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REVIEW article

Front. Microbiol.
Sec. Virology
Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1442321

Viral Contamination in Cell Culture: Analyzing the Impact of Epstein Barr Virus and Ovine Herpesvirus 2

Provisionally accepted
  • 1 Animal Health Research Institute (Egypt), Giza, Giza, Egypt
  • 2 Putra Malaysia University, Selangor Darul Ehsan, Selangor Darul Ehsan, Malaysia
  • 3 Kyushu Institute of Technology, Kitakyushu, Fukuoka, Japan
  • 4 University of Sadat City, Sadat City, Egypt
  • 5 Cairo University, Giza, Giza, Egypt
  • 6 Virology, Lancaster University, Lancaster, United Kingdom

The final, formatted version of the article will be published soon.

    Cell culture techniques are increasingly favored over animal models due to rising costs, time constraints, and ethical concerns regarding animal use. These methods serve critical roles in disease modeling, drug screening, drug discovery, and toxicity analysis.Notably, cell cultures facilitate primary virus isolation, infectivity assays, biochemical studies, and vaccine production. However, viral contamination in cell cultures poses significant challenges, particularly due to the necessity for complex and sophisticated detection methods. Among the prevalent viruses, Epstein Barr virus (EBV) is ubiquitous across human populations, infecting about 98% of individuals. Despite its prevalence, the detection of EBV is often not considered a safety priority, as its detection methods are well-established, including PCR techniques that can identify both active and latent forms of the virus. Conversely, Ovine herpesvirus 2 (OvHV-2), a relative of EBV, presents a critical concern due to its ability to infect a wide range of organs and species, including over 33 animal species and nearly all domestic sheep. This makes the detection of OvHV-2 crucial for the safety of cell cultures across various species. The literature reveals a gap in the comprehensive understanding of OvHV-2 detection in cell culture systems, highlighting an urgent need for developing robust detection methodologies specific to OvHV-2 to ensure bioprocess safety.

    Keywords: Cell Culture Techniques, Viral contamination, ebv, OvHV-2, Detection methods

    Received: 03 Jun 2024; Accepted: 28 Jan 2025.

    Copyright: © 2025 Bastawecy, Abdelmonem, Afify, Saad, Shirosaki, CHE ABDULLAH, F. El Naggar, Rohaim and Munir. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Muhammad Munir, Virology, Lancaster University, Lancaster, 75189, United Kingdom

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.