Adeel Mumtaz Abbasi, Shiza Nasir, Amna Arshad Bajwa, Haroon Akbar, Sara Artigas-Jerónimo, Clara Muñoz-Hernández, Marta Sánchez-Sánchez, Alberto Moraga-Fernández, Isabel G. Fernández de Mera, José de la Fuente, Muhammad Imran Rashid
{"title":"从头组装Hyalomma anatolicum的sialotranscriptome并深入了解其对环状毛癣菌感染的反应表达动态","authors":"Adeel Mumtaz Abbasi, Shiza Nasir, Amna Arshad Bajwa, Haroon Akbar, Sara Artigas-Jerónimo, Clara Muñoz-Hernández, Marta Sánchez-Sánchez, Alberto Moraga-Fernández, Isabel G. Fernández de Mera, José de la Fuente, Muhammad Imran Rashid","doi":"10.1007/s10493-024-00962-z","DOIUrl":null,"url":null,"abstract":"<p><i>Hyalomma anatolicum</i> is a tick of significant one-health importance due to its role as a vector for various pathogens affecting humans, animals and the environment, such as <i>Theileria annulata</i>, which causes tropical theileriosis in cattle, leading to severe economic losses. When infected with pathogens like <i>T. annulata</i>, the salivary glands of <i>H. anatolicum</i> undergo gene expression changes, secrete modified proteins and activate immune responses, all of which facilitate pathogen survival and transmission by modulating the host immune response and optimizing conditions for pathogen development. Understanding these responses is crucial for developing control strategies for tick-borne diseases. To understand the interaction between <i>H. anatolicum</i> and <i>T. annulata,</i> we performed a differential gene expression analysis of <i>H. anatolicum</i> salivary glands. An average of approximately 25 million raw sequencing reads were generated in each replicate using Illumina Sequencing. The sequenced reads were de novo assembled and the assembled transcriptome yielded approximately 50,231 non-redundant transcripts after clustering with CD-HIT using a sequence identity of 95% and alignment coverage of 90%. The assembly quality was evaluated with BUSCO analysis and found to be 86% complete using the Arachnida dataset and then blasted against non-redundant protein sequence database from NCBI followed by counting of reads and differential expression analysis. Overall, around 2400 and 400 genes were found differentially expressed with logFC > 1 and logFC > 2 respectively at FDR < 0.05. Top up-regulated genes included Calpain, Papilin, Neprilysin, and Ankyrin repeat-containing protein. Top down-regulated genes included Scoloptoxin, and Selenoprotein S and other uncharacterized proteins. Many other up-regulated proteins with high significance were uncharacterized suggesting room for further <i>H. anatolicum</i> functional and structural characterization studies. To our best knowledge, this is the first study of <i>H. anatolicum</i> sialotranscriptome which greatly contributes to sialotranscriptome information not only as sequence database but also indicates the potential targets for development of vaccine against ticks and transmission-blocking vaccines against <i>T. annulata</i>.</p>","PeriodicalId":12088,"journal":{"name":"Experimental and Applied Acarology","volume":"19 1","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"De novo assembly of sialotranscriptome of Hyalomma anatolicum and insights into expression dynamics in response to Theileria annulata infection\",\"authors\":\"Adeel Mumtaz Abbasi, Shiza Nasir, Amna Arshad Bajwa, Haroon Akbar, Sara Artigas-Jerónimo, Clara Muñoz-Hernández, Marta Sánchez-Sánchez, Alberto Moraga-Fernández, Isabel G. Fernández de Mera, José de la Fuente, Muhammad Imran Rashid\",\"doi\":\"10.1007/s10493-024-00962-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><i>Hyalomma anatolicum</i> is a tick of significant one-health importance due to its role as a vector for various pathogens affecting humans, animals and the environment, such as <i>Theileria annulata</i>, which causes tropical theileriosis in cattle, leading to severe economic losses. When infected with pathogens like <i>T. annulata</i>, the salivary glands of <i>H. anatolicum</i> undergo gene expression changes, secrete modified proteins and activate immune responses, all of which facilitate pathogen survival and transmission by modulating the host immune response and optimizing conditions for pathogen development. Understanding these responses is crucial for developing control strategies for tick-borne diseases. To