0.1 What are viruses?
1. Origin of viruses
1.1 introduction
1.2 Theories
RNA molecules that existed before cells
cell components
micro-organisms.
1.3 Conclusion: How did viruses originate?
INTRODUCTION:
The first plant virus shown to have a DNA genome and the first shown to replicate by reverse transcription.
Worldwide but only causes significantly losses locally.
It is transmitted by aphids .
Type member of the Caulimovirus genus, contains 11 species and 6 possible members.
significantly impact on plant virology and plant molecular biology.
The virus is an important source of gene regulatory elements, used exclusively in the genetic manipulation of plants.
STRUCTURE:Icosachedral with a diameter of 52Â nm built from 420 capsid protein subunits.
It contains a circular double-stranded DNA molecule of about 8.0 kB .
Dna is interrupted by sitespecific discontinuties resulting from its replication by reverse transcription.
After entering the host, the single stranded nicks in the viral DNA are repaired, forming a supercoiled molecule that binds to histones.
DNA is transcriped into a full length .
Replication
Risk Factors:The Cauliflower mosaic virus promoter (CaMV 35S) is used in most transgenic crops to activate foreign genes which have been artificially inserted into the host plant. It is inserted into transgenic plants in a form which is different from that found when it is present in its natural Brassica plant hosts. This enables it to operate in a wide range of host-organism environments which would otherwise not be possible.
INTRODUCTION:
The first plant virus shown to have a DNA genome and the first shown to replicate by reverse transcription.
Worldwide but only causes significantly losses locally.
It is transmitted by aphids .
Type member of the Caulimovirus genus, contains 11 species and 6 possible members.
significantly impact on plant virology and plant molecular biology.
The virus is an important source of gene regulatory elements, used exclusively in the genetic manipulation of plants.
STRUCTURE:Icosachedral with a diameter of 52Â nm built from 420 capsid protein subunits.
It contains a circular double-stranded DNA molecule of about 8.0 kB .
Dna is interrupted by sitespecific discontinuties resulting from its replication by reverse transcription.
After entering the host, the single stranded nicks in the viral DNA are repaired, forming a supercoiled molecule that binds to histones.
DNA is transcriped into a full length .
Replication
Risk Factors:The Cauliflower mosaic virus promoter (CaMV 35S) is used in most transgenic crops to activate foreign genes which have been artificially inserted into the host plant. It is inserted into transgenic plants in a form which is different from that found when it is present in its natural Brassica plant hosts. This enables it to operate in a wide range of host-organism environments which would otherwise not be possible.
TOBACCO MOSAIC VIRUS (Genome organization &their replication) TMV is a plant virus which infects a wide range of plants, especially tobacco and other members of the family Solanaceae and cucumbers, and a number of ornamental flowers.
Animal viruses are self replicating, intracellular parasites that completely rely on host animal cell for reproduction. They use the host's cellular components to replicate, then leaves the host cell to infect other cells.
Virus isolation in embryonated eggs, cell cultures and animals
Purification by centrifugation, chromatography and electrophoresis
3d models such as organoid cultures is not discussed
inroduction:Plant viruses are viruses that affect plants.
Pathogenic to higher plants.
. Harmless to human and other animals.
Reduce plant crop yield and quality of crops.
Some may be able to multiply within the bodies
Of aphids and nematodes.
History:Beijernick ( 1897) coined the latin name “VIRUS” meaning Poison. He studied plant juices and found they caused healthy plants to become sick.
Wendell Stanley (1935) crystallized sap from sick Tobacco plants. He discovered viruses were made of nucleic acids and proteins.
Geminivirus:one of the family of plant virus.
Currently over 360 species in this family, divided among 9 genera.
Diseases associated with this family include bright yellow mosaic , yellow mosaic, yellow mottle, leaf curling, stunting, streaks, reduced yields.
Ss circular dna diverge in both directions from a virion strand origin of replication (AMBISENSE).
Virus Classification:Group – Group II (ssDNA)
Order - Unassigned
Family - Geminiviridae
Genera – Becurtovirus Grablovirus
Begomovirus Mastrevirus
Capulavirus Topocuvirus
curtovirus Turncurtovirus
Eragrovirus
Structure: have Circular single-stranded DNA.
