Validation of non-fluorescent methods to reliably detect acrosomal and plasma membrane integrity of common marmoset ( Callithrix jacchus) sperm
Simple, rapid and stable sperm evaluation methods which have been optimized for common marmoset ( Callithrix jacchus) are critical for studies involving collection and evaluation of sperm in the field. This is particularly important for new species groups such as Callitrichidae where the sperm have...
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creator | Valle, R.R. Valle, C.M.R. Nichi, M. Muniz, J.A.P.C. Nayudu, P.L. Guimarães, M.A.B.V. |
description | Simple, rapid and stable sperm evaluation methods which have been optimized for common marmoset (
Callithrix jacchus) are critical for studies involving collection and evaluation of sperm in the field. This is particularly important for new species groups such as
Callitrichidae where the sperm have been little studied. Of this family,
C. jacchus is the best known, and has been chosen as a model species for other members of the genus
Callithrix. The fundamental evaluation parameters for sperm of any species are viability and acrosomal status. Semen samples were collected by penile vibratory stimulation. To evaluate sperm plasma membrane integrity, Eosin–Nigrosin was tested here for the common marmoset sperm to be used under field conditions. Further, a non-fluorescent stain for acrosome, the “Simple” stain, developed for domestic and wild cats, was tested on common marmoset sperm. This was compared with a fluorescent staining, Fluorescein isothiocyanate-
Pisum sativum agglutinin (FITC-PSA), routinely used and validated for common marmoset at the German Primate Centre to evaluate acrosomal integrity. Results obtained with the “Simple” stain showed a marked differentiation between sperm with intact and non-intact acrosome both with and without ionophore treatment and closely correlated with results obtained with FITC-PSA. Temperature had no effect on the results with the “Simple” stain and the complete processing is simple enough to be carried out under field conditions. These findings indicated that the “Simple” stain and Eosin–Nigrosin provide rapid and accurate results for
C. jacchus sperm and that those methods can be reliably used as field tools for sperm evaluation for this species. |
doi_str_mv | 10.1016/j.theriogenology.2008.03.011 |
format | Article |
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Callithrix jacchus) are critical for studies involving collection and evaluation of sperm in the field. This is particularly important for new species groups such as
Callitrichidae where the sperm have been little studied. Of this family,
C. jacchus is the best known, and has been chosen as a model species for other members of the genus
Callithrix. The fundamental evaluation parameters for sperm of any species are viability and acrosomal status. Semen samples were collected by penile vibratory stimulation. To evaluate sperm plasma membrane integrity, Eosin–Nigrosin was tested here for the common marmoset sperm to be used under field conditions. Further, a non-fluorescent stain for acrosome, the “Simple” stain, developed for domestic and wild cats, was tested on common marmoset sperm. This was compared with a fluorescent staining, Fluorescein isothiocyanate-
Pisum sativum agglutinin (FITC-PSA), routinely used and validated for common marmoset at the German Primate Centre to evaluate acrosomal integrity. Results obtained with the “Simple” stain showed a marked differentiation between sperm with intact and non-intact acrosome both with and without ionophore treatment and closely correlated with results obtained with FITC-PSA. Temperature had no effect on the results with the “Simple” stain and the complete processing is simple enough to be carried out under field conditions. These findings indicated that the “Simple” stain and Eosin–Nigrosin provide rapid and accurate results for
C. jacchus sperm and that those methods can be reliably used as field tools for sperm evaluation for this species.</description><identifier>ISSN: 0093-691X</identifier><identifier>EISSN: 1879-3231</identifier><identifier>DOI: 10.1016/j.theriogenology.2008.03.011</identifier><identifier>PMID: 18479742</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acrosome ; Acrosome - metabolism ; acrosome reaction ; Aniline Compounds - metabolism ; Animals ; Callithrix ; Callithrix - physiology ; Callithrix jacchus ; Cell Membrane - physiology ; differential staining ; Eosine Yellowish-(YS) - metabolism ; Fluorescein-5-isothiocyanate - metabolism ; ionophores ; Male ; Marmoset ; non-fluorescent stain ; plasma membrane ; Primate ; Reproducibility of Results ; Sperm ; sperm evaluation ; sperm viability ; spermatozoa ; Spermatozoa - physiology ; Staining and Labeling - methods ; Staining and Labeling - veterinary ; viability ; Vibrostimulation</subject><ispartof>Theriogenology, 2008-07, Vol.70 (1), p.115-120</ispartof><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-32f4371ff2b213c67b2ad4d4bc437348e55ebfe4f6bb49faa01a5beaa644dabb3</citedby><cites>FETCH-LOGICAL-c408t-32f4371ff2b213c67b2ad4d4bc437348e55ebfe4f6bb49faa01a5beaa644dabb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0093691X08001349$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18479742$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Valle, R.R.