Block 6 Flashcards

1
Q

the process of growing bacteria or a virus in iterations.
For instance, a virus may be grown in one environment, and then a
portion of that virus population can be removed and put into a new
environment is called?

A

Serial passage

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2
Q

VACCINES ARE PRODUCED FROM:
Name 3 sources

A

VACCINES ARE PRODUCED FROM
1. NATURALLY OCCURRING ATTENUATED
VIRUSES,
2. SERIAL PASSAGE IN CULTURED CELLS, HETEROLOGOUS HOSTS OR
3. COLD-ADAPTED MUTANTS AND RE-ASSORTANTS

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3
Q

RINDERPEST AND CLASSICAL SWINE FEVER

adapted to be growm how? why?

A

RINDERPEST AND CLASSICAL SWINE FEVER WERE ADAPTED TO BE ABLE TO
GROWN IN RABBITS AND AFTER SERIAL PASSAGE BECOME USED AS
VACCINES.

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4
Q

VACCINES PRODUCED FROM INACTIVATED WHOLE VIRIONS, PURIFIED
NATIVE VIRAL PROTEINS are called?

A

NON-REPLICATING VIRUS VACCINES:

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5
Q

vaccines produced by serial passage of viruses in hererologous hosts is a ? vaccine?

A

live-attenuated

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6
Q

Subunit vaccines produced by Expression of viral proteins in Eukaryotic (yeast mammalian, insect), bacteria or plants

( I think that the slide is saying this is an example of…But I don’t understand the slide so double check)

A

VACCINES PRODUCED BY RECOMBINANT DNA AND RELATED
TECHNOLOGIES.

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7
Q

DIVA
stands for what?

A

(DIFFERENTIATING INFECTED
FROM VACCINATED ANIMALS)

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8
Q

DIVA (DIFFERENTIATING INFECTED
FROM VACCINATED ANIMALS)

only uses what portion of the pathogen?

A

ONLY USES SUBUNIT (PORTION) OF THE PATHOGEN

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9
Q

DIVA

IF AN ANTIBODY TO OTHER SUBUNITS OR ANTIGENS
NOT INCLUDED IN THE VACCINE ARE DETECTED, THEN
THE ANIMAL HAS BEEN INFECTED WITH THE PATHOGEN.

what?

A

(NATURAL INFECTION)

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10
Q

DIVA

IF ONLY THE ANTIBODIES TO THE SUBUNIT OF THE
VACCINE ARE DETECTED THEN THE ANIMAL IS NOT
INFECTED.
what?

A

(JUST VACCINATED)

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11
Q

PREVENTION AND

CONTROL

what is the difference between isolation and quarantine?

A

**ISOLATION: **SEPARATING AN ANIMAL IF
THEY SHOW CLINICAL SIGNS AND/OR
TEST POSITIVE ON DIAGNOSTIC TEST.
* QUARANTINE: APPLIES TO THOSE WHO
HAVE BEEN EXPOSED TO A
CONTAGIOUS DISEASE

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12
Q

PREVENTION AND

CONTROL

should you quarantine if THEY AREN’T SHOWING SIGNS
OR THE ANIMALS TEST NEGATIVE ON
DIAGNOSTICS? when?

A

EVEN IF THEY AREN’T SHOWING SIGNS
OR THE ANIMALS TEST NEGATIVE ON
DIAGNOSTICS IF THE DISEASE INVOLVES
CHRONICALLY INFECTED HEALTHY
SHEDDERS.

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13
Q

what is QUARANTINE AND CULLING:

A

TO
SEPARATE AND RESTRICT THE MOVEMENT
OF ANIMALS, KILLING THE ANIMAL AND
PROPER DISPOSITION OF THE CULLED
ANIMALS.

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14
Q

PREVENTION AND CONTROL OF
INFECTIOUS DISEASES

name 4

A

DECONTAMINATION
STERILIZATION
DISINFECTION
ANTISEPSIS

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15
Q

t/f
sterilisation, disinfection and antisepsis are all forms of decontamination?

A

t

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16
Q

APPLICATION OF LIQUID ANTIMICROBIAL TO SKIN
OR LIVING TISSUE TO INHIBIT OR DESTROY MICROORGANISMS.

what?
example?

A

ANTISEPSIS

hand sanitizer

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17
Q

ELIMINATES ALL MICROORGANISMS, **EXCEPT
BACTERIAL SPORES **ON INANIMATE OBJECTS. (LESS EFFECTIVE
THAN STERILIZATION)

what?
example?