Genome is either in two segments.
The non-segmented genome is 2500-3000 nucleotides long, and the segmented genome is 4800-5600 nucleotides long.
The genome encodes for both structural and non-structural proteins.
In geminivirus, both segments must be transmitted to the host for a full systemic infection to occur.
Virion Sturcture:Geminivirus are non-enveloped, icosahedral virions that consists of a capsid.
The capsid is germinate, or twinned, and consists of 22 Capsomers.
The capsid is 30nm long and has a diameter of 18-20nm.
Symptoms:the time of infection, the virus strains and the presence of mixed infections.
Common symptoms are stunting, curling, and twisting of leaves.
Short internodes and stunted appearance , no apical growth caused by early infection.
Replication:Geminivirus encodes only a few proteins, thus they need to dependent host cell factors for replication.
These factors are DNA polymerase and repair polymerase to amplify their genome.
Replicate by a rolling circle mechanism like bacteriophages such as M13, and many plasmids.
Viruses are small, acellular particles that can replicate only in a host cell. They are obligatory intracellular parasites.They
consist of a nucleic acid genome enclosed in a protective protein shell or capsidBacteriophage is the virus that infect bacteria.Bacteriophages were discovered by Frederick Twort(1915)and Felix d'Herelle(1917).
Detailed description about viroid, virusoid and prions are described in a simple and detailed manner, will be very to understand about different plant pathogens
TOBACCO MOSAIC VIRUS (Genome organization &their replication) TMV is a plant virus which infects a wide range of plants, especially tobacco and other members of the family Solanaceae and cucumbers, and a number of ornamental flowers.
Animal viruses are self replicating, intracellular parasites that completely rely on host animal cell for reproduction. They use the host's cellular components to replicate, then leaves the host cell to infect other cells.
Virus isolation in embryonated eggs, cell cultures and animals
Purification by centrifugation, chromatography and electrophoresis
3d models such as organoid cultures is not discussed
inroduction:Plant viruses are viruses that affect plants.
Pathogenic to higher plants.
. Harmless to human and other animals.
Reduce plant crop yield and quality of crops.
Some may be able to multiply within the bodies
Of aphids and nematodes.
History:Beijernick ( 1897) coined the latin name “VIRUS” meaning Poison. He studied plant juices and found they caused healthy plants to become sick.
Wendell Stanley (1935) crystallized sap from sick Tobacco plants. He discovered viruses were made of nucleic acids and proteins.
Geminivirus:one of the family of plant virus.
Currently over 360 species in this family, divided among 9 genera.
Diseases associated with this family include bright yellow mosaic , yellow mosaic, yellow mottle, leaf curling, stunting, streaks, reduced yields.
Ss circular dna diverge in both directions from a virion strand origin of replication (AMBISENSE).
Virus Classification:Group – Group II (ssDNA)
Order - Unassigned
Family - Geminiviridae
Genera – Becurtovirus Grablovirus
Begomovirus Mastrevirus
Capulavirus Topocuvirus
curtovirus Turncurtovirus
Eragrovirus
Structure: have Circular single-stranded DNA.
Genome is either in two segments.
The non-segmented genome is 2500-3000 nucleotides long, and the segmented genome is 4800-5600 nucleotides long.
The genome encodes for both structural and non-structural proteins.
In geminivirus, both segments must be transmitted to the host for a full systemic infection to occur.
Virion Sturcture:Geminivirus are non-enveloped, icosahedral virions that consists of a capsid.
The capsid is germinate, or twinned, and consists of 22 Capsomers.
The capsid is 30nm long and has a diameter of 18-20nm.
Symptoms:the time of infection, the virus strains and the presence of mixed infections.
Common symptoms are stunting, curling, and twisting of leaves.
Short internodes and stunted appearance , no apical growth caused by early infection.
Replication:Geminivirus encodes only a few proteins, thus they need to dependent host cell factors for replication.
These factors are DNA polymerase and repair polymerase to amplify their genome.
Replicate by a rolling circle mechanism like bacteriophages such as M13, and many plasmids.
