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Lysozyme gene expression by hemocytes of Pacific white shrimp, Litopenaeus vannamei, after injection with Vibrio
The purpose of this study was to quantify the gene expression of lysozyme, an important antibacterial protein produced by shrimp hemocytes, within tissues of Litopenaeus vannamei Boone in response to a pathogen challenge. We quantified lysozyme transcripts with a real-time PCR method and used these...
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Published in: | Fish & Shellfish Immunology 2007-04, Vol.22 (4), p.327-339 |
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description | The purpose of this study was to quantify the gene expression of lysozyme, an important antibacterial protein produced by shrimp hemocytes, within tissues of
Litopenaeus vannamei Boone in response to a pathogen challenge. We quantified lysozyme transcripts with a real-time PCR method and used these data, along with total hemocyte counts, to infer patterns of hemocyte trafficking during the immune response. Transcript expression was detected by in situ hybridization of mRNA in circulating hemocytes, and within tissues with high hemocyte concentrations. Lysozyme gene expression was monitored in 5 tissues and in circulating hemocytes for 48
h following challenge with the shrimp pathogen
Vibrio campbellii Baumann. The results suggest that lysozyme is expressed in most if not all hemocytes in circulation and in peripheral tissues. Injection with
V. campbellii produced a significant decrease in transcriptional signal in circulating hemocytes and peripheral tissues 4
h after injection. Over the same early time period lysozyme signal increased significantly in the muscle at the site of injection and remained high for the duration of the time-course, suggesting that hemocytes are recruited to the site of injection early during the course of the immune response. After 4
h, lysozyme signal increased in circulating hemocytes and tissues, with a return to control levels noted for all tissues except the muscle at the site of injection. |
doi_str_mv | 10.1016/j.fsi.2006.06.004 |
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Litopenaeus vannamei Boone in response to a pathogen challenge. We quantified lysozyme transcripts with a real-time PCR method and used these data, along with total hemocyte counts, to infer patterns of hemocyte trafficking during the immune response. Transcript expression was detected by in situ hybridization of mRNA in circulating hemocytes, and within tissues with high hemocyte concentrations. Lysozyme gene expression was monitored in 5 tissues and in circulating hemocytes for 48
h following challenge with the shrimp pathogen
Vibrio campbellii Baumann. The results suggest that lysozyme is expressed in most if not all hemocytes in circulation and in peripheral tissues. Injection with
V. campbellii produced a significant decrease in transcriptional signal in circulating hemocytes and peripheral tissues 4
h after injection. Over the same early time period lysozyme signal increased significantly in the muscle at the site of injection and remained high for the duration of the time-course, suggesting that hemocytes are recruited to the site of injection early during the course of the immune response. After 4
h, lysozyme signal increased in circulating hemocytes and tissues, with a return to control levels noted for all tissues except the muscle at the site of injection.</description><identifier>ISSN: 1050-4648</identifier><identifier>EISSN: 1095-9947</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.1016/j.fsi.2006.06.004</identifier><identifier>PMID: 16916613</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Blood Cell Count - veterinary ; DNA Primers - chemistry ; Gene expression ; Gene Expression Regulation, Enzymologic - immunology ; Hemocyte ; Hemocytes - enzymology ; Hemocytes - immunology ; In situ hybridization ; In Situ Hybridization - veterinary ; Litopenaeus vannamei ; Lymphoid organ ; Lysozyme ; Marine ; Muramidase - analysis ; Muramidase - biosynthesis ; Muramidase - genetics ; Neural Networks (Computer) ; Penaeidae - immunology ; Penaeidae - microbiology ; Quantitative real-time PCR ; Reverse Transcriptase Polymerase Chain Reaction - veterinary ; Shrimp ; Time Factors ; Vibrio ; Vibrio - immunology ; Vibrio campbellii</subject><ispartof>Fish & Shellfish Immunology, 2007-04, Vol.22 (4), p.327-339</ispartof><rights>2006 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-dba82e00b66838f040694b5accf0d9f32896c292ff26967f9d11244e0d98f2fa3</citedby><cites>FETCH-LOGICAL-c382t-dba82e00b66838f040694b5accf0d9f32896c292ff26967f9d11244e0d98f2fa3</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/16916613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Burge, Erin J.