In vivo Immunogenicity and Antigenicity of MAP-8 Peptides Derived from the Structural and Non-Structural Proteins of Canine Parvovirus Type 2
Introduction Canine parvovirus is a viral disease associated with the infection with the canine parvovirus type 2 (CPV-2). Virus-attenuated or inactivated vaccines are commonly used as prophylaxis; still, novel formats such as peptide-based vaccines are a promising alternative due to their safety an...
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creator | Dionicio-Ocampo, Andrea Guadalupe Barrientos-Arevalo, Odalys Ruiz-De los santos, Huehueltolli Cortés-Rodríguez, Dulce Yanet Nicolás-Morales, María Lilia Hurtado-Ortega, Edgar Ramírez-Vargas, Marco Antonio Vences-Velázquez, Amalia Espinoza-Rojo, Mónica Cortés-Sarabia, Karen |
description | Introduction
Canine parvovirus is a viral disease associated with the infection with the canine parvovirus type 2 (CPV-2). Virus-attenuated or inactivated vaccines are commonly used as prophylaxis; still, novel formats such as peptide-based vaccines are a promising alternative due to their safety and capacity to induce an adequate immune response. However, selected peptides must be evaluated in vivo to test their ability to induce immune response and potential side effects.
Materials and Methods
Four peptides derived from the structural and non-structural proteins of CPV-2 were chemically synthesized and used to evaluate the immunogenicity in Balb/C mice. Serum samples were collected and used for the evaluation of humoral immune response. We performed Indirect ELISA and Dot blot to detect antibodies against the peptides. Finally, to evaluate the potential side effects of peptides, we conducted a urinalysis (before sacrifice) and a complete blood count (day 200 since the first inoculation).
Results
From the four used peptides, we detected the presence of IgM and IgG subclasses against all the peptides. The complete blood count showed changes in the levels of hemoglobin, the count of granulocytes and lymphocytes, and the numbers and parameters of platelets between the control and experimental groups. The Dot blot confirmed the peptides’ immunogenicity and the recognition of the native antigen in the commercial vaccine.
Conclusion
The in vivo evaluation in Balb/c mice showed that the peptides derived from the CPV-2 are immunogenic and safe for administration, which can contribute to developing effective and safe vaccines against parvovirus. |
doi_str_mv | 10.1007/s10989-024-10669-9 |
format | Article |
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Canine parvovirus is a viral disease associated with the infection with the canine parvovirus type 2 (CPV-2). Virus-attenuated or inactivated vaccines are commonly used as prophylaxis; still, novel formats such as peptide-based vaccines are a promising alternative due to their safety and capacity to induce an adequate immune response. However, selected peptides must be evaluated in vivo to test their ability to induce immune response and potential side effects.
Materials and Methods
Four peptides derived from the structural and non-structural proteins of CPV-2 were chemically synthesized and used to evaluate the immunogenicity in Balb/C mice. Serum samples were collected and used for the evaluation of humoral immune response. We performed Indirect ELISA and Dot blot to detect antibodies against the peptides. Finally, to evaluate the potential side effects of peptides, we conducted a urinalysis (before sacrifice) and a complete blood count (day 200 since the first inoculation).
Results
From the four used peptides, we detected the presence of IgM and IgG subclasses against all the peptides. The complete blood count showed changes in the levels of hemoglobin, the count of granulocytes and lymphocytes, and the numbers and parameters of platelets between the control and experimental groups. The Dot blot confirmed the peptides’ immunogenicity and the recognition of the native antigen in the commercial vaccine.