Viruses are small, acellular particles that can replicate only in a host cell. They are obligatory intracellular parasites.They
consist of a nucleic acid genome enclosed in a protective protein shell or capsidBacteriophage is the virus that infect bacteria.Bacteriophages were discovered by Frederick Twort(1915)and Felix d'Herelle(1917).
Detailed description about viroid, virusoid and prions are described in a simple and detailed manner, will be very to understand about different plant pathogens
Lung carcinogenesis by tobacco smoke - Arabic presentationHaçan Elhalabi
Lung Carcinogenesis by Tobacco Smoke
أهداف العرض التقديمي
عرض مكونات الدخان ودورها في السرطان.
آليات التأثير على المادة الوراثية وإحداث السرطان.
العلائم الحيوية الدالة على المواد المسرطنة (مراقبة).
تقديم الدلائل للمدخنين على خطورة الإقدام على التدخين (وقاية).
التدخين
الآليّات العامّة لسرطان الرئة المحدث بواسطة دخان التبغ :
Lung Cancer Pathways
مناقشة المكونات كل على حدى
1. النيكوتين
المسرطنات
4. متراكبات الدنا DNA Adduct
5.تبعات تشكل متراكبات الدنا DNA
6. المحددات الحيوية Biomarkers
Conclusion
نتائج مدمرة على صعيد الصحة الشخصية –سرطان الرئة- قد تنتهي بالموت
تم إيضاح آلية حدوث السرطان بشكل جيد في سرطان الرئة ولكن دور العديد من المواد لم يحدد بشكل دقيق بعد (متراكبات الدنا, دور المواد غير السامة جيناً...)
فهم أفضل للسرطان – وقاية أفضل.
Virus, infectious agent of small size and simple composition that can multiply only in living cells of animals, plants, or bacteria. The name is from a Latin word meaning “slimy liquid” or “poison.”
human_papilomma_viruses.
definition, species and category.
the virus has the great health effect on men and women; specially its effect on the reproductive organs.
An infection that causes warts in various parts of the body, depending on the strain.
Human papillomavirus (HPV) is the most common sexually transmitted infection (STI).
Many people with HPV don't develop any symptoms but can still infect others through sexual contact. Symptoms may include warts on the genitals or surrounding skin.
There's no cure for the virus and warts may go away on their own. Treatment focuses on removing the warts. A vaccine that prevents the HPV strains most likely to cause genital warts and cervical cancer is recommended for boys and girls.
HPV infection is a viral infection that commonly causes skin or mucous membrane growths (warts). There are more than 100 varieties of human papillomavirus (HPV). Some types of human papillomavirus (HPV) infection cause warts, and some can cause different types of cancer.
Most HPV infections don't lead to cancer. But some types of genital HPV can cause cancer of the lower part of the uterus that connects to the vagina (cervix). Other types of cancers, including cancers of the anus, penis, vagina, vulva and back of the throat (oropharyngeal), have been linked to HPV infection.
These infections are often transmitted sexually or through other skin-to-skin contact. Vaccines can help protect against the strains of HPV most likely to cause genital warts or cervical cancer.
Cervical cancer
Nearly all cervical cancers are caused by HPV infections, but cervical cancer may take 20 years or longer to develop after an HPV infection. The HPV infection and early cervical cancer typically don't cause noticeable symptoms. Getting vaccinated against HPV infection is your best protection from cervical cancer.
كيف تحمي نفسك من الهجوم الكيمائي؟
الهجوم الكيمائي- السارين
ماهو السارين:
سلاح قوي جداً للحرب الكيماوية يستخدم في الحروب كسم للأعصاب وينتمي إلى زمرة الفوسفات العضوية, يؤدي في الجسم إلى تعطيل إشارات إيقاف التقلص العضلي و بالتالي يؤدي إلى تقلص مستمر (تشنج مستمر) و الخطورة تكمن في توقف العضلات التنفسية عن العمل.
متى استخدم غاز السارين:
كيف يتعرض الناس للسارين؟
ما هي المدة اللازمة لظهور الأعراض على المصابين:
الأعراض و العلامات الفوري/ة التي تظهر على المصاب:
خطوات العلاج:
التصنيف
المرادفات والأسماء الشائعة
نبذة تاريخية
المواد الفعالة
دليل الجرعات
محاذير الاستخدام
ملاحظات حول الاستخدام
وصف النبات
القسم المستعمل
المكونات
المواد الفعالة
What’s a suspension ?
