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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Veröffentlicht in:International journal of biological macromolecules 2024-04, Vol.263 (Pt 2), p.130311-130311, Article 130311
Hauptverfasser: 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
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container_end_page 130311
container_issue Pt 2
container_start_page 130311
container_title International journal of biological macromolecules
container_volume 263
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. [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.
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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><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. 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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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