A

DISINFECTION

alcohol, pastuerization

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18
Q

PROCESS THAT DESTROYS OR ELIMINATES** ALL
FORMS** OF MICROBIAL LIFE/PATHOGENS, INCLUDING BACTERIA
WITH SPORES.

what?
example?

A

STERILIZATION

autoclave

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19
Q

PROCESS MAKING A MEDICAL DEVICE,
INSTRUMENT, OR ENVIRONMENTAL SURFACE SAFE TO HANDLE

what?
exampl?

A

DECONTAMINATION

soap+water

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20
Q

STERILIZATION METHODS

what is an example of moist heat?

A

MOIST HEAT: AUTOCLAVE

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21
Q

STERILIZATION METHODS
what is an example of dry heat?

A

DRY HEAT: HOT AIR OVEN

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22
Q

STERILIZATION METHODS
what is an example of chemical method?

A

CHEMICAL METHODS: GASES LIKE ETHYLENE OXIDE, OZONE.

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23
Q

STERILIZATION METHODS
what are the 2 methods of radiation

examples?

A
  • RADIATION:
  • NON-IONIZING: ULTRAVIOLET RADIATION
  • IONIZING: GAMMA RAYS, X-RAYS
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24
Q

STERILIZATION METHODS

what is STERILE FILTRATION?

