Skip to main content
Pathogens logoLink to Pathogens
editorial
. 2023 Dec 7;12(12):1422. doi: 10.3390/pathogens12121422

Herpesvirus Diseases in Humans and Animals: Recent Developments, Challenges, and Charting Future Paths

Miroslava Šudomová 1,*, Sherif T S Hassan 2
PMCID: PMC10745940  PMID: 38133305

1. Introduction

Herpesviruses, a family of enveloped DNA viruses, pose significant threats to both humans and animals. They cause a spectrum of diseases, ranging from mild, self-limiting conditions to severe, life-threatening illnesses. With the ability to establish lifelong relationships with their hosts and trigger recurrent outbreaks, herpesviruses have emerged as formidable players in the realm of infectious diseases [1,2,3]. Human herpesviruses, including herpes simplex virus (HSV), varicella-zoster virus (VZV), cytomegalovirus (CMV), Epstein–Barr virus (EBV), Kaposi’s sarcoma-associated herpesvirus (KSHV), and others, continue to exert a substantial impact on global public health [4,5]. Likewise, the animal kingdom encounters viral obstacles, as equine, bovine herpesviruses, feline, and canine herpesvirus, pseudorabies virus, and other related viruses cause considerable risks to agriculture and veterinary fields [6,7,8,9].

The overlap between human and animal health features the interconnected challenges presented by these viruses [10].

2. Recent Developments

In recent years, significant strides have been made in elucidating the molecular biology and pathogenesis of human and animal herpesviruses. Advances in genomics, proteomics, and imaging techniques have provided unprecedented insights into the intricate interactions between these viruses and their hosts [1,11]. Furthermore, the identification of viral and host factors influencing the course of infection has opened new avenues for therapeutic interventions [12]. Cutting-edge technologies, from CRISPR-based genome editing to high-throughput sequencing, have empowered scientists to dissect the viral genome, identify novel therapeutic targets, and explore innovative vaccine strategies [13,14,15,16,17]. The development of antiviral drugs, such as acyclovir and its derivatives, has improved patient outcomes. However, concerns about drug resistance and the persistence of latent infections remain [18,19].

Overall, the integration of these diverse approaches has expanded our understanding of herpesviruses and paved the way for more effective strategies in combating these infections.

3. Challenges and Innovative Solutions

Navigating the complex landscape of herpesvirus research reveals a set of challenges that span various facets of virology and medicine. One prominent challenge lies in drug resistance, where, despite the effectiveness of antiviral drugs such as acyclovir, the emergence of drug-resistant strains poses a substantial threat. Ongoing surveillance, and the development of alternative therapeutic strategies, are imperative for addressing this issue [4,20,21].

The challenge of latency and reactivation in herpesvirus infections, characterized by the establishment of latent infections and periodic reactivation, adds complexity to the treatment and prevention efforts. Understanding and targeting latent reservoirs is crucial for curbing recurrent infections, with innovative solutions such as therapies targeting latent reservoirs, gene-editing technologies, and an enhanced understanding of triggers for viral reactivation. Moreover, investigating immunomodulatory agents to enhance immune surveillance shows promise [22,23,24,25]. Furthermore, a possible link between herpesvirus reactivation and various conditions, including long COVID-19 and chronic fatigue syndrome, has been suggested. The stress on the immune system during acute COVID-19 may contribute to reactivation and, in chronic fatigue syndrome, viral reactivation could impact immune regulation and chronic inflammation. Ongoing research aims to establish clearer connections and potential therapeutic approaches for these conditions [26,27,28].

In the dynamic field of vaccine development, despite notable research progress, crafting a safe and effective herpesvirus vaccine proves to be an ongoing challenge. The complex evasion tactics employed by these viruses necessitate innovative strategies to elicit robust and enduring immune responses. Advancements in mRNA vaccine technologies, the identification of conserved viral targets for vaccine development, and the exploration of novel adjuvants are all at the forefront of efforts to conquer this challenge [29,30,31,32,33]. Moderna’s exploration of RNA-based vaccines against EBV and CMV aligns with these innovative approaches, offering potential breakthroughs in the ongoing battle against persistent viral infections [34].

