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Bone Marrow Response to Acute and Chronic Trypanosoma congolense Infection in Multimammate Rats (Mastomys coucha)
The femoral bone marrow of multimammate rats (n=90), aged 3–8 weeks, experimentally infected with different doses of Trypanosoma congolense was examined by light and electron microscopy. Some animals died from trypanosomosis, but groups of 10 were killed at 4–8, 9–16, 20–24, 30, 40, 50 and 60 days p...
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Published in: | Journal of comparative pathology 2001-02, Vol.124 (2-3), p.149-158 |
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description | The femoral bone marrow of multimammate rats (n=90), aged 3–8 weeks, experimentally infected with different doses of Trypanosoma congolense was examined by light and electron microscopy. Some animals died from trypanosomosis, but groups of 10 were killed at 4–8, 9–16, 20–24, 30, 40, 50 and 60 days post-infection (dpi). In the acute stage of infection (4–8 dpi) the bone marrow invariably showed a striking increase in erythropoiesis, characterized by an increase in the number of mitotic figures and erythroblastic islands and by a marked decrease in the myeloid:erythroid cell ratio. Later in the infection, erythropoietic activity decreased, while erythrophagocytosis, granulopoiesis, megakaryopoiesis and plasma cell population increased. In chronic infection (16–60 dpi), erythropoietic activity decreased, while intra- and extra-vascular erythrophagocytosis greatly increased. There was also an increase in the bone marrow stroma cells. Excessive erythrophagocytosis by these cells led to the formation of myelin figures and cytoplasmic telephagolysosomes. Degeneration and necrosis of neutrophils lining the adluminal surfaces of the blood sinuses were observed. It is concluded that in the acute stage of the infection, the bone marrow is responsive to the anaemia and that in the chronic stage, dyserythropoiesis and increased erythrophagocytosis by the expanded and activated cells of the mononuclear phagocytic system play an important role in the production of anaemia. |
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Some animals died from trypanosomosis, but groups of 10 were killed at 4–8, 9–16, 20–24, 30, 40, 50 and 60 days post-infection (dpi). In the acute stage of infection (4–8 dpi) the bone marrow invariably showed a striking increase in erythropoiesis, characterized by an increase in the number of mitotic figures and erythroblastic islands and by a marked decrease in the myeloid:erythroid cell ratio. Later in the infection, erythropoietic activity decreased, while erythrophagocytosis, granulopoiesis, megakaryopoiesis and plasma cell population increased. In chronic infection (16–60 dpi), erythropoietic activity decreased, while intra- and extra-vascular erythrophagocytosis greatly increased. There was also an increase in the bone marrow stroma cells. Excessive erythrophagocytosis by these cells led to the formation of myelin figures and cytoplasmic telephagolysosomes. Degeneration and necrosis of neutrophils lining the adluminal surfaces of the blood sinuses were observed. It is concluded that in the acute stage of the infection, the bone marrow is responsive to the anaemia and that in the chronic stage, dyserythropoiesis and increased erythrophagocytosis by the expanded and activated cells of the mononuclear phagocytic system play an important role in the production of anaemia.</description><identifier>ISSN: 0021-9975</identifier><identifier>EISSN: 1532-3129</identifier><identifier>DOI: 10.1053/jcpa.2000.0445</identifier><identifier>PMID: 11222012</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acute Disease ; Anemia - etiology ; Anemia - pathology ; Animals ; Bone Marrow Diseases - parasitology ; Bone Marrow Diseases - pathology ; Chronic Disease ; Erythroblasts - ultrastructure ; Erythropoiesis ; Femur ; Hematocrit ; Mitosis ; Muridae - parasitology ; Rats ; Rodent Diseases - parasitology ; Rodent Diseases - pathology ; Stromal Cells - ultrastructure ; Trypanosoma congolense - pathogenicity ; Trypanosoma congolense - ultrastructure ; Trypanosomiasis, African - complications ; Trypanosomiasis, African - pathology</subject><ispartof>Journal of comparative pathology, 2001-02, Vol.124 (2-3), p.149-158</ispartof><rights>2001 Harcourt Publishers Ltd</rights><rights>Copyright Harcourt Publishers Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-95dc6bd7ac51340b7876ca8db517bd5dc145b22a48b979812b92a379d5740b153</citedby><cites>FETCH-LOGICAL-c435t-95dc6bd7ac51340b7876ca8db517bd5dc145b22a48b979812b92a379d5740b153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11222012$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ojok, L.