EFFECTS OF FETAL BOVINE SERUM CONCENTRATION AND VENTED FLASK CONDITIONS ON E-11 CELL GROWTH AND TILAPIA LAKE VIRUS PROPAGATION

Authors

  • Nurhamimah Zainal Abidin nurhamimah@uitm.edu.my
  • Muhamad Afiq Aziz Institute of Biological Sciences, Faculty of Science, Universiti Malaya, 50603 Kuala Lumpur, Malaysia
  • Nur Fadiah Wathiqah Fadzillah 1School of Biology,Faculty of Applied Sciences Universiti Teknologi MARA (UiTM), Cawangan Negeri Sembilan, Kampus Kuala Pilah, 72000 Kuala Pilah, Negeri Sembilan, Malaysia
  • Mohammad Noor Amal Azmai Aquatic Animal Health and Therapeutics Laboratory, Institute of Bioscience, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.

DOI:

https://doi.org/10.24191/joa.v14i1.9648

Keywords:

Aquaculture, Tilapia Lake Virus (TiLV), E-11 cells, Cytopathic effect

Abstract

Tilapia Lake Virus (TiLV) is an emerging pathogen threatening global tilapia aquaculture, causing high mortality and significant economic losses. The present study aimed to optimize E-11 cell culture conditions for improved growth and TiLV propagation under different serum and flask ventilation conditions. E-11 cells were cultured in Leibovitz’s L-15 medium supplemented with 10%, 15%, and 20% fetal bovine serum (FBS) and maintained at 25°C in a CO₂-free incubator. Cell viability was assessed over four days using the Trypan Blue exclusion assay, while TiLV propagation was evaluated in both seal-cap and vent-cap flasks through microscopic observation of cytopathic effects (CPE). Results showed that E-11 cells supplemented with 15% FBS exhibited the highest viability (85–90%) and optimal proliferation compared to cells grown in 10% or 20% FBS. Morphologically, all cultures displayed similar epithelial-like characteristics with polygonal cell shapes and intact monolayers under the microscope. No significant differences in viability were observed between open- and closed-vented flasks; however, CPE were detected only in infected E-11 cells maintained in vent-cap flasks by 10 days post-infection (dpi), while cells in seal-cap flasks remained morphologically intact. These findings suggest that a 15% FBS concentration and a vented culture environment support both healthy E-11 cell growth and effective TiLV propagation. This optimized culture system enhances the reliability of in vitro TiLV studies and supports efforts toward sustainable aquaculture and food security.

 

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2026-04-30

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