Microbiology is the study of microorganisms like bacteria, fungi and viruses that are too small to be seen without magnification. There are several types of microorganisms that can be classified based on their shape, staining properties, temperature and nutritional requirements. Bacteria in particular can cause disease when they invade the body, produce toxins or enzymes, or form protective capsules. Factors that affect a host's susceptibility to microbial infections include their immune system status, wounds, medical implants and underlying illnesses. Understanding microbiology is important for controlling the spread of infectious diseases.
The cells of the immune system can be categorized as lymphocytes (T-cells, B-cells and NK cells), neutrophils, and monocytes/macrophages. These are all types of white blood cells. The major proteins of the immune system are predominantly signaling proteins (often called cytokines), antibodies, and complement proteins.
In recent years, antibodies have become increasingly accepted as therapeutics for human diseases, particularly for cancer, viral infection and autoimmune disorders.
Monoclonal antibodies (Mabs) have been used as diagnostic and analytical reagents since hybridoma technology was invented in 1975.
“man-made antibodies.” was named by Cesar Milstein, who was one of the inventors of monoclonal antibody technology.
Until the late 1980’s, antibody technology relied primarily on animal immunization and the expression of engineered antibodies.
Cell mediated immunity also known as T cell immunity. it is developed by cell mediated responses and it does not involve any antibodies. Cell mediated immunity is offered by T lymphocytes and it starts developing when T cells come in contact with the antigens. In the Cell mediated immunity T cell plays one of the important role for the process of crosstalk with other immune system as well as to signal B cells to produce the antibody mediated immune response. Primary function of cell mediated response-
1) Eliminate intracellular pathogens.
2)Eliminate tumor cells.
T cells regulate proliferation and activity of other cells of the immune system : B cells, macrophages, neutrophil, etc.
Antigen processing and presentation by Dr K.Geetha, Associate Professor, Department of Biotechnology, Kamaraj College of Engineering & Technology, Near Virudhunagar, Madurai Dist.
The cells of the immune system can be categorized as lymphocytes (T-cells, B-cells and NK cells), neutrophils, and monocytes/macrophages. These are all types of white blood cells. The major proteins of the immune system are predominantly signaling proteins (often called cytokines), antibodies, and complement proteins.
In recent years, antibodies have become increasingly accepted as therapeutics for human diseases, particularly for cancer, viral infection and autoimmune disorders.
Monoclonal antibodies (Mabs) have been used as diagnostic and analytical reagents since hybridoma technology was invented in 1975.
“man-made antibodies.” was named by Cesar Milstein, who was one of the inventors of monoclonal antibody technology.
Until the late 1980’s, antibody technology relied primarily on animal immunization and the expression of engineered antibodies.
Cell mediated immunity also known as T cell immunity. it is developed by cell mediated responses and it does not involve any antibodies. Cell mediated immunity is offered by T lymphocytes and it starts developing when T cells come in contact with the antigens. In the Cell mediated immunity T cell plays one of the important role for the process of crosstalk with other immune system as well as to signal B cells to produce the antibody mediated immune response. Primary function of cell mediated response-
1) Eliminate intracellular pathogens.
2)Eliminate tumor cells.
T cells regulate proliferation and activity of other cells of the immune system : B cells, macrophages, neutrophil, etc.
Antigen processing and presentation by Dr K.Geetha, Associate Professor, Department of Biotechnology, Kamaraj College of Engineering & Technology, Near Virudhunagar, Madurai Dist.
Microbial cell factories,Biotechnology has found its entry into medicine (red) and agriculture (green), and now a new wave of industry (white), also called industrial biotechnology
This presentation gives you the detailed description of various cells & organs of immune systems that participates (particularly, in combination), make communication between themselves to regulate the whole immune system very precisely.
A number of morphologically and functionally diverse organs and tissue organs and tissue contribute to the development of immune responses .
These organs can be distinguished by function as the primary and secondary lymphoid organs .
Humoral immunity is defined as the immunity mediated by antibodies, which are secreted by B lymphocytes.
B lymphocytes secrete the antibodies into the blood and lymph
Microbial cell factories,Biotechnology has found its entry into medicine (red) and agriculture (green), and now a new wave of industry (white), also called industrial biotechnology
This presentation gives you the detailed description of various cells & organs of immune systems that participates (particularly, in combination), make communication between themselves to regulate the whole immune system very precisely.
A number of morphologically and functionally diverse organs and tissue organs and tissue contribute to the development of immune responses .
These organs can be distinguished by function as the primary and secondary lymphoid organs .
Humoral immunity is defined as the immunity mediated by antibodies, which are secreted by B lymphocytes.
B lymphocytes secrete the antibodies into the blood and lymph
Microbiology is the study of a variety of living things, such as bacteria, fungus, and other tiny creatures, that are not visible to the naked eye. However, these little creatures are the foundation of all life on earth.. all types of living things that are invisible to the unaided eye.
Important categories have been divided based on certain traits in the study of bacteria in food. These classifications have no taxonomic relevance.
Food technology, food safety and hygiene, food poisoning, food genomics, and, more generally,
Microbiology is the study of
living organisms of microscopic
size which includes bacteria ,
Fungi , Algae , Protozoa and Viruses. It is concerned with the forms, structure , reproduction , physiology , metabolism and classification.
Principle Of Microbiology
Medical microbiology deals with the causative agent of the infectious disease of the human , the ways in which they produce disease in the body and essential information for diagnosis and treatment.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
HOT NEW PRODUCT! BIG SALES FAST SHIPPING NOW FROM CHINA!! EU KU DB BK substit...GL Anaacs
Contact us if you are interested:
Email / Skype : kefaya1771@gmail.com
Threema: PXHY5PDH
New BATCH Ku !!! MUCH IN DEMAND FAST SALE EVERY BATCH HAPPY GOOD EFFECT BIG BATCH !
Contact me on Threema or skype to start big business!!
Hot-sale products:
NEW HOT EUTYLONE WHITE CRYSTAL!!
5cl-adba precursor (semi finished )
5cl-adba raw materials
ADBB precursor (semi finished )
ADBB raw materials
APVP powder
5fadb/4f-adb
Jwh018 / Jwh210
Eutylone crystal
Protonitazene (hydrochloride) CAS: 119276-01-6
Flubrotizolam CAS: 57801-95-3
Metonitazene CAS: 14680-51-4
Payment terms: Western Union,MoneyGram,Bitcoin or USDT.
Deliver Time: Usually 7-15days
Shipping method: FedEx, TNT, DHL,UPS etc.Our deliveries are 100% safe, fast, reliable and discreet.
Samples will be sent for your evaluation!If you are interested in, please contact me, let's talk details.
We specializes in exporting high quality Research chemical, medical intermediate, Pharmaceutical chemicals and so on. Products are exported to USA, Canada, France, Korea, Japan,Russia, Southeast Asia and other countries.
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
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.
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.
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
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
1. MICROBIOLOGY
It’s the branch of science that deals with
the study of minute/very
tinny/microscopic organisms which can
not be seen by our naked eyes but only
by using magnifying instruments like
a lens or a microscope
A microorganism is a microscopic
creature that can either be unicellular or
multicellular and relatively complexed
2. TYPES OF MICROORGANISMS
1. Bacteria
2. Fungi
3. Virus
4. Protozoa/parasites
5. Protist
Microorganisms live in all parts of
biosphere where there is liquid, soil
springs, oceans, atmosphere and inside
the rock.
3. IMPORTANCE OF MICRO ORGANISMS
1.They help in recycling other organisms, dead
remains and waste products through
decomposition.
2.Some are important symbiotics e.g eschericia
coli in the stomach which help in vitamin k
processing, lactobacillus accidophillus that help
to keep the vaginal pH acidic
3.They are used in biotechnology during food
and beverage preparations
4. They are used in making soil fertile
4. HISTORY OF MICROBIOLOGY
It began as a speculation that microorganisms
were existing though it was not yet proved and
this was as early as 6th C by a Roman scholar
called marcus varro who suggested that
possibly diseases were spread by yet the
unseen organisms .it was in the 17th C that the
above speculation was proved by Anton Van
Leuwenheuk who discovered the microscope
which revealed the unseen microbes by
marcus hence being the father of micro
biology.
5. -Lazarro spallanzani,found out that boiling broth,would
sterlize it and any microbe in it. He also found out that
new microbes could settle in broth if it was left exposed
in air.
-Leus pasteur discovered the process of food preservation
called pasteurisation
-Fednard julius cohn discovered the science of classifying
bacteria.
-Robert koch established that microbes can cause diseases
and they could spread from one infected person to
another. He also introduced sterilization of surgical
instruments. He found out that TB was caused by myco
bacteria tuberclosis. TB is called kochs disease.
6. Mycology, which refers to the study of fungi.
Virology, the study of viruses.
Serology, which is the study of antibody antigen
reactions.
Parasitology, the study of parasites
Epidemeology, which is the study of disease
outbreak in the community.
Immunology – the science which concerned
with mechanisms of body protection against
pathogenic microorganisms and foreign cells and
substances.
Protozoology – which deals with pathogenic
unicellular animal organisms.
7. BACTERIOLOGY
It is the study of bacteria. Bacteria are
minute, prokaryotic, unicellular
microscopic organisms that live in each
and every environment or space.
Bacteria differ from plants because they
lack chlorophyll and they reproduce by
binary fission where as cells divide into
two atomically equal parts that have the
same genetic composition and structure
and binary fission process (research)
8. Cont’d
Bacteria are widely distributed in water, soil,
and air. Bacteria that cause diseases or
infections are called pathogens and those that
donot are called commensals or non
pathogenic organisms
Note; when commensals are distributed or
disrupted to another part of the body or rather
than their specific site, they cause infections
e.g. e coli is a commensal in the alimentary
canal but when it gains entrance in the urinary
tract , it causes urethritis.
9. Cont’d
All bacteria are pathogenic in blood stream causing a
condition known as septicaemia and when they are found in
CNS they cause meningitis, there is no normal flora in
blood and in CNS
-Normal flora are organisms that do not cause disease in
certain parts or sites of the body but only useful to them.eg
lacto bacilli and e coli
Normal flora may cause infections when immune system of
the person is compromised and these are called
opportunistic infections
Assignment;
1. List examples of normal flora and the parts where they are found
2. Benefits of normal flora to humans
11. CLASSIFICATION OF BACTERIA
Bacteria may be classified in six different
ways i.e.
Basing on shape or cell structure
Basing on staining properties and
reaction
Basing on gas requirement
Basing on biochemical reactions
Basing on temperature dependence
Basing on nutritional requirements
12. CLASSIFICATION OF BACTERIA BASING ON
MORPHOLOGY
1. COCCI
These are bacteria that are spherical,
round or oval shaped. There are many
forms of cocci bacteria i.e.
(i) Diplococci
Thses appear in a pair e.g. Neisseria
gonorrheae and Diplococci
pneumonaea
16. (iv)Some cocci are in chains and
are referred to as streptococci e.g.
streptococi pyogens and
streptococci agalantae, streptococci
pneumoneae
17. (v)Some cocci are in clusters and
are called staphylococci e.g. staph
aureus, staph albus
18. 2. BACILLI/BACILLUS
These are rod or stick shaped
microorganisms e.g.
