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Feline herpesvirus, also known as viral rhinobronchitis, is widely present worldwide and only one serotype has been confirmed, but its virulence varies among different virus strains. The feline herpesvirus replicates and proliferates in the epithelial cells of the conjunctiva and upper respiratory tract, as well as in neuronal cells. Infection with a neural pathogen can lead to lifelong latent infection. Although feline herpesvirus is antigen related to canine herpesvirus, it is not yet known whether they can be transmitted to each other. Feline herpesvirus 1 (FHV-1) is a large virus with a envelope and double stranded DNA. It proliferates in the nucleus and forms nuclear inclusions. The feline herpesvirus is extremely unstable under acidic conditions and is highly sensitive to heat, ether, chloroform, formalin, and phenol. It can survive in dry environments for no more than 12 hours, making it quite fragile in the environment. Conventional disinfectants can effectively disinfect it. The infected object FHV-1 only infects feline animals and has also been isolated from dogs, but its importance is still unclear.
Figure 1. Feline Herpesvirus Infections. (Sykes J E, 2022)
Chronic latent infection is a typical result of acute infection with feline herpesvirus, which intermittently reactivates and releases the virus into oral, nasal, and conjunctival secretions. Unless kept in a cat house, environmental pollution is not the main source of infection. The main sources of infection are cats in the acute infection phase and cats in the chronic latent infection phase that have been reactivated and detoxified. The possibility of placental infection has not been confirmed, but chronic latent infection in female cats is considered an urgent state during delivery and lactation, which can lead to virus reactivation and emission. Therefore, young cats may be exposed to the virus at a very early stage. But the outcome of its infection depends on the amount of maternal transitional antibodies. When there are sufficient transitional antibodies, some cats will be protected by them, resulting in asymptomatic infection and latent infection. If there is insufficient transitional antibodies, clinical symptoms may occur. In healthy small populations, the incidence of virus emissions may be less than 1%, while in symptomatic large populations, the incidence of virus emissions may reach 20%.
FHV-1 infection significantly alters gene expression and signaling pathways in host cells. A transcriptomic study in 2024 identified several key host genes and pathways involved in early activation of infection:
The virus enters the cat's body through the mouth, nose, conjunctiva, and other pathways, causing lytic infection of the nasal mucosal epithelial cells and spreading to the conjunctiva, throat, trachea, bronchi, and bronchioles. The lesions are local multiple necrotic (neutrophil infiltration) and inflammatory lesions, and there have been reports that transient viremia may occur, especially in newborns or low-temperature kittens, because feline herpesvirus likes to replicate at lower temperatures. After 24 hours of infection, the virus begins to be released and lasts for 1-3 weeks. Acute symptoms will be relieved within 10-14 days, while some may develop chronic lesions in the upper respiratory tract and eyes. The virus spreads along the sensory nerves and reaches the neurons, especially in the trigeminal ganglion, which is the main site of latent infection. Almost all infected cats become lifelong carriers of the virus. At present, there is no simple testing method to detect this latent state, as the virus's genes exist in the nucleus of infected neurons and do not replicate.
| Diagnosis | Details |
| Nucleic Acid Detection | A positive result of PCR may represent the emission of a small amount of virus or latent infection of the virus, and may not necessarily indicate that the current clinical symptoms are caused by feline herpesvirus. However, when quantitative real-time PCR is used, the detected virus concentration can provide further information. If there is a high virus concentration in nasal secretions or tears, it indicates active virus replication and is related to clinical symptoms. If the concentration is low, it indicates latent infection. |
| Antibody Detection | The detection of feline herpesvirus antibodies in serum, aqueous humor, and cerebrospinal fluid can be achieved through serum neutralization tests or enzyme immunoassay (ELISA). Mainly due to natural infection and vaccination, the seropositivity rate of cats is high. |
| Immunofluorescence Antibody Staining | Fluorescent antibody staining can be used to detect the presence of feline herpesvirus specific proteins on smears or biopsy samples of the conjunctiva or cornea. Similar to virus isolation, sampling should be performed before fluorescent staining of the eyes, otherwise false positives may occur. The sensitivity of immunofluorescence antibody staining is not as good as virus isolation and PCR, especially in cases of chronic infection. |
| Virus Isolation | Asymptomatic virus carrying cats may be able to undergo virus isolation, but whether the result is positive or negative, it is not very diagnostic. The samples used for virus isolation must be collected before fluorescence staining or rose bengal staining, and the collected samples should be promptly sent to the laboratory or sent under refrigeration. Although virus isolation has diagnostic significance for initial acute infections, it is rarely used in clinical diagnosis and treatment from a logical perspective. |
Severely infected cats may experience loss of potassium ions and bicarbonate due to insufficient food intake and drooling, so it is best to administer intravenous fluids to correct dehydration, ion and acid-base balance in affected animals. Eating is very important for many diseases in cats. Many cats do not eat because of loss of smell and oral ulcers. It is recommended to provide food that is palatable, and to heat and stir it appropriately to increase the cat's desire to eat. Appetite enhancers can also be given. All cases of acute infection are recommended to be treated with broad-spectrum antibiotics with good respiratory penetration to prevent secondary bacterial infections. The secretions in the nasal cavity should be cleaned with physiological saline and coated with Vaseline ointment to prevent them from adhering to the nostrils. Some mucus dissolving drugs, such as bromahexine, can also be given. For the eyes, steroid free antibiotic eye drops or ointments can be given several times a day. Nebulization therapy can increase the dissolution of secretions and maintain respiratory humidity.
Reference
| Target | Cat. No. | Product Name | Host | Isotype | Application | |
| FHV | CABT-RM029 | Mouse Anti-FHV-1 monoclonal antibody, clone IN650 | Mouse | IgG2a, κ | ELISA, WB, IF, IHC | Inquiry |
| DPAB-CS24106 | Feline Anti-FIV Control Serum | Feline | IgG | IF | Inquiry | |
| CABT-CS636 | Magic™ Mouse Anti-FHV Monoclonal Antibody, clone 123A | Mouse | IgG | ELISA (Cap), LFIA | Inquiry | |
| CABT-CS637 | Magic™ Mouse Anti-FHV Monoclonal Antibody, clone 123B | Mouse | IgG | ELISA (Det), LFIA | Inquiry | |
| DPAB-CS24105 | Feline Anti-FHV-1 Control Serum | Feline | IgG | IF | Inquiry |
| Target | Cat. No. | Product Name | Host | |
| FHV | DAG-WT3378 | Native Feline Herpesvirus Antigen | N/A | Inquiry |
| DAG-WT5870 | Feline Herpes Virus (FHV) Stock (Qualitative) | N/A | Inquiry | |
| DAG-WT1135 | Inactivated Feline Herpes Virus (FHV) | N/A | Inquiry |
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