Lab-on-a-chip and SDS-PAGE analysis of hemolymph protein profile from Rhipicephalus microplus (Acari: Ixodidae) infected with entomopathogenic nematode and fungus
In the present study, lab-on-a-chip electrophoresis (LoaC) was suggested as an alternative method to the conventional polyacrylamide gel electrophoresis under denaturing conditions (SDS-PAGE) to analyze raw cell-free tick hemolymph. Rhipicephalus microplus females were exposed to the entomopathogeni...
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creator | Golo, Patrícia Silva dos Santos, Alessa Siqueira de Oliveira Monteiro, Caio Marcio Oliveira Perinotto, Wendell Marcelo de Souza Quinelato, Simone Camargo, Mariana Guedes de Sá, Fillipe Araujo Angelo, Isabele da Costa Martins, Marta Fonseca Prata, Marcia Cristina de Azevedo Bittencourt, Vânia Rita Elias Pinheiro |
description | In the present study, lab-on-a-chip electrophoresis (LoaC) was suggested as an alternative method to the conventional polyacrylamide gel electrophoresis under denaturing conditions (SDS-PAGE) to analyze raw cell-free tick hemolymph.
Rhipicephalus microplus
females were exposed to the entomopathogenic fungus
Metarhizium anisopliae
senso latu IBCB 116 strain and/or to the entomopathogenic nematode
Heterorhabditis indica
LPP1 strain. Hemolymph from not exposed or exposed ticks was collected 16 and 24 h after exposure and analyze by SDS-PAGE or LoaC. SDS-PAGE yielded 15 bands and LoaC electrophoresis 17 bands. Despite the differences in the number of bands, when the hemolymph protein profiles of exposed or unexposed ticks were compared in the same method, no suppressing or additional bands were detected among the treatments regardless the method (i.e., SDS-PAGE or chip electrophoresis using the Protein 230 Kit®). The potential of LoaC electrophoresis to detect protein bands from tick hemolymph was considered more efficient in comparison to the detection obtained using the traditional SDS-PAGE method, especially when it comes to protein subunits heavier than 100 KDa. LoaC electrophoresis provided a very good reproducibility, and is much faster than the conventional SDS-PAGE method, which requires several hours for one analysis. Despite both methods can be used to analyze tick hemolymph composition, LoaC was considered more suitable for cell-free hemolymph protein separation and detection. LoaC hemolymph band percent data reported changes in key proteins (i.e., HeLp and vitellogenin) exceptionally important for tick embryogenesis. This study reported, for the first time, tick hemolymph protein profile using LoaC. |
doi_str_mv | 10.1007/s00436-016-5109-z |
format | Article |
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Rhipicephalus microplus
females were exposed to the entomopathogenic fungus
Metarhizium anisopliae
senso latu IBCB 116 strain and/or to the entomopathogenic nematode
Heterorhabditis indica
LPP1 strain. Hemolymph from not exposed or exposed ticks was collected 16 and 24 h after exposure and analyze by SDS-PAGE or LoaC. SDS-PAGE yielded 15 bands and LoaC electrophoresis 17 bands. Despite the differences in the number of bands, when the hemolymph protein profiles of exposed or unexposed ticks were compared in the same method, no suppressing or additional bands were detected among the treatments regardless the method (i.e., SDS-PAGE or chip electrophoresis using the Protein 230 Kit®). The potential of LoaC electrophoresis to detect protein bands from tick hemolymph was considered more efficient in comparison to the detection obtained using the traditional SDS-PAGE method, especially when it comes to protein subunits heavier than 100 KDa. LoaC electrophoresis provided a very good reproducibility, and is much faster than the conventional SDS-PAGE method, which requires several hours for one analysis. Despite both methods can be used to analyze tick hemolymph composition, LoaC was considered more suitable for cell-free hemolymph protein separation and detection. LoaC hemolymph band percent data reported changes in key proteins (i.e., HeLp and vitellogenin) exceptionally important for tick embryogenesis. This study reported, for the first time, tick hemolymph protein profile using LoaC.