(i)Coryen bacteria diptheriae,
these look like chinese lettery
formation (palisade)
24. CLASSIFICATION OF BACTERIA BASING ON
THE STAINING PROPERTY AND REACTIONS
Staining is the process of subjecting
organisms to different colours or dyes for
proper identification and clarification
Grams staining
This is a staining procedure that is used to
divide or differentiate bacteria into two
groups i.e. gram positive and gram negative
bacteria
25. Cont’d
This staining process of bacteria was
developed by a scientist called Gram, Gram
prepared a dye i.e. crystal violet dye (purple)
He then subjected it to different organisms
where by some organisms could retain it and
others could not get stained with it
Those that retained the dye he called them
gram positive bacteria and those that failed
he called them gram negative
26. GRAM POSITIVE BACTERIA
These are bacteria that have a thicker/thickened
peptidoglycan layer(cell wall) that enables
them to retain the purple dye during the grams
stain process.
Examples of gram positive bacteria include;
Staphylococcus aureus . This organism causes
stye, boils, abscesses, food poisoning, UTI in
young females, skin ulcers and septicaemia
Staph saprophyticans .This cause UTI in
young active females
27. Streptococci pneumoniae. This causes
pneumonia in infants, sinustis, septicaemia,
otitis media and conjuctivitis
Strep agalactiea . This causes pneumonia ,
neonatal septicaemia, meningitis in
neonates and septic abortion
Streptococci pyogens . This causes
pharyngitis, otitis media, impetigo,wound
infection, septicaemia, tensilitis, cellulitis
28. clostridium difficile . This causes
diptheria
bacillus anthracis. This causes pulmonary
anthrax
Clostridium perfringes. This causes gas
gangrene, food poisoning, septicaemia
Coryn bacterium diptheriae . This causes
diptheria
Clostridium tetani. This causes tetanus
29. GRAM NEGATIVE BACTERIA
These are bacteria that have a thin or less
peptidoglycan layer that does not enable them to
retain the grams stain (crystal violet, purple dye)
Examples of gram negative bacteria include;
Haemophillus influenzae . This causes
meningitis, pneumonia, otitis media, sinusitis ,
chronic bronchitis, flue
Haemophillus ducreyii. This causes chancroid
Eschericia coli. This causes uti, septicaemia,
wound infection and neonatal meningitis
30. Shigella spp. These cause shigelosis or dysentry
(bloody stool)
Salmonella spp . These cause enteric fever i.e.
typhoid, food poisoning, septicaemia, abscess of the
spleen
Vibrio cholerae . This causes cholera
Brucella spp eg babortus from cattle and b suis from
pigs, b melitenesis from goats. These cause
brucellosis
Bordetella pertusis . This causes whooping cough
Neisseria meningitidis . This causes meningitis and
septicaemia
31. Cont’d
Neisseria gonorrheae . This causes gonorrhea,
pelvic inflammatory disese , septic arthritis
listeria monocytogens. This cause still Birth or
miscarriages, and septicaemia
Brucella spp e.g. brucella abortus from cattle and
brucella suis from pigs, brucella melitenesis from
goats. These cause brucellosis
Bordetella pertusis . This cause whooping cough
Neisseria meningitidis . This cause mengitis and
septicaemia
32. Neisseria gonorrheae . This
causes gonorrhea, pelvic
inflammatory disease , septic
arthritis
Listeria monocytogens. This
causes still birth or miscarriages,
and septicaemia
33. ZN STAINING PROPERTY/REACTION
This staining procedure was developed by a
scientist called Ziehl Nelseen and it is
used to differentiate between acid alcohol
fast bacillus (AAFBs) from the non
AAFBs
ZN prepared two dyes i.e. strong
carbofuchsin (red) and methlene blue dye
34. Cont’d
He then subjected these dyes to different
bacilli, those that retained Red dye that
was made of acids and alcohols he called
them AAFBs and those that stained blue
dye he called them non AAFBs
AAFBs include;
oMycobacterium tuberculosis
oMycobacterium lepreae
36. CLASSIFICATION OF BACTERIA BASING
ON GASEOUS REQUIREMENTS
1. Obligate/strict aerobes
These are bacteria that require plenty of
oxygen for their growth e.g.
