This document provides an overview of viruses, including:
- The history of virus discovery from Iwanowski's experiments in 1892 showing that the cause of tobacco mosaic disease was able to pass through filters that removed bacteria.
- Characteristics of viruses that distinguish them from living cells, including being acellular and only able to reproduce within host cells.
- The components of viruses, which include nucleic acids and protein capsids, with some viruses also having envelopes.
- The replication cycles of bacteriophages and how they can either undergo lytic or lysogenic cycles, and the replication processes of enveloped DNA, RNA, and retroviruses within host cells.
- Emerging viruses
Viral replication by Kainat Ramzan-SlideShareKainatRamzan3
Virus multiplication are in Following steps: attached, penetration, biosynthesis, maturation, assembly and release and also discribe the life of Bacteriophage by following two life cycle
Present By Kainat Ramzan
Bacteriophage is the most common and extensively studied virus. The life cycle of bacteriophages. The transfer of their genetic system via the process of transduction (Generalised and Specialised) and studying the gene mapping in phages. This theoretical explanation about viruses and their genetic system will help the learner in the fields of biotechnology, microbiology, basic science, life science, and various other fields of biology.
General Characters and Classification of Viruses. Includes ICTV classification and Baltimore classification of viruses. A brief explanation of the Viral structure and Lifecycle.
Morphology, Classification, Cultivation and Replication of VirusKrutika Pardeshi
This presentation is Useful for B. Pharmacy SEM III Students to study the Topic Fungi According to PCI Syllabus.
It Consist of Morpholoy of Fungi, Cultivation , Replication and Classification of Virud
Viral replication by Kainat Ramzan-SlideShareKainatRamzan3
Virus multiplication are in Following steps: attached, penetration, biosynthesis, maturation, assembly and release and also discribe the life of Bacteriophage by following two life cycle
Present By Kainat Ramzan
Bacteriophage is the most common and extensively studied virus. The life cycle of bacteriophages. The transfer of their genetic system via the process of transduction (Generalised and Specialised) and studying the gene mapping in phages. This theoretical explanation about viruses and their genetic system will help the learner in the fields of biotechnology, microbiology, basic science, life science, and various other fields of biology.
General Characters and Classification of Viruses. Includes ICTV classification and Baltimore classification of viruses. A brief explanation of the Viral structure and Lifecycle.
Morphology, Classification, Cultivation and Replication of VirusKrutika Pardeshi
This presentation is Useful for B. Pharmacy SEM III Students to study the Topic Fungi According to PCI Syllabus.
It Consist of Morpholoy of Fungi, Cultivation , Replication and Classification of Virud
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Introduction:
RNA interference (RNAi) or Post-Transcriptional Gene Silencing (PTGS) is an important biological process for modulating eukaryotic gene expression.
It is highly conserved process of posttranscriptional gene silencing by which double stranded RNA (dsRNA) causes sequence-specific degradation of mRNA sequences.
dsRNA-induced gene silencing (RNAi) is reported in a wide range of eukaryotes ranging from worms, insects, mammals and plants.
This process mediates resistance to both endogenous parasitic and exogenous pathogenic nucleic acids, and regulates the expression of protein-coding genes.
What are small ncRNAs?
micro RNA (miRNA)
short interfering RNA (siRNA)
Properties of small non-coding RNA:
Involved in silencing mRNA transcripts.
Called “small” because they are usually only about 21-24 nucleotides long.
Synthesized by first cutting up longer precursor sequences (like the 61nt one that Lee discovered).
Silence an mRNA by base pairing with some sequence on the mRNA.
Discovery of siRNA?
The first small RNA:
In 1993 Rosalind Lee (Victor Ambros lab) was studying a non- coding gene in C. elegans, lin-4, that was involved in silencing of another gene, lin-14, at the appropriate time in the
development of the worm C. elegans.
Two small transcripts of lin-4 (22nt and 61nt) were found to be complementary to a sequence in the 3' UTR of lin-14.