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-016-5109-z</identifier><identifier>PMID: 27174026</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acari ; Animals ; Arthropod Proteins - chemistry ; Arthropod Proteins - metabolism ; Biomedical and Life Sciences ; Biomedicine ; Electrophoresis, Polyacrylamide Gel - instrumentation ; Electrophoresis, Polyacrylamide Gel - methods ; Female ; Fungi - classification ; Fungi - genetics ; Fungi - isolation & purification ; Fungi - physiology ; Health aspects ; Hemolymph - chemistry ; Hemolymph - metabolism ; Heterorhabditis indica ; Immunology ; Ixodidae ; Lab-On-A-Chip Devices ; Medical Microbiology ; Membrane proteins ; Metarhizium anisopliae ; Microbiology ; Nematoda ; Nematoda - classification ; Nematoda - genetics ; Nematoda - isolation & purification ; Nematoda - physiology ; Original Paper ; Reproducibility of Results ; Rhipicephalus ; Rhipicephalus - chemistry ; Rhipicephalus - metabolism ; Rhipicephalus - microbiology ; Rhipicephalus - parasitology ; Roundworms ; Ticks</subject><ispartof>Parasitology research (1987), 2016-09, Vol.115 (9), p.3459-3468</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><rights>COPYRIGHT 2016 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-3ec2f6c668d8c1eddb198ea75cad9a8cbfe17083a6811fbed68a87c947feb6e93</citedby><cites>FETCH-LOGICAL-c416t-3ec2f6c668d8c1eddb198ea75cad9a8cbfe17083a6811fbed68a87c947feb6e93</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/s00436-016-5109-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00436-016-5109-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27174026$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Golo, Patrícia Silva</creatorcontrib><creatorcontrib>dos Santos, Alessa Siqueira de Oliveira</creatorcontrib><creatorcontrib>Monteiro, Caio Marcio Oliveira</creatorcontrib><creatorcontrib>Perinotto, Wendell Marcelo de Souza</creatorcontrib><creatorcontrib>Quinelato, Simone</creatorcontrib><creatorcontrib>Camargo, Mariana Guedes</creatorcontrib><creatorcontrib>de Sá, Fillipe Araujo</creatorcontrib><creatorcontrib>Angelo, Isabele da Costa</creatorcontrib><creatorcontrib>Martins, Marta Fonseca</creatorcontrib><creatorcontrib>Prata, Marcia Cristina de Azevedo</creatorcontrib><creatorcontrib>Bittencourt, Vânia Rita Elias Pinheiro</creatorcontrib><title>Lab-on-a-chip and SDS-PAGE analysis of hemolymph protein profile from Rhipicephalus microplus (Acari: Ixodidae) infected with entomopathogenic nematode and fungus</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>In the present study, lab-on-a-chip electrophoresis (LoaC) was suggested as an alternative method to the conventional polyacrylamide gel electrophoresis under denaturing conditions (SDS-PAGE) to analyze raw cell-free tick hemolymph.
Rhipicephalus microplus
females were exposed to the entomopathogenic fungus
Metarhizium anisopliae
senso latu IBCB 116 strain and/or to the entomopathogenic nematode
Heterorhabditis indica
LPP1 strain. Hemolymph from not exposed or exposed ticks was collected 16 and 24 h after exposure and analyze by SDS-PAGE or LoaC. SDS-PAGE yielded 15 bands and LoaC electrophoresis 17 bands. Despite the differences in the number of bands, when the hemolymph protein profiles of exposed or unexposed ticks were compared in the same method, no suppressing or additional bands were detected among the treatments regardless the method (i.e., SDS-PAGE or chip electrophoresis using the Protein 230 Kit®). The potential of LoaC electrophoresis to detect protein bands from tick hemolymph was considered more efficient in comparison to the detection obtained using the traditional SDS-PAGE method, especially when it comes to protein subunits heavier than 100 KDa. LoaC electrophoresis provided a very good reproducibility, and is much faster than the conventional SDS-PAGE method, which requires several hours for one analysis. Despite both methods can be used to analyze tick hemolymph composition, LoaC was considered more suitable for cell-free hemolymph protein separation and detection. LoaC hemolymph band percent data reported changes in key proteins (i.e., HeLp and vitellogenin) exceptionally important for tick embryogenesis. This study reported, for the first time, tick hemolymph protein profile using LoaC.</description><subject>Acari</subject><subject>Animals</subject><subject>Arthropod Proteins - chemistry</subject><subject>Arthropod Proteins - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Electrophoresis, Polyacrylamide Gel - instrumentation</subject><subject>Electrophoresis, Polyacrylamide Gel - methods</subject><subject>Female</subject><subject>Fungi - classification</subject><subject>Fungi - genetics</subject><subject>Fungi - isolation & purification</subject><subject>Fungi - physiology</subject><subject>Health aspects</subject><subject>Hemolymph - chemistry</subject><subject>Hemolymph - metabolism</subject><subject>Heterorhabditis indica</subject><subject>Immunology</subject><subject>Ixodidae</subject><subject>Lab-On-A-Chip Devices</subject><subject>Medical Microbiology</subject><subject>Membrane proteins</subject><subject>Metarhizium anisopliae</subject><subject>Microbiology</subject><subject>Nematoda</subject><subject>Nematoda - classification</subject><subject>Nematoda - genetics</subject><subject>Nematoda - isolation & purification</subject><subject>Nematoda - physiology</subject><subject>Original Paper</subject><subject>Reproducibility of Results</subject><subject>Rhipicephalus</subject><subject>Rhipicephalus - chemistry</subject><subject>Rhipicephalus - metabolism</subject><subject>Rhipicephalus - microbiology</subject><subject>Rhipicephalus - parasitology</subject><subject>Roundworms</subject><subject>Ticks</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFu1DAQhiMEokvhAbggH8vBxZN4HYfbqrSl0kogCmfLsccbV4kd4kSwfZw-KV62cETIh7Hl_x_N_F9RvAZ2DozV7xJjvBKUgaBrYA29f1KsgFclhWa9flqsWJPvDKA6KV6kdMcY1ILz58VJWUPNWSlWxcNWtzQGqqnp_Eh0sOT2wy39vLm-zA_d75NPJDrS4RD7_TB2ZJzijD4cqvM9EjfFgXzJZm9w7HS_JDJ4M8XxcDvbGD359-TmZ7TeanxLfHBoZrTkh587gmGOQxz13MUdBm9IwEHP0eLvSdwSdkt6WTxzuk_46rGeFt-uLr9efKTbT9c3F5stNRzETCs0pRNGCGmlAbS2hUairtdG20ZL0zqEmslKCwngWrRCalmbhtcOW4FNdVqcHfvmzb4vmGY1-GSw73XAuCQFUsgqR7iW_yEFKJuSlyJLz4_Sne5R5e3jPGmTj8UcUwx4CFFteM24kLxk2QBHQ84wpQmdGic_6GmvgKkDdnXErjJ2dcCu7rPnzeM8Szug_ev4wzkLyqMg5a-ww0ndxWXKfNM_uv4C-2C7Pg</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Golo, Patrícia Silva</creator><creator>dos Santos, Alessa Siqueira de Oliveira</creator><creator>Monteiro, Caio Marcio Oliveira</creator><creator>Perinotto, Wendell Marcelo de Souza</creator><creator>Quinelato, Simone</creator><creator>Camargo, Mariana Guedes</creator><creator>de Sá, Fillipe Araujo</creator><creator>Angelo, Isabele da Costa</creator><creator>Martins, Marta Fonseca</creator><creator>Prata, Marcia Cristina de Azevedo</creator><creator>Bittencourt, Vânia Rita Elias Pinheiro</creator><general>Springer Berlin Heidelberg</general><general>Springer</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><scope>7SS</scope><scope>M7N</scope></search><sort><creationdate>20160901</creationdate><title>Lab-on-a-chip and SDS-PAGE analysis of hemolymph protein profile from Rhipicephalus microplus (Acari: Ixodidae) infected with entomopathogenic nematode and fungus</title><author>Golo, Patrícia Silva ; dos Santos, Alessa Siqueira de Oliveira ; Monteiro, Caio Marcio Oliveira ; Perinotto, Wendell Marcelo de Souza ; Quinelato, Simone ; Camargo, Mariana Guedes ; de Sá, Fillipe Araujo ; Angelo, Isabele da Costa ; Martins, Marta Fonseca ; Prata, Marcia Cristina de Azevedo ; Bittencourt, Vânia Rita Elias Pinheiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-3ec2f6c668d8c1eddb198ea75cad9a8cbfe17083a6811fbed68a87c947feb6e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acari</topic><topic>Animals</topic><topic>Arthropod Proteins - chemistry</topic><topic>Arthropod Proteins - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Electrophoresis, Polyacrylamide Gel - instrumentation</topic><topic>Electrophoresis, Polyacrylamide Gel - methods</topic><topic>Female</topic><topic>Fungi - classification</topic><topic>Fungi - genetics</topic><topic>Fungi - isolation & purification</topic><topic>Fungi - physiology</topic><topic>Health aspects</topic><topic>Hemolymph - chemistry</topic><topic>Hemolymph - metabolism</topic><topic>Heterorhabditis indica</topic><topic>Immunology</topic><topic>Ixodidae</topic><topic>Lab-On-A-Chip Devices</topic><topic>Medical Microbiology</topic><topic>Membrane proteins</topic><topic>Metarhizium anisopliae</topic><topic>Microbiology</topic><topic>Nematoda</topic><topic>Nematoda - classification</topic><topic>Nematoda - genetics</topic><topic>Nematoda - isolation & purification</topic><topic>Nematoda - physiology</topic><topic>Original Paper</topic><topic>Reproducibility of Results</topic><topic>Rhipicephalus</topic><topic>Rhipicephalus - chemistry</topic><topic>Rhipicephalus - metabolism</topic><topic>Rhipicephalus - microbiology</topic><topic>Rhipicephalus - parasitology</topic><topic>Roundworms</topic><topic>Ticks</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Golo, Patrícia Silva</creatorcontrib><creatorcontrib>dos Santos, Alessa Siqueira de Oliveira</creatorcontrib><creatorcontrib>Monteiro, Caio Marcio Oliveira</creatorcontrib><creatorcontrib>Perinotto, Wendell Marcelo de