Zeinab Aboezz, Hassan M Mahsoub, Ehab El-Nahas, Saad Sharawi, Ayman S El-Habbaa, Gabr F El-Bagoury, Frank W Pierson
{"title":"Toward a transcriptional map of the turkey adenovirus 3 (TAdV-3) genome.","authors":"Zeinab Aboezz, Hassan M Mahsoub, Ehab El-Nahas, Saad Sharawi, Ayman S El-Habbaa, Gabr F El-Bagoury, Frank W Pierson","doi":"10.1080/03079457.2026.2658512","DOIUrl":null,"url":null,"abstract":"<p><p>Turkey adenovirus 3 (TAdV-3), <i>Siadenovirus gallopavotertii</i>, historically referred to as turkey haemorrhagic enteritis virus (THEV), causes immunosuppression and haemorrhagic enteritis in turkey poults. Although an avirulent TAdV-3 strain is used as a live vaccine, its immunosuppressive properties remain poorly understood at the molecular level. Here, we employed Rapid Amplification of cDNA Ends (RACE) and Sanger sequencing to generate a transcriptomic map of TAdV-3 in infected MDTC-RP19 cells at 24 h post infection. Using RACE and virus-specific primers, we obtained full-length annotation of 14 out of 23 predicted viral transcripts. Analysis of late structural genes revealed a conserved tripartite leader (TPL) sequence shared across all late transcripts, providing new insights into their transcription start sites, splicing events, and promoter architecture. Additionally, we identified alternative leader exons - for instance, DBP mRNA contains a bipartite leader, whereas <i>Hyd</i> mRNA utilizes the TPL - and observed coordinated 3' end processing via shared polyadenylation signals between certain transcripts (e.g. ORF1 and <i>Hyd</i>). This precise annotation of TAdV-3 mRNAs lays the groundwork for linking transcript structure to protein function, enhancing our understanding of TAdV-3's immunosuppressive strategies and informing future development of TAdV-3 based gene delivery platforms.</p>","PeriodicalId":8788,"journal":{"name":"Avian Pathology","volume":" ","pages":"380-388"},"PeriodicalIF":2.7000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Avian Pathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1080/03079457.2026.2658512","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Turkey adenovirus 3 (TAdV-3), Siadenovirus gallopavotertii, historically referred to as turkey haemorrhagic enteritis virus (THEV), causes immunosuppression and haemorrhagic enteritis in turkey poults. Although an avirulent TAdV-3 strain is used as a live vaccine, its immunosuppressive properties remain poorly understood at the molecular level. Here, we employed Rapid Amplification of cDNA Ends (RACE) and Sanger sequencing to generate a transcriptomic map of TAdV-3 in infected MDTC-RP19 cells at 24 h post infection. Using RACE and virus-specific primers, we obtained full-length annotation of 14 out of 23 predicted viral transcripts. Analysis of late structural genes revealed a conserved tripartite leader (TPL) sequence shared across all late transcripts, providing new insights into their transcription start sites, splicing events, and promoter architecture. Additionally, we identified alternative leader exons - for instance, DBP mRNA contains a bipartite leader, whereas Hyd mRNA utilizes the TPL - and observed coordinated 3' end processing via shared polyadenylation signals between certain transcripts (e.g. ORF1 and Hyd). This precise annotation of TAdV-3 mRNAs lays the groundwork for linking transcript structure to protein function, enhancing our understanding of TAdV-3's immunosuppressive strategies and informing future development of TAdV-3 based gene delivery platforms.
期刊介绍:
Avian Pathology is the official journal of the World Veterinary Poultry Association and, since its first publication in 1972, has been a leading international journal for poultry disease scientists. It publishes material relevant to the entire field of infectious and non-infectious diseases of poultry and other birds. Accepted manuscripts will contribute novel data of interest to an international readership and will add significantly to knowledge and understanding of diseases, old or new. Subject areas include pathology, diagnosis, detection and characterisation of pathogens, infections of possible zoonotic importance, epidemiology, innate and immune responses, vaccines, gene sequences, genetics in relation to disease and physiological and biochemical changes in response to disease. First and subsequent reports of well-recognized diseases within a country are not acceptable unless they also include substantial new information about the disease or pathogen. Manuscripts on wild or pet birds should describe disease or pathogens in a significant number of birds, recognizing/suggesting serious potential impact on that species or that the disease or pathogen is of demonstrable relevance to poultry. Manuscripts on food-borne microorganisms acquired during or after processing, and those that catalogue the occurrence or properties of microorganisms, are unlikely to be considered for publication in the absence of data linking them to avian disease.