In laboratory animals, maintaining the health status in very alarming situations very difficult. Both SPF and Gnotobiotic animals have laboratory significance for which their management is a valid aspect.
Production method of germ free lab animalsPankaj Gaonkar
This document describes the production method of germ free lab animals. It discusses the definition of germ free animals and the equipment needed to produce them, such as isolators and transfer chambers. The key steps of the method are ensuring availability of germ free surrogate mothers, transferring pregnant donor mice to the isolator on day 17-20, performing caesarean sections in the transfer chamber to remove the uterine packages, and mixing the donor pups with the surrogate mother's litter in the isolator. Producing germ free animals allows their use to study reactions to diets, infectious disease pathogenesis, and other research.
This document discusses the management of specific pathogen free (SPF) and gnotobiotic laboratory animals. It defines SPF animals as those free of specified microorganisms and parasites. Gnotobiotic animals are derived via cesarean section and maintained germfree. The document outlines the purchase, housing, breeding, and screening of SPF and gnotobiotic animals. It emphasizes strict biosecurity protocols to prevent contamination, including staff training, barrier facilities, and routine screening of animals and facilities. Proper care, record keeping, and environmental conditions are also necessary to maintain these specialized research colonies.
Gnotobiosis (from Greek roots gnostos "known" and bios "life") refers to an engineered state of an organism in which all forms of life (i.e., microorganisms) in or on it, including its microbiota, have been identified.[1] The term gnotobiotic organism, or gnotobiote, can refer to a model organism that is colonized with a specific community of known microorganisms (isobiotic or defined flora animal) or that contains no microorganisms (germ-free) often for experimental purposes.[2][3][4][5] The study of gnotobiosis and the generation of various types of gnotobiotic model organisms as tools for studying interactions between host organisms and microorganisms is referred to as gnotobiology.
Gnotobiotics is the scientific study of animals or other organisms that are raised in germ free environments or ones that contain only specifically known germs. The gnotobiotic laboratory animal is potentially a very valuable tool for investigating any suspected interaction between the host and its associated microflora or between different components of that flora. However, like many other good ideas, the production of gnotobiotes is simple in concept but complicated in execution. In the early stages the greatest obstacles to the general use of germ free animals were the expense and the restricted amount of space that could be maintained free from contaminants. Nowadays, with modern isolators and facilities it is easier to produce gnotobiotic animals at relatively modest price.
Gnotobiotic animals or Gnotobiote are an animal stock or strain in which only certain known strains of bacteria and other microorganisms are present. Technically the term also includes germ free animals as the status of their microbial communities is also known (Reyniers, 1959). Gnotobiotic animals are derived by aseptic hysterotomy or hysterectomy, embryo transfer or sterile hatching of eggs and are continuously maintained using aseptic technique where the microbial status of the animal is fully defined; includes both germ free and defined flora animals. Animals reared in a gnotobiotic colony are devoid of normal flora, has poorly developed immune systems, lower cardiac output, thin intestinal walls, low antibody titers low metabolism rate and high susceptibility to infectious pathogens (Wostmann et al., 1996). Lower amounts of serum gamma globulins have been observed in germ free animals of several species and the quantity increases on association with microorganisms. Nuttall and Thierfelder are considered pioneers of gnotobiotics and germ free research. Germ free mice have adapted anatomically and physiologically to life without microbes
The gnotobiotic principles used in the production of infection free laboratory animals evolved from the efforts to rear and study animals in the absence of microbes or in association with one or more pure cultures of microbes . The gnotobiotic animal is potentially a very valuable tool for Scientitist.
Foot and mouth disease is a highly contagious viral disease that affects cloven-hooved animals. It is characterized by blisters in the mouth and feet, excessive salivation, and lameness. The disease spreads through direct contact, aerosols, contaminated equipment and materials, people, predators, food, and semen. There is no treatment, but vaccination, sanitation, and biosecurity measures can control and prevent the spread.
Immunodiffusion -Different Types,Principle,procedureand application. it is a diagnostic technique for the detection or measurements of antibodies and antigens by their precipitation which involves diffusion through a substances such as agar or gel agarose .common types -oudin procedure,oakley fulthorpe procedure ,mancini technique ,ouchterlony double immuno diffusion
This document provides information on procedures for examining urine, skin scrapings, and milk from various animal species. It describes how to collect and store samples, and outlines the steps for chemical, microscopic, and cultural examinations. Key points covered include normal versus abnormal findings for pH, glucose, protein, ketones, bilirubin, blood, and sediments in urine. Examination of milk involves assessing color, odor, consistency, and performing white slide and California mastitis tests to detect inflammation.
The viral neutralization test is a serological method that detects the presence of viral neutralizing antibodies. It involves mixing dilutions of antibodies with a standardized amount of virus, incubating them, and observing for cytopathic effects in cell cultures. If the antibodies neutralize the virus, no cytopathic effects will be observed as the cells remain intact. While the viral neutralization test is highly sensitive and specific, it is also slow, intensive, and requires skilled technicians. It remains the gold standard method for diagnosing viral infections in the laboratory by comparing other test methods to it.
Production method of germ free lab animalsPankaj Gaonkar
This document describes the production method of germ free lab animals. It discusses the definition of germ free animals and the equipment needed to produce them, such as isolators and transfer chambers. The key steps of the method are ensuring availability of germ free surrogate mothers, transferring pregnant donor mice to the isolator on day 17-20, performing caesarean sections in the transfer chamber to remove the uterine packages, and mixing the donor pups with the surrogate mother's litter in the isolator. Producing germ free animals allows their use to study reactions to diets, infectious disease pathogenesis, and other research.
This document discusses the management of specific pathogen free (SPF) and gnotobiotic laboratory animals. It defines SPF animals as those free of specified microorganisms and parasites. Gnotobiotic animals are derived via cesarean section and maintained germfree. The document outlines the purchase, housing, breeding, and screening of SPF and gnotobiotic animals. It emphasizes strict biosecurity protocols to prevent contamination, including staff training, barrier facilities, and routine screening of animals and facilities. Proper care, record keeping, and environmental conditions are also necessary to maintain these specialized research colonies.