M.tuberculosis , Proteus aeruginosa
2. Obligate/strict anaerobes
these are microbes that require an
environment that is free of oxygen e.g.
clostridium. tetani
37. 3. Carboxyphilic bacteria
These are bacteria that require an atmosphere of
5 to 10 % co₂ for their growth e.g. neisseria
gonorrhoea
4. Facultative anaerobes
These are bacteria that can survive in an
environment that has o₂ or not e.g.
e .coli
6. Micro aerophillic organisms
These are microbes that can grow best in an
atmosphere that has a trace of o₂ e.g. h.
influenza
38. CLASSIFICATION OF BACTERIA BASING
ON TEMPERATURE DEPENDANCE
1. Thermophillic
Thsese are temperature loving bacteria that can
survive to up to a temp of 45c and above
2. Mesothermic bacteria
These survive in a medium temperature of 25-45
3. Hypoctermic bacteria.
These survive at low temperature of 8 and below
39. CLASSIFICATION OF BACTERIA BASING ON
NUTRITIONAL REQUIREMENTS
1. Autotrophs
These are bacteria that make or prepare their
own food due to presence of chlophyll like
pigment that can perform photosynthesis eg v.
cholerae
2. Chemoautotrophs
These make their own food by use of energy
obtained from chemical sources. They differ
from autotrophs in that they do not need
sunlight
40. 3. Heterotrophs
These are bacteria which do not make their own
food but obtain it from others ie already made
4. Symbiotics bacteria
These are bacteria which obtain food by living
together with other organism e.g. Rhizobium
bacteria in legumes and Entero bacteria in
intestines
5. Saprophytic bacteria
These bacteria survive by eating on rotten
materials
41. REQUIREMENTS FOR BACTERIAL GROWTH
These are factors or states that assist in bacterial
growth , these factors are divided into physical
and chemical requirements
Physical requirements
1.Temperature
Bacteria need warmth and moderate temp for
their growth and development
2. Moisture
Many bacteria grow well in moist environment
than in dry areas
42. 3. PH
This is the degree of alkalinity or acidity of the
environment. Most bacteria do grow well in a
neutral ph of 7 though acidophiles require a ph
of 0-5.5 and neultaphiles require a ph of 8.5-
11.5
4.Osmotic pressure
This is the pressure exerted on bacteria by their
surroundings , when this pressure is variated it
affects the bacterial growth
44. FACTORS THAT ENABLE BACTERIA TO
CAUSE DISEASES
These are particulars or properties that the bacteria
poses, use to cause diseases or infections to
people and animals
1. Invasiveness property
This is the ability of an organism to enter inside the
hosts tissues .
Pathogenic bacteria have this ability hence enabling
them to cause disease and infections
45. 2. Virulence
This is the ability of an organism to quickly multiply
and effectively destroy body tissues
after inversion into the hosts tissue many bacteria
use this property to spread and cause infections
3. Possession or secretion of capsule
This is a very rough and rigid layer produced by some
bacteria especially in adverse conditions
It acts as a protective barrier, many bacteria produce or
have this coating which protects them from
antibodies, phagocytic cells and chemical reactions
hence being able to cause or spread diseases to
humans e.g. streptococcus pneumoniae
46. 3. Production of toxins
Toxins are poisonous substances produced by some
bacteria that case changes with in the hosts tissues
Some toxins are fetal e.g. tetani produces a
nuerotoxin which usually affects the cells of CNS
systems causing spasms and a disease called
tetanus or lock jaw disease
Endo toxins are toxins produced or released when
the organism is dead while Exo toxins are produce
by live organisms
47. 4. Production of enzymes
Some of the enzymes produced by these
bacteria cause antibody destruction e.g.
collagenase enzymes break down the
collagen fibres found in tendons,
cartilages and in bones; kinase enzyme
breaks the fibrin which is formed by the
host as a protective barrier
lipase
protease
48. 5.Possession of pilli
These are appendages found on the
surfaces of bacterial cells and are used for
attachment to the hosts tissues hence
enabling the bacteria to cause infections
in or the hosts tissues
6. Possession of the flagella
the flagella aids in movement from one
site of the body to another spreading its
toxins and affecting different sites
49. 7. spore formation
Spores are small metabolic dormant
cells with thick walls which can be
destroyed by antibodies and
phagocytic cells. So bacteria that
posses this ability can cause
infections on and over a long period
of time
50. FACTORS THAT MAKE HOSTS SUSCEPTIBLE
TO INFECTIONS/DISEASES
Malnutrition
Poor hygiene
Immunity
Age
Environment
Life style
Hereditary
51. INFECTION PREVENTION AND CONTROL
Infection
This is the invasion and multiplication of microbes in
or on the body tissues with or with out signs and
symptoms
CLASSES OF INFECTIONS
Localised infections
These are infections which are confined to a smaller
part or portion of the body
Disseminated infections
These spread widely and affects the body beyond the
usual site of infection
52. Systemic infections
Infections spread through blood and lymphatic
system
Primary infections
This is the 1st disease noted in an illness e.g. skin
rash, running nose in measles
Secondary infections
This occur when the body weaken by a primary
infection e.g. measles to pneumonia
Mixed infections
This occurs when the disease is caused by two or
more organisms
53. Zoonoses
are infections that affect animals but
can be transmitted to humans
through direct contact with infected
animals tissues , consumption of
animal products which are affected
and in halation of pathogens e.g.
rabies. Anthrax, marbug, brucelosis
and bovin tuberculosis
54. TYPES OF INFECTIONS
Urinary tract infection
Respiratory tract infection
STDS
Tropical infections
SOURCES OF INFECTIONS
Human
Environment
Animals
Birds
55. PHASES FOR INFECTION DEVELOPMENT
1.Entry phase
This is a time when a microbe enters into the
body tissues through invasiveness property
2. Incubation period
is the time between the entry of the microbe
and the appearance of the fast signs and
symptoms of the disease
3. Prodrome phase
is the period when the patient presents with
mild but non specific symptoms that signal the
onset of the disease
56. 4. clinical phase
This is the period when a patient experiences
typical signs and symptoms of the disease. In
this stage the organism is actively destroying
the hosts cells
5. Recovery phase
is the time when symptoms disappears , tissues
heal and the body regains strength i.e.
overcomes the infection
57. Note.
Asymptomatic patients are people
who do not show signs and
symptoms though they have the
infection
symptomatic patients are people
who show signs and symptoms of
the infection they have
58. MODE OF TRANSMISION OF THE
INFECTIONS
These are the means by which pathogens pass or
move from the source to a new susceptible
host
1. Contact transmission or transfer
This is divided into two i.e. direct contact e.g.
via hand to hand or body to body and indirect
contact e.g. from clothes, beddings and
communal equipments
59. 2. Air borne transfer
This involves inhalation of organisms Of organisms
which are found in droplets from one individual
to another during kissing, coughing, sneezing
3.Common vehicle/oral transfer
This is through eating and drinking contaminated
food
4.Vector borne transfer
This is via arthropodes e.g. ticks and mosquitoes
5. Blood borne transfer
This is via blood transmission e.g. hepatitis and
syphills
60. ROUTES OF ENTRY OF
MICROBES/ INFECTIONS TO
HUMAN BODIES
Almentary tract
Skin and mucus membranes
Transplacentally or vertical route
Respiratory tract
61. CROSS INFECTIONS
These are infections that can be transferred
from one person to another who
originally had no infection of that type
SOURCES OF CROSS INFECTIONS
Unsterilized equipments
Body exudates
Infected patients
Wastes
62. WAYS OF PREVENTING CROSS
INFECTIONS
Wash hands before and after attending to a
patient
Decontaminating wastes before disposal
Proper segregation of wastes according to
their bins and liners before disposal i.e.
highly infectious materials are put in red
bin, e.g. all anatomic wastes/blood stained
materials
63. Infectious material are put in yellow bin
e.g. used gauze/gloves/cotton and
infusions
All sharps are put in yellow safety box
All non infectious materials are put in
black bin/green e.g. papers/glass
bottles/food items
All pharmaceuticals are put in brown
bins
64. Use of sterile equipments on patients
use of protective wear while attending to
patients and handling samples
Wiping away spillages with suitable
disinfectant
Isolation of patients
Note;
Community acquired infections are
infections obtained from the community
65. NOSOCOMIAL INFECTIONS
These are infections that are acquired from the
hospital or health care facility when the patient
is admitted for any other reason
The common pathogens that can cause these
infections are
• Staph. Aureus
• Pseudomonas
• E.coli
• Mycobacterium Tb
66. SOURCES OF HOSPITALACQUIRED INFECTIONS
Acutely ill patients
Asymptomatic patients
Inadequate sterilized equipments
Hospital staff during patient care
FACTORS CONTRIBUTING TO NOSOCOMIAL
INFECTIONS
Failure of health worker to follow infection
Control guidelines
Presence of resistant pathogens which are not
affected by common disinfectants
67. Increasing number of patients with
weakened immunity
Over crowding of patients in the
hospital
Over use and improper use of catheters
Prolonged and over stay in the hospital
Assignment;
What are the ways of prevention of
Nosocomial infections?
68. PRINCIPLES OF INFECTION CONTROL
1.Aattacking source of the infection
This includes the following;
• Treatment of the cases and carriers
• Isolation of cases
• Control of reservoir host e.g. stray
dogs
69. 2. Interrupting the route of transmission
through
Observing environmental sanitation,
Personal hygiene and
Behavior changes
Vector control
Immunization
3. Protecting the host
Chemotherapy
Sterilization and disinfection
better nutrition
Personal protection e.g. gloving
71. This is the study of medically
important parasites and the disease
they cause or spread
A parasite, is an organism that live
on or inside another organism/host
for nourishment or shelter.
A host, is an organism where the
parasite get its nourishment and
shelter
72. Symbiosis, is a feeding relationship
between two organisms of different
species while parasitism is a form of
symbiotic relationship where one
organism benefits at the expense of the
other
TYPES OF PARASITES
Exo parasites
These live on the surface or superficial
parts of the body e.g. ticks
73. Endo parasites
These live inside the hosts tissues e.g.
• Ascaris lumblicoid
• Giardia lumbria
• Tunga penetrans
Facultative parasites
These show both parasitic and non parasitic
mode of life e.g. ticks
Obligate /strict parasites
These cant survive without a host
74. TYPES OF HOSTS
Definitive host
It’s a host in which sexual reproduction
of a parasite take place
Intermediate host
It’s a host that harbors larval stages of
a parasite or where the asexual
development of a parasite takes place
Reservoir host
This stores parasites and act as a
source of transmission to other hosts
78. Immunology
This is the study of the body’s
immune system
Immunity. Is the body’s ability to
resist or fight against diseases and
the disease causing germs
79. The body’s immunity is divided
into two systems, viz
1. Innate/ non specific
immunity
2. Adaptive immunity/specific
immunity
81. The physical body barriers against disease
causing germs include
Skin
The skin is very rough and rigid hence avoiding
easy penetration of the microbes into the body
Cilia
These are hair like projection found in the
deferent parts of the body like in the respiratory
system, these help in trapping organisms
preventing them from entering into the body
hence a protection
82. The chemical barriers are;
Mucus
This is found also in the respiratory system and its
aim is to trap and kill microbes since it contains anti
microbial agents hence providing protection
Hcl
This chemical kills microbes in the stomach that
may have entered the GIT along with the food
Lysol
This chemical component is found in the tears, it
contains ingredients that kill microbes that land in
the eyes
83. The acidic PH in the vagina which kill the organisms
that may enter the body through that route
Sebum
This is the oily chemical produced by the skin, this oil has
the ability of trapping and killing microbes hence giving
protection
Cellular involvement
The phagocytic cells and the macrophages play a big role
of attacking and destroying any organism that may gain
its way into the body and this is seen in the process of
phagocytosis
Inflammation and protein complement actions
These act as an alarm or signal to the body defenses that
the body has been invaded by a pathogen or an enemy
84. ADAPTIVE/SPECIFIC IMMUNITY
It’s divided into two and these are;
1. Passive immunity
2. Active immunity
PASSIVE IMMUNITY
This is the type of immunity acquired when
already made antibodies are introduced into the
body to help it fight against a specific antigen.
