Divergence in toxin antigenicity and venom enzymes in Tityus melici, a medically important scorpion, despite transcriptomic and phylogenetic affinities with problematic Brazilian species
The Brazilian scorpion Tityus melici, native to Minas Gerais and Bahia, is morphologically related to Tityus serrulatus, the most medically significant species in Brazil. Despite inhabiting scorpion-envenomation endemic regions, T. melici venom remains unexplored. This work evaluates T. melici venom...
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creator | Kalapothakis, Yan Miranda, Kelton Aragão, Matheus Larangote, Débora Braga-Pereira, Gracielle Noetzold, Marina Molina, Denis Langer, Rafael Conceição, Izabela Mamede Guerra-Duarte, Clara Chávez-Olórtegui, Carlos Kalapothakis, Evanguedes Borges, Adolfo |
description | The Brazilian scorpion Tityus melici, native to Minas Gerais and Bahia, is morphologically related to Tityus serrulatus, the most medically significant species in Brazil. Despite inhabiting scorpion-envenomation endemic regions, T. melici venom remains unexplored. This work evaluates T. melici venom composition and function using transcriptomics, enzymatic activities, and in vivo and in vitro immunological analyses. Next-Generation Sequencing unveiled 86 components putatively involved in venom toxicity: 39 toxins, 28 metalloproteases, seven disulfide isomerases, six hyaluronidases, three phospholipases and three amidating enzymes. T. serrulatus showed the highest number of toxin matches with 80–100 % sequence similarity. T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice. We demonstrated venom phospholipase A2 activity, and elevated hyaluronidase and metalloprotease activities compared to T. serrulatus, paralleling our transcriptomic findings. Comparison of transcriptional levels for T. serrulatus and T. melici venom metalloenzymes suggests species-specific expression patterns in Tityus. Despite close phylogenetic association with T. serrulatus inferred from COI sequences and toxin similarities, partial neutralization of T. melici venom toxicity was achieved when using the anti-T. serrulatus antivenom, implying antigenic divergence among their toxins. We suggest that the Brazilian therapeutic scorpion antivenom could be improved to effectively neutralize T. melici venom.
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•T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice.•Next-Generation Sequencing revealed 86 components potentially involved in toxicity.•High hyaluronidase and proteolytic activity were found compared to T. serrulatus.•Venom lethality was partially neutralized by the anti-T. serrulatus antivenom.•Diverse metalloenzyme transcriptional levels were noted compared to T. serrulatus. |
doi_str_mv | 10.1016/j.ijbiomac.2024.130311 |
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•T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice.•Next-Generation Sequencing revealed 86 components potentially involved in toxicity.•High hyaluronidase and proteolytic activity were found compared to T. serrulatus.•Venom lethality was partially neutralized by the anti-T. serrulatus antivenom.•Diverse metalloenzyme transcriptional levels were noted compared to T. serrulatus.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2024.130311</identifier><identifier>PMID: 38403220</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Animals ; Animals, Poisonous ; Antivenins ; antivenoms ; Brazil ; Cytochrome oxidase ; disulfides ; Gene Expression Profiling ; hyaluronoglucosaminidase ; Hyaluronoglucosaminidase - genetics ; Hyaluronoglucosaminidase - metabolism ; isomerases ; metalloproteinases ; Mice ; neutralization ; phospholipase A2 ; phospholipases ; Phylogeny ; Scorpion antivenom ; Scorpion Venoms - genetics ; Scorpion Venoms - metabolism ; Scorpions - genetics ; sequence homology ; species ; therapeutics ; Tityus ; Tityus serrulatus ; toxicity ; Toxin divergence ; toxins ; Toxins, Biological ; transcription (genetics) ; Transcriptome ; transcriptomics ; Venom neutralization ; Venom toxicity ; Venoms</subject><ispartof>International journal of biological macromolecules, 2024-04, Vol.263 (Pt 2), p.130311-130311, Article 130311</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c348t-f8e29e26a25ccf654d4539a3f8867e1b28855f286ea3069604226b20fe690d733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0141813024011140$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38403220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kalapothakis, Yan</creatorcontrib><creatorcontrib>Miranda, Kelton</creatorcontrib><creatorcontrib>Aragão, Matheus</creatorcontrib><creatorcontrib>Larangote, Débora</creatorcontrib><creatorcontrib>Braga-Pereira, Gracielle</creatorcontrib><creatorcontrib>Noetzold, Marina</creatorcontrib><creatorcontrib>Molina, Denis</creatorcontrib><creatorcontrib>Langer, Rafael</creatorcontrib><creatorcontrib>Conceição, Izabela Mamede</creatorcontrib><creatorcontrib>Guerra-Duarte, Clara</creatorcontrib><creatorcontrib>Chávez-Olórtegui, Carlos</creatorcontrib><creatorcontrib>Kalapothakis, Evanguedes</creatorcontrib><creatorcontrib>Borges, Adolfo</creatorcontrib><title>Divergence in toxin antigenicity and venom enzymes in Tityus melici, a medically important scorpion, despite transcriptomic and phylogenetic affinities with problematic Brazilian species</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>The Brazilian scorpion Tityus melici, native to Minas Gerais and Bahia, is morphologically related to Tityus serrulatus, the most medically significant species in Brazil. Despite inhabiting scorpion-envenomation endemic regions, T. melici venom remains unexplored. This work evaluates T. melici venom composition and function using transcriptomics, enzymatic activities, and in vivo and in vitro immunological analyses. Next-Generation Sequencing unveiled 86 components putatively involved in venom toxicity: 39 toxins, 28 metalloproteases, seven disulfide isomerases, six hyaluronidases, three phospholipases and three amidating enzymes. T. serrulatus showed the highest number of toxin matches with 80–100 % sequence similarity. T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice. We demonstrated venom phospholipase A2 activity, and elevated hyaluronidase and metalloprotease activities compared to T. serrulatus, paralleling our transcriptomic findings. Comparison of transcriptional levels for T. serrulatus and T. melici venom metalloenzymes suggests species-specific expression patterns in Tityus. Despite close phylogenetic association with T. serrulatus inferred from COI sequences and toxin similarities, partial neutralization of T. melici venom toxicity was achieved when using the anti-T. serrulatus antivenom, implying antigenic divergence among their toxins. We suggest that the Brazilian therapeutic scorpion antivenom could be improved to effectively neutralize T. melici venom.
[Display omitted]
•T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice.•Next-Generation Sequencing revealed 86 components potentially involved in toxicity.•High hyaluronidase and proteolytic activity were found compared to T. serrulatus.•Venom lethality was partially neutralized by the anti-T. serrulatus antivenom.•Diverse metalloenzyme transcriptional levels were noted compared to T. serrulatus.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Animals, Poisonous</subject><subject>Antivenins</subject><subject>antivenoms</subject><subject>Brazil</subject><subject>Cytochrome oxidase</subject><subject>disulfides</subject><subject>Gene Expression Profiling</subject><subject>hyaluronoglucosaminidase</subject><subject>Hyaluronoglucosaminidase - genetics</subject><subject>Hyaluronoglucosaminidase - metabolism</subject><subject>isomerases</subject><subject>metalloproteinases</subject><subject>Mice</subject><subject>neutralization</subject><subject>phospholipase A2</subject><subject>phospholipases</subject><subject>Phylogeny</subject><subject>Scorpion antivenom</subject><subject>Scorpion Venoms - genetics</subject><subject>Scorpion Venoms - metabolism</subject><subject>Scorpions - genetics</subject><subject>sequence homology</subject><subject>species</subject><subject>therapeutics</subject><subject>Tityus</subject><subject>Tityus serrulatus</subject><subject>toxicity</subject><subject>Toxin divergence</subject><subject>toxins</subject><subject>Toxins, Biological</subject><subject>transcription (genetics)</subject><subject>Transcriptome</subject><subject>transcriptomics</subject><subject>Venom neutralization</subject><subject>Venom toxicity</subject><subject>Venoms</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1v1DAQtRCILoW_UPnIoVn8kXidG1A-pUpcytlynAmdVWIH27uQ_jR-HQ7bcu3F9sy8ec96j5ALzraccfVmv8V9h2GybiuYqLdcMsn5E7LhetdWjDH5lGwYr3mly-iMvEhpX7qq4fo5OZO6ZlIItiF_PuAR4g_wDih6msPvclqfsbTQYV5K0dMj-DBR8HfLBGnF3ZTJIdEJxgK6pLa8enR2HBeK0xxiLhQ0uRBnDP6S9pBmzEBztD65iHMOE7p_1PPtMoYiBnltDAN6zFhEfmG-pXMM3QiTXWfvo73DEa2naQZXIC_Js8GOCV7d3-fk-6ePN1dfqutvn79evbuunKx1rgYNogWhrGicG1RT93UjWysHrdUOeCe0bppBaAVWMtUqVguhOsEGUC3rd1Kek9cn3vKbnwdI2UyYHIyj9RAOyUjeyKZt2uL5Y1DRSsH4TrGVVZ2gLoaUIgxmjjjZuBjOzBqx2ZuHiM0asTlFXBYv7jUOXXH9_9pDpgXw9gSAYsoRIZpU7CoB9xjBZdMHfEzjL_KDvxM</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Kalapothakis, Yan</creator><creator>Miranda, Kelton</creator><creator>Aragão, Matheus</creator><creator>Larangote, Débora</creator><creator>Braga-Pereira, Gracielle</creator><creator>Noetzold, Marina</creator><creator>Molina, Denis</creator><creator>Langer, Rafael</creator><creator>Conceição, Izabela Mamede</creator><creator>Guerra-Duarte, Clara</creator><creator>Chávez-Olórtegui, Carlos</creator><creator>Kalapothakis, Evanguedes</creator><creator>Borges, Adolfo</creator><general>Elsevier B.V</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>7S9</scope><scope>L.6</scope></search><sort><creationdate>202404</creationdate><title>Divergence in toxin antigenicity and venom enzymes in Tityus melici, a medically important scorpion, despite transcriptomic and phylogenetic affinities with problematic Brazilian species</title><author>Kalapothakis, Yan ; Miranda, Kelton ; Aragão, Matheus ; Larangote, Débora ; Braga-Pereira, Gracielle ; Noetzold, Marina ; Molina, Denis ; Langer, Rafael ; Conceição, Izabela Mamede ; Guerra-Duarte, Clara ; Chávez-Olórtegui, Carlos ; Kalapothakis, Evanguedes ; Borges, Adolfo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-f8e29e26a25ccf654d4539a3f8867e1b28855f286ea3069604226b20fe690d733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Animals, Poisonous</topic><topic>Antivenins</topic><topic>antivenoms</topic><topic>Brazil</topic><topic>Cytochrome oxidase</topic><topic>disulfides</topic><topic>Gene Expression Profiling</topic><topic>hyaluronoglucosaminidase</topic><topic>Hyaluronoglucosaminidase - genetics</topic><topic>Hyaluronoglucosaminidase - metabolism</topic><topic>isomerases</topic><topic>metalloproteinases</topic><topic>Mice</topic><topic>neutralization</topic><topic>phospholipase A2</topic><topic>phospholipases</topic><topic>Phylogeny</topic><topic>Scorpion antivenom</topic><topic>Scorpion Venoms - genetics</topic><topic>Scorpion Venoms - metabolism</topic><topic>Scorpions - genetics</topic><topic>sequence homology</topic><topic>species</topic><topic>therapeutics</topic><topic>Tityus</topic><topic>Tityus serrulatus</topic><topic>toxicity</topic><topic>Toxin divergence</topic><topic>toxins</topic><topic>Toxins, Biological</topic><topic>transcription (genetics)</topic><topic>Transcriptome</topic><topic>transcriptomics</topic><topic>Venom neutralization</topic><topic>Venom toxicity</topic><topic>Venoms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalapothakis, Yan</creatorcontrib><creatorcontrib>Miranda, Kelton</creatorcontrib><creatorcontrib>Aragão, Matheus</creatorcontrib><creatorcontrib>Larangote, Débora</creatorcontrib><creatorcontrib>Braga-Pereira, Gracielle</creatorcontrib><creatorcontrib>Noetzold, Marina</creatorcontrib><creatorcontrib>Molina, Denis</creatorcontrib><creatorcontrib>Langer, Rafael</creatorcontrib><creatorcontrib>Conceição, Izabela