Gnotobiosis (from Greek roots gnostos "known" and bios "life") refers to an engineered state of an organism in which all forms of life (i.e., microorganisms) in or on it, including its microbiota, have been identified.[1] The term gnotobiotic organism, or gnotobiote, can refer to a model organism that is colonized with a specific community of known microorganisms (isobiotic or defined flora animal) or that contains no microorganisms (germ-free) often for experimental purposes.[2][3][4][5] The study of gnotobiosis and the generation of various types of gnotobiotic model organisms as tools for studying interactions between host organisms and microorganisms is referred to as gnotobiology.
Gnotobiotics is the scientific study of animals or other organisms that are raised in germ free environments or ones that contain only specifically known germs. The gnotobiotic laboratory animal is potentially a very valuable tool for investigating any suspected interaction between the host and its associated microflora or between different components of that flora. However, like many other good ideas, the production of gnotobiotes is simple in concept but complicated in execution. In the early stages the greatest obstacles to the general use of germ free animals were the expense and the restricted amount of space that could be maintained free from contaminants. Nowadays, with modern isolators and facilities it is easier to produce gnotobiotic animals at relatively modest price.
Gnotobiotic animals or Gnotobiote are an animal stock or strain in which only certain known strains of bacteria and other microorganisms are present. Technically the term also includes germ free animals as the status of their microbial communities is also known (Reyniers, 1959). Gnotobiotic animals are derived by aseptic hysterotomy or hysterectomy, embryo transfer or sterile hatching of eggs and are continuously maintained using aseptic technique where the microbial status of the animal is fully defined; includes both germ free and defined flora animals. Animals reared in a gnotobiotic colony are devoid of normal flora, has poorly developed immune systems, lower cardiac output, thin intestinal walls, low antibody titers low metabolism rate and high susceptibility to infectious pathogens (Wostmann et al., 1996). Lower amounts of serum gamma globulins have been observed in germ free animals of several species and the quantity increases on association with microorganisms. Nuttall and Thierfelder are considered pioneers of gnotobiotics and germ free research. Germ free mice have adapted anatomically and physiologically to life without microbes
The gnotobiotic principles used in the production of infection free laboratory animals evolved from the efforts to rear and study animals in the absence of microbes or in association with one or more pure cultures of microbes . The gnotobiotic animal is potentially a very valuable tool for Scientitist.
Foot and mouth disease is a highly contagious viral disease that affects cloven-hooved animals. It is characterized by blisters in the mouth and feet, excessive salivation, and lameness. The disease spreads through direct contact, aerosols, contaminated equipment and materials, people, predators, food, and semen. There is no treatment, but vaccination, sanitation, and biosecurity measures can control and prevent the spread.
Immunodiffusion -Different Types,Principle,procedureand application. it is a diagnostic technique for the detection or measurements of antibodies and antigens by their precipitation which involves diffusion through a substances such as agar or gel agarose .common types -oudin procedure,oakley fulthorpe procedure ,mancini technique ,ouchterlony double immuno diffusion
This document provides information on procedures for examining urine, skin scrapings, and milk from various animal species. It describes how to collect and store samples, and outlines the steps for chemical, microscopic, and cultural examinations. Key points covered include normal versus abnormal findings for pH, glucose, protein, ketones, bilirubin, blood, and sediments in urine. Examination of milk involves assessing color, odor, consistency, and performing white slide and California mastitis tests to detect inflammation.
The viral neutralization test is a serological method that detects the presence of viral neutralizing antibodies. It involves mixing dilutions of antibodies with a standardized amount of virus, incubating them, and observing for cytopathic effects in cell cultures. If the antibodies neutralize the virus, no cytopathic effects will be observed as the cells remain intact. While the viral neutralization test is highly sensitive and specific, it is also slow, intensive, and requires skilled technicians. It remains the gold standard method for diagnosing viral infections in the laboratory by comparing other test methods to it.
Care and handling of laboratory animals – rabbit, guinea pigKEVENLIAM
This document provides information on the care and handling of laboratory rabbits and guinea pigs. It discusses their physiology, common uses in experiments, and guidelines for proper handling and housing. Rabbits and guinea pigs are often used as they are small, inexpensive, and similar to humans physiologically. Proper care is important to ensure the health and welfare of these laboratory animals.
This document discusses commonly used laboratory animals in research. It describes that mice, rats, hamsters, guinea pigs, rabbits, monkeys, dogs, zebrafish, and transgenic flies are frequently employed. Mice and rats are most popular due to their similarities to humans. Each animal type has distinct characteristics that make them suitable for different areas of research like medicine development, safety testing, and studying disease mechanisms and physiology. The document provides details on the typical strains, uses, advantages, and biological data of several common laboratory animal species.
This document provides information on cell culture techniques. It discusses:
1. Primary cell culture involves directly culturing cells separated from tissues using enzymatic or mechanical methods. Adherent cells attach to surfaces while suspension cells remain floating.
2. Secondary cell cultures are produced when primary cells are subcultured. Cell lines can be either finite, with limited life spans, or continuous, capable of indefinite growth.
3. Cell culture media must provide nutrients and an appropriate environment for cell growth. Serum-containing and serum-free media are commonly used. Equipment like incubators, storage units, and cryogenic tanks are also needed to maintain cell cultures.
Blood parasites have been subject of extensive research since the beginning of the 20th century. The presence of haemoparasites in animals is very common. In this presentation I presented the most common parasites.
Dr. Fakhar-e-Alam Kulyar
DVM, M.Phil CMS
University of Agriculture Faisalabad
Barr bodies are inactive X chromosomes that appear as darkly stained structures in the nuclei of female somatic cells. A buccal smear involves scraping cheek cells and staining them to identify Barr bodies and determine sex. Giemsa stain produces violet Barr bodies within pink nuclei. Thionin is a sensitive DNA stain that clearly shows dark blue or black Barr bodies near the nuclear envelope in female cells. The presence of one or more Barr bodies corresponds to the number of X chromosomes.
This document describes the HOTIS test, which is used to detect mastitis in bovine milk by detecting the presence of Streptococcus agalactiae. The test involves mixing milk with a pH indicator dye, bromocresol purple, in a test tube. If streptococci that cause mastitis are present, they will produce acid during incubation that changes the color of the dye from purple to yellow, indicating a positive result. Colonies of S. agalactiae appear as canary yellow flakes or balls deposited on the sides of the test tube. The HOTIS test was discovered in 1943 and is a diagnostic procedure for detecting mastitis-causing streptococci in milk.
Rocket immunoelectrophoresis is a quantitative technique used to detect antigen-antibody complexes. It involves placing antigen samples in wells cut into an agarose gel containing immobilized antibodies. An electric current is passed through the gel, causing the antigens to migrate. As antigens interact with antibodies, precipitin lines form in the shape of cones or "rockets". The height of the rockets is proportional to antigen concentration, allowing quantification. Rocket immunoelectrophoresis is used to estimate protein concentrations and study antigenic relationships between organisms.
Clostridial infections in animals in IndiaBhoj Raj Singh
Clostridial infection are rising at steady pace in India with inclusion of antibiotics in feed and intensive farming as well as indiscriminate therapeutic use of antibiotics in animals and birds.
SAFETY RULE AND REGULATION IN MICROBIOLOGICAL LABOURATORYvivek kumar
Safety rules and regulations are necessary in microbiology laboratories to prevent adverse health effects. Key safety procedures include:
- Following good lab practices like wearing protective equipment, properly labeling samples, and disinfecting work surfaces.
- Using aseptic techniques to prevent contamination of cultures.
- Properly disposing of contaminated waste through autoclaving or using sharps containers.
- Knowing emergency procedures like the locations of eye washes, showers, and how to handle spills.
- Adhering to biosafety levels which are determined by the risk of pathogens being studied.
This document discusses different types of incubators and their applications. It begins by describing laboratory incubators, which maintain optimal temperature, humidity, and gases to grow cell and microbiological cultures. The market is divided into gassed CO2 incubators and non-gassed types. Incubators provide controlled environments for cultures and protect cells from temperature and atmospheric changes. Types discussed include standard, cooled, humidity-controlled, CO2, shaking, and hybridization incubators. Factors like volume, materials, temperature control, and safety features are considered when choosing an incubator. Applications include growing cell cultures, microbiological analyses, breeding insects, storing samples, and growing protein crystals.
CO2 incubators are designed to provide ideal tissue culturing conditions with high resistance to contamination through control over contamination with simple operation and reliable performance. They allow growth of organisms in optimal conditions of temperature, carbon dioxide and humidity. Incubators generally come in three configurations: air jacket, dry wall, and water jacket. They have inner chambers made of stainless steel and outer walls of heavy gauge steel, with temperature control through a programmable controller that maintains the inside between 5 degrees C above ambient and 60 degrees C.
This document discusses various methods for testing the efficacy of disinfectants, including carrier tests, suspension tests, and practical tests. Carrier tests involve contaminating carriers like threads with bacteria and exposing them to disinfectants. Suspension tests involve exposing a bacterial suspension directly to the disinfectant. Practical tests evaluate disinfectants under real-world conditions. The document also describes factors that can influence disinfection like temperature, pH, and the presence of organic matter or other substances. Specific tests discussed in detail include the AOAC use-dilution test, Kelsey-Sykes capacity test, and surface disinfection tests.
This document discusses various methods for preserving microorganisms in pure culture, including periodic transfer to fresh media, lyophilization (freeze drying), cryopreservation, storage under oil or in saline suspension, and drying in vacuum. The key objectives of preservation are to maintain isolated pure cultures for extended periods while avoiding contamination or genetic changes. Lyophilization and cryopreservation in liquid nitrogen are commonly used techniques that allow long-term viable storage for decades by stopping microbial growth and metabolism. Periodic transfer risks contamination and genetic variation over time.
The document summarizes manufacturing processes and strategies for lateral flow assay production. Key steps include reagent application and drying, lamination of components, inspection and marking, cutting, quality control, and assembly/packaging. Batch manufacturing uses equipment like dispensers, laminators, and cutters in a process line layout. In-line manufacturing utilizes reel-to-reel handling and dispensing for higher throughput of 60 million+ tests per year with only 2-5 operators.
The document describes the Ascoli test, a precipitin test used for the serological diagnosis of anthrax. The test uses antiserum raised in rabbits against Bacillus anthracis to detect thermostable antigens from the bacteria. A positive result is indicated by the formation of a visible precipitate band within 15 minutes when the antiserum is layered with a filtrate obtained from boiling and filtering a sample suspected to contain B. anthracis antigens.
Foot and mouth disease is a highly contagious viral disease that affects cloven-hooved animals like cattle, pigs, sheep and goats. It is caused by an aphthovirus from the family Picornaviridae. The virus can be transmitted between animals through direct contact or contact with contaminated materials. Clinical signs include blisters and sores in the mouth and on the feet. Young animals are more susceptible to death from myocarditis. Farmers are advised to promptly isolate and report suspected cases of foot and mouth disease to prevent its spread.
This presentation was given at the Delmarva Small Ruminant Conference All Worms All Day on December 8, 2018, in Keedysville, Maryland. The presenter was Susan Schoenian.
The document discusses proper procedures for sample preparation and transportation for laboratory analysis. It covers sampling of water, feed, poultry sheds, and animals. Key points include taking water samples from the water source, collecting feed samples in sterile containers, using sterile swabs to sample surfaces in poultry sheds, and following aseptic techniques when sampling organs from animals. The document also outlines packaging and transportation requirements to prevent contamination and preserve sample quality during transport.
Biochemistry is a basic science which deals with chemical nature and chemical behaviour of living matter and with the reactions and processes they undergo.
Biochemistry involves the study of:
Chemical constituents of living matter.
Chemical changes which occur in the organism during digestion, absorption and excretion.
Chemical changes which occur during growth and multiplication of the organism.
Transformation of one form of chemical constituent to the other.
Energy changes involved in such transformation.
Note:- The term “Biochemistry” was first introduced by German chemist Carl Neuberg in 1903 from Greek word “bios” means “life”.
It is mainly deals with the biochemical aspects that are involved in several conditions.
The results of qualitative and quantitative analysis of body fluids assist the clinicians in the diagnosis, treatment and prevention of the disease and drug monitoring, tissue and organ transplantation, forensic investigations and so on.
Various biological fluids subjected to chemical tests and assays include blood, plasma, serum, urine, cerebrospinal fluid (CSF), ascetic fluid, pleural fluid, faeces, calculi and tissues.