</creatorcontrib><creatorcontrib>Madigan, Daniel J.</creatorcontrib><creatorcontrib>Burnett, Louis E.</creatorcontrib><creatorcontrib>Burnett, Karen G.</creatorcontrib><title>Lysozyme gene expression by hemocytes of Pacific white shrimp, Litopenaeus vannamei, after injection with Vibrio</title><title>Fish & Shellfish Immunology</title><addtitle>Fish Shellfish Immunol</addtitle><description>The purpose of this study was to quantify the gene expression of lysozyme, an important antibacterial protein produced by shrimp hemocytes, within tissues of
Litopenaeus vannamei Boone in response to a pathogen challenge. We quantified lysozyme transcripts with a real-time PCR method and used these data, along with total hemocyte counts, to infer patterns of hemocyte trafficking during the immune response. Transcript expression was detected by in situ hybridization of mRNA in circulating hemocytes, and within tissues with high hemocyte concentrations. Lysozyme gene expression was monitored in 5 tissues and in circulating hemocytes for 48
h following challenge with the shrimp pathogen
Vibrio campbellii Baumann. The results suggest that lysozyme is expressed in most if not all hemocytes in circulation and in peripheral tissues. Injection with
V. campbellii produced a significant decrease in transcriptional signal in circulating hemocytes and peripheral tissues 4
h after injection. Over the same early time period lysozyme signal increased significantly in the muscle at the site of injection and remained high for the duration of the time-course, suggesting that hemocytes are recruited to the site of injection early during the course of the immune response. After 4
h, lysozyme signal increased in circulating hemocytes and tissues, with a return to control levels noted for all tissues except the muscle at the site of injection.</description><subject>Animals</subject><subject>Blood Cell Count - veterinary</subject><subject>DNA Primers - chemistry</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Enzymologic - immunology</subject><subject>Hemocyte</subject><subject>Hemocytes - enzymology</subject><subject>Hemocytes - immunology</subject><subject>In situ hybridization</subject><subject>In Situ Hybridization - veterinary</subject><subject>Litopenaeus vannamei</subject><subject>Lymphoid organ</subject><subject>Lysozyme</subject><subject>Marine</subject><subject>Muramidase - analysis</subject><subject>Muramidase - biosynthesis</subject><subject>Muramidase - genetics</subject><subject>Neural Networks (Computer)</subject><subject>Penaeidae - immunology</subject><subject>Penaeidae - microbiology</subject><subject>Quantitative real-time PCR</subject><subject>Reverse Transcriptase Polymerase Chain Reaction - veterinary</subject><subject>Shrimp</subject><subject>Time Factors</subject><subject>Vibrio</subject><subject>Vibrio - immunology</subject><subject>Vibrio campbellii</subject><issn>1050-4648</issn><issn>1095-9947</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkU1r3DAQhkVJaT7aH9BL0SmneCvJsmyRUwltElhoD22vQpZH3VnWliN5k7i_PjK7kFsLAxLMM8_hfQn5yNmKM64-b1c-4UowplbLMPmGnHGmq0JrWZ8s_4oVUsnmlJyntGUZLBV7R0650lwpXp6RcT2n8Hfugf6BASg8jxFSwjDQdqYb6IObJ0g0ePrDOvTo6NMGJ6BpE7Efr-gapzDCYGGf6KMdBtsDXlHrJ4gUhy24aXE94bShv7GNGN6Tt97uEnw4vhfk17evP2_uivX32_ubL-vClY2Yiq61jQDGWqWasvFMMqVlW1nnPOu0L0WjlRNaeC-UVrXXHedCSsjLxgtvywtyefCOMTzsIU2mx-Rgt7MDhH0yWVvLWlb_BbluKinrBeQH0MWQUgRvxpyBjbPhzCx9mK3JfZilD7MMk_nm01G-b3voXi-OBWTg-gBAzuIRIZrkEAYHHcYcnukC_kP_AqgynKI</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Burge, Erin J.</creator><creator>Madigan, Daniel J.</creator><creator>Burnett, Louis E.</creator><creator>Burnett, Karen G.