A

STERILE FILTRATION: MICROFILTRATION USING MEMBRANE
FILTERS

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25
# STERILIZATION METHODS name 5
moist heat dry heat chemical method radiation x2 sterile filtration
26
LARGE, SOMETIMES ENVELOPED, DNA VIRUSES WITH COMPLEX STRUCTURES (SYMMETRY) what are they?
POXVIRUSES
27
POXVIRUSES describe how does that differ if they are genus parapoxvirus?
MOST ARE PLEOMORPHIC, USUALLY BRICK SHAPED WITH AN IRREGULAR SURFACE OR IF OF THE GENUS PARAPOXVIRUS: OVOID (CRISS-CROSS PATTERN IN AN ORGANIZED PATTERN)
28
POXVIRUSES THERE ARE TWO INFECTIOUS FORMS: what are they?
INTRACELLULAR MATURE VIRUS (IMV) EXTRACELLULAR ENVELOPED VIRUS (EEV)
29
POXVIRUSES what is the difference between INTRACELLULAR MATURE VIRUS (IMV) and EXTRACELLULAR ENVELOPED VIRUS (EEV)
* INTRACELLULAR MATURE VIRUS (IMV) WHICH **ONLY HAVE AN INNER MEMBRANE **AND RELEASED VIA CELL DESTRUCTION * EXTRACELLULAR ENVELOPED VIRUS (EEV) WHICH CONTAIN **TWO MEMBRANES** (ENVELOPE AND INNER MEMBRANE) –AND RELEASED VIA BUDDING.
30
what is a virion?
a complete virus particle that consist of an RNA or DNA core with a protein coat sometimes with an external envelope and is th extracellular ineffectibe form of the virus (outside the host cell)
31
POXVIRUSES HAVE COMPLEX SYMMETRY * VIRION describe
VIRION OUTER LAYER ENCLOSES A DUMBBELL -SHAPED CORE AND 2 LATERAL BODIES. THE CORE HAS VIRAL DNA WITH SEVERAL PROTEINS.
32
POXVIRUSES how many genes in genome? how many encoded proteins?
POXVIRUSES HAVE MORE THAN 200 GENES IN THEIR GENOME AND AS MANY AS 100 ENCODE PROTEINS THAT CONTAINS VIRIONS.
33
POXVIRUSES how many genes in genome? how many encoded proteins?
POXVIRUSES HAVE MORE THAN 200 GENES IN THEIR GENOME AND AS MANY AS 100 ENCODE PROTEINS THAT CONTAINS VIRIONS.
34
# POXVIRUSES where does replication occur? why?
REPLICATION OCCURS PREDOMINANTLY IN THE **CYTOPLASM** **BECAUSE** ENZYMES HAVE THE ABILITY TO REPLICATE AND TRANSCRIBE IN THE GENOME.
35
POXVIRUSES THE GENOME CONSISTS OF A SINGLE MOLECULE OF ?
THE GENOME CONSISTS OF A SINGLE MOLECULE OF LINEAR DOUBLE STRANDED DNA
36
# STABILITY OF POXVIRUSES are they stable? how long do they stay infectious? why? what relevance to disinfectants?
THEY ARE **EXTREMELY STABLE** IN THE ENVIRONMENT AND REMAIN INFECTIOUS FOR **SEVERAL MONTHS** OUTSIDE A HOST BODY **BECAUSE OF THEIR LOW LIPID CONTENT **MAKING THEM **MORE RESILIENT** TO SOLVENTS/DISINFECTANTS.
37
# STABILITY OF POXVIRUSES do they have a high resistence to drying? why is this relevant?
THEY ALSO HAVE A VERY HIGH RESISTANCE TO DRYING AND CAN SURVIVE FOR YEARS IN DRIED SCABS (WHICH ARE VERY INFECTIOUS) OR OTHER VIRUS-LADEN MATERIAL.
38
which virus has an enveloped form that stable in the environment?
poxvirus, BUT poxvirs not an answer choice, so know what virus are pox viruses ex. coupox
39
# TRANSMISSION OF POXVIRUSES what are the 3 ways? examples?
* SKIN: MUST BE BROKEN SKIN. THIS IS THE MOST COMMON ROUTE * RESPIRATORY: INHALATION OF AEROSOL (SHEEPPOX VIRUS) * MECHANICALLY: ATHROPOD BITES (MYXOMA AND AVIPOXCIRUSES)
40
# POXVIRUS PATHOGENESIS/IMMUNITY t/f POXVIRUSES ARE NOT HIGHLY EPITHELIOTROPIC
F POXVIRUSES **ARE** HIGHLY EPITHELIOTROPIC CAUSING CUTANEOUS LESION!
41
POXVIRUS PATHOGENESIS/IMMUNITY ARE THEY ALL HOST SPECIFIC?