Because lin-4 encoded no protein, she deduced that it must be these transcripts that are causing the silencing by RNA-RNA interactions.
Types of RNAi ( non coding RNA)
MiRNA
Length (23-25 nt)
Trans acting
Binds with target MRNA in mismatch
Translation inhibition
Si RNA
Length 21 nt.
Cis acting
Bind with target Mrna in perfect complementary sequence
Piwi-RNA
Length ; 25 to 36 nt.
Expressed in Germ Cells
Regulates trnasposomes activity
MECHANISM OF RNAI:
First the double-stranded RNA teams up with a protein complex named Dicer, which cuts the long RNA into short pieces.
Then another protein complex called RISC (RNA-induced silencing complex) discards one of the two RNA strands.
The RISC-docked, single-stranded RNA then pairs with the homologous mRNA and destroys it.
THE RISC COMPLEX:
RISC is large(>500kD) RNA multi- protein Binding complex which triggers MRNA degradation in response to MRNA
Unwinding of double stranded Si RNA by ATP independent Helicase
Active component of RISC is Ago proteins( ENDONUCLEASE) which cleave target MRNA.
DICER: endonuclease (RNase Family III)
Argonaute: Central Component of the RNA-Induced Silencing Complex (RISC)
One strand of the dsRNA produced by Dicer is retained in the RISC complex in association with Argonaute
ARGONAUTE PROTEIN :
1.PAZ(PIWI/Argonaute/ Zwille)- Recognition of target MRNA
2.PIWI (p-element induced wimpy Testis)- breaks Phosphodiester bond of mRNA.)RNAse H activity.
MiRNA:
The Double-stranded RNAs are naturally produced in eukaryotic cells during development, and they have a key role in regulating gene expression .
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
2. Learning objectives
i. Describe the history of virus discovery.
ii. Contrast the characteristic of a virus as compared to
a living cell.
iii. Understand the origin of virus.
iv. Explain virus component and shape.
v. Characterize a bacteriophage.
vi. Contrast bacteriophage lytic and lysogenic life cycle.
vii. Describe the life cycle of an enveloped DNA and
RNA virus.
viii. State the characteristic of viriods and prions.
3. History of virus discovery
❖ In the late 1800s, botanists had
been trying to find the cause of
tobacco mosaic disease.
❖ In 1892, D. IWANOWSKI
tried to filter the sap of infected
tobacco plants (Filter capable
of removing particles the size
of all known bacteria).
5. History of virus discovery
❖ The filtrate was FULLY CAPABLE of
producing the ORIGINAL DISEASE
in new hosts.
❖ Nothing could be seen in the filtrates
using the most powerful microscopes,
nor could anything be cultivated from
the filtrates.
❖ Iwanowski concluded that the bacteria
was so small / or they made a filterable
toxin.
6. History of virus discovery
● A Dutch botanist named Martinus Beijerink
ruled out the filterable toxin conclusion
because the filtered sap are capable of causing
undiluted infection.
● The agent cannot be cultivated on nutrient
media (need a host)
● In 1935, Stanley
discovered this agent
after crystallization
7.
8. Virus characteristics
❖ Viruses are not classified into any of the
biological classification system.
❖ They lie in the threshold of life and
nonlife.
9. Virus characteristics
Non-Life
❖ They are acellular, with no
cell nucleus, organelles
or cytoplasm. Therefore,
they do not have the
components necessary to
carry metabolic activities
independently.
❖ Viruses cannot move and
reproduce on their own.
Life
❖ They could only reproduce
within the living cells that
they infect. They use their
genetic information to force
the host cell to replicate
themselves (obligate
intracellular parasite) .
10. Virus size
❖ Viruses are smaller than
bacteria.
❖ Viruses are too small even
to be seen by a light
microscope.
❖ The biggest size virus is
about 240-300nm (1/10 of
red blood cells/ size of the
smallest bacteria)
❖ The tiniest virus is 20nm –
smaller than a ribosome
11.
12. Virus origin ❖ According to a hypothesis,
viruses are bits of nucleic acid
that ‘escaped’ from cellular
organism.
❖ Some traces are from animal
cells, plant cells and bacterial
cells.
❖ Their multiple origins explain
why viruses are species-specific.
❖ However, some other have
broader range of host cells
13. Virus component
❖Virus consist of only
I) Nucleic acid (DNA or RNA) The DNA /RNA
could be single or double stranded.
II) A capsid or a protein coat which functions in
protecting the genetic material during the viral
infection process.
III) In some viruses, there is an outer envelope
that encloses the coat, and is made of parts of
the previously infected cells.
(A complete virus that consist of the genetic material, the protein
coat and an envelope is called the virion)
15. Virus shape
Virus shape can be based on the capsid
i. Helical (rod-shaped) e.g. tobacco mosaic
virus
ii. Polyhedral / Icosahedral (many-sided
shaped) e.g. adenovirus.
iii. Complex combination of both by having
structures like tail (helical and polyhedral)
e.g. bacteriophage
iv. Most enveloped virus have spherical shape
e.g. influenza virus
16.
17.
18. Virus classification
❖ Before, viruses are classified according to the type of host that
they infected.
❖ The current system reflect phenotypic characteristics.
❖ The Baltimore classification system distinguish viruses based
on their
- Method of replication
- Genome type (DNA or RNA)
❖ The International Committee on Taxonomy of Viruses
devised and implemented several rules on the naming and
classification of viruses early in the 1990s.
❖ It started at the level of order and ends at genus
20. Bacteriophage
❖ Much of the knowledge comes from studying
bacteriophage, because they can be cultured easily
within living bacteria.
❖ Bacteriophage possess dsDNA inside their capsid
(protein head). The capsid functions as protection of
their genetic material.
❖ Their tail fibers are the base used to attach themselves
to bacterial host cell
❖ The tail is the channel for their genetic material to be
injected to the host cell.
22. Bacteriophage replication
❖ There are two types of bacteriophage
replication, LYTIC and LYSOGENIC cycles.
❖ In a lytic cycle, the virus destroys the host cell.
It is a rapid process where the host cell
undergoes lysis.
❖ In a lysogenic cycle, the viral genome usually
becomes integrated into the host cell.
23. Virus lytic cycle
There are five steps in a typical bacteriophage lytic
reproduction,
i. Attachment-A virus will attach to a suitable
host cell
ii. Penetration- The whole virus or only the
genetic material (nucleic acid) will penetrate the
cell’s cytoplasm. A bacteriophage capsid
remains on the outside of the bacterial cell
whereas many viruses that infect animal cell
enter a host cell intact.
25. Virus lytic cycle
iii. Replication and synthesis - The viral
DNA/RNA directs the host cell to produce
many copies of viral nucleic acids and proteins
necessary for its replication.
iv. Assembly - The viral nucleic acids and
proteins are assembled together to form new
infectious particles.
v. Release - Newly generated viral particles are
released from the host cell.
26.
27.
28.
29.
30.
31. Virus lysogenic cycle
❖ The infection will enter a latent period. The host cell
is not killed in this process, but the viral nucleic acid
will undergo genetic recombination with the host
cell’s chromosome. This integrated structure is
called a prophage.
❖ When the bacterial DNA replicates, the prophage
also replicates.
❖ Certain external condition such as UV light and
x-rays cause viruses to revert to a lytic cycle and
then destroy their hosts.
34. Reproductive Cycles of Animal
Viruses
• There are two key variables used to classify
viruses that infect animals:
● DNA or RNA?
● Single-stranded or double-stranded?
35. Replication of an enveloped DNA virus
❖ Enveloped virus has a different way of infecting eukaryotic
cells.
❖ After attachment to a host-cell receptor, some enveloped
viruses fuse with the animal cell’s plasma membrane. The
viral capsid and nucleic acid will then be released into the
animal cell.