Note:- Modern day medical practice is highly dependent on the laboratory analysis of body fluids, especially the blood. The disease manifestations are reflected in the composition of blood and other tissues.
Hence, the demarcation of abnormal from normal constituents of the body is another aim of the study of clinical biochemistry.
Care and handling of laboratory animals – rabbit, guinea pigKEVENLIAM
This document provides information on the care and handling of laboratory rabbits and guinea pigs. It discusses their physiology, common uses in experiments, and guidelines for proper handling and housing. Rabbits and guinea pigs are often used as they are small, inexpensive, and similar to humans physiologically. Proper care is important to ensure the health and welfare of these laboratory animals.
This document discusses commonly used laboratory animals in research. It describes that mice, rats, hamsters, guinea pigs, rabbits, monkeys, dogs, zebrafish, and transgenic flies are frequently employed. Mice and rats are most popular due to their similarities to humans. Each animal type has distinct characteristics that make them suitable for different areas of research like medicine development, safety testing, and studying disease mechanisms and physiology. The document provides details on the typical strains, uses, advantages, and biological data of several common laboratory animal species.
This document provides information on cell culture techniques. It discusses:
1. Primary cell culture involves directly culturing cells separated from tissues using enzymatic or mechanical methods. Adherent cells attach to surfaces while suspension cells remain floating.
2. Secondary cell cultures are produced when primary cells are subcultured. Cell lines can be either finite, with limited life spans, or continuous, capable of indefinite growth.
3. Cell culture media must provide nutrients and an appropriate environment for cell growth. Serum-containing and serum-free media are commonly used. Equipment like incubators, storage units, and cryogenic tanks are also needed to maintain cell cultures.
Blood parasites have been subject of extensive research since the beginning of the 20th century. The presence of haemoparasites in animals is very common. In this presentation I presented the most common parasites.
Dr. Fakhar-e-Alam Kulyar
DVM, M.Phil CMS
University of Agriculture Faisalabad
Barr bodies are inactive X chromosomes that appear as darkly stained structures in the nuclei of female somatic cells. A buccal smear involves scraping cheek cells and staining them to identify Barr bodies and determine sex. Giemsa stain produces violet Barr bodies within pink nuclei. Thionin is a sensitive DNA stain that clearly shows dark blue or black Barr bodies near the nuclear envelope in female cells. The presence of one or more Barr bodies corresponds to the number of X chromosomes.
This document describes the HOTIS test, which is used to detect mastitis in bovine milk by detecting the presence of Streptococcus agalactiae. The test involves mixing milk with a pH indicator dye, bromocresol purple, in a test tube. If streptococci that cause mastitis are present, they will produce acid during incubation that changes the color of the dye from purple to yellow, indicating a positive result. Colonies of S. agalactiae appear as canary yellow flakes or balls deposited on the sides of the test tube. The HOTIS test was discovered in 1943 and is a diagnostic procedure for detecting mastitis-causing streptococci in milk.
Rocket immunoelectrophoresis is a quantitative technique used to detect antigen-antibody complexes. It involves placing antigen samples in wells cut into an agarose gel containing immobilized antibodies. An electric current is passed through the gel, causing the antigens to migrate. As antigens interact with antibodies, precipitin lines form in the shape of cones or "rockets". The height of the rockets is proportional to antigen concentration, allowing quantification. Rocket immunoelectrophoresis is used to estimate protein concentrations and study antigenic relationships between organisms.
Clostridial infections in animals in IndiaBhoj Raj Singh
Clostridial infection are rising at steady pace in India with inclusion of antibiotics in feed and intensive farming as well as indiscriminate therapeutic use of antibiotics in animals and birds.
SAFETY RULE AND REGULATION IN MICROBIOLOGICAL LABOURATORYvivek kumar
Safety rules and regulations are necessary in microbiology laboratories to prevent adverse health effects. Key safety procedures include:
- Following good lab practices like wearing protective equipment, properly labeling samples, and disinfecting work surfaces.
- Using aseptic techniques to prevent contamination of cultures.
- Properly disposing of contaminated waste through autoclaving or using sharps containers.
- Knowing emergency procedures like the locations of eye washes, showers, and how to handle spills.
- Adhering to biosafety levels which are determined by the risk of pathogens being studied.
This document discusses different types of incubators and their applications. It begins by describing laboratory incubators, which maintain optimal temperature, humidity, and gases to grow cell and microbiological cultures. The market is divided into gassed CO2 incubators and non-gassed types. Incubators provide controlled environments for cultures and protect cells from temperature and atmospheric changes. Types discussed include standard, cooled, humidity-controlled, CO2, shaking, and hybridization incubators. Factors like volume, materials, temperature control, and safety features are considered when choosing an incubator. Applications include growing cell cultures, microbiological analyses, breeding insects, storing samples, and growing protein crystals.
CO2 incubators are designed to provide ideal tissue culturing conditions with high resistance to contamination through control over contamination with simple operation and reliable performance. They allow growth of organisms in optimal conditions of temperature, carbon dioxide and humidity. Incubators generally come in three configurations: air jacket, dry wall, and water jacket. They have inner chambers made of stainless steel and outer walls of heavy gauge steel, with temperature control through a programmable controller that maintains the inside between 5 degrees C above ambient and 60 degrees C.
This document discusses various methods for testing the efficacy of disinfectants, including carrier tests, suspension tests, and practical tests. Carrier tests involve contaminating carriers like threads with bacteria and exposing them to disinfectants. Suspension tests involve exposing a bacterial suspension directly to the disinfectant. Practical tests evaluate disinfectants under real-world conditions. The document also describes factors that can influence disinfection like temperature, pH, and the presence of organic matter or other substances. Specific tests discussed in detail include the AOAC use-dilution test, Kelsey-Sykes capacity test, and surface disinfection tests.
This document discusses various methods for preserving microorganisms in pure culture, including periodic transfer to fresh media, lyophilization (freeze drying), cryopreservation, storage under oil or in saline suspension, and drying in vacuum. The key objectives of preservation are to maintain isolated pure cultures for extended periods while avoiding contamination or genetic changes. Lyophilization and cryopreservation in liquid nitrogen are commonly used techniques that allow long-term viable storage for decades by stopping microbial growth and metabolism. Periodic transfer risks contamination and genetic variation over time.
The document summarizes manufacturing processes and strategies for lateral flow assay production. Key steps include reagent application and drying, lamination of components, inspection and marking, cutting, quality control, and assembly/packaging. Batch manufacturing uses equipment like dispensers, laminators, and cutters in a process line layout. In-line manufacturing utilizes reel-to-reel handling and dispensing for higher throughput of 60 million+ tests per year with only 2-5 operators.
The document describes the Ascoli test, a precipitin test used for the serological diagnosis of anthrax. The test uses antiserum raised in rabbits against Bacillus anthracis to detect thermostable antigens from the bacteria. A positive result is indicated by the formation of a visible precipitate band within 15 minutes when the antiserum is layered with a filtrate obtained from boiling and filtering a sample suspected to contain B. anthracis antigens.
Foot and mouth disease is a highly contagious viral disease that affects cloven-hooved animals like cattle, pigs, sheep and goats. It is caused by an aphthovirus from the family Picornaviridae. The virus can be transmitted between animals through direct contact or contact with contaminated materials. Clinical signs include blisters and sores in the mouth and on the feet. Young animals are more susceptible to death from myocarditis. Farmers are advised to promptly isolate and report suspected cases of foot and mouth disease to prevent its spread.
This presentation was given at the Delmarva Small Ruminant Conference All Worms All Day on December 8, 2018, in Keedysville, Maryland. The presenter was Susan Schoenian.
The document discusses proper procedures for sample preparation and transportation for laboratory analysis. It covers sampling of water, feed, poultry sheds, and animals. Key points include taking water samples from the water source, collecting feed samples in sterile containers, using sterile swabs to sample surfaces in poultry sheds, and following aseptic techniques when sampling organs from animals. The document also outlines packaging and transportation requirements to prevent contamination and preserve sample quality during transport.
Biochemistry is a basic science which deals with chemical nature and chemical behaviour of living matter and with the reactions and processes they undergo.
Biochemistry involves the study of:
Chemical constituents of living matter.
Chemical changes which occur in the organism during digestion, absorption and excretion.
Chemical changes which occur during growth and multiplication of the organism.
Transformation of one form of chemical constituent to the other.
Energy changes involved in such transformation.
Note:- The term “Biochemistry” was first introduced by German chemist Carl Neuberg in 1903 from Greek word “bios” means “life”.
It is mainly deals with the biochemical aspects that are involved in several conditions.
The results of qualitative and quantitative analysis of body fluids assist the clinicians in the diagnosis, treatment and prevention of the disease and drug monitoring, tissue and organ transplantation, forensic investigations and so on.
Various biological fluids subjected to chemical tests and assays include blood, plasma, serum, urine, cerebrospinal fluid (CSF), ascetic fluid, pleural fluid, faeces, calculi and tissues.
Note:- Modern day medical practice is highly dependent on the laboratory analysis of body fluids, especially the blood. The disease manifestations are reflected in the composition of blood and other tissues.
Hence, the demarcation of abnormal from normal constituents of the body is another aim of the study of clinical biochemistry.
This document provides information on implementing a swine herd health program, including disease prevention, vaccination, and waste disposal. It discusses key concepts like the epidemiological triad of disease, common swine diseases and their symptoms, and developing herd health programs tailored for different groups of pigs. Guidelines are provided for proper vaccination techniques, safe handling of biologics and drugs, and establishing a waste disposal system. The goal of a herd health program is to keep pigs healthy and prevent disease spread through measures like vaccination, deworming, nutrition, biosecurity, and proper waste management.
This document discusses various clinical bacteriology tests used to detect and identify bacteria that may be causing infections. It describes how samples are collected from parts of the body and cultured to allow bacterial growth. Common tests mentioned include throat, sputum, urine and blood cultures to detect bacteria in respiratory, urinary or blood infections. Antibiotic sensitivity testing helps determine the most effective antibiotic for treatment. Gram staining can identify bacteria as either gram-positive or gram-negative. The document provides details on sample collection and processing of bacteriology tests to diagnose bacterial infections.
The entomopathogenic bacteria is isolated from insect cadavers or soil samples by heat treating the samples to kill vegetative cells and enrich for bacterial spores, plating the samples on growth media to obtain isolated colonies, and transferring colonies to liquid culture. The bacteria is mass cultured in flasks containing UG medium on an orbital shaker to induce sporulation and production of parasporal crystals. The spores and crystals are harvested through centrifugation, washing, and resuspension in water or saline for use in bioassays or storage.
Microbiology is the study of microorganisms like bacteria, fungi, and protozoa. Pharmaceutical microbiology applies microbiology to the production of medicines, focusing on microbes involved in antibiotics, vaccines, and other drugs. It ensures product safety through testing, limits on contamination, and sterilization. Proper controls are vital for pharmaceutical quality and preventing infectious disease.
pharmaceutical application of microbial technology.pptxberciyalgolda1
This document discusses key aspects of pharmaceutical microbiology. It begins by defining pharmaceutical microbiology as the study of microorganisms related to production of pharmaceutical products like antibiotics, enzymes and vaccines. It then describes several factors involved in pharmaceutical microbiology like microbial contamination, limits testing, antimicrobial preservation and sterilization techniques. The document emphasizes the importance of controlling microbes during drug manufacturing and storage to ensure product safety and quality.
cpcsea guidelines for laboratory animal facility-pptxANIKETH SURVE
The document discusses guidelines for the humane care and use of animals in research. It states that adequate veterinary care is required and is the responsibility of a veterinarian or trained person. Effective quarantine procedures should be used to limit the transmission of diseases between newly received and existing animals. All animals must be observed daily for signs of illness and abnormal behavior and receive proper medical care. Proper facilities and protective equipment must be provided to animal house staff.
safety data sheet, an introduction to cell culture, safety equipment, safe laboratory practices, ascetic techniques, sterile work area, good personal hygiene, sterile reagents and media, sterile handling, planning of cell culture labs.
Different Methods used in Integrated-Plant-Disease-Management.pptxshahzaibanwar11
its about different methods used in integrated plant disease management. it is a holistic approach that use a combination of different methods to manage diseases and to minimize the effect on environment and main crop health.it minimizes the use of chemicals and forces the use of natural methods.
This document discusses key concepts in pharmaceutics and drug development. It covers:
1. The branches of pharmaceutics including pharmacokinetics, pharmacodynamics, biopharmaceutics, and pharmaceutical technology.
2. The process of drug discovery and development, from identifying drug targets through preclinical and clinical testing.
3. The different phases of clinical trials and timelines for drug approval.
4. The definitions of key terms used in drug development like target, hit, lead, candidate, and product.
5. The differences between brand drugs, generics, and biosimilars.
This document provides an introduction to botanical medicines, covering their history, science, uses, and dangers. It discusses how botanicals are extracted and prepared as medicines, as well as how their effectiveness is studied through in vitro, in vivo, and clinical trials. While botanicals have been used for thousands of years, the book notes that research on their effects is still developing and opinions vary on their role in medicine. It emphasizes the need for more rigorous clinical research and cooperation between conventional and complementary practitioners to establish the safety and efficacy of herbal medicines.
This document describes a study conducted by students on the antimicrobial activities of plant extracts. It includes an introduction discussing the increasing resistance of microbes to antibiotics and the need to find alternatives. The document outlines the methodology used, which involved collecting 9 different plant parts and testing their ethanol, acetone and petroleum ether extracts against various bacteria and fungi. The results and discussion section analyzes the effectiveness of the different plant extracts.
Farmers use antibiotics to keep livestock healthy and food safe. Antibiotics treat and prevent bacterial infections in animals just as they do in humans. The FDA approves antibiotics for use in animals and determines withdrawal periods to ensure meat is antibiotic-free. Multiple agencies regularly test food to ensure it is safe. While antibiotic overuse can lead to resistance, farmers and veterinarians are working to prevent this through judicious use and separating medically important human antibiotics.
A vaccine is a biological preparation that provides active acquired immunity to a particular infectious disease.Vaccine contains certain agents that not only resembles a disease-causing microorganism but it also stimulates body’s immune system recognize the foreign agents.Vaccines can be prophylactic or therapeutic.
The administration of vaccines is called vaccination.
British physician Edward Jenner, who in 1796 used the cowpox virus (Latin variola vaccinia) to confer protection against smallpox. In 1885 the French microbiologist Louis Pasteur and Emile Roux developed the first vaccine against rabies.
There are several types of vaccines like Whole-Organism vaccine, recombinant vaccine,dna vaccine, multivalent subunit vaccines etc.
This document provides an overview of diagnostic testing in microbiology laboratories. It discusses basic microbiology principles like media and culture, direct and indirect testing methods, sterile vs. non-sterile body sites, sensitivity and specificity. It then walks through the process of handling a specimen from receipt to reporting results, including appropriate collection, transport, inoculation, isolation, identification and documentation. Finally, it discusses a case study of testing a blood sample and issues around laboratory staffing.
Discuss one cause of foodborne illness..Not E coli ... State why it .pdfarishmarketing21
Discuss one cause of foodborne illness..Not E coli ... State why it is a public health problem?
The discuss why this problem occurs, Also discuss current control measures recommended and
used to prevent and control the foodborne illness that is the focus of your discussion. Finally, you
should propose a new control strategy or measure(s) that, if implemented, you believe would
reduce or eliminate the problem that you have characterized earlier Your proposal for improved
prevention and control practice should utilize terms and concepts,You should explain how your
proposal relates to the problem that you identified earlier in the paper, why you believe that it
will work, and how your proposed measure(s) fill gaps in the current public health response.
Solution
- Listeriosis is a serious infection caused by the germ Listeria monocytogenes. People usually
become ill with listeriosis after eating contaminated food. The disease primarily affects pregnant
women, newborns, older adults, and people with weakened immune systems. It\'s rare for people
in other groups to get sick with Listeria infection.
Listeriosis is usually a mild illness for pregnant women, but it causes severe disease in the fetus
or newborn baby. Adults 65 years and older and people with weakened immune systems most
commonly develop severe infections of the bloodstream (causing sepsis) or brain (causing
meningitis or encephalitis). Listeria infections can sometimes affect other parts of the body,
including bones, joints, and sites in the chest and abdomen.
- it is a public health problem because Recognized as an important public health problem in the
United States, Listeria monocytogenes is a ubiquitous, intracellular pathogen known to cause
food-contaminating outbreaks. These microorganisms have the ability to multiply within host
cells and spread from cell to cell
- control measures -
Avoiding Outbreaks
A clean, dry environment is of utmost importance in controlling Listeria. Common processing
facility contamination sites include floors, walls, ceilings, food contact surfaces, cleaning aids,
drains/wash areas, and heating, ventilation, and air conditioning (HVAC) systems. Potential
problem areas should be identified at each processing facility
Without meticulous and proper cleaning, plant equipment, including any equipment used for
refrigeration and HVAC, can become breeding grounds for microorganisms. Intermittent defrost
systems, which are subject to frequent washdowns, encourage microbial growth. Because they
often contain moisture from standing water or condensation, special attention should be paid to
these systems to prevent their contamination.
Among the many general guidelines for keeping a food processing facility clean, visual
inspection and routine testing are important. While regular cleaning can help prevent outbreaks,
continuous monitoring is needed to assess further control measures. Determine sample points
and frequency for routine environmental testing, food cont.
This document summarizes the key differences between in vitro and in vivo experiments. In vitro refers to experiments performed outside of a living organism in artificial laboratory conditions, such as cell cultures or test tubes. In vivo experiments are conducted within living organisms under natural physiological conditions. Some key differences highlighted are that in vitro experiments are less expensive and faster but also less precise, while in vivo can provide more accurate results but are more time-consuming and costly. Examples of each type of experiment are also provided.
Through culture growth and effects on agar plates, Streptococci can be identified and differentiated. Alpha-hemolytic colonies from respiratory specimens are considered normal flora, while beta-hemolytic colonies are tested to identify the antigenic group as A or B. Identification can also be made by the ability of S. pyogenes to hydrolyze PYR, turning it bright red. Rapid immunoassay testing is also available to detect group A streptococci from throat swabs.
The document discusses infection control in pathological laboratories. It begins by defining infection control and its importance in healthcare settings. It then discusses how infection control was established in the 1950s and focuses on surveillance and risk factor identification. The document outlines sources of infection in laboratories, including inhalation, needle sticks, and ingestion. It provides several prevention and safety measures, such as hand washing, masks, vaccinations, and safe sharps practices. Finally, it discusses monitoring infection control through observations, interviews, inspections, and data analysis to maintain a safe environment.
Similar to Production of Specific Pathogen Free and Gnotobiotic animals (20)
Vaccination schedule of animals and poultryRameswar Panda
Vaccination is a preventive measure for controlling the disease outbreak. To be the vaccination a successful one, the components of vaccination program should be strictly followed. Vaccination aid is not available for all the diseases, rather for the disease which is contagious and causes a havoc
This document classifies livestock feed and forages into several categories: cultivated fodder including green/succulent, dry, and supplements/additives; natural vegetation including grasslands, pasture, and trees; concentrates that are rich in carbohydrates, protein, or both moderate; and roughages versus concentrates based on their crude fiber and nutrient content. It further categorizes roughages into maintenance type for cereal fodder and hay, production type for leguminous fodder and hay, and sustenance type for straw and stovers based on their digestible crude protein percentage.
This document summarizes several common breeds of ducks. It divides ducks into meat, egg, and ornamental types and describes the key characteristics of popular breeds like Pekin, Aylesbury, Muscovy, Rouen, Cayuga, Khaki Campbell, Indian Runner, and some ornamental and Indian breeds. The Pekin is one of the most popular breeds worldwide, originating from China. It is efficient and lays around 160 eggs. The Muscovy is native to South America and males are twice the female size and have distinctive knobs on their heads. Indian Runner ducks come in white, fawn, and penciled varieties and can lay up to 250 eggs while foraging outside all day
For better poultry farming, cognizance about different breeds should be important. To go either layer or broiler farming, breeds are the considerable factors. All are differentiated in terms of their geographical distribution, utility, colour etc.
After brooding stage, grower stage happens to every poultry species. many parallel manage-mental events is undertaken to make the birds good layers. feeding is the most essential part in this stage
Advances in vitamin & mineral nutrition in livestockRameswar Panda
feeding management cannot be ignored under any circumstances. This presentation depicts the tangential and burning points related to the role and significance of Vitamins and minerals for the livestock
Housing of wild animals is as essential as that of livestock species. The matter is so deepening in terms of its conservation especially in the context of India
The document summarizes several milch (dairy) cattle breeds found in India, including Gir, Sahiwal, Red Sindhi, and Deoni. It provides details on the origins, appearance, milk production capabilities, and reproductive characteristics of each breed. On average, Gir cows produce the most milk at 3,175 kg per lactation period, while Sindhi cows are the most economical producers. The breeds vary in traits like size, coloration, milk yield, temperament, and suitability for different climates and work.
In India, as not much of attention is paid so far as to this important aspect- animal housing, we find different types of animal houses constructed without careful planning and designing.
Livestock sector is an important sector in indian economy. To boost the productive performance of existing livestock population in india, biotechnolgy plays a key role to fullfill this.
The matter is not how the horses are transported, it is the welfare aspect of the horses which are to be taken in to account. There are legal frameworks in European countries regarding horse transportation which were effective from january 2007. In india also the transportation is legalized. there is a rule called Animal transport rules act. 1978, under which there are 6 schedules. and among them schedule 5 bears the transportation rules of horses.
Rfid a modern technique in animal identificationRameswar Panda
Radio frequency identification (RFID) is an efficient animal identification technology that uses radio waves to identify and track animals. RFID systems consist of transponders attached to animals, transceivers to read the transponders, and a computer system to store identification data. RFID ear tags, rumen boluses, and microchips implanted under the skin are common methods to attach transponders to animals. RFID technologies help automate dairy farm operations like weighing, milking, and health monitoring of individual animals. Standards like ISO 11784 and 11785 regulate RFID frequencies and transponder coding to ensure compatibility worldwide.
Ruminant livestock like cattle can produce a significant amount of methane per day, contributing to global warming. Many factors influence the methane emissions from cattle, including their diet and the addition of certain feeds. Manipulating these factors through mitigation strategies can help reduce the methane losses from cattle. A variety of techniques exist to measure methane emissions from individual animals or groups, both in indoor and outdoor enclosures, to help identify ways to decrease cattle's contributions to atmospheric methane levels.
Current Ms word generated power point presentation covers major details about the micronuclei test. It's significance and assays to conduct it. It is used to detect the micronuclei formation inside the cells of nearly every multicellular organism. It's formation takes place during chromosomal sepration at metaphase.
The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
Although Artemia has been known to man for centuries, its use as a food for the culture of larval organisms apparently began only in the 1930s, when several investigators found that it made an excellent food for newly hatched fish larvae (Litvinenko et al., 2023). As aquaculture developed in the 1960s and ‘70s, the use of Artemia also became more widespread, due both to its convenience and to its nutritional value for larval organisms (Arenas-Pardo et al., 2024). The fact that Artemia dormant cysts can be stored for long periods in cans, and then used as an off-the-shelf food requiring only 24 h of incubation makes them the most convenient, least labor-intensive, live food available for aquaculture (Sorgeloos & Roubach, 2021). The nutritional value of Artemia, especially for marine organisms, is not constant, but varies both geographically and temporally. During the last decade, however, both the causes of Artemia nutritional variability and methods to improve poorquality Artemia have been identified (Loufi et al., 2024).
Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
When I was asked to give a companion lecture in support of ‘The Philosophy of Science’ (https://shorturl.at/4pUXz) I decided not to walk through the detail of the many methodologies in order of use. Instead, I chose to employ a long standing, and ongoing, scientific development as an exemplar. And so, I chose the ever evolving story of Thermodynamics as a scientific investigation at its best.
Conducted over a period of >200 years, Thermodynamics R&D, and application, benefitted from the highest levels of professionalism, collaboration, and technical thoroughness. New layers of application, methodology, and practice were made possible by the progressive advance of technology. In turn, this has seen measurement and modelling accuracy continually improved at a micro and macro level.
Perhaps most importantly, Thermodynamics rapidly became a primary tool in the advance of applied science/engineering/technology, spanning micro-tech, to aerospace and cosmology. I can think of no better a story to illustrate the breadth of scientific methodologies and applications at their best.
The binding of cosmological structures by massless topological defectsSérgio Sacani
Assuming spherical symmetry and weak field, it is shown that if one solves the Poisson equation or the Einstein field
equations sourced by a topological defect, i.e. a singularity of a very specific form, the result is a localized gravitational
field capable of driving flat rotation (i.e. Keplerian circular orbits at a constant speed for all radii) of test masses on a thin
spherical shell without any underlying mass. Moreover, a large-scale structure which exploits this solution by assembling
concentrically a number of such topological defects can establish a flat stellar or galactic rotation curve, and can also deflect
light in the same manner as an equipotential (isothermal) sphere. Thus, the need for dark matter or modified gravity theory is
mitigated, at least in part.
Or: Beyond linear.
Abstract: Equivariant neural networks are neural networks that incorporate symmetries. The nonlinear activation functions in these networks result in interesting nonlinear equivariant maps between simple representations, and motivate the key player of this talk: piecewise linear representation theory.
Disclaimer: No one is perfect, so please mind that there might be mistakes and typos.
dtubbenhauer@gmail.com
Corrected slides: dtubbenhauer.com/talks.html
EWOCS-I: The catalog of X-ray sources in Westerlund 1 from the Extended Weste...Sérgio Sacani
Context. With a mass exceeding several 104 M⊙ and a rich and dense population of massive stars, supermassive young star clusters
represent the most massive star-forming environment that is dominated by the feedback from massive stars and gravitational interactions
among stars.
Aims. In this paper we present the Extended Westerlund 1 and 2 Open Clusters Survey (EWOCS) project, which aims to investigate
the influence of the starburst environment on the formation of stars and planets, and on the evolution of both low and high mass stars.
The primary targets of this project are Westerlund 1 and 2, the closest supermassive star clusters to the Sun.
Methods. The project is based primarily on recent observations conducted with the Chandra and JWST observatories. Specifically,
the Chandra survey of Westerlund 1 consists of 36 new ACIS-I observations, nearly co-pointed, for a total exposure time of 1 Msec.
Additionally, we included 8 archival Chandra/ACIS-S observations. This paper presents the resulting catalog of X-ray sources within
and around Westerlund 1. Sources were detected by combining various existing methods, and photon extraction and source validation
were carried out using the ACIS-Extract software.
Results. The EWOCS X-ray catalog comprises 5963 validated sources out of the 9420 initially provided to ACIS-Extract, reaching a
photon flux threshold of approximately 2 × 10−8 photons cm−2
s
−1
. The X-ray sources exhibit a highly concentrated spatial distribution,
with 1075 sources located within the central 1 arcmin. We have successfully detected X-ray emissions from 126 out of the 166 known
massive stars of the cluster, and we have collected over 71 000 photons from the magnetar CXO J164710.20-455217.
Describing and Interpreting an Immersive Learning Case with the Immersion Cub...Leonel Morgado
Current descriptions of immersive learning cases are often difficult or impossible to compare. This is due to a myriad of different options on what details to include, which aspects are relevant, and on the descriptive approaches employed. Also, these aspects often combine very specific details with more general guidelines or indicate intents and rationales without clarifying their implementation. In this paper we provide a method to describe immersive learning cases that is structured to enable comparisons, yet flexible enough to allow researchers and practitioners to decide which aspects to include. This method leverages a taxonomy that classifies educational aspects at three levels (uses, practices, and strategies) and then utilizes two frameworks, the Immersive Learning Brain and the Immersion Cube, to enable a structured description and interpretation of immersive learning cases. The method is then demonstrated on a published immersive learning case on training for wind turbine maintenance using virtual reality. Applying the method results in a structured artifact, the Immersive Learning Case Sheet, that tags the case with its proximal uses, practices, and strategies, and refines the free text case description to ensure that matching details are included. This contribution is thus a case description method in support of future comparative research of immersive learning cases. We then discuss how the resulting description and interpretation can be leveraged to change immersion learning cases, by enriching them (considering low-effort changes or additions) or innovating (exploring more challenging avenues of transformation). The method holds significant promise to support better-grounded research in immersive learning.
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Authoring a personal GPT for your research and practice: How we created the Q...Leonel Morgado
Thematic analysis in qualitative research is a time-consuming and systematic task, typically done using teams. Team members must ground their activities on common understandings of the major concepts underlying the thematic analysis, and define criteria for its development. However, conceptual misunderstandings, equivocations, and lack of adherence to criteria are challenges to the quality and speed of this process. Given the distributed and uncertain nature of this process, we wondered if the tasks in thematic analysis could be supported by readily available artificial intelligence chatbots. Our early efforts point to potential benefits: not just saving time in the coding process but better adherence to criteria and grounding, by increasing triangulation between humans and artificial intelligence. This tutorial will provide a description and demonstration of the process we followed, as two academic researchers, to develop a custom ChatGPT to assist with qualitative coding in the thematic data analysis process of immersive learning accounts in a survey of the academic literature: QUAL-E Immersive Learning Thematic Analysis Helper. In the hands-on time, participants will try out QUAL-E and develop their ideas for their own qualitative coding ChatGPT. Participants that have the paid ChatGPT Plus subscription can create a draft of their assistants. The organizers will provide course materials and slide deck that participants will be able to utilize to continue development of their custom GPT. The paid subscription to ChatGPT Plus is not required to participate in this workshop, just for trying out personal GPTs during it.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
Production of Specific Pathogen Free and Gnotobiotic animals
1.
2.
3. Free of particular pathogens
Example.
The animal should not have any
respiratory diseases while testing the
effects of drugs on lungs.
4. High monitoring system
During purchasing, the buyer should
make query about the list of the
diseases affecting the animals and the
recent history of health screening with
the type of health programme
monitoring so as to decide whether
that particular item is matching up to
the expermental purpose or not.
5. Special care during caesarian section.
Use of sterile isolation units with
positive pressure potential build up so
as to prevent the entry of pathogen
from outside.
6. Entry of sterilized food and water
through the isolation unit.
Airlock should be disinfected prior to
the entry of above items.
7.
8. Only certain strains of bacteria are
present.
They are only carrying the organisms
on which researchers want to do
experiment.
Used to study the symbiotic
relationship between the animal and
the inhabiting organisms.
9. Important for microbiologist as it
establishes some specific symbiotic
relationship between animal and
micro-organisms