Next Article in Journal
A Pre- and Within-Pandemic Survey of SARS-CoV-2 RNA in Saliva Swabs from Stray Cats in Switzerland
Previous Article in Journal
Variation in Thermal Stability among Respiratory Syncytial Virus Clinical Isolates under Non-Freezing Conditions
Previous Article in Special Issue
High Phenotypic Variation between an In Vitro-Passaged Fowl Adenovirus Serotype 1 (FAdV-1) and Its Virulent Progenitor Strain despite Almost Complete Sequence Identity of the Whole Genomes
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Special Issue: Avian Adenoviruses

1
Christian Doppler Laboratory for Innovative Poultry Vaccines (IPOV), University of Veterinary Medicine, 1210 Vienna, Austria
2
Clinic for Poultry and Fish Medicine, Department for Farm Animals and Veterinary Public Health, University of Veterinary Medicine (Vetmeduni Vienna), 1210 Vienna, Austria
*
Author to whom correspondence should be addressed.
Viruses 2022, 14(4), 680; https://doi.org/10.3390/v14040680
Submission received: 18 March 2022 / Accepted: 24 March 2022 / Published: 25 March 2022
(This article belongs to the Special Issue Avian Adenovirus Infections)
For years, research on avian adenoviruses, here fowl adenoviruses (FAdVs), received less attention, mainly due to limited clinical relevance in poultry production. However, along with a change in this situation in the last two decades, a paradigm shift has occurred, which has paved the way towards intensified research and scientific activities [1]. Today, FAdVs are important pathogens in the field, causing diseases with substantial impact on poultry health and welfare. Various reviews published in recent years provide a record of this development [2,3,4,5]. The number of submitted manuscripts devoted to FAdVs and the avid resonance to this Special Issue also underline the interest and topicality of the subject. In that regard, the guest editors wish to thank everyone who contributed, either by preparing an article or assisting in the review process, to the successful realization of this volume.
For a long time after the first discovery of FAdVs in the middle of the last century, single outbreaks of associated diseases were reported without major spread, except for hepatitis-hydropericardium syndrome (HHS), which appeared in 1989. Since then, HHS and the causative agent FAdV-4 became endemic in certain countries. The disease gained even more importance with its recent emergence in China, where it also spread to other poultry species, especially ducks, kept for production purposes [6,7]. Together with an increasing record of outbreaks of inclusion body hepatitis (IBH) occurring worldwide, the demand to protect birds by vaccination became evident. With a need to cover both HHS and IBH, this also increased the number of serotypes attributed to pathologies, complicating vaccine development on the side of much-desired cross-protection. Field data on this challenging question are very limited, and this Special Issue contributes with a detailed review on the Korean situation monitored over a period of 15 years [8]. In this study, not only a switch in serotypes in the field was noticed in response to pre-existing immunity, but the findings also pointed towards a lack of cross-protection between different serotypes. With the increasing importance of HHS and IBH, it can be predicted that more of such studies will be published in the future. In parallel, new vaccine technologies will be applied in order to increase the panel of available vaccines, for example, live vaccines developed by creating recombinant viruses [9,10]. This will also contribute to the understanding of the underlying mechanisms of pathogenicity, as