Conclusion
The in vivo evaluation in Balb/c mice showed that the peptides derived from the CPV-2 are immunogenic and safe for administration, which can contribute to developing effective and safe vaccines against parvovirus.</description><identifier>ISSN: 1573-3904</identifier><identifier>ISSN: 1573-3149</identifier><identifier>EISSN: 1573-3904</identifier><identifier>DOI: 10.1007/s10989-024-10669-9</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animal Anatomy ; Antigenicity ; Biochemistry ; Biomedical and Life Sciences ; Blood levels ; Blood tests ; Enzyme-linked immunosorbent assay ; Hemoglobin ; Histology ; Immune response (humoral) ; Immunogenicity ; Immunoglobulin G ; Immunoglobulin M ; Inoculation ; Leukocytes (granulocytic) ; Life Sciences ; Lymphocytes ; Molecular Medicine ; Morphology ; Parvoviruses ; Peptides ; Pharmaceutical Sciences/Technology ; Pharmacology/Toxicology ; Polymer Sciences ; Prophylaxis ; Side effects ; Structural proteins ; Urinalysis ; Vaccines ; Viral diseases</subject><ispartof>International journal of peptide research and therapeutics, 2024-11, Vol.31 (1), p.8, Article 8</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2024 Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>Copyright Springer Nature B.V. Jan 2025</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c200t-cb5fc7884cee40d0d4da046ddb334d0e371a268de827dab8a69d3b4b1976bb7b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10989-024-10669-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10989-024-10669-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Dionicio-Ocampo, Andrea Guadalupe</creatorcontrib><creatorcontrib>Barrientos-Arevalo, Odalys</creatorcontrib><creatorcontrib>Ruiz-De los santos, Huehueltolli</creatorcontrib><creatorcontrib>Cortés-Rodríguez, Dulce Yanet</creatorcontrib><creatorcontrib>Nicolás-Morales, María Lilia</creatorcontrib><creatorcontrib>Hurtado-Ortega, Edgar</creatorcontrib><creatorcontrib>Ramírez-Vargas, Marco Antonio</creatorcontrib><creatorcontrib>Vences-Velázquez, Amalia</creatorcontrib><creatorcontrib>Espinoza-Rojo, Mónica</creatorcontrib><creatorcontrib>Cortés-Sarabia, Karen</creatorcontrib><title>In vivo Immunogenicity and Antigenicity of MAP-8 Peptides Derived from the Structural and Non-Structural Proteins of Canine Parvovirus Type 2</title><title>International journal of peptide research and therapeutics</title><addtitle>Int J Pept Res Ther</addtitle><description>Introduction
Canine parvovirus is a viral disease associated with the infection with the canine parvovirus type 2 (CPV-2). Virus-attenuated or inactivated vaccines are commonly used as prophylaxis; still, novel formats such as peptide-based vaccines are a promising alternative due to their safety and capacity to induce an adequate immune response. However, selected peptides must be evaluated in vivo to test their ability to induce immune response and potential side effects.
Materials and Methods
Four peptides derived from the structural and non-structural proteins of CPV-2 were chemically synthesized and used to evaluate the immunogenicity in Balb/C mice. Serum samples were collected and used for the evaluation of humoral immune response. We performed Indirect ELISA and Dot blot to detect antibodies against the peptides. Finally, to evaluate the potential side effects of peptides, we conducted a urinalysis (before sacrifice) and a complete blood count (day 200 since the first inoculation).
Results
From the four used peptides, we detected the presence of IgM and IgG subclasses against all the peptides. The complete blood count showed changes in the levels of hemoglobin, the count of granulocytes and lymphocytes, and the numbers and parameters of platelets between the control and experimental groups. The Dot blot confirmed the peptides’ immunogenicity and the recognition of the native antigen in the commercial vaccine.
Conclusion
The in vivo evaluation in Balb/c mice showed that the peptides derived from the CPV-2 are immunogenic and safe for administration, which can contribute to developing effective and safe vaccines against parvovirus.</description><subject>Animal Anatomy</subject><subject>Antigenicity</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Blood levels</subject><subject>Blood tests</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Hemoglobin</subject><subject>Histology</subject><subject>Immune response (humoral)</subject><subject>Immunogenicity</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Inoculation</subject><subject>Leukocytes (granulocytic)</subject><subject>Life Sciences</subject><subject>Lymphocytes</subject><subject>Molecular Medicine</subject><subject>Morphology</subject><subject>Parvoviruses</subject><subject>Peptides</subject><subject>Pharmaceutical Sciences/Technology</subject><subject>Pharmacology/Toxicology</subject><subject>Polymer Sciences</subject><subject>Prophylaxis</subject><subject>Side effects</subject><subject>Structural proteins</subject><subject>Urinalysis</subject><subject>Vaccines</subject><subject>Viral diseases</subject><issn>1573-3904</issn><issn>1573-3149</issn><issn>1573-3904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRSMEEs8fYGWJtWEcp3G8rMqrEo9KwNpy4klxRe1iO5H6EfwzKUXAitWMRvfckU6WnTI4ZwDiIjKQlaSQF5RBWUoqd7IDNhKccgnF7p99PzuMcQEwygWDg-xj6khve0-my2Xn_BydbWxaE-0MGbtkfw6-JffjGa3IDFfJGozkEoPt0ZA2-CVJr0ieUuia1AX99oU_eEf_nGbBJ7Qubpom2lmHZKZD73sbukie1ysk-XG21-q3iCff8yh7ub56ntzSu8eb6WR8R5scINGmHrWNqKqiQSzAgCmMhqI0pua8MIBcMJ2XlcEqF0bXlS6l4XVRMynKuhY1P8rOtr2r4N87jEktfBfc8FJxlstKAC9HQyrfpprgYwzYqlWwSx3WioHaaFdb7WrQrr60KzlAfAvFIezmGH6r_6E-AWe3h6E</recordid><startdate>20241118</startdate><enddate>20241118</enddate><creator>Dionicio-Ocampo, Andrea Guadalupe</creator><creator>Barrientos-Arevalo, Odalys</creator><creator>Ruiz-De los santos, Huehueltolli</creator><creator>Cortés-Rodríguez, Dulce Yanet</creator><creator>Nicolás-Morales, María Lilia</creator><creator>Hurtado-Ortega, Edgar</creator><creator>Ramírez-Vargas, Marco Antonio</creator><creator>Vences-Velázquez, Amalia</creator><creator>Espinoza-Rojo, Mónica</creator><creator>Cortés-Sarabia, Karen</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope></search><sort><creationdate>20241118</creationdate><title>In vivo Immunogenicity and Antigenicity of MAP-8 Peptides Derived from the Structural and Non-Structural Proteins of Canine Parvovirus Type 2</title><author>Dionicio-Ocampo, Andrea Guadalupe ; Barrientos-Arevalo, Odalys ; Ruiz-De los santos, Huehueltolli ; Cortés-Rodríguez, Dulce Yanet ; Nicolás-Morales, María Lilia ; Hurtado-Ortega, Edgar ; Ramírez-Vargas, Marco Antonio ; Vences-Velázquez, Amalia ; Espinoza-Rojo, Mónica ; Cortés-Sarabia, Karen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c200t-cb5fc7884cee40d0d4da046ddb334d0e371a268de827dab8a69d3b4b1976bb7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animal Anatomy</topic><topic>Antigenicity</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Blood levels</topic><topic>Blood tests</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Hemoglobin</topic><topic>Histology</topic><topic>Immune response (humoral)</topic><topic>Immunogenicity</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin M</topic><topic>Inoculation</topic><topic>Leukocytes (granulocytic)</topic><topic>Life Sciences</topic><topic>Lymphocytes</topic><topic>Molecular Medicine</topic><topic>Morphology</topic><topic>Parvoviruses</topic><topic>Peptides</topic><topic>Pharmaceutical Sciences/Technology</topic><topic>Pharmacology/Toxicology</topic><topic>Polymer Sciences</topic><topic>Prophylaxis</topic><topic>Side effects</topic><topic>Structural proteins</topic><topic>Urinalysis</topic><topic>Vaccines</topic><topic>Viral diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dionicio-Ocampo, Andrea Guadalupe</creatorcontrib><creatorcontrib>Barrientos-Arevalo, Odalys</creatorcontrib><creatorcontrib>Ruiz-De