</creatorcontrib><creatorcontrib>Kaeufer-Weiss, I.</creatorcontrib><creatorcontrib>Weiss, E.</creatorcontrib><title>Bone Marrow Response to Acute and Chronic Trypanosoma congolense Infection in Multimammate Rats (Mastomys coucha)</title><title>Journal of comparative pathology</title><addtitle>J Comp Pathol</addtitle><description>The femoral bone marrow of multimammate rats (n=90), aged 3–8 weeks, experimentally infected with different doses of Trypanosoma congolense was examined by light and electron microscopy. Some animals died from trypanosomosis, but groups of 10 were killed at 4–8, 9–16, 20–24, 30, 40, 50 and 60 days post-infection (dpi). In the acute stage of infection (4–8 dpi) the bone marrow invariably showed a striking increase in erythropoiesis, characterized by an increase in the number of mitotic figures and erythroblastic islands and by a marked decrease in the myeloid:erythroid cell ratio. Later in the infection, erythropoietic activity decreased, while erythrophagocytosis, granulopoiesis, megakaryopoiesis and plasma cell population increased. In chronic infection (16–60 dpi), erythropoietic activity decreased, while intra- and extra-vascular erythrophagocytosis greatly increased. There was also an increase in the bone marrow stroma cells. Excessive erythrophagocytosis by these cells led to the formation of myelin figures and cytoplasmic telephagolysosomes. Degeneration and necrosis of neutrophils lining the adluminal surfaces of the blood sinuses were observed. It is concluded that in the acute stage of the infection, the bone marrow is responsive to the anaemia and that in the chronic stage, dyserythropoiesis and increased erythrophagocytosis by the expanded and activated cells of the mononuclear phagocytic system play an important role in the production of anaemia.</description><subject>Acute Disease</subject><subject>Anemia - etiology</subject><subject>Anemia - pathology</subject><subject>Animals</subject><subject>Bone Marrow Diseases - parasitology</subject><subject>Bone Marrow Diseases - pathology</subject><subject>Chronic Disease</subject><subject>Erythroblasts - ultrastructure</subject><subject>Erythropoiesis</subject><subject>Femur</subject><subject>Hematocrit</subject><subject>Mitosis</subject><subject>Muridae - parasitology</subject><subject>Rats</subject><subject>Rodent Diseases - parasitology</subject><subject>Rodent Diseases - pathology</subject><subject>Stromal Cells - ultrastructure</subject><subject>Trypanosoma congolense - pathogenicity</subject><subject>Trypanosoma congolense - ultrastructure</subject><subject>Trypanosomiasis, African - complications</subject><subject>Trypanosomiasis, African - pathology</subject><issn>0021-9975</issn><issn>1532-3129</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp1kM9LwzAYhoMobk6vHiUn0UNnkjZLe5zDH4MNYcxzSJPMZbRJl7TK_ntTNvAkfPAdvud94XsAuMVojBFNn3ayEWOCEBqjLKNnYIhpSpIUk-IcDBEiOCkKRgfgKoRdpPKckkswwJgQgjAZgv2zsxouhffuB650aJwNGrYOTmXXaiisgrOtd9ZIuPaHRlgXXC2gdPbLVbpn53ajZWuchcbCZVe1phZ1LWJ4JdoAH5YitK4-hJjp5FY8XoOLjaiCvjntEfh8fVnP3pPFx9t8Nl0kMktpmxRUyUmpmJAUpxkqWc4mUuSqpJiVKh5xRktCRJaXBStyTMqCiJQVirJIRwsjcH_sbbzbdzq0vDZB6qoSVrsucIYmFMeJ4PgISu9C8HrDGx9_8AeOEe8l814y7yXzXnIM3J2au7LW6g8_WY1AfgR0_O_baM-DNNpKrYyPrrhy5r_uX96ki70</recordid><startdate>20010201</startdate><enddate>20010201</enddate><creator>Ojok, L.</creator><creator>Kaeufer-Weiss, I.</creator><creator>Weiss, E.