Souza</creatorcontrib><creatorcontrib>Quinelato, Simone</creatorcontrib><creatorcontrib>Camargo, Mariana Guedes</creatorcontrib><creatorcontrib>de Sá, Fillipe Araujo</creatorcontrib><creatorcontrib>Angelo, Isabele da Costa</creatorcontrib><creatorcontrib>Martins, Marta Fonseca</creatorcontrib><creatorcontrib>Prata, Marcia Cristina de Azevedo</creatorcontrib><creatorcontrib>Bittencourt, Vânia Rita Elias Pinheiro</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><collection>Entomology Abstracts (Full archive)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Golo, Patrícia Silva</au><au>dos Santos, Alessa Siqueira de Oliveira</au><au>Monteiro, Caio Marcio Oliveira</au><au>Perinotto, Wendell Marcelo de Souza</au><au>Quinelato, Simone</au><au>Camargo, Mariana Guedes</au><au>de Sá, Fillipe Araujo</au><au>Angelo, Isabele da Costa</au><au>Martins, Marta Fonseca</au><au>Prata, Marcia Cristina de Azevedo</au><au>Bittencourt, Vânia Rita Elias Pinheiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lab-on-a-chip and SDS-PAGE analysis of hemolymph protein profile from Rhipicephalus microplus (Acari: Ixodidae) infected with entomopathogenic nematode and fungus</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>115</volume><issue>9</issue><spage>3459</spage><epage>3468</epage><pages>3459-3468</pages><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>In the present study, lab-on-a-chip electrophoresis (LoaC) was suggested as an alternative method to the conventional polyacrylamide gel electrophoresis under denaturing conditions (SDS-PAGE) to analyze raw cell-free tick hemolymph.
Rhipicephalus microplus
females were exposed to the entomopathogenic fungus
Metarhizium anisopliae
senso latu IBCB 116 strain and/or to the entomopathogenic nematode
Heterorhabditis indica
LPP1 strain. Hemolymph from not exposed or exposed ticks was collected 16 and 24 h after exposure and analyze by SDS-PAGE or LoaC. SDS-PAGE yielded 15 bands and LoaC electrophoresis 17 bands. Despite the differences in the number of bands, when the hemolymph protein profiles of exposed or unexposed ticks were compared in the same method, no suppressing or additional bands were detected among the treatments regardless the method (i.e., SDS-PAGE or chip electrophoresis using the Protein 230 Kit®). The potential of LoaC electrophoresis to detect protein bands from tick hemolymph was considered more efficient in comparison to the detection obtained using the traditional SDS-PAGE method, especially when it comes to protein subunits heavier than 100 KDa. LoaC electrophoresis provided a very good reproducibility, and is much faster than the conventional SDS-PAGE method, which requires several hours for one analysis. Despite both methods can be used to analyze tick hemolymph composition, LoaC was considered more suitable for cell-free hemolymph protein separation and detection. LoaC hemolymph band percent data reported changes in key proteins (i.e., HeLp and vitellogenin) exceptionally important for tick embryogenesis. This study reported, for the first time, tick hemolymph protein profile using LoaC.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>27174026</pmid><doi>10.1007/s00436-016-5109-z</doi><tpages>10</tpages></addata></record> |
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ispartof | Parasitology research (1987), 2016-09, Vol.115 (9), p.3459-3468 |
issn | 0932-0113 1432-1955 |
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source | MEDLINE; SpringerLink Journals |
subjects | Acari Animals Arthropod Proteins - chemistry Arthropod Proteins - metabolism Biomedical and Life Sciences Biomedicine Electrophoresis, Polyacrylamide Gel - instrumentation Electrophoresis, Polyacrylamide Gel - methods Female Fungi - classification Fungi - genetics Fungi - isolation & purification Fungi - physiology Health aspects Hemolymph - chemistry Hemolymph - metabolism Heterorhabditis indica Immunology Ixodidae Lab-On-A-Chip Devices Medical Microbiology Membrane proteins Metarhizium anisopliae Microbiology Nematoda Nematoda - classification Nematoda - genetics Nematoda - isolation & purification Nematoda - physiology Original Paper Reproducibility of Results Rhipicephalus Rhipicephalus - chemistry Rhipicephalus - metabolism Rhipicephalus - microbiology Rhipicephalus - parasitology Roundworms Ticks |
title | Lab-on-a-chip and SDS-PAGE analysis of hemolymph protein profile from Rhipicephalus microplus (Acari: Ixodidae) infected with entomopathogenic nematode and fungus |
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