Mamede</creatorcontrib><creatorcontrib>Guerra-Duarte, Clara</creatorcontrib><creatorcontrib>Chávez-Olórtegui, Carlos</creatorcontrib><creatorcontrib>Kalapothakis, Evanguedes</creatorcontrib><creatorcontrib>Borges, Adolfo</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>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalapothakis, Yan</au><au>Miranda, Kelton</au><au>Aragão, Matheus</au><au>Larangote, Débora</au><au>Braga-Pereira, Gracielle</au><au>Noetzold, Marina</au><au>Molina, Denis</au><au>Langer, Rafael</au><au>Conceição, Izabela Mamede</au><au>Guerra-Duarte, Clara</au><au>Chávez-Olórtegui, Carlos</au><au>Kalapothakis, Evanguedes</au><au>Borges, Adolfo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergence in toxin antigenicity and venom enzymes in Tityus melici, a medically important scorpion, despite transcriptomic and phylogenetic affinities with problematic Brazilian species</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2024-04</date><risdate>2024</risdate><volume>263</volume><issue>Pt 2</issue><spage>130311</spage><epage>130311</epage><pages>130311-130311</pages><artnum>130311</artnum><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>The Brazilian scorpion Tityus melici, native to Minas Gerais and Bahia, is morphologically related to Tityus serrulatus, the most medically significant species in Brazil. Despite inhabiting scorpion-envenomation endemic regions, T. melici venom remains unexplored. This work evaluates T. melici venom composition and function using transcriptomics, enzymatic activities, and in vivo and in vitro immunological analyses. Next-Generation Sequencing unveiled 86 components putatively involved in venom toxicity: 39 toxins, 28 metalloproteases, seven disulfide isomerases, six hyaluronidases, three phospholipases and three amidating enzymes. T. serrulatus showed the highest number of toxin matches with 80–100 % sequence similarity. T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice. We demonstrated venom phospholipase A2 activity, and elevated hyaluronidase and metalloprotease activities compared to T. serrulatus, paralleling our transcriptomic findings. Comparison of transcriptional levels for T. serrulatus and T. melici venom metalloenzymes suggests species-specific expression patterns in Tityus. Despite close phylogenetic association with T. serrulatus inferred from COI sequences and toxin similarities, partial neutralization of T. melici venom toxicity was achieved when using the anti-T. serrulatus antivenom, implying antigenic divergence among their toxins. We suggest that the Brazilian therapeutic scorpion antivenom could be improved to effectively neutralize T. melici venom.
[Display omitted]
•T. melici is of medical importance as it has a venom LD50 of 0.85 mg/kg in mice.•Next-Generation Sequencing revealed 86 components potentially involved in toxicity.•High hyaluronidase and proteolytic activity were found compared to T. serrulatus.•Venom lethality was partially neutralized by the anti-T. serrulatus antivenom.•Diverse metalloenzyme transcriptional levels were noted compared to T. serrulatus.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38403220</pmid><doi>10.1016/j.ijbiomac.2024.130311</doi><tpages>1</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Animals, Poisonous Antivenins antivenoms Brazil Cytochrome oxidase disulfides Gene Expression Profiling hyaluronoglucosaminidase Hyaluronoglucosaminidase - genetics Hyaluronoglucosaminidase - metabolism isomerases metalloproteinases Mice neutralization phospholipase A2 phospholipases Phylogeny Scorpion antivenom Scorpion Venoms - genetics Scorpion Venoms - metabolism Scorpions - genetics sequence homology species therapeutics Tityus Tityus serrulatus toxicity Toxin divergence toxins Toxins, Biological transcription (genetics) Transcriptome transcriptomics Venom neutralization Venom toxicity Venoms |
title | Divergence in toxin antigenicity and venom enzymes in Tityus melici, a medically important scorpion, despite transcriptomic and phylogenetic affinities with problematic Brazilian species |
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