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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Veröffentlicht in:Comparative medicine 2001-08, Vol.51 (4), p.357-360
Hauptverfasser: Criley, Jennifer M., Carty, Anthony J., Besch-Williford, Cynthia L., Franklin, Craig L.
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Carty, Anthony J.
Besch-Williford, Cynthia L.
Franklin, Craig L.
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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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. 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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 &amp; 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. ; 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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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