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Plasmodium vivax transcriptomics: What is new?
Malaria is the leading human parasitosis and is transmitted through the bite of anopheline mosquitoes infected with parasites of the genus Plasmodium spp. Among the seven species that cause malaria in humans, Plasmodium vivax is the most prevalent species in Latin America. In recent years, there hav...
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Published in: | Experimental Biology and Medicine 2023-10, Vol.248 (19), p.1645-1656 |
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description | Malaria is the leading human parasitosis and is transmitted through the bite of anopheline mosquitoes infected with parasites of the genus Plasmodium spp. Among the seven species that cause malaria in humans, Plasmodium vivax is the most prevalent species in Latin America. In recent years, there have been an increasing number of reports of clinical complications caused by P. vivax infections, which were previously neglected and underestimated. P. vivax biology remains with large gaps. The emergence of next-generation sequencing technology has ensured a breakthrough in species knowledge. Coupled with this, the deposition of the P. vivax Sal-1 reference genome allowed an increase in transcriptomics projects by accessing messenger RNA. Thus, the regulation of differential gene expression according to the parasite life stage was verified, and several expressed genes were linked to different biological functions. Today, with the progress associated with RNA sequencing technologies, it is possible to detect nuances and obtain robust results. Discoveries provided by transcriptomic studies allow us to understand topics such as RNA expression and regulation and proteins and metabolic pathways involved during different stages of the parasite life cycle. The information obtained enables a better comprehension of immune system evasion mechanisms; invasion and adhesion strategies used by the parasite; as well as new vaccine targets, potential molecular markers, and others therapeutic targets. In this review, we provide new insights into P. vivax biology by summarizing recent findings in transcriptomic studies. |
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In recent years, there have been an increasing number of reports of clinical complications caused by P. vivax infections, which were previously neglected and underestimated. P. vivax biology remains with large gaps. The emergence of next-generation sequencing technology has ensured a breakthrough in species knowledge. Coupled with this, the deposition of the P. vivax Sal-1 reference genome allowed an increase in transcriptomics projects by accessing messenger RNA. Thus, the regulation of differential gene expression according to the parasite life stage was verified, and several expressed genes were linked to different biological functions. Today, with the progress associated with RNA sequencing technologies, it is possible to detect nuances and obtain robust results. Discoveries provided by transcriptomic studies allow us to understand topics such as RNA expression and regulation and proteins and metabolic pathways involved during different stages of the parasite life cycle. The information obtained enables a better comprehension of immune system evasion mechanisms; invasion and adhesion strategies used by the parasite; as well as new vaccine targets, potential molecular markers, and others therapeutic targets. 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The information obtained enables a better comprehension of immune system evasion mechanisms; invasion and adhesion strategies used by the parasite; as well as new vaccine targets, potential molecular markers, and others therapeutic targets. In this review, we provide new insights into P. vivax biology by summarizing recent findings in transcriptomic studies.</description><subject>Animals</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Malaria</subject><subject>Malaria, Vivax - genetics</subject><subject>Malaria, Vivax - parasitology</subject><subject>Minireview</subject><subject>Parasites</subject><subject>Plasmodium vivax - genetics</subject><issn>1535-3702</issn><issn>1535-3699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kF1LwzAUhoMobk5_gDfSS28689E0rTdDhl8w0AvFy5C2p1tG28ykrfrvzdgHiiAhnEPyvO85vAidEzwmRIgrwhlnAlPKCEkTLPABGq7fQhan6eGu98AAnTi3xJhwQeNjNGBCJHHK-RCNnyvlalPorg563avPoLWqcbnVq9bUOnfXwdtCtYF2QQMfk1N0VKrKwdm2jtDr3e3L9CGcPd0_Tm9mYc6ipA2zrMRZRAvOIIJUYV5EOKJpTAGrCIMSZUYSFRMF3JeyjKi_JYmFyCABztgITTa-qy6rocih8WtVcmV1reyXNErL3z-NXsi56SXBgjLszwhdbh2see_AtbLWLoeqUg2YzkmaCEoSzAXxKNmguTXOWSj3cwiW66Dln6C95uLngnvFLlkPjDeAU3OQS9PZxgf2j-M3j5qGAA</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Ferraboli, Julia Weber</creator><creator>Soares da Veiga, Gisele Tatiane</creator><creator>Albrecht, Letusa</creator><general>SAGE Publications</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>5PM</scope><orcidid>https://orcid.org/0009-0001-8652-9997</orcidid><orcidid>https://orcid.org/0000-0001-6406-2057</orcidid><orcidid>https://orcid.org/0000-0003-1434-0922</orcidid></search><sort><creationdate>20231001</creationdate><title>Plasmodium vivax transcriptomics: What is new?</title><author>Ferraboli, Julia Weber ; Soares da Veiga, Gisele Tatiane ; Albrecht, Letusa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-bbf0b42d53e4e9a05d4042962e0a40ea7fb18a61ae58a6ff42ff4f1677be8e533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Malaria</topic><topic>Malaria, Vivax - genetics</topic><topic>Malaria, Vivax - parasitology</topic><topic>Minireview</topic><topic>Parasites</topic><topic>Plasmodium vivax - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferraboli, Julia Weber</creatorcontrib><creatorcontrib>Soares da Veiga, Gisele Tatiane</creatorcontrib><creatorcontrib>Albrecht, Letusa</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>PubMed Central (Full Participant titles)</collection><jtitle>Experimental Biology and Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferraboli, Julia Weber</au><au>Soares da Veiga, Gisele Tatiane</au><au>Albrecht, Letusa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasmodium vivax transcriptomics: What is new?</atitle><jtitle>Experimental Biology and Medicine</jtitle><addtitle>Exp Biol Med (Maywood)</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>248</volume><issue>19</issue><spage>1645</spage><epage>1656</epage><pages>1645-1656</pages><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>Malaria is the leading human parasitosis and is transmitted through the bite of anopheline mosquitoes infected with parasites of the genus Plasmodium spp. Among the seven species that cause malaria in humans, Plasmodium vivax is the most prevalent species in Latin America. 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subjects | Animals Gene Expression Profiling Humans Malaria Malaria, Vivax - genetics Malaria, Vivax - parasitology Minireview Parasites Plasmodium vivax - genetics |
title | Plasmodium vivax transcriptomics: What is new? |
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