</creatorcontrib><creatorcontrib>Valle, C.M.R.</creatorcontrib><creatorcontrib>Nichi, M.</creatorcontrib><creatorcontrib>Muniz, J.A.P.C.</creatorcontrib><creatorcontrib>Nayudu, P.L.</creatorcontrib><creatorcontrib>Guimarães, M.A.B.V.</creatorcontrib><title>Validation of non-fluorescent methods to reliably detect acrosomal and plasma membrane integrity of common marmoset ( Callithrix jacchus) sperm</title><title>Theriogenology</title><addtitle>Theriogenology</addtitle><description>Simple, rapid and stable sperm evaluation methods which have been optimized for common marmoset (
Callithrix jacchus) are critical for studies involving collection and evaluation of sperm in the field. This is particularly important for new species groups such as
Callitrichidae where the sperm have been little studied. Of this family,
C. jacchus is the best known, and has been chosen as a model species for other members of the genus
Callithrix. The fundamental evaluation parameters for sperm of any species are viability and acrosomal status. Semen samples were collected by penile vibratory stimulation. To evaluate sperm plasma membrane integrity, Eosin–Nigrosin was tested here for the common marmoset sperm to be used under field conditions. Further, a non-fluorescent stain for acrosome, the “Simple” stain, developed for domestic and wild cats, was tested on common marmoset sperm. This was compared with a fluorescent staining, Fluorescein isothiocyanate-
Pisum sativum agglutinin (FITC-PSA), routinely used and validated for common marmoset at the German Primate Centre to evaluate acrosomal integrity. Results obtained with the “Simple” stain showed a marked differentiation between sperm with intact and non-intact acrosome both with and without ionophore treatment and closely correlated with results obtained with FITC-PSA. Temperature had no effect on the results with the “Simple” stain and the complete processing is simple enough to be carried out under field conditions. These findings indicated that the “Simple” stain and Eosin–Nigrosin provide rapid and accurate results for
C. jacchus sperm and that those methods can be reliably used as field tools for sperm evaluation for this species.</description><subject>Acrosome</subject><subject>Acrosome - metabolism</subject><subject>acrosome reaction</subject><subject>Aniline Compounds - metabolism</subject><subject>Animals</subject><subject>Callithrix</subject><subject>Callithrix - physiology</subject><subject>Callithrix jacchus</subject><subject>Cell Membrane - physiology</subject><subject>differential staining</subject><subject>Eosine Yellowish-(YS) - metabolism</subject><subject>Fluorescein-5-isothiocyanate - metabolism</subject><subject>ionophores</subject><subject>Male</subject><subject>Marmoset</subject><subject>non-fluorescent stain</subject><subject>plasma membrane</subject><subject>Primate</subject><subject>Reproducibility of Results</subject><subject>Sperm</subject><subject>sperm evaluation</subject><subject>sperm viability</subject><subject>spermatozoa</subject><subject>Spermatozoa - physiology</subject><subject>Staining and Labeling - methods</subject><subject>Staining and Labeling - veterinary</subject><subject>viability</subject><subject>Vibrostimulation</subject><issn>0093-691X</issn><issn>1879-3231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc-KFDEQhxtR3HH1FTQHET1Mm3TS_2AvMrgqLHjQFW-hkq7MZEg6Y5IW5yl8ZTPMgHjzFCi-qtSvvqp6yWjNKOve7uu8w2jDFufgwvZYN5QONeU1ZexBtWJDP655w9nDakXpyNfdyL5fVU9S2lNKedexx9UVG0Q_9qJZVb-_gbMTZBtmEgyZw7w2bgkRk8Y5E495F6ZEciARnQXljmTCjDoT0DGk4MERmCdycJA8FN6rCDMSO2fcRpuPp6k6eF_me4g-JMzkNdmAczbvov1F9qD1bklvSDpg9E-rRwZcwmeX97q6v33_dfNxfff5w6fNu7u1FnTIJaARvGfGNKphXHe9amASk1C6lLkYsG1RGRSmU0qMBoAyaBUCdEJMoBS_rl6d5x5i-LFgytLbEtm5snxYkuxZJ5qhaQp4cwZPcVNEIw_RliRHyag8CZF7-a8QeRIiKZdFSGl_fvlnUR6nv80XAwV4cQYMBAnlZEnef2ko40UebUXbFeL2TGC5x0-LUSZtcdY42VhEyCnY_9vlD3gIs4c</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Valle, R.R.</creator><creator>Valle, C.M.R.</creator><creator>Nichi, M.</creator><creator>Muniz, J.A.P.C.</creator><creator>Nayudu, P.L.</creator><creator>Guimarães, M.A.B.V.