Severe neurological complications, including HSV-induced encephalitis, present another challenge for herpesvirus research. Unraveling the mechanisms behind viral invasion of the nervous system is essential for preventing and treating these complications. Innovative solutions include developing antiviral drugs with enhanced blood–brain barrier penetration, exploring neuroprotective agents, and understanding the host factors influencing neurological outcomes [35,36,37,38,39].

The association of certain herpesviruses with an increased risk of cancers adds a layer of complexity to the research landscape. Innovative strategies targeting viral oncogenes, immuno-therapies for cancer prevention, and the advancement of understanding viral-induced cellular changes are key solutions to address this challenge [40,41,42].

Furthermore, the interplay between human and animal health, exemplified by simian herpesviruses, emphasizes the intricate link between them. Predicting and preventing cross-species transmission events requires a holistic One Health Approach. Strengthening surveillance at the human–animal interface, promoting interdisciplinary collaborations, and developing targeted interventions emerge as innovative solutions to break the chain of transmission between species [10,43,44].

4. Charting Future Paths

As we delve into the complex realm of herpesvirus diseases in humans and animals, envisioning future frontiers becomes pivotal in shaping effective strategies for their prevention, treatment, and overall management. The convergence of cutting-edge technologies, such as advanced genomics and targeted antiviral therapies, promises to revolutionize our approach. Personalized medicine tailored to individual immune responses, coupled with the development of broad-spectrum antivirals, stands out as a potential frontier. Moreover, the integration of artificial intelligence in predictive modeling and vaccine design holds potential for staying ahead of the evolving herpesvirus strains. Collaborative, interdisciplinary efforts spanning virology, immunology, and computational sciences will be essential in navigating these frontiers. As we chart a course forward, a holistic understanding that transcends species boundaries will be key, fostering a future where innovative solutions ensure the effective control and mitigation of herpesvirus diseases in both human and animal populations.

Acknowledgments

The authors wish to express their gratitude to their respective institutions for facilitating access to subscribed databases that enabled the collection of essential information needed for crafting this Editorial.