los santos, Huehueltolli</creatorcontrib><creatorcontrib>Cortés-Rodríguez, Dulce Yanet</creatorcontrib><creatorcontrib>Nicolás-Morales, María Lilia</creatorcontrib><creatorcontrib>Hurtado-Ortega, Edgar</creatorcontrib><creatorcontrib>Ramírez-Vargas, Marco Antonio</creatorcontrib><creatorcontrib>Vences-Velázquez, Amalia</creatorcontrib><creatorcontrib>Espinoza-Rojo, Mónica</creatorcontrib><creatorcontrib>Cortés-Sarabia, Karen</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>International journal of peptide research and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dionicio-Ocampo, Andrea Guadalupe</au><au>Barrientos-Arevalo, Odalys</au><au>Ruiz-De los santos, Huehueltolli</au><au>Cortés-Rodríguez, Dulce Yanet</au><au>Nicolás-Morales, María Lilia</au><au>Hurtado-Ortega, Edgar</au><au>Ramírez-Vargas, Marco Antonio</au><au>Vences-Velázquez, Amalia</au><au>Espinoza-Rojo, Mónica</au><au>Cortés-Sarabia, Karen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo Immunogenicity and Antigenicity of MAP-8 Peptides Derived from the Structural and Non-Structural Proteins of Canine Parvovirus Type 2</atitle><jtitle>International journal of peptide research and therapeutics</jtitle><stitle>Int J Pept Res Ther</stitle><date>2024-11-18</date><risdate>2024</risdate><volume>31</volume><issue>1</issue><spage>8</spage><pages>8-</pages><artnum>8</artnum><issn>1573-3904</issn><issn>1573-3149</issn><eissn>1573-3904</eissn><abstract>Introduction
Canine parvovirus is a viral disease associated with the infection with the canine parvovirus type 2 (CPV-2). Virus-attenuated or inactivated vaccines are commonly used as prophylaxis; still, novel formats such as peptide-based vaccines are a promising alternative due to their safety and capacity to induce an adequate immune response. However, selected peptides must be evaluated in vivo to test their ability to induce immune response and potential side effects.
Materials and Methods
Four peptides derived from the structural and non-structural proteins of CPV-2 were chemically synthesized and used to evaluate the immunogenicity in Balb/C mice. Serum samples were collected and used for the evaluation of humoral immune response. We performed Indirect ELISA and Dot blot to detect antibodies against the peptides. Finally, to evaluate the potential side effects of peptides, we conducted a urinalysis (before sacrifice) and a complete blood count (day 200 since the first inoculation).
Results
From the four used peptides, we detected the presence of IgM and IgG subclasses against all the peptides. The complete blood count showed changes in the levels of hemoglobin, the count of granulocytes and lymphocytes, and the numbers and parameters of platelets between the control and experimental groups. The Dot blot confirmed the peptides’ immunogenicity and the recognition of the native antigen in the commercial vaccine.
Conclusion
The in vivo evaluation in Balb/c mice showed that the peptides derived from the CPV-2 are immunogenic and safe for administration, which can contribute to developing effective and safe vaccines against parvovirus.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10989-024-10669-9</doi></addata></record> |
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subjects | Animal Anatomy Antigenicity Biochemistry Biomedical and Life Sciences Blood levels Blood tests Enzyme-linked immunosorbent assay Hemoglobin Histology Immune response (humoral) Immunogenicity Immunoglobulin G Immunoglobulin M Inoculation Leukocytes (granulocytic) Life Sciences Lymphocytes Molecular Medicine Morphology Parvoviruses Peptides Pharmaceutical Sciences/Technology Pharmacology/Toxicology Polymer Sciences Prophylaxis Side effects Structural proteins Urinalysis Vaccines Viral diseases |
title | In vivo Immunogenicity and Antigenicity of MAP-8 Peptides Derived from the Structural and Non-Structural Proteins of Canine Parvovirus Type 2 |
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