36. Enveloped virus penetration step
❖ Some virus enter the cell through endocytosis.
❖ In this process, the plasma membrane of the animal cell
invaginates to form a membrane-bounded vesicle that
contains a virus.
37. Replication of an enveloped DNA virus
❖ The viral DNA will be replicated and transcribed by the
host cell.
❖ After the viral genes are transcribed, the viral structural
proteins are synthesized through translation outside
nucleus.
❖ The new virus particles are then assembled.
❖ Enveloped viruses obtain their glycoprotein spikes on the
envelopes by picking up a fragment of the host plasma
membrane as they leave the infected cell.
38. 1. After entering the cell, the viral
DNA uses host nucleotides and
enzymes to replicate itself
2. The viral DNA use other host
resources to produce its capsid
proteins by transcription and
translation
3. The new viral DNA and capsid
protein assembled into new virus
particle, which leave the cell
1 2
3
Self-assembly of new
virus particles and
their exit from cell
39.
40. Replication of an enveloped RNA virus
❖ The viral genome (single stranded RNA) function as
a template for synthesis of complementary RNA
strand
❖ Some complementary strands became mRNA that
will translated
❖ Viral genome RNA are made using complementary
strands
❖ After translation, assembly and release step be done
in proper sequence
41. 1. Glycoprotiens bind to specific
receptor on the surface of the host
cell
2. Capsid and viral genome enter the
cell
3. Cellular enzyme remove the capsid
4. The viral genome functions as a
template for making complementary
RNA strands which have two
functions
5. Serves as templates for making new
copies of genome RNA
6. Serves as mRNA which will be
translated into both capsid proteins
and glycoprotein for the viral
enveloped
7. Vesicle transport (ER) the
glycoproteins to the cell’s plasma
membrane
8. A capsid assembled around each
viral genome molecule
1
2
3
4
5 6
7
8
42.
43. Replication of an RNA virus (retrovirus)
● Virus attach through specific glycoprotein and enter
through endocytosis
● Digestion of capsid through cellular enzyme
● Viral RNA ia a template for complementary DNA sense
by reverse transcriptase
● Second DNA strand will be synthesized by reverse
transcriptase
● Ds DNA incorporated with the cell’s DNA as a provirus
● The genes are replicated, transcribed and translated to
build the components for the RNA virus assembly
before being released
44. 1. The virus fuses with the cell’s plasma
membrane. The capsid proteins are removed,
releasing the viral genome.
2. Reverse transcriptase catalyzes the synthesis of
a DNA strand complimentary to the viral RNA.
3. Reverse transcriptase catalylzes the synthesis of
the second DNA strand complimentary to the
first.
4. The double stranded DNA is incorporated as a
provirus into the cell’s DNA (chromosomal DNA)
5. Proviral gene are transcribed into RNA
molecules.
6. RNA transcribed from the provirus serves as
mRNA for translation into HIV proteins and as
genome for the next viral generations.
7. Capsids are assembled around viral genomes
and reverse transcriptase molecules.
8. The new viruses bud off from the host cell.
1
2
3
4
5
6
7
8
45.
46.
47. H1N1 virus
● H1N1 virus isolated
from patients found that
it is made up of genetic
elements from four
different flu viruses –
North American
Mexican influenza,
North American avian
influenza, human
influenza, and swine
influenza virus
48. Viruslike agents
❖ Viruses is considered as the smallest living /
nonliving microbe.
❖ However, there are even smaller infectious
agents found – viroids and prions.
49. Viroids
❖ In 1961, an infective agent in potatoes has been
discovered. The agent is called viroid and it is
smaller than viruses with no protein coats.
❖ Viroids are infectious RNA particle that may cause
plant diseases by interfering with mRNA processing.
50. Prions
❖ Prions are infectious particles made of protein. Research
indicates that prions are normal proteins that become folded
incorrectly.
❖ Prions could cause neurological degenerative diseases such
as mad cow disease and Scrapie.