Author Contributions

Conceptualization, M.Š. and S.T.S.H.; writing—original draft preparation, M.Š. and S.T.S.H.; writing—review and editing, M.Š. and S.T.S.H. All authors have read and agreed to the published version of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Adler B., Sattler C., Adler H. Herpesviruses and Their Host Cells: A Successful Liaison. Trends Microbiol. 2017;25:229–241. doi: 10.1016/j.tim.2016.11.009. [DOI] [PubMed] [Google Scholar]
  • 2.Paludan S.R., Bowie A.G., Horan K.A., Fitzgerald K.A. Recognition of Herpesviruses by the Innate Immune System. Nat. Rev. Immunol. 2011;11:143–154. doi: 10.1038/nri2937. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Okoh G.R., Lockhart M., Grimsey J., Whitmore D., Ariel E., Butler J., Horwood P.F. Development of Subfamily-Based Consensus PCR Assays for the Detection of Human and Animal Herpesviruses. Eur. J. Clin. Microbiol. Infect. Dis. 2023;42:741–746. doi: 10.1007/s10096-023-04605-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Šudomová M., Berchová-Bímová K., Mazurakova A., Šamec D., Kubatka P., Hassan S.T.S. Flavonoids Target Human Herpesviruses That Infect the Nervous System: Mechanisms of Action and Therapeutic Insights. Viruses. 2022;14:592. doi: 10.3390/v14030592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Šudomová M., Hassan S.T.S. Nutraceutical Curcumin with Promising Protection against Herpesvirus Infections and Their Associated Inflammation: Mechanisms and Pathways. Microorganisms. 2021;9:292. doi: 10.3390/microorganisms9020292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.de Almeida Campos A.C., Cicolo S., de Oliveira C.M., Molina C.V., Navas-Suárez P.E., Poltronieri Dos Santos T., da Silveira V.B., Barbosa C.M., Baccarin R.Y.A., Durigon E.L., et al. Potential Outbreak by Herpesvirus in Equines: Detection, Clinical, and Genetic Analysis of Equid Gammaherpesvirus 2 (EHV-2) Braz. J. Microbiol. 2023;54:1137–1143. doi: 10.1007/s42770-022-00890-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Ostler J.B., Jones C. The Bovine Herpesvirus 1 Latency-Reactivation Cycle, a Chronic Problem in the Cattle Industry. Viruses. 2023;15:552. doi: 10.3390/v15020552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Žlabravec Z., Vrezec A., Slavec B., Kuhar U., Zorman Rojs O., Račnik J. Herpesvirus Infection in a Breeding Population of Two Coexisting Strix Owls. Animals. 2021;11:2519. doi: 10.3390/ani11092519. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Hanson L., Dishon A., Kotler M. Herpesviruses That Infect Fish. Viruses. 2011;3:2160–2191. doi: 10.3390/v3112160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Woźniakowski G., Samorek-Salamonowicz E. Animal Herpesviruses and Their Zoonotic Potential for Cross-Species Infection. Ann. Agric. Environ. Med. 2015;22:191–194. doi: 10.5604/12321966.1152063. [DOI] [PubMed] [Google Scholar]
  • 11.Azab W., Dayaram A., Greenwood A.D., Osterrieder N. How Host Specific Are Herpesviruses? Lessons from Herpesviruses Infecting Wild and Endangered Mammals. Annu. Rev. Virol. 2018;5:53–68. doi: 10.1146/annurev-virology-092917-043227. [DOI] [PubMed] [Google Scholar]
  • 12.Asha K., Sharma-Walia N. Targeting Host Cellular Factors as a Strategy of Therapeutic Intervention for Herpesvirus Infections. Front. Cell. Infect. Microbiol. 2021;11:603309. doi: 10.3389/fcimb.2021.603309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Chen Y.-C., Sheng J., Trang P., Liu F. Potential Application of the CRISPR/Cas9 System against Herpesvirus Infections. Viruses. 2018;10:291. doi: 10.3390/v10060291. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Yuen K.-S., Chan C.-P., Kok K.-H., Jin D.-Y. Mutagenesis and Genome Engineering of Epstein–Barr Virus in Cultured Human Cells by CRISPR/Cas9. In: Reeves A., editor. In Vitro Mutagenesis. Volume 1498. Springer; New York, NY, USA: 2017. pp. 23–31. Methods in Molecular Biology. [DOI] [PubMed] [Google Scholar]