Therefore this means that the body is not involved
in making and producing these antibodies or
immunity
85. Passive immunity is further divided into two types
vis
Natural passive immunity
Artificial passive immunity
Natural passive immunity is the type of immunity
acquired when already made antibodies are passed on the
baby from the mother through the placenta and breast
milk
Artificial passive immunity is the type of immunity
acquired when the serum/vaccine containing artificially
made antibodies is introduced into some one’s body to
protect him or her from a specific organism or disease
Advantages and disadvantages of passive immunity
(research work)
86. ACTIVE IMMUNITY
This is the type of immunity that occurs when an
individual’s body is actively involved in making its own
antibody against a specific antigen. This type of
immunity is also further divided into;
1. Natural active immunity
2. Artificial active immunity
Natural active immunity is the type of immunity
acquired after suffering from an infection or disease.
This means that when a person gets an infection, the
body responds by producing antibodies against that
antigen, some of the produced antibodies will be used in
the elimination process and others will remain as
memory antibodies or cells
87. So when the body is attacked again by
the same antigen, it uses the memory
antibodies to eliminate that antigen
Artificial active immunity
This is the type of immunity acquired
when an antigenic substance has been
introduced into the body through
immunization to provoke or stimulate
it to produce antibodies against that
specific introduced antigen
88. Merits and demerits of active
immunity(research)
differences between active
and passive immunity
89. Active immunity Passive immunity
It is produced with the help of
the bodies immune system
The body is not actively
involved in the formation of
the immunity
Immunity developed is long
lasting
Immunity lasts for a short
period of time
Immunity takes time to be
developed
Provides immediate immunity
Immunological memory is
used
Its not used
Its not applicable in immune
suppressed clients
Its applicable
90. IMMUNISATION AND VACCINATION
Immunization is the process of
creating/introducing immunity against
specific antigen or infection
Or
Is the process of introducing vaccines
in the body to help it fight against
disease causing germs
91. VACCINES
This refers to the substance that
contains antigenic material and when
introduced in the body it boosts or
stimulates antibody production
the vaccine may contain living or
killed microbes, bacteria, toxoid or
antigenic material
92. TYPES/CLASSES OF VACCINES
1. Live attenuated vaccines
2. killed/ inactivated vaccines
3. Toxoid vaccine
4. Conjugated vaccines
KILED VACCINES
These are from pathogens that have
been killed with chemicals or heat and
they need multiple doses to induce
adequate immune response
93. Examples of killed vaccines
Hepatitis vaccine
Influenza vaccine
Rabies vaccine,
Polio vaccine
Pertusis vaccine
Merits
1. They are stable and easy to store
2. They have along duration of potency
94. Demerits
1. Multiple doses are required in order to
generate adequate immune response
2. May turn into an infection if inactivation
was not completed
LIVE ATTENUATED VACCINES
These are made by weakening the pathogen
using the process of attenuation
the weakened pathogen continues to
multiply inside the human host and