strain variation within FAdV serotypes is quite substantial. In this context, perception of the role of hexon is very new and it remains to be elucidated whether this can be transferred to other serotypes as well and if it can even be narrowed down to a single amino acid change [11,12]. Unsurprisingly, other genes are participating in pathogenicity as well, especially fibers as reported for FAdV-4 [13,14,15]. In a contribution to this Special Issue, Grafl et al., 2022, for instance, show that FAdV-1 pathogenicity is driven by factors outside hexon and that even strains with near-identical genomes possess very different in vivo properties [16]. A somewhat slower replication cycle in vitro is correlated with the pathogenicity in vivo. Remarkably, in another study of this Special Issue, it was shown that the replication cycle in vitro not only differs between FAdVs but also influences the expression of MHC-I [17]. Using FAdV-9, it was further shown that this feature, which is well-known from human adenoviruses, is mediated by the left end of the genome. This also underlines the complexity of the FAdV genomes, which needs further research to fully elucidate the host–pathogen interaction on the level of individual genes. While whole genome sequences are mandatory for such detailed analyses, they may be insufficient to assign serotypes, for which cross-neutralization tests remain the unrivaled gold standard, as shown for FAdV-5, the sole serotype representative of fowl aviadenovirus species B [18]. In addition to important implications for taxonomy, such studies also contribute to our understanding of FAdV evolution.
Aligning neatly with the spectrum of published studies, and following up on some of the most compelling questions in the research field, the contents of the Special Issue showcase the diverse range of subjects investigated in FAdVs. It is with great pleasure that we bring to you the final product of those collective efforts and we hope you enjoy an interesting read.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Schachner, A.; Grafl, B.; Hess, M. Spotlight on avian pathology: Fowl adenovirus (FAdV) in chickens and beyond—an unresolved host-pathogen interplay. Avian Pathol. 2021, 50, 2–5. [Google Scholar] [CrossRef] [PubMed]
  2. Li, P.H.; Zheng, P.P.; Zhang, T.F.; Wen, G.Y.; Shao, H.B.; Luo, Q.P. Fowl adenovirus serotype 4: Epidemiology, pathogenesis, diagnostic detection, and vaccine strategies. Poult. Sci. 2017, 96, 2630–2640. [Google Scholar] [CrossRef] [PubMed]
  3. Schachner, A.; Matos, M.; Grafl, B.; Hess, M. Fowl adenovirus-induced diseases and strategies for their control—a review on the current global situation. Avian Pathol. 2018, 47, 111–126. [Google Scholar] [CrossRef] [PubMed]
  4. Shah, M.S.; Ashraf, A.; Khan, M.I.; Rahman, M.; Habib, M.; Chughtai, M.I.; Qureshi, J.A. Fowl adenovirus: History, emergence, biology and development of a vaccine against hydropericardium syndrome. Arch. Virol. 2017, 162, 1833–1843. [Google Scholar] [CrossRef] [PubMed]
  5. Wang, Z.; Zhao, J. Pathogenesis of Hypervirulent Fowl Adenovirus Serotype 4: The Contributions of Viral and Host Factors. Viruses 2019, 11, 741. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Chen, H.; Dou, Y.; Zheng, X.; Tang, Y.; Zhang, M.; Zhang, Y.; Wang, Z.; Diao, Y. Hydropericardium Hepatitis Syndrome Emerged in Cherry Valley Ducks in China. Transbound. Emerg. Dis. 2016, 64, 1262–1267. [Google Scholar] [CrossRef] [PubMed]
  7. Zhao, J.; Zhong, Q.; Zhao, Y.; Hu, Y.-X.; Zhang, G.-Z. Pathogenicity and Complete Genome Characterization of Fowl Adenoviruses Isolated from Chickens Associated with Inclusion Body Hepatitis and Hydropericardium Syndrome in China. PLoS ONE 2015, 10, e0133073. [Google Scholar] [CrossRef] [PubMed]
  8. Mo, J. Historical Investigation of Fowl Adenovirus Outbreaks in South Korea from 2007 to 2021: A Comprehensive Review. Viruses 2021, 13, 2256. [Google Scholar] [CrossRef] [PubMed]
  9. Pan, Q.; Wang, J.; Gao, Y.; Cui, H.; Liu, C.; Qi, X.; Zhang, Y.; Wang, Y.; Li, K.; Gao, L.; et al. Development and application of a novel ELISA for detecting antibodies against group I fowl adenoviruses. Appl. Microbiol. Biotechnol. 2019, 104, 853–859. [Google Scholar] [CrossRef] [PubMed]
  10. Tian, K.-Y.; Guo, H.-F.; Li, N.; Zhang, Y.-H.; Wang, Z.; Wang, B.; Yang, X.; Li, Y.-T.; Zhao, J. Protection of chickens against hepatitis-hydropericardium syndrome and Newcastle disease with a recombinant Newcastle disease virus vaccine expressing the fowl adenovirus serotype 4 fiber-2 protein. Vaccine 2020, 38, 1989–1997. [Google Scholar] [CrossRef] [PubMed]
  11. Zhang, Y.; Liu, A.; Wang, Y.; Cui, H.; Gao, Y.; Qi, X.; Liu, C.; Zhang, Y.; Li, K.; Gao, L.; et al. A Single Amino Acid at Residue 188 of the Hexon Protein Is Responsible for the Pathogenicity of the Emerging Novel Virus Fowl Adenovirus 4. J. Virol. 2021, 95, JVI0060321. [Google Scholar] [CrossRef] [PubMed]
  12. Zhang, Y.; Pan, Q.; Guo, R.; Liu, A.; Xu, Z.; Gao, Y.; Cui, H.; Liu, C.; Qi, X.; Zhang, Y.; et al. Immunogenicity of Novel Live Vaccine Based on an Artificial rHN20 Strain against Emerging Fowl Adenovirus 4. Viruses 2021, 13, 2153. [Google Scholar] [CrossRef] [PubMed]
  13. Mu, Y.; Xie, Q.; Wang, W.; Lu, H.; Lian, M.; Gao, W.; Li, T.; Wan, Z.; Shao, H.; Qin, A.; et al. A Novel Fiber-1-Edited and Highly Attenuated Recombinant Serotype 4 Fowl Adenovirus Confers Efficient Protection Against Lethal Challenge. Front. Veter. Sci. 2021, 8, 759418. [Google Scholar] [CrossRef] [PubMed]
  14. Wang, W.; Liu, Q.; Li, T.; Geng, T.; Chen, H.; Xie, Q.; Shao, H.; Wan, Z.; Qin, A.; Ye, J. Fiber-1, Not Fiber-2, Directly Mediates the Infection of the Pathogenic Serotype 4 Fowl Adenovirus via Its Shaft and Knob Domains. J. Virol. 2020, 94, e00954-20. [Google Scholar] [CrossRef] [PubMed]
  15. Xie, Q.; Cao, S.; Zhang, W.; Wang, W.; Li, L.; Kan, Q.; Fu, H.; Geng, T.; Li, T.; Wan, Z.; et al. A novel fiber-2-edited live attenuated vaccine candidate against the highly pathogenic serotype 4 fowl adenovirus. Veter. Res. 2021, 52, 35. [Google Scholar] [CrossRef] [PubMed]
  16. Grafl, B.; Schachner, A.; Hess, M. High Phenotypic Variation between an In Vitro-Passaged Fowl Adenovirus Serotype 1 (FAdV-1) and Its Virulent Progenitor Strain despite Almost Complete Sequence Identity of the Whole Genomes. Viruses 2022, 14, 358. [Google Scholar] [CrossRef] [PubMed]
  17. Griffin, B.D.; Corredor, J.C.; Pei, Y.; Nagy, É. Downregulation of Cell Surface Major Histocompatibility Complex Class I Expression Is Mediated by the Left-End Transcription Unit of Fowl Adenovirus 9. Viruses 2021, 13, 2211. [Google Scholar] [CrossRef] [PubMed]
  18. Kaján, G.L.; Schachner, A.; Gellért, Á.; Hess, M. Species Fowl aviadenovirus B Consists of a Single Serotype despite Genetic Distance of FAdV-5 Isolates. Viruses 2022, 14, 248. [Google Scholar] [CrossRef] [PubMed]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Schachner, A.; Hess, M. Special Issue: Avian Adenoviruses. Viruses 2022, 14, 680. https://doi.org/10.3390/v14040680

AMA Style

Schachner A, Hess M. Special Issue: Avian Adenoviruses. Viruses. 2022; 14(4):680. https://doi.org/10.3390/v14040680

Chicago/Turabian Style

Schachner, Anna, and Michael Hess. 2022. "Special Issue: Avian Adenoviruses" Viruses 14, no. 4: 680. https://doi.org/10.3390/v14040680

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop