Feline herpesvirus-1 (FeHV-1) in cats with ophthalmic problems: attempted propagation in CRFK cell lines
Year 2023,
Volume: 8 Issue: 3, 200 - 205, 31.12.2023
Hasbi Sait Saltık
,
Yaren Fidan
Abstract
Feline herpesvirus-1 (FeHV-1) is classified within the Varicellovirus genus and is frequently seen in cats. Ocular complications, such as conjunctivitis, keratitis, and corneal ulcers, are common and have the potential to result in latency and permanent visual loss if not appropriately diagnosed and monitored. This study aimed to isolate FeHV-1 from cats with ocular lesions using the CRFK cell line.
This study included a total of ten cats that tested positive for FeHV-1 and showed symptoms, including ocular and nasal discharge (8/10), conjunctivitis (6/10), and keratitis (5/10). Conjunctival samples were collected and processed for nucleic acid extraction. The CRFK cell line was propagated, and all positive samples were inoculated in 6-well plates. Surprisingly, no CPE was observed in the CRFK cell cultures during the observation period. Following post-inoculation in cell culture, the PCR analysis conducted on the supernatants obtained from the cultures found negative for FeHV-1.
This study points out the challenges faced in isolating FeHV-1 in the CRFK from ocular samples of naturally infected cats. This highlights the requirement for future comprehensive in vitro studies to enhance the efficacy of FeHV-1 isolation techniques and explore potential approaches for FeHV-1 diagnosis.
Supporting Institution
TUBITAK
Project Number
2209, 1919B012112628
Thanks
We gratefully acknowledge the support of TUBITAK, which provided financing for the research.
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Year 2023,
Volume: 8 Issue: 3, 200 - 205, 31.12.2023
Hasbi Sait Saltık
,
Yaren Fidan
Project Number
2209, 1919B012112628
References
- Bol S, Bunnik EM (2015). Lysine supplementation is not effective for the prevention or treatment of feline herpesvirus 1 infection in cats: a systematic review. BMC Vet Res 11, 1-15. https://doi.org/10.1186/s12917-015-0594-3
- Burgesser KM, Hotaling S, Schiebel A, Ashbaugh SE, Roberts SM, Collins JK (1999). Comparison of PCR, virus isolation, and indirect fluorescent antibody staining in the detection of naturally occurring feline herpesvirus infections. J Vet Diagn Investig 11(2), 122-126. https://doi.org/10.1177/104063879901100203
- Cannon MJ, Schmid DS, Hyde TB (2010). Review of cytomegalovirus seroprevalence and demographic characteristics associated with infection. Rev Med Virol 20(4), 202-213. https://doi.org/10.1002/rmv.655
- de Parseval A, Ngo S, Sun P, Elder JH (2004). Factors that increase the effective concentration of CXCR4 dictate feline immunodeficiency virus tropism and kinetics of replication. J Virol 78(17), 9132-9143. https://doi.org/10.1128/jvi.78.17.9132-9143.2004
- Gaskell R, Dawson S, Radford A, Thiry E (2007). Feline herpesvirus. Vet Res 38 337-3354. https://doi.org/ 10.1051/vetres:2006063
- Gould D (2011). Feline herpesvirus-1: ocular manifestations, diagnosis and treatment options. J Feline Med Surg. 13(5):333-46. https://doi: 10.1016/j.jfms.2011.03.010.
- Haid C, Kaps S, Gönczi E, Hässig M, Metzler A, Spiess BM, Richter M (2007). Pretreatment with feline interferon omega and the course of subsequent infection with feline herpesvirus in cats. Vet Ophthalmol 10(5), 278-284. https://doi.org/10.1111/j.1463-5224.2007.00550.x
- Henzel A, Brum MCS, Lautert C, Martins M, Lovato LT, Weiblen R (2012). Isolation and identification of feline calicivirus and feline herpesvirus in Southern Brazil. Braz J Microbiol 43, 560-568. https://doi.org/10.1590/S1517-83822012000200017
- Lee Y, Maes R, Tai SHS, Hussey GS (2019). Viral replication and innate immunity of feline herpesvirus-1 virulence-associated genes in feline respiratory epithelial cells. Virus Res 264, 56-67. https://doi.org/10.1016/j.virusres.2019.02.013
- Leeming G, Meli ML, Cripps P, Vaughan-Thomas A, Lutz H, Gaskell R, Kipar A (2006). Tracheal organ cultures as a useful tool to study Felid herpesvirus 1 infection in respiratory epithelium. J Virol Methods 138(1-2), 191-195. https://doi.org/10.1016/j.jviromet.2006.07.010
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- Lister A, Wu CC, Leutenegger CM (2015). Detection of feline upper respiratory tract disease pathogens using a commercially available real-time PCR test. Vet J, 206(2), 149-153. https://doi.org/10.1016/j.tvjl.2015.08.001
- Maes R. Felid Herpesvirus Type 1 Infection in Cats: A Natural Host Model for Alphaherpesvirus Pathogenesis. ISRN Vet Sci. 2012: 495830. https://doi.org/10.5402/2012/495830.
- Maggs DJ, Collins BK, Thorne JG, Nasisse MP (2000). Effects of L-lysine and L-arginine on in vitro replication of feline herpesvirus type-1. Am J Vet Res;61(12):1474–8. https://doi.org/10.2460/ajvr.2000.61.1474.
- Magouz A, Lokman MS, Albrakati A, Elmahallawy EK (2022). First Report of Isolation and Molecular Characterization of Felid Herpesvirus-1 from Symptomatic Domestic Cats in Egypt. Vet Sci 9(2), 81.
- Povey RC (1979). A review of feline viral rhinotracheitis (feline herpesvirus I infection). Comp Immunol Microbiol Infect Dis 2(2-3), 373-387. https://doi.org/10.1016/0147-9571(79)90023-7
- Reubel GH, Ramos RA, Hickman MA, Rimstad E, Hoffmann DE, Pedersen NC (1993). Detection of active and latent feline herpesvirus 1 infections using the polymerase chain reaction. Arch Virol 132, 409-420. https://doi.org/10.1007/BF01309549.
- Sandmeyer LS, Waldner CL, Bauer BS, Wen X, Bienzle D (2010). Comparison of polymerase chain reaction tests for diagnosis of feline herpesvirus, Chlamydophila felis, and Mycoplasma spp. infection in cats with ocular disease in Canada. Can Vet J 51(6), 629
- Schulz C, Hartmann K, Mueller RS, Helps C, Schulz BS (2015). Sampling sites for detection of feline herpesvirus-1, feline calicivirus and Chlamydia felis in cats with feline upper respiratory tract disease. J Feline Med Surg 17(12), 1012-1019.
- Stiles J (2014). Ocular manifestations of feline viral diseases. Vet J 201(2), 166-173. https://doi.org/10.1016/j.tvjl.2013.11.018
- Storey ES, Gerding PA, Scherba G, Schaeffer DJ (2002). Survival of equine herpesvirus‐4, feline herpesvirus‐1, and feline calicivirus in multidose ophthalmic solutions. Vet Ophthalmol 5(4), 263-267. https://doi.org/10.1046/j.1463-5224.2002.00234.x
- Sun H, Li Y, Jiao W, Liu C et al (2014). Isolation and identification of feline herpesvirus type 1 from a South China tiger in China. Viruses 6(3), 1004-1014. https://doi.org/10.3390/v6031004
- Sykes JE, Browning GF, Anderson G, Studdert VP, Smith HV (1997). Differential sensitivity of culture and the polymerase chain reaction for detection of feline herpesvirus 1 in vaccinated and unvaccinated cats. Arch Virol 142(1), 65-74. https://doi.org/10.1007/s007050050059
- Sykes JE, Shelley CR (2013) Isolation in cell culture. In: Sykes JE (ed) Canine and feline infectious diseases, 1rd edn. Elsevier Saunders, Missouri, pp 2-9
- Tan Y, Dong G, Xu H et al (2020). Development of a cross-priming isothermal amplification assay based on the glycoprotein B gene for instant and rapid detection of feline herpesvirus type 1. Arch Virol 165(3), 743-747. https://doi.org/10.1007/s00705-020-04526-5
- Veir JK, Ruch-Gallie R, Spindel ME et al (2008). Prevalence of selected infectious organisms and comparison of two anatomic sampling sites in shelter cats with upper respiratory tract disease. J Feline Med Surg 10: 551–557. https://doi.org/10.1016/j.jfms.2008.04.002
- Walter J, Foley P, Yason C, Vanderstichel R, Muckle A (2020). Prevalence of feline herpesvirus-1, feline calicivirus, Chlamydia felis, and Bordetella bronchiseptica in a population of shelter cats on Prince Edward Island. Can J Vet Res 84(3), 181-188
- Yang DK, Kim HH, Park YR, et al (2020). Isolation and molecular characterization of feline herpesvirus 1 from naturally infected Korean cats. J Bacteriol Virol 50(4), 263-272. https://doi.org/10.4167/jbv.2020.50.4.263