eChapters

Horse

The lumbosacral plexus in horse is formed by last three lumbar and first two sacral nerves, similar to that in ox. The caudal gluteal nerve divides into two branches. The medial branch supplies the superficial gluteal muscle in addition to the middle and deep gluteal and biceps femoris muscles. The lateral branch reaches the level of tuber ischii and terminates into the semitendinosus muscle at the perineal region. The sciatic nerve is almost similar to that of ox in the disposition and distribution of its branches. The superficial and deep peroneal nerves are also similar to those of ox. The tibial nerve divides at the distal third of the leg into medial and lateral plantar nerves. Each plantar nerve divides at the fetlock into cranial, middle and caudal digital nerves.

Dog

The lumbosacral plexus in dog is formed by the last four or five lumbar and first two or three sacral nerves. The cranial gluteal nerve receives fibres from sixth and seventh lumbar and first and second sacral nerves. The caudal gluteal nerve arises from sixth and seventh lumbar and first sacral nerves. The sciatic nerve derives fibres from sixth and seventh lumbar and first and second sacral nerves. The lateral cutaneous nerve arises either from sciatic or from the peroneal nerve. The peroneal nerve divides into superficial and deep branches, similar to those of ox. The tibial nerve divides into medial and lateral plantar nerves at the level of distal third of the leg. The medial plantar nerve divides at the metatarsus into medial and lateral branches. The medial branch becomes the first plantar common digital nerve. It divides to form the plantar proper digital nerves of the first and second digits. The lateral branch divides into three plantar metatarsal nerves which unite, in the intermetatarsal space with the three plantar common digital nerves of the lateral plantar nerve. Each of these united plantar common digital nerves descends and after reaching at the metatarso-phalangeal articulation into three plantar proper digital nerves. The lateral plantar nerve, divides into three plantar common digital nerves which join the three plantar metatarsal nerves and form the plantar (caudal) proper digital nerves. The united proper digital nerves supply the second to fifth digit and terminate into the corresponding intermetatarsal space.

Sites for surgical interventions

Luxation of patella in cattle and horses

The luxation of patella is a condition wherein the patella of the stifle joint (femoropatellar articulation) is locked above the medial ridge of the trochlea of the femur.

Anatomy of femoropatellar articulation of the stifle joint

The stifle joint is a composite joint formed in two parts. One of these is an articulation between the condyles of distal extremity of femur and the condyles of the proximal extremity of tibia (femoro-tibial articulation) and the other is the articulation between the trochlea of the distal extremity of the femur and the articular surface of the patella (femoro-patellar articulation).

The trochlea of the femur consists of two asymmetrical ridges separated by a groove. The medial ridge is more prominent, wider and a little more extended dorsally than the lateral ridge. The two ridges converge ventrally. The articular surface of the patella is more or less quadrilateral or triangular with the base above and apex below. It has a vertical ridge in the middle and it separates the two concave areas of which the medial one is larger than the lateral. The patella is fastened against the trochlea with the help of three types of ligaments. One of these is the capsular ligament which is attached to the periphery of the articular areas of the two segments of the joint. The other one is the medial and lateral collateral ligaments. The third set of ligaments is the patellar (straight) ligaments.

Soil sample collection is the first and most important step for soil quality analysis. A soil sample collected with due care and proper procedure is essential for getting reliable result of the analysis. The sample should represent the field and for practical purposes, an area of about 0.5 hectare is considered as one sampling unit. In case of conspicuous variation observed in the field in terms of texture, colour, slope etc, separate samples should be collected from areas differing in these attributes. In other words, sample should be collected from an area in the field with similar characteristics as seen through normal visual observation. Sampling should thus be avoided from areas like near trees, permanent vegetations, manure pits, manure piles or recently fertilized fields.