</creator><general>Elsevier Inc</general><general>[Oxford]: Butterworth-Heinemann; [New York]: Elsevier Science</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>20080701</creationdate><title>Validation of non-fluorescent methods to reliably detect acrosomal and plasma membrane integrity of common marmoset ( Callithrix jacchus) sperm</title><author>Valle, R.R. ; Valle, C.M.R. ; Nichi, M. ; Muniz, J.A.P.C. ; Nayudu, P.L. ; Guimarães, M.A.B.V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-32f4371ff2b213c67b2ad4d4bc437348e55ebfe4f6bb49faa01a5beaa644dabb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acrosome</topic><topic>Acrosome - metabolism</topic><topic>acrosome reaction</topic><topic>Aniline Compounds - metabolism</topic><topic>Animals</topic><topic>Callithrix</topic><topic>Callithrix - physiology</topic><topic>Callithrix jacchus</topic><topic>Cell Membrane - physiology</topic><topic>differential staining</topic><topic>Eosine Yellowish-(YS) - metabolism</topic><topic>Fluorescein-5-isothiocyanate - metabolism</topic><topic>ionophores</topic><topic>Male</topic><topic>Marmoset</topic><topic>non-fluorescent stain</topic><topic>plasma membrane</topic><topic>Primate</topic><topic>Reproducibility of Results</topic><topic>Sperm</topic><topic>sperm evaluation</topic><topic>sperm viability</topic><topic>spermatozoa</topic><topic>Spermatozoa - physiology</topic><topic>Staining and Labeling - methods</topic><topic>Staining and Labeling - veterinary</topic><topic>viability</topic><topic>Vibrostimulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Valle, R.R.</creatorcontrib><creatorcontrib>Valle, C.M.R.</creatorcontrib><creatorcontrib>Nichi, M.</creatorcontrib><creatorcontrib>Muniz, J.A.P.C.</creatorcontrib><creatorcontrib>Nayudu, P.L.</creatorcontrib><creatorcontrib>Guimarães, M.A.B.V.</creatorcontrib><collection>AGRIS</collection><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>Theriogenology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Valle, R.R.</au><au>Valle, C.M.R.</au><au>Nichi, M.</au><au>Muniz, J.A.P.C.</au><au>Nayudu, P.L.</au><au>Guimarães, M.A.B.V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validation of non-fluorescent methods to reliably detect acrosomal and plasma membrane integrity of common marmoset ( Callithrix jacchus) sperm</atitle><jtitle>Theriogenology</jtitle><addtitle>Theriogenology</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>70</volume><issue>1</issue><spage>115</spage><epage>120</epage><pages>115-120</pages><issn>0093-691X</issn><eissn>1879-3231</eissn><abstract>Simple, rapid and stable sperm evaluation methods which have been optimized for common marmoset (
Callithrix jacchus) are critical for studies involving collection and evaluation of sperm in the field. This is particularly important for new species groups such as
Callitrichidae where the sperm have been little studied. Of this family,
C. jacchus is the best known, and has been chosen as a model species for other members of the genus
Callithrix. The fundamental evaluation parameters for sperm of any species are viability and acrosomal status. Semen samples were collected by penile vibratory stimulation. To evaluate sperm plasma membrane integrity, Eosin–Nigrosin was tested here for the common marmoset sperm to be used under field conditions. Further, a non-fluorescent stain for acrosome, the “Simple” stain, developed for domestic and wild cats, was tested on common marmoset sperm. This was compared with a fluorescent staining, Fluorescein isothiocyanate-
Pisum sativum agglutinin (FITC-PSA), routinely used and validated for common marmoset at the German Primate Centre to evaluate acrosomal integrity. Results obtained with the “Simple” stain showed a marked differentiation between sperm with intact and non-intact acrosome both with and without ionophore treatment and closely correlated with results obtained with FITC-PSA. Temperature had no effect on the results with the “Simple” stain and the complete processing is simple enough to be carried out under field conditions. These findings indicated that the “Simple” stain and Eosin–Nigrosin provide rapid and accurate results for
C. jacchus sperm and that those methods can be reliably used as field tools for sperm evaluation for this species.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18479742</pmid><doi>10.1016/j.theriogenology.2008.03.011</doi><tpages>6</tpages></addata></record> |
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subjects | Acrosome Acrosome - metabolism acrosome reaction Aniline Compounds - metabolism Animals Callithrix Callithrix - physiology Callithrix jacchus Cell Membrane - physiology differential staining Eosine Yellowish-(YS) - metabolism Fluorescein-5-isothiocyanate - metabolism ionophores Male Marmoset non-fluorescent stain plasma membrane Primate Reproducibility of Results Sperm sperm evaluation sperm viability spermatozoa Spermatozoa - physiology Staining and Labeling - methods Staining and Labeling - veterinary viability Vibrostimulation |
title | Validation of non-fluorescent methods to reliably detect acrosomal and plasma membrane integrity of common marmoset ( Callithrix jacchus) sperm |
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