THEY ARE HOST SPECIFIC, **EXCEPT** ORTHOPOXVIRUSES WHICH INFECT A WIDE RANGE OF SPECIES!
42
POXVIRUS PATHOGENESIS/IMMUNITY CAN THEY CAUSE SYSTEMIC DISEASES? IN WHAT? EXAMPLE?
CAN CAUSE SYSTEMIC DISEASES IN BIRDS AND WILD ANIMALS (SHEEPPOX AND GOATPOX)
43
POXVIRUS PATHOGENESIS/IMMUNITY INVADE THE SKIN AND ACCESS WHAT ? BY WHAT SYSTEM?
INVADES THE SKIN AND ACCESSES THE SYSTEMIC CIRCULATION VIA THE LYMPHATIC SYSTEM.
44
POXVIRUS PATHOGENESIS/IMMUNITY USES SECONDARY VIREMIA TO DO WHAT?
USES SECONDARY VIREMIA TO GET THE VIRUS BACK TO THE SKIN AND OTHER TARGET ORGANS
45
# ORTHOPOXVIRUS COW VIRUS-DISTRIBUTION?
DISTRIBUTION: ENDEMIC ONLY TO EUROPE AND ASIA
46
ORTHOPOXVIRUS HOSTS?
HOSTS: CATTLE, WILD AND DOMESTIC CATS, HUMANS, ZOO ANIMALS, ETC.
47
ORTHOPOXVIRUS RESERVOIR HOSTS
RESERVOIR HOSTS: RODENTS
48
ORTHOPOXVIRUS TRANSMISSION:
TRANSMISSION: * COW TO COW: THROUGH INFECTED MILER’S HANDS OR TEAT CUPS * INFECTED FARM CATS CAN ALSO TRANSMIT THE DISEASE * RODENTS SERVE AS THE RESERVOIR AND CAN TRANSMIT THE DISEASE
49
ORTHOPOXVIRUS CLINICAL SIGNS IN CATTLE:
CLINICAL SIGNS IN CATTLE: PAPULES ON TEATS/UDDERS. SUCKLING CALVES MAY ALSO DEVELOP LESIONS IN MOUTH
50
# COWPOX IN CATS * TRANSMISSION:
TRANSMISSION: * SKIN INOCULATION (TYPICALLY THROUGH A BITE OR SKIN WOUND) RODENTS ARE A COMMON SOURCE OF INFECTION. * ORO-NASAL ROUTE IS ALSO POSSIBLE * IN CHEETAHS VIRAL PNEUMONIA MAY BE EVIDENT AS WELL
51
# COWPOX IN CATS CLINICAL SIGNS PRIMARY LESIONS: SECONDARY LESIONS:
**PRIMARY LESIONS:** * A SINGLE PRIMARY LESION TYPICALLY ON THE HEAD, NECK OR FORELIMB * CAN BE A SMALL SCABBED WOUND ALL THE WAY TO A LARGE ABSCESS **SECONDARY LESIONS:** * OCCURS 7-10 DAYS AFTER THE PRIMARY LESION * ULCERATION AND SCABS * CAN HEAL IN 6 WEEKS
52
# COWPOX IN CATS CS ?
TYPICALLY, NO OTHER CS OTHER THAN SKIN LESIONS * 20% CAN GET MILD CORYZA/CONJUNCTIVITIS (INFLAMMATION OF MUCOUS MEMBRANES)
53
# COWPOX IN CATS COMPLICATIONS ?
COMPLICATIONS FROM SECONDARY BACTERIAL INFECTION
54
COWPOX IN HUMANS TRANSMISSION?
TRANSMISSION: * **MAINLY CAUSED BY DIRECT CONTACT TO “CUDDLY” CATS** * RARELY FROM RODENTS * HUMANS GET IT MORE FROM CATS THAN COWS!
55
# COWPOX IN HUMANS CLINICAL SIGNS:
MACROPAPULAR LESIONS ARE SEEN ON THE HANDS AND FACE THEN LATER DEVELOP INTO VESICULAR AND THEN ULCERATIVE LESIONS * RESULT IN ENLARGED PAINFUL LOCAL LYMPH NODES * PATIENTS REPORT FEVER, VOMITING AND SORE THROAT
56
# MONKEYPOX FOUND WHERE?
NORMALLY SEEN IN AFRICA
57
# MONKEYPOX IN HUMANS: SYMPTOMS?
IN HUMANS: A VIRAL ZOONOSIS WITH SYMPTOMS IN HUMANS SIMILAR TO THOSE SEEN IN THE PAST WITH SMALLPOX
58
# MONKEYPOX TRANSMISSION: PRIMARY INFECTION? SECONDARY INFECTION?
**PRIMARY INFECTION:** FROM INFECTED BODY FLUIDS OF AN INFECTED ANIMAL. HANDLING MONKEYS, GAMBIAN RATS OR SQUIRRELS * **SECONDARY INFECTION:** HUMAN-HUMAN VIA INFECTED RESPIRATORY EXCRETIONS, SKIN LESIONS OR CONTAMINATED OBJECT
59
# PARAPOXVIRUSES **PSEUDOCOWPOX** EXPLAIN?
(CATTLE, HUMANS) ZOONOTIC
60
PARAPOXVIRUSES CONTAGIOUS ECTHYMA/ORF VIRUS EXPLAIN
CONTAGIOUS ECTHYMA (DISEASE IN ANIMALS) ORF VIRUS (DISEASE IN HUMANS) SHEEP, GOATS, HUMANS
61
BOCVNE PAPULAR STOMATITIS VIRUS EXPLAIN
(CATTLE, HUMANS) - NOT AS IMPORTANT
62
A VIRAL SKIN DISEASE CAUSES MILD SORES ON THE TEATS AND UDDERS OF CATTLE. WHAT IS IT?
PSEUDOCOWPOX
63
PSEUDOCOWPOX WHAT ABOUT HUMANS?
CAN ALSO INFECT HUMANS! (MILKER’S NODULE) ZOONOTIC
64
PSEUDOCOWPOX WHERE?
REPORTED FROM MOST COUNTRIES.
65
PSEUDOCOWPOX TRANSMISSION
TRANSMISSION: * FROM INFECTED COWS, INFECTED MILKERS HANDS, INFECTED TEAT CUPS * BITING INSECTS * HORIZONTALLY FROM COW TO CALF VIA MILK * SEMEN OF BULLS-LESS KNOWN
66
PSEUDOCOWPOX PATHOGENESIS:
PATHOGENESIS: LESIONS ARE CHARACTERIZED BY HYPERPLASIA OF SQUAMOUS EPITHELIUM.
67
PSEUDOCOWPOX CLINICAL SIGNS: ACUTE SIGNS? CHRONIC LESIONS?
* INFECTIONS ARE GENERAL MILD * ACUTE LESIONS: * **ERYTHEMA(RED SKIN)→PAPULES(EMPTY RAISED BUMP)→VESICLE(RAISED BUMP W/CLEAR FLUID) OR PUSTULE(RAISED BUMP W/ PUSS FLUID)→RUPTURE→THICK SCAB** * A THICK SCAB (0.5-25CM IN DIAMETER ) THAT BECOMES ELEVATED WITH GRANULATION TISSUE. * AFTER 7-10 DAYS A **HORSESHOE-SHAPED SCABS** WILL FORM * CHRONIC LESIONS * STARTS AS ERYTHEMA AND LEADS TO YELLOW- GRAY SCABS, BUT IS PAINLESS, PERSISTS FOR MONTHS.
68
# PSEUDOCOWPOX DIAGNOSIS:
* **HORSESHOE-SHAPED RING LIKE LESION.** PATHOGNOMONIC * ISOLATION AND DETECTION OF THE VIRUS VIA VARIOUS DIAGNOSTIC LAB METHODS FROM VESICULAR FLUID OR FROM TEAT SKIN
69
# PSEUDOCOWPOX TREATMENT:
* REMOVAL OF SCABS (VERY INFECTIOUS!) * **BURN THE SCABS** * APPLY AN EMOLLIENT OINTMENT BEFORE MILKING * APPLY ASTRINGENT PREPARATION AFTER MILKING (TIGHTENS THE SKIN AND LIMITS SPREAD)
70
# PSEUDOCOWPOX DIFFERENTIAL DIAGNOSIS:
DIFFERENTIAL DIAGNOSIS: *** COWPOX VIRUS * BOVINE HERPESVIRUS ULCERATIVE MAMMILITIS * VESICULAR STOMATITIS** * UDDER IMPETIGO * TEAT CHAPS AND FROSTBITE * BLACK SPOT
71
# PSEUDOCOWPOX PREVENTION:
* DISINFECTION (IODOPHOR TEAT DIP) * ISOLATION AND TREATMENT OF INFECTED COWS * REDUCE TEAT TRAUMA
72
# CONTAGIOUS ECTHYMA (ORF) ETIOLOGY:
ORF VIRUS, GENUS PARAPOXVIRUS
73
# CONTAGIOUS ECTHYMA (ORF) TRANSMISSION:
* SCABS FALL OFF AND CAN **REMAIN INFECTIOUS IN THE ENVIRONMENT FOR EXTENDED TIME** * CONTAMINATED INSTRUMENTS (TAIL DOCKING/EAR TAGGING) * INFECTS VIA DAMAGED SKIN * **ORAL LESIONS ON LAMB CAN TRANSFER TO THE MOTHERS TEAT AND BACK** * SPREADS RAPIDLY
74
# CONTAGIOUS ECTHYMA (ORF) HOST:
HOST: SHEEP AND GOATS-PRIMARILY LAMBS AND GOAT KIDS
75
# CONTAGIOUS ECTHYMA (ORF) DISTRIBUTION:
WORLDWIDE
76
# CONTAGIOUS ECTHYMA (ORF) PATHOGENESIS:
* SKIN: CELLULAR RESPONSE WITH NECROSIS AND SLOUGHING * CUTANEOUS: DELAYED HYPERSENSITIVITY AND INFLUX INFLAMMATORY CELLS. * **MACULE→PAPULE→VESICLE→PUSTULE→ULCE R→SCAB**
77
# CONTAGIOUS ECTHYMA (ORF) CLINICAL SIGNS:
* THE FIRST LESION DEVELOPS IN THE **MUCOCUTANEOUS JUNCTION** AND ARE ACCOMPANIED WITH SWOLLEN LIPS * LESIONS THEN SPREADS TO THE MUZZLE AND NOSTRILS CAUSING ANIMALS TO HAVE DIFFICULTY EATING LEADING TO ANOREXIA AND WEIGHT LOSS. * LESIONS ON THE TEATS MAY LEAD TO A SECONDARY BACTERIAL INFECTION RESULTING IN MASTITIS DUE TO THE INVASION OF THE LESIONS VIA FLY LARVAE. * SEVERE CASES MAY RESULT IN LESIONS ON THE GENITALS (LEADING TO INFERTILITY IF ON THE SCROTUM), FEET (LEADING TO LAMENESS), EARS.
78