Soil Sampling procedure

1. For a particular field unit, one composite soil sample is prepared out of the samples collected from 7-8 spots distributed across the field unit. The entire field is covered by moving in a zig-zag manner from each sampling spot.
2. For each sampling point or spot, scrapping off the surface litter such as grasses or crop residues is done. Then, a “V” shaped pit of 15-20 cm length and of equal width is made. Depth of sampling depends upon the requirement and on the type of crop. For field crops like paddy, wheat etc, samples are collected from 15 cm depth. From the “V” shaped pits, take outslice of ½ inch thickness from both sides of the exposed pit surfaces from top to bottom.
3. The soil samples so collected from the 7-8 points are mixed thoroughly by hand and then is reduced to about 500 g by quartering process. The quartering process consists of a procedure in which the entire soil mass is divided into four quarters; the two opposite ones are discarded and the remaining two are remixed. This process is repeated till about 500g soil is obtained.

Soil pH is the measure of hydronium ion (H₃O⁺) or more commonly hydrogen ion (H⁺) activity in the soil suspension. Soil pH can be measured in soil-water suspension, saturation extract or in 0.01 M CaCl₂ solution. Saturation extract is used to identify specific soil problems such as salinity or sodicity. Measurement of pH using 0.01 M CaCl₂ solution gives more reproducible results than measured through soil-water suspension. It also provides a good approximation of field conditions as the electrolytic composition of 0.01 M CaCl₂ is considered similar to that of soil solution. However, among the three methods, soil-water suspension is most commonly used in research laboratories as well as for fertilizer recommendation as it is simpler and more convenient.

Electrical conductivity (EC) is a useful indicator of soil salinity. Relationships have been developed between EC and salinity classes for a 1:1 soil: water suspension. With increase in salt content in a soil, the EC increases. Thus, for salt affected soils, measurement of EC is vital as accumulation of salts in the root zone is detrimental to plant growth. EC is a measure of the ability of a soil solution to conduct electrical current.

Equipment and Reagents

1. Digital Conductivity meter
2. 0.01 M potassium chloride (KCl) solution: Dissolve 0.7456 g dry KCl in distilled water and make up the volume to 1.0 litre. This solution has an electrical conductivity of 1.413 dS m_-1 at 25ºC.

Ion exchange is a reversible process by which a cation or anion held on the solid phase is exchanged with another cation or anion in the liquid phase. Soil mineral and organic colloidal particles have negative valence charges that hold dissociable cations. The power to retain cations at the surface of soil colloids is referred to as the cation exchange capacity (CEC). Cation exchange is a reversible reaction in soil solution, dependent upon negative charges of soil components arising from permanently charged or pH-dependent sites on organic matter and mineral colloid surfaces. The CEC is the sum of cations held by a kilogram of soil and is expressed in Cmol (p₊)/kg soil. In most agricultural soils, the cation-exchange capacity (CEC) is generally higher than the anion exchange capacity (AEC).

Exchanges sodium (Na+) is animportantparameter forsalt affected soils. This is estimated by extraction with ammonium acetate and then measuring the extract inflamephotometer.

Reagents

1. Neutral normal ammonium acetate solution (1 N CH₃COONH₄ of pH 7): Dissolve 77.09 g of ammonium acetate in distilled water and make up the volume to one litre. Adjust the pH of the solution to 7 with ammonia solution or acetic acid.
2. Standard solution of Na (500 mg/L Na): Dissolve 1.271 g of NaCl in distilled water and make up the volume to one litre.
3. Working standard solution of Na (100 mg/L): Dilute 200 ml of 500 mg/L stock solution to 1000 ml.

Soil texture refers to the relative distribution of sand, silt and clay on a sample of <2 mm size. It is an intrinsic soil property and basically refers to the particle size distribution in a soil. A number of physical characteristics and chemical properties of a soil are influenced by texture or particle size distribution. To estimate the content of sand, silt and clay particles, the soil samples are first brought into a dispersed state by mechanical and chemical treatments so that different binding agents are removed. In the dispersed soil samples, the soil particles settle down at a differential settling rate according to their size. In laboratory, the common methods for analysis for particle size distribution are : Buyoucos hydrometer method and International pipette method. In this chapter, the procedure of Buyoucos hydrometer method is described.