Suspension Requirements?
Why a suspension?
Stability;
HOW TO MAKE A FINE POWDER? (10-50 MICRON)
Fluid Energy
Preparing Flocculated suspensions
Formulation considerations for orally administered suspension:
Rheology
Rheology for Pharmacists
Excipients used in the formulation of suspensions for oral administration:
Excipients used in the formulation of suspensions for oral administration:
Some subdosage forms of suspensions
Extemporaneous Prepration:
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
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Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
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The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
3. TABLE OF CONTENTS SECTION 1
•0.1 What are viruses?
•1. Origin of viruses
• 1.1 introduction
• 1.2 Theories
• RNA molecules that existed before cells
• cell components
• micro-organisms.
• 1.3 Conclusion: How did viruses originate?
5. WHERE DID VIRUSES COME FORM?
THE MAIN QUESTION NEEDS TO BE
ANWERED IS:
6. WHAT ARE VIRUSES?
• Parasites, selective infection.
• Living or not?
• Genetics:
• RNA viruses
• DNA viruses
• Structure:
• Capsid
• Genome
7. 1.1 INTRODUTION
• Where did viruses come from?
• Fossils-origin relationship.
• Speculation on how viruses may have
orginated.
• How old are Viruses? Related to
Bacteria?
• The age of Eukaryotic viruses vs. the
age of prokaryotic?
9. THEORIES ON THE ORIGIN OF VIRUSES
• 1. Molecular precursors of cellular organisms
• 2. Components of cells
• 3. Intracellular micro-organisms.
10. 1. MOLECULAR PRECURSORS OF
CELLULAR ORGANISMS
• RNAs were originated before cells
and had many features.
• What happened as cells evolved?
11. 2. COMPONENTS OF CELLS
• 1. Independent from host cell
control, components could
replicate?
• 2. Structural similarities between
mRNA and some viruses.
Covalently:
• 3. Could some DNA viruses be
descendant of plasmids?
• 4. Or Transposons maybe?
12. 2. COMPONENTS OF CELLS
• 5. Are we made of viruses?:
• Chicken-and-egg situation
between
retrotransposons and
retroviruses!!
• HGSP: 8% of genom is LTR-flanked
14. CONCLUSION:
THE MAIN QUESTION’S STILL UNANSWERED
• Multiple sugessted ancestors, unknown origin
• Many processes may have participated
• Viruses selectivity to host may refer to the origin.
15. Evolution is the constant change of
a viral population in the face of
selection pressures
16.
17.
18. Evolution has 4 main
drivers:
Large number of progeny
Large number of mutants
Quasi-species effects
Selection
19. Evolution has 4 main
drivers:
Large number of
progeny
Large number of
mutants
Quasi-species effects
Selection
Large number of progeny
20. Evolution has 4 main
drivers:
Large number of
progeny
Large number of
mutants
Quasi-species effects
Selection
Large number of mutants
Diversity
Successful
Viruses
DNA
DS
SS
RNA
SS
DS
21. A quasispecies is a well-defined distribution
of mutants that is generated by a mutation-
selection process.
Evolution has 4 main
drivers:
Large number of
progeny
Large number of
mutants
Quasi-species effects
Selection
Quasi-species effects
22. Evolution has 4 main
drivers:
Large number of
progeny
Large number of
mutants
Quasi-species effects
Selection
Selection
Survival of the fittest
Survival of the
survivors
29. New viruses can only arise from viruses that are
already existed, not de novo
30. Constrains on virus evolution:
Viral genome is constrain
Physical nature of capsid
Extreme alteration in viral consensus
genome do not survive selection
31. REFERENCES
• 1. Virology principles and application, JHON CARTER AND
VENETIA SAUNDERS.
• 2. The origin and Evolution of Viruses, ESTEBAN DOMINGO AND
JOHN J. HOLLAND.
• 3.
First I’d like to welcome you all to our virology presentation.
Today’s class is about the origin and evolution of viruses.
I’m going to discuss Origin section and my colugue Dima is going to discuss the evolution section.
Estimated time is 90 minutes devided into two parts and a coffe break between.
Before we start we’ll remember viruses:
Parasites, selective to an organisms or a group causing infections
In an attempt to determin the origin, we know that origins of many cellular organisms can be inferred from fossils, but there is very little fossil record of viruses.
The discussion of the possible origins of viruses will be highly speculative.
The answer to the question ‘Where did viruses
come from?’ is ‘Basically, we do not know!’. We
can, however, speculate about possible ancestors of
viruses;
Viruses by definition are parasites of cells, so there
could be no viruses until cells had evolved.
There is evidence for the presence of living cells about 3.9 billion years ago.
It is likely that viruses developed at an early stage in these primitive prokaryotes, but the extent to which
the viruses of the modern prokaryotes resemble these early viruses is unknown
Here’s a timeline for earth’s history. The approximate time of various groups of organisms are indicated.
And now let’s move to the theories pertaining our subject:
first: RNA molecules that existed before cells
The second one
At an early stages of erath RNA molecules
evolved and developed enzyme activities (ribozymes)
and the ability to replicate themselves
perhaps some were parasitized by some of
these RNA molecules,
Once cells had Evolved which somehow acquired capsid
protein genes
Perhaps some cellular components evolved abilities to
replicate themselves, independent of host cell control,
and thus became parasites of those cells.
candidates for precursors of viruses include mRNA
molecules and DNA molecules such as plasmids and
Transposons
Could some phages, such as the filamentous
phages or some of the tailed phages (Chapter 19), be
descended from ancient plasmids and their sex pili?
Transposons are sequences of mobile DNA in the
genomes of prokaryotes and eukaryotes
Retrotranspososns: which are retovirus-like sequences in eukaryotic
cell genomes
consists of two
long terminal repeats which contain genes some of which encodes reverse trancriptase
Reverse
transcription produces a new copy of the retrotransposon,
which can be inserted into another site in the cell
genome. Retrotransposons are found in the genomes of
humans (Figure 20.3), other vertebrates, invertebrates,
plants and fungi.
that retroviruses originated from retrotransposons
It is likely that retroviruses originated from retrotransposons,
though this is a chicken-and-egg situation
and it is also likely that some retrotransposons
are descended from retroviral proviruses
Retrotransposons
are described as autonomous elements because
they have a pol gene that enables them to replicate
Results from the human genome sequencing project
indicate that about eight per cent of our genome is
composed of LTR-flanked sequences, which are often
referred to as endogenous retroviruses
It is assumed that
the ancestors of these organelles adopted parasitic modes of life in host cells
over time they became increasingly dependent
on their hosts,
Perhaps a similar evolutionary process
continued further, leading to greater degeneracy and loss of functions such as protein synthesis
Until it had becom
The answer to this question is that we do not know!
The great variety of virion structures and of virus
genome types and replication strategies indicates that
viruses had multiple origins
Small simple viruses, such
as parvoviruses and picornaviruses, perhaps evolved
from molecular precursors, while some large complex
viruses, such as the mimivirus, perhaps evolved from
cellular precursors
We can
now note that certain structural types of virus are
restricted to particular categories of host: naked, rodshaped
ssRNA viruses are restricted to plant hosts,
while viruses with a head-plus-tail structure are rarely
found outside the prokaryotes. The reasons for these
distributions presumably concern diverse origins of the
viruses in these very different hosts
cellular nucleotides interact with, exchange with, and coevolve with the DNA and RNA viruses, transposons, retrotransposons, and other mobile genetic elements.Novel viruses are among the “new” life forms that evolve from such interaction, and the originating of viruses is therefore a never-ending process Transposon ■ noun Genetics a segment of DNA that can be translocated as a whole from a site in one genome to another site in the same genome or to a different genome.
■ noun Genetics a transposon whose sequence shows homology with that of a retrovirus
The myth of consensus genome sequences
The λ phage or bacteriophage lambda is a virus that infects the Escherichia coli bacteria, discovered in 1950. It is a complex linear double-stranded DNA virus.