically implanted with fetal bovine liver, thymus, and lymph
node. At necropsy, marked splenomegaly and mild hepatomegaly were observed in both animals. Large areas of necrosis and inflammation, with associated intracytoplasmic granular basophilic inclusions, were observed in histologic sections of multiple organs. Aerobic and anaerobic culturing of
the liver yielded negative results. Six months after the initial case, four more reconstituted scid-bg mice from a different fetal donor had identical clinical, gross, and histologic signs of disease. To determine whether the basophilic inclusions represented an infective agent, 4-month-old
immune-naïve C. B-17 scid-bg mice were inoculated intraperitoneally with a liver and spleen homogenate from an affected mouse. Two weeks after inoculation, mice developed clinical signs of disease and lesions identical to those seen in the signal mice. On ultrastructural examination
of the liver, pleomorphic bacteria were found in large cytoplasmic vacuoles of hepatocytes. Bacterial DNA was amplified from the liver, using primers that amplify a segment of the16S rRNA gene from many bacterial species. Sequencing of the polymerase chain reaction (PCR) product revealed gene
sequence identical to that of Coxiella burnetii, the agent of Q-fever. These results highlight the need to consider infective agents of the donor species when working with xenografted animals.</description><subject>Abdomen</subject><subject>Animals</subject><subject>Cattle</subject><subject>Cattle Diseases - microbiology</subject><subject>Coxiella burnetii - genetics</subject><subject>Coxiella burnetii - isolation & purification</subject><subject>DNA, Bacterial - analysis</subject><subject>Environmental Microbiology</subject><subject>Equipment Contamination</subject><subject>Female</subject><subject>Fetal Tissue Transplantation</subject><subject>Hepatitis, Chronic - etiology</subject><subject>Hepatitis, Chronic - microbiology</subject><subject>Hepatitis, Chronic - pathology</subject><subject>Immunocompromised Host</subject><subject>Liver - embryology</subject><subject>Liver - microbiology</subject><subject>Liver Transplantation</subject><subject>Lymph Nodes - embryology</subject><subject>Lymph Nodes - microbiology</subject><subject>Lymph Nodes - transplantation</subject><subject>Mice</subject><subject>Mice, SCID - microbiology</subject><subject>Mice, SCID - surgery</subject><subject>Polymerase Chain Reaction</subject><subject>Postoperative Complications - microbiology</subject><subject>Postoperative Complications - pathology</subject><subject>Q Fever - microbiology</subject><subject>Q Fever - pathology</subject><subject>Q Fever - transmission</subject><subject>Thymus Gland - embryology</subject><subject>Thymus Gland - microbiology</subject><subject>Thymus Gland - transplantation</subject><subject>Transplantation Chimera - microbiology</subject><subject>Transplantation, Heterologous</subject><subject>Transplantation, Heterotopic</subject><issn>1532-0820</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRbMAUV6_gLxiF-SxE1zvgIqXVAQSILFAsqbOpLhKnRI75fH1uLQsmc2dxdHRzN3KdqGUIudDwQfZXggzzoXWXOxkAwAtCqXL3ex11H46ahpkk77zFJ1jt74mG13rmfNsdHKRg2KP1lX5ZMrunCX2Qr6NHfqwaNBHqtiHi2_siiI27KJdOk_syYXQ00G2XWMT6HCT-9nz1eXT6CYf31_fjs7HuZNSxRw0WKwLXQCXp0iFsChqDagE1LXSlVQSNSLSqUznI5-UaCsQxIUigRXJ_ex47V107XtPIZq5C3b1lae2D0aB5KUcQgKPNmA_mVNlFp2bY_dl_vpIwMMacH5KPqKZtamWdLtx1iA2GMyq1FWnZlmCL4zgAvgQVHLA0FRUY99EE7Ez028TQCTl2T_Ktc_Ok4OD4b9T_i28MNjFlEnxA-LsiWE</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Criley, Jennifer M.</creator><creator>Carty, Anthony J.</creator><creator>Besch-Williford, Cynthia L.</creator><creator>Franklin, Craig L.</creator><general>American Association for Laboratory Animal Science</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>Coxiella burnetii Infection in C.B-17 Scid-bg Mice Xenotransplanted with Fetal Bovine Tissue</title><author>Criley, Jennifer M. ; Carty, Anthony J. ; Besch-Williford, Cynthia L. ; Franklin, Craig L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i337t-191caf4941036ae42ca2f91a721ff79d373a9aaae63902a0b5acd12e027e2ade3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Abdomen</topic><topic>Animals</topic><topic>Cattle</topic><topic>Cattle Diseases - microbiology</topic><topic>Coxiella burnetii - genetics</topic><topic>Coxiella burnetii - isolation & purification</topic><topic>DNA, Bacterial - analysis</topic><topic>Environmental Microbiology</topic><topic>Equipment Contamination</topic><topic>Female</topic><topic>Fetal Tissue Transplantation</topic><topic>Hepatitis, Chronic - etiology</topic><topic>Hepatitis, Chronic - microbiology</topic><topic>Hepatitis, Chronic - pathology</topic><topic>Immunocompromised Host</topic><topic>Liver - embryology</topic><topic>Liver - microbiology</topic><topic>Liver Transplantation</topic><topic>Lymph Nodes - embryology</topic><topic>Lymph Nodes - microbiology</topic><topic>Lymph Nodes - transplantation</topic><topic>Mice</topic><topic>Mice, SCID - microbiology</topic><topic>Mice, SCID - surgery</topic><topic>Polymerase Chain Reaction</topic><topic>Postoperative Complications - microbiology</topic><topic>Postoperative Complications - pathology</topic><topic>Q Fever - microbiology</topic><topic>Q Fever - pathology</topic><topic>Q Fever - transmission</topic><topic>Thymus Gland - embryology</topic><topic>Thymus Gland - microbiology</topic><topic>Thymus Gland - transplantation</topic><topic>Transplantation Chimera - microbiology</topic><topic>Transplantation, Heterologous</topic><topic>Transplantation, Heterotopic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Criley, Jennifer M.</creatorcontrib><creatorcontrib>Carty, Anthony J.</creatorcontrib><creatorcontrib>Besch-Williford, Cynthia L.</creatorcontrib><creatorcontrib>Franklin, Craig L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Comparative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Criley, Jennifer M.</au><au>Carty, Anthony J.</au><au>Besch-Williford, Cynthia L.</au><au>Franklin, Craig L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coxiella burnetii Infection in C.B-17 Scid-bg Mice Xenotransplanted with Fetal Bovine Tissue</atitle><jtitle>Comparative medicine</jtitle><stitle>Comp Med</stitle><addtitle>Comp Med</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>51</volume><issue>4</issue><spage>357</spage><epage>360</epage><pages>357-360</pages><issn>1532-0820</issn><abstract>Two from a group of approximately 50 C. B-17 scid-bg mice were examined because of lethargy, dehydration, and rough coat. Three months prior to development of clinical signs of disease, mice of this study had been surgically implanted with fetal bovine liver, thymus, and lymph
node. At necropsy, marked splenomegaly and mild hepatomegaly were observed in both animals. Large areas of necrosis and inflammation, with associated intracytoplasmic granular basophilic inclusions, were observed in histologic sections of multiple organs. Aerobic and anaerobic culturing of
the liver yielded negative results. Six months after the initial case, four more reconstituted scid-bg mice from a different fetal donor had identical clinical, gross, and histologic signs of disease. To determine whether the basophilic inclusions represented an infective agent, 4-month-old
immune-naïve C. B-17 scid-bg mice were inoculated intraperitoneally with a liver and spleen homogenate from an affected mouse. Two weeks after inoculation, mice developed clinical signs of disease and lesions identical to those seen in the signal mice. On ultrastructural examination
of the liver, pleomorphic bacteria were found in large cytoplasmic vacuoles of hepatocytes. Bacterial DNA was amplified from the liver, using primers that amplify a segment of the16S rRNA gene from many bacterial species. Sequencing of the polymerase chain reaction (PCR) product revealed gene
sequence identical to that of Coxiella burnetii, the agent of Q-fever. These results highlight the need to consider infective agents of the donor species when working with xenografted animals.</abstract><cop>United States</cop><pub>American Association for Laboratory Animal Science</pub><pmid>11924795</pmid><tpages>4</tpages></addata></record> |
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subjects | Abdomen Animals Cattle Cattle Diseases - microbiology Coxiella burnetii - genetics Coxiella burnetii - isolation & purification DNA, Bacterial - analysis Environmental Microbiology Equipment Contamination Female Fetal Tissue Transplantation Hepatitis, Chronic - etiology Hepatitis, Chronic - microbiology Hepatitis, Chronic - pathology Immunocompromised Host Liver - embryology Liver - microbiology Liver Transplantation Lymph Nodes - embryology Lymph Nodes - microbiology Lymph Nodes - transplantation Mice Mice, SCID - microbiology Mice, SCID - surgery Polymerase Chain Reaction Postoperative Complications - microbiology Postoperative Complications - pathology Q Fever - microbiology Q Fever - pathology Q Fever - transmission Thymus Gland - embryology Thymus Gland - microbiology Thymus Gland - transplantation Transplantation Chimera - microbiology Transplantation, Heterologous Transplantation, Heterotopic |
title | Coxiella burnetii Infection in C.B-17 Scid-bg Mice Xenotransplanted with Fetal Bovine Tissue |
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