Principle

This method is based on the principle of variable rate of settling of particles as per their size and as described by Stokes’Law. Large particles shall settle fast. The measurement of density of the suspension is done at different times using a hydrometer (ASTM 152H-Type hydrometer is preferred). The measurement in this hydrometer is based on a standard temperature of 20 _oC and a particle density of 2.65 Mg m_-3 and the units are expressed in grams of soil per liter.The principal source of error in this procedure is the incomplete dispersion of soil clays as the clay particles are cemented by agents such as organic matter, CaCO and iron oxides. Incomplete dispersion results in low values for clay and high values for silt and sand. Thus, soils with higher organic matter (>1.0%) should be first treated with 6% hydrogen peroxide (H₂O₂) for removal of organic carbon. The rate of sedimentation is also affected by temperature and the density of the dispersing solution.

Soil bulk density (BD) or apparent density is determined in -situ by core method. Stainless steel or metallic cores of cylindrical shape with known height and diameter are inserted into the soil till the rim of the core. The soil core is then excavated and the soil sample is oven dried to get the dry weight. The ratio of the oven dry weight to the total volume of the core gives the bulk density of the soil.

Aggregation is a direct indicator of soil structure. Ahealthy soil is considered to have well aggregated structure. Though not routinely followed during soil testing and chemical analysis, aggregation is one of the major indicators of soil physical health. Wet sieve method (Yoder, 1936) is usually followed for soil aggregate analysis. This involves gently raising and lowering a nest of sieves in water to assess the stability of aggregates to rapid wetting. However, the Yoder’s wet sieving method has been modified to make it simpler and currently, the method of Kemper and Rosenau, 1986 is being commonly used in research laboratories. One of the pre-requisites in these methods is the availability of wet sieving apparatus and further, these methods are laborious and time consuming. On the other hand, the method described by Cambardella and Elliott (1993) is considered very ideal because of its simplicity and is being widely used for aggregate bound soil carbon fraction study. The soil sample is wet sieved with a series of three sieves (2000, 250 and 53 micron size).

Aggregation is one of the basic physical characteristics of soil. Under natural conditions, primary soil particles, particularly clays, tend to join together to form secondary units called aggregates. Size distribution of soil aggregates is important because the size of the aggregates determines their susceptibility to water and wind erosion. Also, their size is important in determining the pore size distribution and regulating pore space in cultivated soils.

There are a variety of procedures being in use to test the stability of aggregates and aggregate size distribution. However, choice of the method for analysis of aggregate size distribution is determined by the purpose of analysis. The developed measures are relative and purpose specific. This chapter discusses dry aggregate analysis.

Thisprocedure estimates aggregatestabilitytoimpact ofraindropsand water erosion. Wet sieving procedure was originally proposed by Yoder, 1936. Later, the procedure was modified byKemper and Rosenau, 1986.

Equipment

1. Yoder type sieve shaking electrically operated machine (3/4 inch stroke at 30 strokes per minute)
2. Concentric sieves of various sizes of pores to fit properly into the machine.
3. Weighing balance

Wet sieving procedure separates soil into different size aggregates. However, for comparing the aggregate size distribution among management treatments and soil types, it is convenient to use indices. Mean weight diameter (MWD) and water stable aggregate percentage are some of the common indices used in aggregate stability studies.

Mean Weight Diameter (MWD)

This index was proposed by Van Bavel (1949) and is being used widely. The entire soil sample is passed through an 8 mm sieve prior to analysis and is subjected to wet sieving procedure as described before. The parameter which Van Bavel (1949) called the MWD is equal to the sum of the product of (a) the mean diameter (d ) of each size fraction and (b) the proportion of the total sample weight (w ) occurring in the corresponding size fraction. The summation is carried out over all ‘n’ size fraction including the one that passes through the finest sieve.

In dry combustion technique, the combustion of soil sample (about 250 mg and mm sieved) is carried out at high temperature (about 1000 ºC) through feeding in an inert boat in the electric furnace. The CO₂ produced from the oxidation of carbon present in the soil sample at high temperature is carried towards non dispersive infrared detector (NDIR) by a carrier gas where it is quantified and total carbon content is determined.

This is one of the commonly used method to estimate organic carbon content in soil. In this wet digestion method, soil organic matter is oxidised with a mixture of K₂Cr₂O₇ and concentrated H₂SO₄ utilizing the heat of dilution of H₂SO₄. The unused K₂Cr₂O₇ is back titrated with ferrous sulphate or ferrous ammonium sulphate.

Labile fractions of soil carbon (C) refer to the fraction of soil carbon that are easily altered by microbial activities. These fractions serve as sensitive indicators to changes in management induced soil quality and are grouped under active soil C pool. The method described by Weil et al. (2003)estimates changes in biologically active soil C using a dilute KMnO . This is an improvement over the method used by Blair et al (1995), where a very high concentration (0.333 M) of KMnO₄ was used.

Organic carbon present in soil can be very labile, labile or non-labile. This procedure measures the extent of lability of soil organic carbon through relative degree of oxidation by K₂Cr₂O₇.

Particulate soil organic matter (POM) is one of the important soil organic matter (SOM) pools and matches the characteristics of a slow, decomposable or stabilized SOM pool. The POM fraction is considered as one of the indicators to changes in management and thus has been used in soil quality assessment studies.

Soil respiration is a good estimator of overall biological activity and thus is often used for describing soil quality. Soil respiration is estimated as the flux of CO₂ emitted from the soil surface. It represents the sum of CO₂ produced by root respiration and by heterotrophic decomposition. This procedure is a laboratory method where soil is incubated for a given period of days and the released CO is trapped by sodiumhydroxide (NaoH). This is also known as alkali trap method.

This is a distillation method proposed by Subbiah and Asija (1956), where the soil is distilled with alkaline KMnO solution. The ammonia liberated is trapped in boric acid and then determined by titration against a standard acid. This procedure estimates the easily mineralizable nitrogen in soil.

Estimation of plant available phosphorus content in soil has been attempted using several extractants. However, Bray’s reagent and Olsen’s reagent are the two common extractants used in India. Bray’s reagent (0.03 N NH₄F and N HCl) is used for acid soils, where, the fluoride ion complexes with Fe and Al in soil and thus releases the bound P. The Olsen’s reagent (0.5 M NaHCO₃) is used for neutral-alkaline soils.

In soil system, potassium (K) exists as water soluble, exchangeable, non- exchangeable and lattice K. The plant available K refers to the sum of water soluble and exchangeable K. Estimation of available K is usually done using neutral normal ammonium acetate as the extractant.

In this method, plant available sulphur (S) is extracted with 0.15% CaCl₂ and the soluble sulphate is estimated on a colorimeter.

The hot water soluble method is the most common method to estimate available B content in soil

Reagents

1. Azomethine-H: Dissolve 0.45 g azomethine-H and 1.0 g L-ascorbic acid in about 100 ml de-ionized or redistilled water. If solution is not clear, it should be heated gently on water bath at about 30ºC till it dissolves. A fresh solution should be prepared every week and kept in a refrigerator.
2. Buffer solution: Dissolve 250 g ammonium acetate in 500 ml de-ionized or redistilled water. Adjust the pH to about 5.5 by slowly adding approximately 100 ml glacial acetic acid, with constant stirring.
3. EDTA reagent (0.025 M): Dissolve 9.3 g EDTA in de-ionized or redistilled water and makes the volume up to 1 litre.
4. Standard Boron solution: Dissolve 0.571 g boric acid (H₃BO₃) AR grade in a small volume of deionized water and make volume to 1000 ml to obtain a stock solution of 100 mg B/L.

This procedure uses Diethylene Tri-amine Penta Acetic acid (DTPA) as the chelating agent, which combines with free metal ions in soil solution and forms soluble complexes.

Analytical methods for study of soil microbes

The analytical techniques for study of soil microbes are grouped under the following heads :

• Determination of form and arrangement of microorganisms in soil
• Isolation and characterization of soil microorganisms
• Detection of microbial activity in soil
• Determination of microbial biomass.

For the above, the different analytical methods used are described below.

Enumeration of microbial flora present in soil is done by dilution plating technique. The technique is based on the fact of diluting the source inoculums to the extent that after plating the known volume of inoculums on appropriate media, the colonies will appear in countable range and each colony will be assumed to have been derived from a single cell/colony forming unit. Three numerically dominant groups of soil microbes are bacteria, actinobacteria and fungi. The most commonly used culture media for their enumeration include

Nutrient Agar-for heterotrophic bacteria,

Actinomycetes isolation Agar or Kenknight and Munaier’s agar for actinobacteria

Martin’s Rose Bengal Agar for fungi.

Biological activity or index of a soil is the function of number of organisms present in soil and their physiological efficiency. The rate of respiration can be used as an index of the biological activity of soil as it reflects the physiological efficiency of the organisms. Monitoring of dehydrogenase, which are respiratory enzymes and integral part of all soil organisms, will give a measure of biological activity of soil at a given time.

During respiration biological oxidation of reduced compounds occur which is catalyzed by dehydrogenase. In the process TTC gets reduced to a pink coloured compound Triphenyl formazan (TPF) which can be quantitatively extracted by methanol and measured colorimeterically. The soil dehydrogenase activity in the current experiment was measured as per the methods of Cassida, (1977).

Fluorescein diacetate (3’ 6’-diacetyl-fluorescein) is a fluorescein conjugated to two acetate radicals. This colourless compound is hydrolysed by both free (exoenzymes) and membrane bound enzymes, releasing a coloured end product, fluorescein. This end product absorbs strongly in the visible wavelength (490 nm) and can be measured by spectrophotometry. The enzymes responsible for FDA hydrolysis are plentiful in the soil environment. Non-specific esterases, proteases and lipases, have been shown to hydrolyse FDA. The hydrolysis of FDA by soil enzymes can be estimated by methods of Adam and Duncan (2001).

Principle

β-Glucosidase (BG) plays a major role in the degradation of soil organic matter and plant residues. It catalyzes the hydrolysis of β-d-glucopyranosides, the final, rate-limiting step in the degradation of cellulose, the most abundant polysaccharide providing simple sugars for the soil microbial population. BG has been shown to be sensitive to changes in soil and residue management as well as an early indicator of changes in SOC before these changes are reflected in total or organic C analyses. The method is based on colorimetric determination of the p-nirtrophenol released by β-glucosidase when soil is incubated with buffered PNG solution and toluene.

Acid and alkaline phosphatase enzymes are among the extensively studied phosphatases and classified so because of their optimum activities in acid and alkaline pH ranges, respectively. Acid phosphatase is predominant in acid soil while alkaline phosphatase is dominant in alkaline soils. The colorimetric assay of phosphatase is based on release of p-nitrophenol from hydrolysis of p-nitrophenyl phosphate byaction of phosphatase enzyme in buffered soil solution (buffer pH 6.5 for acid and 11 for alkaline phosphatase assay).

Principle

Different ions migrate at different speed dictated by their size and by the amount of charges they carry. As a result, different ions can be separated from each other by electrophoresis. The magnitude of the electric force F exerted on the charged particle when subjected to electrophoresis is product of the charge q of the particle and the electric field E generated between the two electrodes.

Mole

A mole is defined as the amount of chemical substance containing exactly 6.022 140 76 × 10₂₃ numbers of constitutive particles such as atoms, ions and molecules. This number is a fundamental constant named Avogadro’s number in honor of Italian scientist Amedeo Avogadro. This constant is properly reported with an explicit unit of “per mole,” and rounded version being 6.022 × 10₂₃/mol.

This definition has been adopted since November, 2018 revising the old definition based on the number of atoms in a sample of pure ₁₂C weighing exactly 12 g. Thus, as per the definition, 1 mole of any element contains the same number of atoms as 1 mole of any other element. However, the mass of 1 mole of a particular element is different from that of another element.

Molar mass

Molar mass of an element (or compound) is the mass in grams of 1 mole of that substance, a property expressed in units of grams per mole (g/mol).

Histology

Cell: Structural and functional unit of an organism

M. Schleiden & Theodor Schwan – proposed cell theory

- All living being made up of cell

Tissue: Group of cell and their extracellular product organized to perform a particular function

M. Malpighii – Father of histology

Partitioning of Energy in Livestock

Energy Partitioning

Partitioning of energy involves loss and distribution of feed energy into different body functions.

Gross energy is calculated from the heat produced when a sample of feed or feces is subjected to complete combustion in a bomb calorimeter under a pressurized oxygen atmosphere.

Apparent digestible energy is the difference between the gross energy of the feed consumed and the gross energy of the feces excreted. Digestion is accompanied by the production of gases in both fore- and hindgut and by the urinary excretion of metabolites.

Metabolizable energy is the difference between digestible energy and energy lost to gases and urine. Metabolic processes and physical activity produce heat (heat of production) which may warm the animal in cold weather. In hot weather, energy may be required to expel excess heat of production, through panting and increased respiratory rate.

Net energy is the remaining energy available for maintenance, reproduction and production. The diagram on the left illustrates energy partitioning for a particular cow near the end of her lactation. Energetic efficiency of this cow is about 29%, expressed as output in the form of milk, gain and fetal growth divided by gross energy input. Although their energy requirements are significantly greater, higher producing cows are also more energetically efficient.

1665 Robert Hooke had successfully invented the microscope. Because of this discovery, Robert Hooke was the first one to have a close look of a cell appears to be. His description of these cells was published in Micrographia. However, the cell walls observed by Hooke gave no indication of the nucleus and other organelles found in most living cells.

1674 Anton van Leeuwenhoek witnessed a live cell (plant) under a microscope.

1775 Antoine Lavoisier first proposed a mechanism for photosynthesis, a process wherein plants plants take in carbon dioxide and release oxygen. Lavoisier was also the first to investigate cell respiration in animals.

1777-83 Chemistry became dominated by the phlogiston theory, or the hypothetical principle of fire wherein all the combustible material was part composed. In this principle, burning (oxidation) was caused by liberating phlogiston, with ash as the dephlogistigated substance.

1836 The proponent of the cell theory in Biology, Theodore Schwann, proposed that the process of fermentation is solely limited to living yeast cells in 1836. Liebig did not agree to this and instead, he proposed another alternative theory of fermentation.

1856 Louis Pasteur opposed Liebig’s chemical theory. In his experiment, he showed that fermentation depends highly on the physiological functions that occur in bacteria and in living yeast cells. This work of Pasteur in 1856 received general recognition.

1860s The view on the chemistry of life highly different from the chemistry of nonliving things. During this period, the view is that the gelatinous and homogenous form of matter in organisms or more commonly known as the protoplasm carries out all the intracellular processes. These include respiration, biosynthesis of molecules, and the breakdown of matter.

Animal Biotechnology

Biotechnology is defined as “the application of biological organisms, systems or processes to manufacturing and service industries” (Coombs, 1984).

It is also defined as “the application of scientific and engineering principles to the processing of materials by biological agents to produce goods and services” (Coleman, 1986).

Animalbiotechnologyis the application of scientific and engineeringprinciples to the processing or production of materials by animals to provide goods and services to human kind.

Farming System of India

Based on how income is derived from a farming enterprise: Specialized farming, diversified farming and mixed farming.

Based on mode of ownership and organization of farms: Individually owned, co-operative farming and collective farming

Based on scale of operations: Small scale farming and Large scale farming.

Embry Transfer Technology (ETT)

Definition: The process of removing one or more embryos from the reproductive tract of a donor female and transferring them to one or more recipient females.

General Terminologies in Livestock Production

Meat is considered as well balanced diet because it is good source of macro and micro nutrients.

Macronutrients-required in large quantity in body i.e proteins, fat and carbohydrates.

Micronutrients-required in lesser quantity by human body i.e vitamins, minerals and fibers.

Organ meat like liver is a good source of glycogen, viatm-A, B1 and nicotinic acid.

Fresh meat is unprocessed.

Raw meat is a fresh meat undergone chilling and freezing.

Refrigeration and rapid cooling can delay the onset of rigor mortis

Foot-and-Mouth Disease

Loeffler and Frosch in 1897. Apthovirus of Picornaviridae. Strain O, A, C, Asia-1, SAT-1, 2, 3.

Cattle as Indicator host, Pig as amplifier, Sheep as maintenance host.

Musculature of heart in calves will have striped appearance termed as TIGER HEART.

Panting is common feature or sequel following FMD due to disturb endocrine function.

Preferred cell line for virus isolation in BHK-21.

Our general environment is loaded with tiny invisible living things that influence us consistently. Microbiology is a specialized area of science that deals with living things typicallytoo little to be seen without magnification. Suchmicroscopic life forms are collectively referred to as microorganisms. Microbial kingdom incorporates the study of bacteria, rickettsiae, viruses, fungi, algae and protozo a. Virology the study of viruses, mycology study of fungi and protozoology deals with protozoa.Credit for prologue to microbial world goes to ‘Antony van Leeuwenhoek’ and to vistas of microbial activities to ‘Louis Pasteur’ and ‘Robert Koch’. This period is reffered as the “Golden Era” of microbiology on account of the significant discoveries viz: microbial fermentations, discovery of various disease-causing agents, microbes’ cultivations, differences in metabolic activities, development of attenuated strains and their use as immunoprophylactic agents. The techniques used to study bacteria and different microorganisms embody direct microscopic examination, cultivation, biochemical tests, animal inoculation, serological reactivity and recent molecular biological techniques.Definitive evidence for the cause of a given infection is established by Koch that are still used to this day to definitively prove that a microorganism causes a particular disease. Koch’s four postulates are:

Parasite- The word parasite is derived from the Greek. Para- beside and sitos- food. Parasites are those living organism which reside on or inside the body of some other species of living organism.

Host- Those organisms which provide food shelter and conducive environment to parasite for their growth, development and reproduction. e.g. Tape worm in small intestine of man and animals.

Disease = dis + aise (see + ease) old French word

Transmission- Movement of biological agents (Virus, Bacteria, Rickettsial, Fungi & Parasites) from one place to another place via vector or vehicle/ tools

Vector- Latin word- bearer

Vector is a living organism (usually an arthropod) which transfers infective forms of a parasite from one host to the other.

Chemotherapy

Chemotherapy is branch of pharmacology that deals with study of chemical substance intended to kills or inhibits the growth of invading microorganism or foreign cell without harm to host cells. Paul Ehrlich coined the term chemotherapy and is known as father of chemotherapy. Gerhard Johannes Paul Domagk discovered sulphonamide (sulfonamidochrysoidine). First commercially available sulphonamide marketed in the form of Prontosil dye, for which he received the 1939 Nobel Prize in Physiology or Medicine. SelmanAbraham Waksman discover streptomycin and several other antibiotics from soil actinomycetes and actinomycetes is called treasurer house of antibiotics.

α-lactam antibiotics- includes penicillins, cephalosporins, carbapenems, monobectum and beta-lactamase inhibitors. It inhibits bacterial cell wall synthesis due to inhibition of transpeptidation reaction thus inhibits peptidoglycan synthesis. Penicillins contain 6-animopenicillanic acid (((lactam ring + thiazolidine ring) eg. natural penicillins, beta-lactamase-resistant agents, aminopenicillins, carboxypenicillins, and ureidopenicillins. Discovery of penicillin was done by Alexender fleming from penicillium mold in 1928 from Penicillium notatum. Now a day’s Penicillium chrysogenum mold is a major source of penicillin production. Benzathine penicillin G is a repository salt of penicillin. Probenicid competitively inhibit renal tubular secretion of penicillin and increase the half- life of penicillin. Procaine penicillin G should not administer by i.v. route due to adversely affect the cardiac conducting system. Beta-lactamses inhibitors are calvulenic acid (Streptomyces clavuligerus), salbactum, tazobactam. They are called suicidal /progressive inhibitors. Main adverse effect associate with penicillin is immediate type of hypersensitivity reaction due to Antigen+ IgE antibody reaction.

Veterinary physiology deals with the study of normal functions of animal systems. It includes the study of how animals work and the physical and chemical processes that occur within animals. The examples of various biological processes in animals include gas exchange, blood and circulation, osmoregulation, digestion, nervous and muscle systems, respiration, growth, reproduction, endocrine function and how animals behave and function in different environmental conditions. This also includes the possible manipulation of the reproductive processes by means of hormone manipulation techniques for more efficient livestock and poultry production.

Zoonoses

Zoonoses are those diseases and infections which are transmitted between vertebrate animals and humans under natural conditions. The emergence of a pathogen into a new host species is called disease invasion or “disease emergence”.

Anthrax is a notifiable disease and primarily occurs in herbivores but it is a type of bio-terrorism agent and called as malignant pustule, malignant edema, woolsorters disease, ragpickers disease, maladi charbon, splenic fever etc. Causative agent is Bacillus anthracis contains vegetative spore and lethal dose is 2,500 to 55,000 spores.

Brucellosis is one of the world’s most widespread zoonoses caused by the genus Brucella. In human it is called Malta fever, Undulant fever, Mediterranean fever, Rock Fever of Gibraltar and Gastric Fever while in animals it is called Bang’s disease, Enzootic abortion, Epizootic abortion, Slinking of calves, Ram epididymitis and Contagious abortion etc. it is also called occupational disease.

Leptospirosis is a disease of animal sand humanbeings caused by genus Leptospira and called as Weil’s syndrome, Canicola fever, Canefield fever, 7-day fever, Rat Catcher’s Yellows, Autumn fever, black jaundice). Fletcher’s EMJH media is used to culture the organism.

Pathology is derived from Greek word (Pathos=disease + logos=study). It is study of structure and function of body in disease.

Veterinary Pathology is the study of anatomical, chemical and physiological alterations in comparison to normal due to disease in animals. Pathology has responsibility to forms a vital bridge between preclinical sciences (Anatomy, Physiology, Biochemistry) and clinical branches of medicine and surgery.

General Pathology deals with the basic alterations of tissues as a result of disease. e.g. fatty changes, thrombosis, amyloidosis, embolism, necrosis etc.

Systemic Pathology is related to the alterations in tissues/organs of a particular system. e.g. respiratory system, genital system etc.

Special Pathology is the application of the basic reactions of gene general pathology to various specific diseases.

Gross or Macroscopic Pathology is the examination of tissue without the help of a microscope.

Veterinary surgery: The surgery which is practiced on animals. It deals with the treatment of deformities, injuries, or disease conditions by manipulation with the hands. The term “Surgery” is derived from a Greek word – Chirurgia (Cheir – Hand, Ergon – work).

The papyri of Egypt contained information on treatment of fractures and superficial wounds.

In Vedic era, Salihotra and Palakapya were the greatest ancient Indian veterinarians. Salihotra treated horses and Palakaya elephants.

“Susruta Samhita’ is the earliest known work dealing with the medical science especially surgery.

Hobday wrote first comprehensive text on surgical diseases of the dog and cat.

The theory and practice of asepsis was introduced by Joseph Lister.

W.S. Halsted introduced the principles of surgery and use of rubber gloves.

History of Genetics

Lamarck (1744-1829): Proposed theory of “Inheritance of acquired characters”.

Charles Robert Darwin (1809-1882): published his classic book “Origin of Species” in 1859 and proposed theory of evolution and survival of the fittest.

Johann Greger Mendel : Gave laws of heredity in 1866 and is considered as Father of Genetics.

W. Flemming: The term mitosis was first used by Fleming in 1882.

W. Waldeyer: Coined the term “Chromosome” in 1888.

August Weisman: Gave the “Theory of Germplasm” in 1889.