# CONTAGIOUS ECTHYMA (ORF) VACCINATION: DOES IT LAST? SHOULD ALL ANIMALS GET IT? WHAT ABOUT INSPECTING THE LAMB? WHAT ABOUT PREGNANT EWES
* **DOES NOT OFFER LONG-LASTING IMMUNITY.** AT MOST 1-2 YEARS. * VACCINES **SHOULD NOT** BE USED ON FARMS THAT DO NOT HAVE A PROBLEM WITH ORF * **YOU SHOULD INSPECT THE LAMB 1 WEEK AFTER VACCINATION FOR LOCAL REACTIONS** * IN PROBLEM FLOCKS/HERS, THE LAMBS/KIDS MAY NEED TO BE VACCINATED AT 6-8 WEEKS. * **VACCINATE PREGNANT EWES BEFORE LAMBING**
79
# CONTAGIOUS ECTHYMA (ORF) IN HUMANS:
* MACRO-POPULAR LESIONS AND LARGE NODULAR LESIONS IN THE FINGER, THE HAND, THE ARM, FACE, AND EVEN THE PENIS. VERY PAINFUL * SECONDARY BACTERIAL INFECTIONS OF LESIONS MAY CAUSE COMPLICATIONS
80
# GENUS: CAPRIPOXVIRUS SHEEPPOX (SPV) AND GOAT POX (GPV) DISTRIBUTION
DISTRIBUTION: ENDEMIC IN AFRICA, ASIA AND PARTS OF EUROPE
81
SHEEPPOX (SPV) AND GOAT POX (GPV) HOW MANY VIRUS?
USED TO BE CONSIDERED ONE VIRUS, WITH GENETIC SEQUENCING IT WAS DETERMINED TO BE TWO SEPARATE VIRUSES.
82
SHEEPPOX (SPV) AND GOAT POX (GPV) CAN THEY BE DISTINGUISHED?
THEY CANNOT BE DISTINGUISHED FROM ONE ANOTHER WITH SEROLOGICAL TECHNIQUES.
83
SHEEPPOX (SPV) AND GOAT POX (GPV) WHAT RELATION TO LSDV?
CLOSELY RELATED TO LSDV BUT THERE IS NO EVIDENCE LSDV CAUSES DISEASE IN SHEEPS AND GOATS.
84
# CAPRIPOXVIRUS LUMPY SKIN DISEASE OF CATTLE (LSDV) DISTRIBUTION:
DISTRIBUTION: ENZOOTIC IN SUB-SAHARAN AFRICA AND MIDDLE EAST WITH RECENT INCURSION IN IRAQ **not asia**
85
LUMPY SKIN DISEASE OF CATTLE (LSDV) TRANSMISSION:
TRANSMISSION: ARTHROPOD VECTOR (MOST COMMON), DIRECT CONTACT
86
LUMPY SKIN DISEASE OF CATTLE (LSDV) HOST:
HOST: CATTLE
87
LUMPY SKIN DISEASE OF CATTLE (LSDV) CLINICAL SIGNS:
CLINICAL SIGNS: FEVER, MULTIPLE **NODULAR LESIONS ON SKIN** AND MUCOUS MEMBRANE, LYMPHADENOPATHY
88
SHEEPPOX AND GOATPOX where?
africa, asia europe
89
SHEEPPOX AND GOATPOX TRANSMISSION: how contagious? how acquired? where found on animal? relevance of scabs?
* **HIGHLY **CONTAGIOUS * **ENTERS THE RESPIRATORY TRACT VIS AEROSOL (MOST COMMON).** CAN ALSO OCCUR IN THE MM VIA DIRECT CONTENT FROM CONTAMINATED IATROGENIC MATERIALS AS WELL AS MECHANICAL TRANSMISSION BY BITING ARTHROPODS. * VIRUSES IS PRESENT IN NASAL AND ORAL SECRETIONS FOR SEVERAL WEEKS AFTER INFECTION. * CAN SURVIVE IN DRY** SCABS FOR MONTHS**
90
SHEEPPOX PATHOGENESIS:
PATHOGENESIS: * SHEEPPOX IS A **SYSTEMIC DISEASE *** AFTER INCUBATION, **LEUKOCYTE-ASSOCIATED **VIREMIA INCURS. * VIRUS WILL LOCALIZE IN THE SKIN AND OTHER INTERNAL ORGANS. intestines, lungs et. * RESULTS IN SEVERE **NECROTIZING VASCULITIS** IN THE ARTERIOLES AND POSTCAPILLARY VENULES OF THE SKIN, **reportable
91
# SHEEPPOX clinical signs malignant form? benign form?
CLINICAL SIGNS: * MALIGNANT FORM: * SEEN IN LAMBS AND HAVE A HIGH MORTALITY RATE * LESIONS START ON SKIN AND MOVE INTO LARYNX/PHARYNX/LUNGS. SECONDARY PNEUMONIA IS COMMON WHILE ABORTION IS RARE * STAR SHAPED SCAR FORMED FREE OF HAIR OR WOOL BENIGN FORM * MORE COMMON IN ADULTS * ONLY SKIN LESIONS OCCUR * MORTALITY IS LOW 0
92
# SHEEPPOX PREVENTION AND CONTROL:
* **NOTIFIABLE DISEASE** IN MOST COUNTRIES OF THE WORLD * **VACCINATION:** * THERE IS A LARGE VARIETY OF VACCINES AVAILABLE BUT A **LIVE ATTENUATED VACCINES** OFFER EXCELLENT PROTECTION FOR MORE THAN A YEAR.
93
# GOAT POX found where? is it reportable? clinically similar to what? how does it differ between kids and adults?
Occurs in Africa, Asia and parts of Europe A **reportable** disease Clinically very similar to sheep pox Young kids suffer systemic disease while adults exhibit a milder form.
94
# SUIPOXVIRUS SWINEPOX distribution?
DISTRIBUTION: WORLDWIDE, WIDESPREAD SPORADIC DISEASE
95
# SUIPOXVIRUS SWINEPOX HOST: what is the difference in older pigs vs. piglets?
HOST: PIGS * OLDER PIGS-**GENERALLY BENIGN. LOW MORTALITY AND LOW** MORBIDITY * CONGENITALLY INFECTED AND VERY YOUNG SUCKLING PIGLETS-HIGH FATALITY
96
# SWINEPOX TRANSMISSION: what 3 ways? what 3 results?
1-DIRECT CONTACT WITH SKIN INJURY (THE VIRUS SURVIVES IN SCABS FOR YEARS) 2 MECHANICAL TRANSMISSION VIA PIG LOUSE-HAEMATOPINUS SUIS (HARBORS THE VIRUS FOR A LONG TIMES), FLIES AND INSECTS. 3**TRANSPLACENTAL INFECTION** OF NEONATAL PIGS-HIGH MORTALITY.
97
# SWINEPOX CLINICAL SIGNS
* TYPICAL POX LESIONS THAT CAN OCCUR ANYWHERE BUT USUALLY ON THE ABDOMEN AND INNER THIGH * GREASY PIG DISEASE AND SECONDARY BACTERIAL DERMATITIS CAN OCCUR SECONDARILY * IN SEVERE INFECTIONS, LESIONS MAY OCCUR IN UPPER RESPIRATORY AND DIGESTIVE TRACTS
98
# SWINEPOX CONTROL
* ERADICATION OF LICE FROM PIGGERY * **NO VACCINE AVAILABLE**
99
# GENUS: AVIPOXVIRUS FOWLPOX HOST:
HOST: HIGHLY INFECTIOUS DISEASE OF POULTRY AND TURKEYS
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# FOWLPOX DISTRIBUTION:
WORLDWIDE
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# FOWLPOX TRANSMISSION:
* SKIN * MECHANICALLY VIA MOSQUITOES, LICE AND TICKS * AEROSOL
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# FOWLPOX is it resistent?
**EXTREMELY RESISTANT** TO DESICCATION AND CAN SURVIVE IN SCABS FOR A LONG TIME.
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# FOWLPOX THREE FORMS:
* CUTANEOUS (DRY FORM) MOST COMMON * DIPHTHERITIC (WET FORM) LEAST COMMON BUT MORE SEVERE * OCULAR FORM
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# FOWLPOX INCLUSION BODIES name 2
1-BOLLINGER BODIES * EOSINOPHILIC, CYTOPLASMIC 2- BARREL BODIES * INSIDE OF BOLLINGER BODIES * SPHERICAL FROM TRYPTIC DIGESTION OF BOLLINGER BODIES
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# FOWLPOX which form is this? * MOST COMMON * LOW MORTALITY * SMALL PAPULES ON THE COMB, WATTLES AND BEAK BUT CAN DEVELOP ON LEGS, FEET AND AROUND THE CLOACA HAVING NODULES BECOME YELLOWISH AND PROGRESS TO A HIGHLY INFECTIOUS THICK SCAB. * SHARP FALL IN EGG PRODUCTION * IF THE CASE IS UNCOMPLICATED, WILL RECOVER IN 4 WEEKS.
THE CUTANEOUS FORM (THE DRY FORM)
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# FOWLPOX which form is this? * DEADLY * CAUSED BY DROPLET INFECTIONS * LESIONS ARE FOUND ON THE MUCOUS MEMBRANES OF MOUTH, PHARYNX, LARYNX AND TRACHEA BUT USUALLY COALESCE AND RESULT IN NECROTIC PSEUDOMEMBRANE (BLOCKING THE AIRWAY) LEADING TO DEAD VIA ASPHYXIATION. * PROGNOSIS IS QUITE POOR.
DIPHTHERIC FOWLPOX (WET FORM)
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# FOWLPOX Which form is this? * CONJUNCTIVITIS * CHEESY EXUDATE ACCUMULATES UNDER THE EYELID AND BECOMES BLIND
FOWL POX OCULAR FORM
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FOWLPOX CONTROL
Vaccination: Modified live fowlpox Control mosquito population and other biting insects.
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UNCLASSIFIED POXVIRUSES ULCERATIVE DERMATOSIS OF SHEEP transmission? clinical forms? hint name 2
