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Replication Cycle

Viral replication and transcription of associated virus orthomyxovirus.

Attachment and Entry

There is limited information of the replication cycle specific to TiLV, but it is known to be in the family Orthomyxoviridae due to its single-stranded negative-sense RNA genome. Typical Orthomyxoviridae carry several surface glycoproteins that recognize and bind to sialic acid receptors on the target cell membrane. The target cell transports the virus into the cell by receptor-mediated endocytosis, initiating endosome acidification. This acidification results in a conformational change of the viral glycoprotein, initiating membrane fusion of the viral envelope and endosomal membrane. Once fusion is complete, the viral genome, accessory proteins, and RNA dependent RNA polymerase are released into the host cell cytoplasm.

Viral Replication and Transcription

Through in situ hybridization, it is found that transcription of the TiLV viral genome occurs in the nucleus, this is common among all Orthomyxoviridae. The nucleocapsid of an orthomyxovirus is transported to the nucleus where it is transcribed by viral enzymes resulting in the production of viral mRNA. Cap sequences are taken from the host cell mRNA during transcription and bound to viral mRNA, this allows the viral mRNA to exit the nucleus and return to the cytoplasm of the host cell where it will by recognized and translated into proteins by host cell ribosomes. The 5' and 3' noncoding termini of TiLV include 13 similar nucleotides, this enables base pairing and replication, transcription, and packaging of viral RNA as a result of the formation of secondary structures. In addition, all of the 5′ ends of TiLV genomic RNA segments contain a brief uridine stretch (3 to 5 bases long). This short uninterrupted sequence resembles that of the 5 to 7 uridine nucleotides found in many other orthomyxoviridae, this occurs when the viral polymerase "stutters" while assembling poly(A) tails.

Assembly and Release

Orthomyxovirus viral glycoproteins then travel to the cell membrane where they form a spherical bud to transport negative-stranded vRNA out of the host cell. After the new viral material leaves the host cell, the host cell is terminated.

Interactions with Host

In cell culture, the affected cells exhibit significant cytopathic effect (CPE), structural changes of the host cell due to viral infection. Clear and rapid CPE development occurs primarily at the E-11 cell line, cell lines of the brain and liver have been shown to be highly permissive at propagating TiLV. Cases of infection note syncytium formation, the fusion of infected neighboring cells to produce multi-nucleated cells. Syncytial cells of this species are characterized by swollen mitochondria. Hepatocytes of infected tilapia are swollen and dissociated, with significant cytoplasmic accumulation of yellow to brown pigment (MMC) in both the spleen and liver of naturally and experimentally infected fish. 'in addition, experimental infection shows histologic lesions on the brain such as edema, focal hemorrhages in the leptomeninges, and capillary congestion in both the white and gray matter.

Studies have shown that upon experimental infection of TiLV, histopathological lesions have been found similar to those seen in natural outbreaks. These natural outbreaks have been characterized with lethargy, discoloration, ocular alterations, skin patches, and ulcerations of the digestive tract. The main organs where pathology is observed are the brain, eyes, and liver. Gross lesions are commonly visible in infected species such as ocular opacity of the cataract, and skin erosions such as, loss of scales or discoloration, skin hemorrhages, abdominal swelling, scale protrusion, and exophthalmia.

Associated Diseases

There is little known of the relationship of TiLV to other viral aquaculture diseases, but viruses such as infectious salmon anemia orthomyxoviruses, infectious hematopoietic necrosis virus, and viral hemorrhagic septicemia virus are common causes of illness and death in cultured fish. Salmon anemia orthomyxoviruses, influenza, and Thogoto have also been said to be have similar replication to that of TiLV due to organization of nucleotide sequences in transcription enabling base pairing. Specific to tilapia, Tilapia iridovirus is the only significant viral pathogen known to cause severe disease and die-offs. Other pathogens known to cause viral diseases in this species are betanodavirus and herpes-like virus.

Viral Transmission and Control

The virus is found to be transmitted through direct horizontal transmission by cohabitation or transfer of live aquatic animals, although these viral pathogens have been found in fresh and preserved tilapia. There is limited information on the biophysical properties and risks of TiLV associated with animal product but research suggests that the eye, brain and liver are likely to contain highest concentrations of TiLV and thus solid and liquid waste are likely to be contaminated. There is currently no evidence of vertical transmission of TiLV.

Restriction of the movement of live tilapines between farms or fisheries is thought to limit the spread of the viral disease to new species, as well as maintaining clean practices and sanitizing equipment in these areas. There is still no evidence that there are practices to limit viral spread in an infected farm.