Satellite viruses are viruses which have small
RNA genome and a protein coat.
Defective viruses can multiply only by
association with a helper virus which
complements the defective gene.
In satellite viruses, the satellite nucleic acid
codes for its own coat protein.
They usually act as parasites of associated
helper viruses.
Satellite viruses have a single-stranded RNA of
800 to 1200 nucleotides.
They are isometric, 17-nm diameter particles,
built of 60 protein subunits,that differs from
their HV.
In addition to the open reading frame (ORF)
encoding their coat protein, some satellite
viruses contain further ORFs.
There are two subgroups in this type
subgroup 1- Chronic bee-paralysis virus-
associated satellite virus-Chronic bee-paralysis
satellite virus
Subgroup 2-Tobacco necrosis satellite viruses,
Maize white-line mosaic satellite virus ,
Panicum mosaic satellite virus ,
Tobacco mosaic satellite virus ,
Tobacco necrosis satellite virus .
Helper viruses
Aureusvirus, Panicovirus, Tobamovirus, and
Necrovirus.
These satellite viruses share no sequence
similarities with each other.
Satellite tobacco mosaic virus (STMV) has a
rod-shaped virus as the helper.
The RNA of Satellite viruses found associated
with chronic bee-paralysis virus (CPV) consists
of three species, about 1.1 kb.
which can be encapsidated in 17-nm isometric
particles built of coat proteins encoded by the
satellite or by CPV.
The satellite interferes with CPV replication.
The STNV subgroup has 1000 to 1200
nucleotide RNA.
It has no methylated cap structure or genome-
linked protein at its 5′-end.
Unlike most plant virus RNAs, it has a
phosphorylated 5′-terminus.
The particles of STNV may also contain a
noncoding satellite RNA of about 620
nucleotides.
This depends on TNV for its replication and on
STNV for its encapsidation.
Satellite RNA are small linear or circular RNA
found inside the virions of certain
multicomponent virus.
They depend on cognate helper viruses for
replication, encapsidation, movement, and
transmission.
Satellite RNAs range in size from 200
nucleotides (nt) to approximately 1,500 nt.
Certain satRNAs code for nonstructural
proteins, but most satRNAs do not encode any
functional protein products.
Therefore exert their biological functions
through direct RNA interactions.
Subgroup 1: Large satellite RNAs
Arabis mosaic virus large satellite RNA
Bamboo mosaic virus satellite RNA
Chicory yellow mottle virus large satellite RNA
Grapevine Bulgarian latent virus satellite RNA
Grapevine fanleaf virus satellite RNA
Myrobalan latent ringspot virus satellite RNA
Tomato black ring virus satellite RNA
Beet ringspot virus satellite RNA
They contains large satRNAs of about 0.7 to 1.5
kb that encode at least one nonstructural
protein.
Hence referred to as messenger-type satRNAs.
They direct protein synthesis both in vitro and in
vivo from a single ORF.
Most of the Btype satellites are found associated
with nepoviruses, and one has been found associated
with the potexvirus(BaMV).
Large satellite RNAs, B-type satellites are
dependent upon the helper virus for replication and
encapsidation.
They are small, linear RNAs of less than 800
nucleotides and with no circular forms that do
not exhibit any biologically significant
messenger activity.
Most satellite RNAs in this subgroup modify
the symptoms induced by the HV.
The most frequent modification is symptom
attenuation, but modulation to more severe
symptoms (eg intense chlorosis or necrosis)
also occurs.
They have small (shorter than 400 nt), circular
RNA genome without biologically significant
messenger activity.
These satellite RNAs occur as both circular and
linear molecules.
The HV may encapsidate circular forms (for
sobemoviruses) or linear forms (for
nepoviruses and luteoviruses).
Small circular single-stranded RNA satellites
interfere with the accumulation and symptoms
induced by the HV.
Modulate − attenuate or exacerbate − the
symptoms caused by their cognate helper
viruses
Do not encode their own RNA-dependent RNA
polymerases(RdRps) for their own replication.
Replication machineries are similar to helper
viruses.
Study of the replication mechanisms of their
cognate helper viruses.
Reduce − the accumulation of their cognate
helper viral RNAs.
Molecular parasites of the helper viruses.
They can accumulate to high levels in host
plants and thus in some cases can be developed
into high-level expression vectors for foreign
genes.
Good biological system for study of molecular
biology of the viruses.
Development of satRNA-based vector systems
for the expression of foreign genes in plants.
In comparison with plasmids and viral
Vectors it has advantages:
i) ease of manipulation,
ii) high in vivo stability,
iii) high expression level.
Because of the relatively small size they are
simpler systems to use for cloning, sequencing,
genetic modification, and regular maintenance.
Most satRNAs are highly structured and thus
significantly more resistant to degradation by
nucleases in vivo than are other viral RNA-based
vector systems. Eg satCMVs
Most satRNAs and satellite viruses can accumulate
to high levels in host plants, which leads to the
increase in level of proteins translated from the
messenger-type RNAs of the satellites.