* TRANSMISSION: SKIN * CLINICAL FORMS: LESIONS ARE TYPICALLY ULCERS WITH A RAW CRATER THAT BLEED EASILY * TWO FORMS 1 LIP AND LEG ULCERATION 2 VENEREAL FORM-TRANSMITS ULCERATION OF THE PREPUCE AND PENIS OR THE VULVA
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what is the host for unclassified poxvirul transmitted by coitus?
sheep
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DIAGNOSING POXVIRUS 7 steps
1. Clinical signs 2. Samplings-from the skin lesions, vesicular fluids (Highly infectious!), crusts or scabs 3. Electron microscopy 4. Histopathology: Characteristic intracytoplasmic inclusion bodies 5. Pock Lesions 6. Serological Assays (ELISA) 7. PCR
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DIAGNOSING POXVIRUS histopathology type A? Type b?
**Type A or ATI Inclusion bodies:** (cowpox and ectromelia virus) strongly eosinophilic **Type B-**most poxviruses. Slightly eosinophilic and composed of viral particles and protein aggregates Bollinger and Borrel bodies in avipoxvirus
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# CIRCOVIRIDAE what is it? PORCINE CIRCOVIRUS TYPE 1? PORCINE CIRCOVIRUS TYPE-2?
* PSITTACINE BEAK AND FEATHER DISEASE VIRUS * PORCINE CIRCOVIRUS TYPE 1 (NON-PATHOGENIC) * PORCINE CIRCOVIRUS TYPE-2 (POST-WEANING MULTISYSTEMIC WASTING SYNDROME [PMWS]) Porcine dermatitis and nephropathy syndrome PDNS
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# CIRCOVIRIDAE what kind of genomes? what does it look like how does replication occur? is it stable?
* SINGULAR SINGLE STRANDED DNA GENOMES * CHICKEN INFECTIOUS ANEMIA VIRUS HAS TRUMPET LIKE PROJECTIONS * REPLICATION OCCURS IN ACTIVELY DIVIDING CELLS * VERY STABLE IN THE ENVIRONMENT
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POST-WEANING MULTISYSTEMIC WASTING SYNDROME (PMWS) what is this called?
porcine coronavirus 2
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POST-WEANING MULTISYSTEMIC WASTING SYNDROME (PMWS) CLINICAL SIGNS:
* **SUBCLINICAL INFECTION IS MOST COMMON** * LETHARGY, PROGRESSIVE WEIGHT LOSS, COUGH, SLOW GROWTH (FAILURE TO THRIVE) * CO-INFECTION CAN CAUSE SEVERE DISEASE AND MORE PRONOUNCED LESIONS.
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POST-WEANING MULTISYSTEMIC WASTING SYNDROME (PMWS) DIANOSIS
* SEROLOGICAL ASSAYS-MOST ARE SEROPOSITIVE SO ANTIGEN DETECTION IS NOT OF MUCH VALUE * DETECTION OF PCV-2 NUCLEIC ACIDS BY PCR
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POST-WEANING MULTISYSTEMIC WASTING SYNDROME (PMWS) VACCINATION:
* CHIMERIC VACCINE USING PCV-1 WITH PCV-2 CAPSID PROTEIN * INACTIVATED OR BACULOVIRUS-EXPRESSED VACCINES * VIRUS-LIKE PARTICLES WITH PCV-2 CAPSID PROTEIN * **VACCINATE SOW ANTEPARTUM** ** not the same as swine pox
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PORCINE DERMATITIS AND NEPHROPATHY SYNDROME (PDNS) also called
porcine coronavrus 2
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PORCINE DERMATITIS AND NEPHROPATHY SYNDROME (PDNS) associated with? continual or sporadic? reported in what age pigs? findings?
* ASSOCIATED WITH PCV2 * SPORADIC * REPORTED IN OLDER PIGLETS * FINDINGS: * NECROTIZING SKIN LESIONS, VASCULITIS AND NECROTIZING AND FIBRINOUS GLOMERULONEPHRITIS