understand the interaction between <i>H. anatolicum</i> and <i>T. annulata,</i> we performed a differential gene expression analysis of <i>H. anatolicum</i> salivary glands. An average of approximately 25 million raw sequencing reads were generated in each replicate using Illumina Sequencing. The sequenced reads were de novo assembled and the assembled transcriptome yielded approximately 50,231 non-redundant transcripts after clustering with CD-HIT using a sequence identity of 95% and alignment coverage of 90%. The assembly quality was evaluated with BUSCO analysis and found to be 86% complete using the Arachnida dataset and then blasted against non-redundant protein sequence database from NCBI followed by counting of reads and differential expression analysis. Overall, around 2400 and 400 genes were found differentially expressed with logFC > 1 and logFC > 2 respectively at FDR < 0.05. Top up-regulated genes included Calpain, Papilin, Neprilysin, and Ankyrin repeat-containing protein. Top down-regulated genes included Scoloptoxin, and Selenoprotein S and other uncharacterized proteins. Many other up-regulated proteins with high significance were uncharacterized suggesting room for further <i>H. anatolicum</i> functional and structural characterization studies. 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De novo assembly of sialotranscriptome of Hyalomma anatolicum and insights into expression dynamics in response to Theileria annulata infection
Hyalomma anatolicum is a tick of significant one-health importance due to its role as a vector for various pathogens affecting humans, animals and the environment, such as Theileria annulata, which causes tropical theileriosis in cattle, leading to severe economic losses. When infected with pathogens like T. annulata, the salivary glands of H. anatolicum undergo gene expression changes, secrete modified proteins and activate immune responses, all of which facilitate pathogen survival and transmission by modulating the host immune response and optimizing conditions for pathogen development. Understanding these responses is crucial for developing control strategies for tick-borne diseases. To understand the interaction between H. anatolicum and T. annulata, we performed a differential gene expression analysis of H. anatolicum salivary glands. An average of approximately 25 million raw sequencing reads were generated in each replicate using Illumina Sequencing. The sequenced reads were de novo assembled and the assembled transcriptome yielded approximately 50,231 non-redundant transcripts after clustering with CD-HIT using a sequence identity of 95% and alignment coverage of 90%. The assembly quality was evaluated with BUSCO analysis and found to be 86% complete using the Arachnida dataset and then blasted against non-redundant protein sequence database from NCBI followed by counting of reads and differential expression analysis. Overall, around 2400 and 400 genes were found differentially expressed with logFC > 1 and logFC > 2 respectively at FDR < 0.05. Top up-regulated genes included Calpain, Papilin, Neprilysin, and Ankyrin repeat-containing protein. Top down-regulated genes included Scoloptoxin, and Selenoprotein S and other uncharacterized proteins. Many other up-regulated proteins with high significance were uncharacterized suggesting room for further H. anatolicum functional and structural characterization studies. To our best knowledge, this is the first study of H. anatolicum sialotranscriptome which greatly contributes to sialotranscriptome information not only as sequence database but also indicates the potential targets for development of vaccine against ticks and transmission-blocking vaccines against T. annulata.
期刊介绍:
Experimental and Applied Acarology publishes peer-reviewed original papers describing advances in basic and applied research on mites and ticks. Coverage encompasses all Acari, including those of environmental, agricultural, medical and veterinary importance, and all the ways in which they interact with other organisms (plants, arthropods and other animals). The subject matter draws upon a wide variety of disciplines, including evolutionary biology, ecology, epidemiology, physiology, biochemistry, toxicology, immunology, genetics, molecular biology and pest management sciences.