Taxonomy and Virion Structure
The rabies virus belongs to the family Rhabdoviridae, genus Lyssavirus. This genus also includes related bat viruses (e.g., Lagos bat, Mokola, and Duvenhage viruses) that share a similar morphology with the classic pathogen and are isolated primarily in Africa.
The virion has a characteristic bullet-like shape, with dimensions ranging from 75 to 180 nm. Its internal structure includes:
- Core: A helical ribonucleocapsid.
- Envelope: A lipoprotein supercapsid covered with glycoprotein spikes on its surface.
Genome and Proteins: The genetic material is represented by a single-stranded linear negative-sense RNA. Associated with it is the nucleoprotein (N protein), which forms the capsid. Beneath the lipoprotein envelope lies the matrix protein M. Surface spikes consist of glycoprotein G. Additionally, the virus contains a polymerase complex, including a large L protein and a phosphoprotein P (or NS), which are responsible for viral RNA synthesis.
Antigenic Properties and Immune Response
The main antigen of the rabies virus is glycoprotein G. It forms the surface spikes of the virion and performs crucial functions:
- ensures adsorption (attachment) to target cell receptors;
- facilitates viral entry into the cell;
- possesses high antigenic and immunogenic properties.
In response to viral invasion, the body produces specific virus-neutralizing antibodies directed precisely against glycoprotein G. These antibodies can be detected using a neutralization test.
Internal proteins (ribonucleocapsid) act as group-specific antigens. To detect viral antigens, the direct fluorescent antibody (DFA) test, complement fixation test (CFT), and precipitation test are used.
Life Cycle (Replication)
The replication process of the rabies virus occurs in the cell cytoplasm and includes several stages:
- Adsorption and Penetration: The virus binds via glycoproteins to cellular receptors and enters the cell through clathrin-mediated endocytosis.
- Uncoating: Viral uncoating occurs within endosomes, after which the ribonucleocapsid is released into the cytoplasm.
- Biosynthesis (Transcription and Replication): Viral RNA-dependent RNA polymerase synthesizes short positive-sense strands (mRNA) for protein translation and full-length positive-sense strands that serve as templates to create new genomic negative-sense RNAs.
- Translation and Processing: Viral proteins are synthesized on cellular ribosomes. Glycoprotein G undergoes complex modification in the endoplasmic reticulum and Golgi apparatus before being inserted into the cell membrane.
- Assembly and Release: New copies of negative-sense RNA bind with proteins to form the ribonucleocapsid. Mature virions exit the cell via budding through membrane areas containing viral glycoproteins.
Variants and Diagnostics
Two variants of the rabies virus are distinguished; they are identical in antigenic structure but differ in biological properties:
- Street virus — circulates in nature, highly pathogenic for humans and animals.
- Fixed virus (virus fixe) — a laboratory strain artificially obtained by Louis Pasteur (via rabbit passages). It has lost pathogenicity for humans, is not secreted in saliva, does not form specific intracellular inclusions, and is used to create vaccines.
Intracerebral inoculation of laboratory animals or cell cultures is used to cultivate the virus. A key diagnostic feature of the street virus is the formation of specific eosinophilic cytoplasmic inclusions in brain neurons — Negri bodies (1–15 µm in size), which consist of viral ribonucleoprotein.
Pathogens are rapidly inactivated by UV irradiation, heating (above 60 °C), alkalis, lipid solvents, and proteolytic enzymes, but they survive well at low temperatures (–20 °C to –70 °C).