  • 15.Lee C.-H., Grey F. Systems Virology and Human Cytomegalovirus: Using High Throughput Approaches to Identify Novel Host-Virus Interactions during Lytic Infection. Front. Cell Infect. Microbiol. 2020;10:280. doi: 10.3389/fcimb.2020.00280. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Liao Y., Bajwa K., Reddy S.M., Lupiani B. Methods for the Manipulation of Herpesvirus Genome and the Application to Marek’s Disease Virus Research. Microorganisms. 2021;9:1260. doi: 10.3390/microorganisms9061260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Vijayakrishnan S., McElwee M., Loney C., Rixon F., Bhella D. In Situ Structure of Virus Capsids within Cell Nuclei by Correlative Light and Cryo-Electron Tomography. Sci. Rep. 2020;10:17596. doi: 10.1038/s41598-020-74104-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Dong H., Wang Z., Zhao D., Leng X., Zhao Y. Antiviral Strategies Targeting Herpesviruses. J. Virus Erad. 2021;7:100047. doi: 10.1016/j.jve.2021.100047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Kłysik K., Pietraszek A., Karewicz A., Nowakowska M. Acyclovir in the Treatment of Herpes Viruses—A Review. Curr. Med. Chem. 2020;27:4118–4137. doi: 10.2174/0929867325666180309105519. [DOI] [PubMed] [Google Scholar]
  • 20.Piret J., Boivin G. Antiviral Drug Discovery and Development. Volume 1322. Springer; Singapore: 2021. Antiviral Drugs against Herpesviruses; pp. 1–30. Advances in Experimental Medicine and Biology. [DOI] [PubMed] [Google Scholar]
  • 21.Piret J., Boivin G. DNA Polymerases of Herpesviruses and Their Inhibitors. Enzymes. 2021;50:79–132. doi: 10.1016/bs.enz.2021.07.003. [DOI] [PubMed] [Google Scholar]
  • 22.Cohen J.I. Herpesvirus Latency. J. Clin. Investig. 2020;130:3361–3369. doi: 10.1172/JCI136225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Reese T.A. Coinfections: Another Variable in the Herpesvirus Latency-Reactivation Dynamic. J. Virol. 2016;90:5534–5537. doi: 10.1128/JVI.01865-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lum K.K., Cristea I.M. Host Innate Immune Response and Viral Immune Evasion during Alphaherpesvirus Infection. Curr. Issues Mol. Biol. 2021;42:635–686. doi: 10.21775/cimb.042.635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Teng M., Zhou Z.-Y., Yao Y., Nair V., Zhang G.-P., Luo J. A New Strategy for Efficient Screening and Identification of Monoclonal Antibodies against Oncogenic Avian Herpesvirus Utilizing CRISPR/Cas9-Based Gene-Editing Technology. Viruses. 2022;14:2045. doi: 10.3390/v14092045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Shafiee A., Teymouri Athar M.M., Amini M.J., Hajishah H., Siahvoshi S., Jalali M., Jahanbakhshi B., Mozhgani S.-H. Reactivation of Herpesviruses during COVID-19: A Systematic Review and Meta-Analysis. Rev. Med. Virol. 2023;33:e2437. doi: 10.1002/rmv.2437. [DOI] [PubMed] [Google Scholar]
  • 27.Vojdani A., Vojdani E., Saidara E., Maes M. Persistent SARS-CoV-2 Infection, EBV, HHV-6 and Other Factors May Contribute to Inflammation and Autoimmunity in Long COVID. Viruses. 2023;15:400. doi: 10.3390/v15020400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Schreiner P., Harrer T., Scheibenbogen C., Lamer S., Schlosser A., Naviaux R.K., Prusty B.K. Human Herpesvirus-6 Reactivation, Mitochondrial Fragmentation, and the Coordination of Antiviral and Metabolic Phenotypes in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Immunohorizons. 2020;4:201–215. doi: 10.4049/immunohorizons.2000006. [DOI] [PubMed] [Google Scholar]
  • 29.Wu T.-T., Qian J., Ang J., Sun R. Vaccine Prospect of Kaposi Sarcoma-Associated Herpesvirus. Curr. Opin. Virol. 2012;2:482–488. doi: 10.1016/j.coviro.2012.06.005. [DOI] [PubMed] [Google Scholar]