</creator><general>Elsevier Ltd</general><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>7X8</scope></search><sort><creationdate>20010201</creationdate><title>Bone Marrow Response to Acute and Chronic Trypanosoma congolense Infection in Multimammate Rats (Mastomys coucha)</title><author>Ojok, L. ; Kaeufer-Weiss, I. ; Weiss, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-95dc6bd7ac51340b7876ca8db517bd5dc145b22a48b979812b92a379d5740b153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acute Disease</topic><topic>Anemia - etiology</topic><topic>Anemia - pathology</topic><topic>Animals</topic><topic>Bone Marrow Diseases - parasitology</topic><topic>Bone Marrow Diseases - pathology</topic><topic>Chronic Disease</topic><topic>Erythroblasts - ultrastructure</topic><topic>Erythropoiesis</topic><topic>Femur</topic><topic>Hematocrit</topic><topic>Mitosis</topic><topic>Muridae - parasitology</topic><topic>Rats</topic><topic>Rodent Diseases - parasitology</topic><topic>Rodent Diseases - pathology</topic><topic>Stromal Cells - ultrastructure</topic><topic>Trypanosoma congolense - pathogenicity</topic><topic>Trypanosoma congolense - ultrastructure</topic><topic>Trypanosomiasis, African - complications</topic><topic>Trypanosomiasis, African - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ojok, L.</creatorcontrib><creatorcontrib>Kaeufer-Weiss, I.</creatorcontrib><creatorcontrib>Weiss, E.</creatorcontrib><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 comparative pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ojok, L.</au><au>Kaeufer-Weiss, I.</au><au>Weiss, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone Marrow Response to Acute and Chronic Trypanosoma congolense Infection in Multimammate Rats (Mastomys coucha)</atitle><jtitle>Journal of comparative pathology</jtitle><addtitle>J Comp Pathol</addtitle><date>2001-02-01</date><risdate>2001</risdate><volume>124</volume><issue>2-3</issue><spage>149</spage><epage>158</epage><pages>149-158</pages><issn>0021-9975</issn><eissn>1532-3129</eissn><abstract>The femoral bone marrow of multimammate rats (n=90), aged 3–8 weeks, experimentally infected with different doses of Trypanosoma congolense was examined by light and electron microscopy. Some animals died from trypanosomosis, but groups of 10 were killed at 4–8, 9–16, 20–24, 30, 40, 50 and 60 days post-infection (dpi). In the acute stage of infection (4–8 dpi) the bone marrow invariably showed a striking increase in erythropoiesis, characterized by an increase in the number of mitotic figures and erythroblastic islands and by a marked decrease in the myeloid:erythroid cell ratio. Later in the infection, erythropoietic activity decreased, while erythrophagocytosis, granulopoiesis, megakaryopoiesis and plasma cell population increased. In chronic infection (16–60 dpi), erythropoietic activity decreased, while intra- and extra-vascular erythrophagocytosis greatly increased. There was also an increase in the bone marrow stroma cells. Excessive erythrophagocytosis by these cells led to the formation of myelin figures and cytoplasmic telephagolysosomes. Degeneration and necrosis of neutrophils lining the adluminal surfaces of the blood sinuses were observed. It is concluded that in the acute stage of the infection, the bone marrow is responsive to the anaemia and that in the chronic stage, dyserythropoiesis and increased erythrophagocytosis by the expanded and activated cells of the mononuclear phagocytic system play an important role in the production of anaemia.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>11222012</pmid><doi>10.1053/jcpa.2000.0445</doi><tpages>10</tpages></addata></record> |
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subjects | Acute Disease Anemia - etiology Anemia - pathology Animals Bone Marrow Diseases - parasitology Bone Marrow Diseases - pathology Chronic Disease Erythroblasts - ultrastructure Erythropoiesis Femur Hematocrit Mitosis Muridae - parasitology Rats Rodent Diseases - parasitology Rodent Diseases - pathology Stromal Cells - ultrastructure Trypanosoma congolense - pathogenicity Trypanosoma congolense - ultrastructure Trypanosomiasis, African - complications Trypanosomiasis, African - pathology |
title | Bone Marrow Response to Acute and Chronic Trypanosoma congolense Infection in Multimammate Rats (Mastomys coucha) |
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