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How Does Viral Rna Enter An Animal Cell

The following points highlight the 6 primary stages involved in the replication of animal viruses. The stages are: one. Adsorption 2. Penetration iii. Un-Coating 4. Replication of Viral Genome 5. Synthesis and Associates of Virus Capsids vi. Release of New Virus.

Phase # i. Adsorption:

Adsorption to the host cell surface is the first stride in reproduction cycle of animal viruses. Adsorption of virion to the host cell surface takes identify through a random collision of virion with a plasma membrane receptor site; the receptor is a poly peptide, and frequently a glycoprotein. Animal viruses, like bacteriophages, possess attachment sides with the help of which it attaches to the receptor site.

Besides of glycoprotein receptors, sometimes, a complex carbohydrate (eastward.m., heparan sulfate) is the receptor, these receptors vary in their distribution pattern on plasma membrane and this distribution variation plays a key office in tissue and host specificity of beast viruses.

For instance, poliovirus receptors are constitute only in man nasopharynx, gut, and cells of spinal cord. While receptors of measles virus occur in virtually tissues.

Differences in nature of polio and measles can be explained through the dissimilarities in the distribution of receptor proteins of host cells to which viruses get adsorbed. In some naked viruses (e.g. adenoviruses) the attachment sites are small fibres at the corners of icosahedron. In enveloped viruses (e.g. myxoviruses) the attachment sites are the spikes nowadays on the surface of envelope.

For example, flu virus has two types of spikes: H (haemagglutinin) spikes and Due north (neuraminidase) spikes. The H spikes attach to the host cell receptor site by recognising sialic acid (Due north-acetyl neuraminic acid), the sugar derivative of glucoprotein.

Influenza neuraminidase helps the virus in penetrating the nasal and respiratory tract secretions past degrading mucosal polysaccharides. However, the receptor sites also vary from person to person.

Stage # ii. Penetration :

Creature viruses penetrate the host cell shortly later adsorption.

Though the detailed machinery of penetration in not articulate, the following three modes are the almost favoured past the researchers:

1. Straight penetration:

Some naked fauna viruses (e.g., picornaviruses, adenoviruses) use vesicle acidification that causes a major change in capsid construction after adsorption to plasma membrane. This altered capsid contacts the vesicle membrane and either releases the viral genome into the cytoplasm through a membrane pore (picornaviruses) or ruptures the membrane to release the viral genome (adenovirus) into the cytoplasm (Fig. 14.3).

Direct penetration by naked virus

2. Fusion with plasma membrane:

The envelop of enveloped virus (e.thou., paramyxoviruses) fuses directly with host plasma membrane. Fusion may involve special envelop fusion proteins that bind to plasma membrane proteins. Finally, the nucleocapsid enters the cytoplasmic matrix where un-coating is washed (Fig. 14.4). A virus polymerase associated with the nucleocapsid, transcribes the virus RNA while the latter is nevertheless within the capsid.

Entry of enveloped virus by fusion with plasma membrane

3. Endocytosis:

Many of the enveloped viruses and certain non-enveloped viruses enter the host cell through engulfment by receptor-mediated endocytosis and form coated vesicles.

The virions attach to coated pits with the protein clathrin and the pits then pinch off to form coated vesicles filled with viruses. These vesicles fuse with lysosomes afterward the clathrin has been removed. Lysosomal enzymes assist in un-coating of virion inside the cytoplasm. (Fig. 14.5).

Entry of enveloped virus by endocytosis

Stage # iii. Un-Coating :

Un-blanket is the procedure of separation of viral genome from the protein glaze. Though the process of un-blanket is not fully understood, information technology is proclaimed that the lysosomal enzymes help in animal virus un-coating past degrading the capsid and low endosomal pHs ofttimes trigger the process of un-coating.

Information technology has been reported in some cases that the viral envelop fuses with the lysosomal membrane and the partially degraded capsid along with viral genome (nucleocapsid) is released into the host cytoplasm. Once in the cytoplasm, viral genome may be released from the capsid upon completion of un-coating or may part while still attacked to capsid components.

Phase # four. Replication of Viral Genome :

The replication process of DNA viruses differs from that of RNA viruses. Even so, in some Dna viruses the replication takes place in cytoplasm (e.g., poxviruses) and in some others in the nucleus of host (e.g., parvoviruses, papovaviruses, adenoviruses, herpes viruses).

Replication of viral genome in RNA viruses is more or less the same as in DNA viruses except the machinery of germination of mRNA among the different group.

Stage # 5. Synthesis and Associates of Virus Capsids :

Sure late genes directly the synthesis of capsid proteins. The latter spontaneously self-assemble to form the capsid. It appears that in instance of icosahedral viruses the capsid protein assembly first forms procapsid in which the viral genome is inserted by some unknown machinery. However, in example of enveloped viruses the capsid poly peptide assembly is generally similar to that of naked viruses (poxvirus is exception).

The capsids of these viruses are assembled in the prison cell cytoplasm by a lengthy, circuitous procedure that begins with the enclosure of a portion of cytoplasmic matrix through construction of a new membrane. Now the newly synthesized viral DNA condenses, passes through the membrane, and moves to the middle of the immature virus.

Phase # vi. Release of New Virus :

Release of newly formed animal viruses from the host cell differs betwixt naked and enveloped viruses. The naked brute viruses are released nearly often past the lysis of the host cell. In enveloped viruses, notwithstanding, the virus-encoded proteins are incorporated in the plasma membrane and and so the nucleocapsid is simultaneously released; the envelop is formed past membrane-budding.

Source: https://www.biologydiscussion.com/viruses/replication-of-animal-viruses-6-main-stages/54919

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