  • 30.Plotkin S.A., Wang D., Oualim A., Diamond D.J., Kotton C.N., Mossman S., Carfi A., Anderson D., Dormitzer P.R. The Status of Vaccine Development Against the Human Cytomegalovirus. J. Infect. Dis. 2020;221:S113–S122. doi: 10.1093/infdis/jiz447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Rühl J., Leung C.S., Münz C. Vaccination against the Epstein-Barr Virus. Cell Mol. Life Sci. 2020;77:4315–4324. doi: 10.1007/s00018-020-03538-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Gagliardi A.M., Andriolo B.N., Torloni M.R., Soares B.G., de Oliveira Gomes J., Andriolo R.B., Canteiro Cruz E. Vaccines for Preventing Herpes Zoster in Older Adults. Cochrane Database Syst. Rev. 2019;2019:CD008858. doi: 10.1002/14651858.CD008858.pub4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Freuling C.M., Müller T.F., Mettenleiter T.C. Vaccines against Pseudorabies Virus (PrV) Vet. Microbiol. 2017;206:3–9. doi: 10.1016/j.vetmic.2016.11.019. [DOI] [PubMed] [Google Scholar]
  • 34.Moderna Announces First Participant Dosed in Phase 1 Study of Its mRNA Epstein-Barr Virus (EBV) Vaccine. [(accessed on 25 November 2023)]. Available online: https://investors.modernatx.com/news/news-details/2022/Moderna-Announces-First-Participant-Dosed-in-Phase-1-Study-of-its-mRNA-Epstein-Barr-Virus-EBV-Vaccine/default.aspx.
  • 35.Armangué T., Olivé-Cirera G., Martínez-Hernandez E., Rodes M., Peris-Sempere V., Guasp M., Ruiz R., Palou E., González A., Marcos M.Á., et al. Neurologic Complications in Herpes Simplex Encephalitis: Clinical, Immunological and Genetic Studies. Brain. 2023;146:4306–4319. doi: 10.1093/brain/awad238. [DOI] [PubMed] [Google Scholar]
  • 36.Baldwin K.J., Cummings C.L. Herpesvirus Infections of the Nervous System. Continuum. 2018;24:1349–1369. doi: 10.1212/CON.0000000000000661. [DOI] [PubMed] [Google Scholar]
  • 37.Zhang X.-Y., Fang F. Congenital Human Cytomegalovirus Infection and Neurologic Diseases in Newborns. Chin. Med. J. 2019;132:2109–2118. doi: 10.1097/CM9.0000000000000404. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Jha H.C., Mehta D., Lu J., El-Naccache D., Shukla S.K., Kovacsics C., Kolson D., Robertson E.S. Gammaherpesvirus Infection of Human Neuronal Cells. mBio. 2015;6:e01844-15. doi: 10.1128/mBio.01844-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Lecollinet S., Pronost S., Coulpier M., Beck C., Gonzalez G., Leblond A., Tritz P. Viral Equine Encephalitis, a Growing Threat to the Horse Population in Europe? Viruses. 2019;12:23. doi: 10.3390/v12010023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Hassan S.T.S., Šudomová M. Molecular Mechanisms of Flavonoids against Tumor Gamma-Herpesviruses and Their Correlated Cancers—A Focus on EBV and KSHV Life Cycles and Carcinogenesis. Int. J. Mol. Sci. 2022;24:247. doi: 10.3390/ijms24010247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Wołącewicz M., Becht R., Grywalska E., Niedźwiedzka-Rystwej P. Herpesviruses in Head and Neck Cancers. Viruses. 2020;12:172. doi: 10.3390/v12020172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Yu C., He S., Zhu W., Ru P., Ge X., Govindasamy K. Human Cytomegalovirus in Cancer: The Mechanism of HCMV-Induced Carcinogenesis and Its Therapeutic Potential. Front. Cell Infect. Microbiol. 2023;13:1202138. doi: 10.3389/fcimb.2023.1202138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Estep R.D., Messaoudi I., Wong S.W. Simian Herpesviruses and Their Risk to Humans. Vaccine. 2010;28:B78–B84. doi: 10.1016/j.vaccine.2009.11.026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Kelly T.R., Karesh W.B., Johnson C.K., Gilardi K.V.K., Anthony S.J., Goldstein T., Olson S.H., Machalaba C., PREDICT Consortium. Mazet J.A.K. One Health Proof of Concept: Bringing a Transdisciplinary Approach to Surveillance for Zoonotic Viruses at the Human-Wild Animal Interface. Prev. Vet. Med. 2017;137:112–118. doi: 10.1016/j.prevetmed.2016.11.023. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Pathogens are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES