This document discusses the examination of the udder and milk for signs of mastitis in dairy cattle. It describes the normal anatomy of the udder and teats. Mastitis is defined as inflammation of the mammary gland and can be subclinical or clinical. It causes significant economic losses to dairy farmers. Mastitis is usually caused by bacteria that enter through the teat canal. It is diagnosed based on physical examination of the udder for signs of inflammation, California Mastitis Tests of milk samples, and culture analysis. Examination of milk samples can reveal clots or discoloration indicating mastitis.
Successful management of delayed case of mastitis in cowsuren vet
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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 .
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
Richard's entangled aventures in wonderlandRichard 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.
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
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(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
This pdf is about the Schizophrenia.
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Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
2. •The udder is responsible for milk production and
delivery of milk.
•Milk is the main source of income in dairy herds,
and conditions that reduce the quality or quantity
of milk will adversely affect the profit margin.
•In addition, conditions that affect the milking
process will increase the milking time and may
predispose the udder to mastitis.
•This lesson will describe the clinical examination
of the ligaments and the skin of the udder, the
teats, the mammary gland and the milk.
3. •The udder is composed of four mammary glands, each with its own
teat.
•The weight of the udder is supported by the medial and superficial and
deep lateral ligaments.
•These ligaments are attached to the pelvis and/or the abdominal
muscles.
•Each gland is composed of milk producing alveolar cells, a reservoir for
the milk produced called the gland cistern and a teat.
4. •The teat has an an- nular fold at the base which partially
separates the gland cistern from the teat cistern.
•The teat cistern is intermittently filled with milk from the gland
cistern during milking.
•At the apex of the teat is the streak (teat canal) and the teat
orifice through which milk passes during milking.
•The teat canal has a muscular sphincter which opens during
milking but which is sealed during the dry period.
•There is a specialised area at the proximal end of the streak
canal called the rosette of Furstenberg which is concerned with
de- fence against infection.
•The skin covering the teat is hairless and strongly adherent to
the underlying tis-sues.
•The supramammary lymph nodes are palpable from the rear
5. Clinical Examination of the Udder
Pelvic
symphysis
Symphyseal
tendon
Lateral
suspensory
ligaments
l suspensory
ents
Gland
sinus
Annular
ring
Teat
sinus
Rosette of
Furstenberg
Streak
canal
Figure 12.2 Cross-section of a normal teat.
6. Difference between normal
udder and mastitis
Udder
• Palpate left quarters of the
mammary gland
– Heat
– Hardness (swelling)
– Edema
– Teat lesions
Normal
Mastitis
7. What’s mastitis ?
Inflammation of one or more quarters of the udderWhat’s mastitis ?
Inflammation of one or more quarters of
the udder
Normal Inflamed
Swelling
pain
warm
redness
Mammae = breast
-itis = Latin suffix for
inflammation
8. What’s the significance of bovine
mastitis ?
• Causes significant economic losses to
the dairy industry.
• The most costly disease affecting dairy
dairy cattle throughout the world
ance of bovine
ant economic losses
ustry in the US
What’s the significance of bovine
mastitis ?
Causes significant economic losses
to the dairy industry in the US
$ 200/cow/year
$ 2 billion/year
The most
costly
disease
affecting
dairy dairy
cattle
throughout
the world
cull RIP
9. What are the health concerns of
mastitis ?
Animal health
Loss of functional quarter Lowered milk production
Death of cow
Human health
Poor quality milk antibiotic residues in milk
hat are the health concerns
mastitis ?
Animal health
Loss of functional quarter
Lowered milk production
Death of cow
10. Types of mastitis
How severe can mastitis be ?
Subclinical Mastitis
~ 90 -95% of all mastitis cases
Udder appears normal
Milk appears normal
Elevated SCC (score 3-5)
Lowered milk output (~ 10%)
Longer duration
Clinical Mastitis
~ 5 - 10% of all mastitis cases
Inflamed udder
Clumps and clots in milk
Acute type
major type of clinical mastitis
bad milk
loss of appetite
depression
prompt attention needed
Chronic type
bad milk
cow appears healthy
11. causes mastitis ?
Bacteria ( ~ 70%)
Yeasts and molds ( ~ 2%)
Unknown ( ~ 28%)
physical
trauma
weather extremes
What causes mastitis ?
Bacteria ( ~ 70%)
Yeasts and molds ( ~ 2%)
Unknown ( ~ 28%)
physical
trauma
weather extremes
Where do these organism
come from ?
Infected udder
Environment
bedding
soil
water
manure
Replacement animals
Where do these organisms
come from ?
Infected udder
Environment
bedding
soil
water
manure
Replacement animals
e do these organisms
from ?
ected udder
vironment
bedding
soil
water
manure
placement animals
12. How does mastitis develop ?
Cow
Predisposing conditions
Existing trauma (milking machine, heat
or cold, injury)
Teat end injury
Lowered immunity (following calving,
surgery)
Nutrition
Organisms
EnvironmentEnvironment
Organism
does mastitis develop ?
Cow
Predisposing conditions
Existing trauma (milking machine, heat
or cold, injury)
Teat end injury
Lowered immunity (following calving,
surgery)
Nutrition
Organisms
Environment
Environment
Organism
Cow
13. Process of infection
Organisms invade the udder through
teat canal
Migrate up the teat canal and colonize the
secretory cells
Colonized organisms produce toxic substances
harmful to the milk producing cells
14. The cow’s immune system send white blood cells
(Somatic cells) to fight the organisms
recovery clinical subclinical
15. Diagnosis of mastitisHow is mastitis diagnosed ?
Physical examination
Signs of inflammation
Empty udder
Differences in firmness
Unbalanced quarters
Cowside tests
California Mastitis test
Physical examination
Signs of inflammation
Empty udder
Differences in firmness
Unbalanced quarters
Cowside tests
California Mastitis test
16. How is mastitis diagnosed ?
Culture analysis
The most reliable
and accurate
method
costly ($ 5- 12)
17. Examination of milk
•Milk samples from all four quarters of mastitic cases should be
examined for signs of mastitis.
•Visual appraisal is facilitated by placing the milk sample onto a
black surface.
•Strip cups are very useful for this purpose as they minimise
environmental contamination.
•washing and disinfecting should follow.
•In clinical mastitis, clots caused by cellular debris derived from
gland inflammation are often present.
•The clots may have been detected by the herdsman.
• Other gross changes include milk which is more watery and
discoloured.
18. •The discolouration may be yellow, port wine or red. Red
indicates blood in the milk and/or colostrum.
•This is seen in a proportion of newly calved cows.
•One, several or all quarters may be affected.
•This condition is of no pathological significance, although
it must be differentiated from acute mastitis (e.g. Bacillus
cereus) that can sometimes present with a haemorrhagic
milk sample which has a darker port wine appearance.
•Identification of the infected quarter is further assisted by
using a CMT to identify which quarter(s) have a high
somatic cell count indicating mastitis. This is described
below.
19.
20. 1-Bloody milk due to leptospira
Clinical signs
•flaccid udder & flappy
•the blood come from all
quarter
•No inflammation of the udder
•Has bloody urine
21. •Normal udder blood from
4 quarter
• May be hypophosphatemia
• Blood from one quarter
• May be due trauma
• Inflamed quarter with bloody milk Mastitis