</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>7QL</scope><scope>7T5</scope><scope>7TN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>Lysozyme gene expression by hemocytes of Pacific white shrimp, Litopenaeus vannamei, after injection with Vibrio</title><author>Burge, Erin J. ; Madigan, Daniel J. ; Burnett, Louis E. ; Burnett, Karen G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-dba82e00b66838f040694b5accf0d9f32896c292ff26967f9d11244e0d98f2fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Blood Cell Count - veterinary</topic><topic>DNA Primers - chemistry</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Enzymologic - immunology</topic><topic>Hemocyte</topic><topic>Hemocytes - enzymology</topic><topic>Hemocytes - immunology</topic><topic>In situ hybridization</topic><topic>In Situ Hybridization - veterinary</topic><topic>Litopenaeus vannamei</topic><topic>Lymphoid organ</topic><topic>Lysozyme</topic><topic>Marine</topic><topic>Muramidase - analysis</topic><topic>Muramidase - biosynthesis</topic><topic>Muramidase - genetics</topic><topic>Neural Networks (Computer)</topic><topic>Penaeidae - immunology</topic><topic>Penaeidae - microbiology</topic><topic>Quantitative real-time PCR</topic><topic>Reverse Transcriptase Polymerase Chain Reaction - veterinary</topic><topic>Shrimp</topic><topic>Time Factors</topic><topic>Vibrio</topic><topic>Vibrio - immunology</topic><topic>Vibrio campbellii</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Burge, Erin J.</creatorcontrib><creatorcontrib>Madigan, Daniel J.</creatorcontrib><creatorcontrib>Burnett, Louis E.</creatorcontrib><creatorcontrib>Burnett, Karen G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Fish & Shellfish Immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Burge, Erin J.</au><au>Madigan, Daniel J.</au><au>Burnett, Louis E.</au><au>Burnett, Karen G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lysozyme gene expression by hemocytes of Pacific white shrimp, Litopenaeus vannamei, after injection with Vibrio</atitle><jtitle>Fish & Shellfish Immunology</jtitle><addtitle>Fish Shellfish Immunol</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>22</volume><issue>4</issue><spage>327</spage><epage>339</epage><pages>327-339</pages><issn>1050-4648</issn><eissn>1095-9947</eissn><eissn>1365-2567</eissn><abstract>The purpose of this study was to quantify the gene expression of lysozyme, an important antibacterial protein produced by shrimp hemocytes, within tissues of
Litopenaeus vannamei Boone in response to a pathogen challenge. We quantified lysozyme transcripts with a real-time PCR method and used these data, along with total hemocyte counts, to infer patterns of hemocyte trafficking during the immune response. Transcript expression was detected by in situ hybridization of mRNA in circulating hemocytes, and within tissues with high hemocyte concentrations. Lysozyme gene expression was monitored in 5 tissues and in circulating hemocytes for 48
h following challenge with the shrimp pathogen
Vibrio campbellii Baumann. The results suggest that lysozyme is expressed in most if not all hemocytes in circulation and in peripheral tissues. Injection with
V. campbellii produced a significant decrease in transcriptional signal in circulating hemocytes and peripheral tissues 4
h after injection. Over the same early time period lysozyme signal increased significantly in the muscle at the site of injection and remained high for the duration of the time-course, suggesting that hemocytes are recruited to the site of injection early during the course of the immune response. After 4
h, lysozyme signal increased in circulating hemocytes and tissues, with a return to control levels noted for all tissues except the muscle at the site of injection.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16916613</pmid><doi>10.1016/j.fsi.2006.06.004</doi><tpages>13</tpages></addata></record> |
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subjects | Animals Blood Cell Count - veterinary DNA Primers - chemistry Gene expression Gene Expression Regulation, Enzymologic - immunology Hemocyte Hemocytes - enzymology Hemocytes - immunology In situ hybridization In Situ Hybridization - veterinary Litopenaeus vannamei Lymphoid organ Lysozyme Marine Muramidase - analysis Muramidase - biosynthesis Muramidase - genetics Neural Networks (Computer) Penaeidae - immunology Penaeidae - microbiology Quantitative real-time PCR Reverse Transcriptase Polymerase Chain Reaction - veterinary Shrimp Time Factors Vibrio Vibrio - immunology Vibrio campbellii |
title | Lysozyme gene expression by hemocytes of Pacific white shrimp, Litopenaeus vannamei, after injection with Vibrio |
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