Strains and Stocks Flashcards
A
Albino
Age-related hearing loss
Research use: carcinogen-induced lung tumors, developmental biology (cleft palate), muscular dystrophy (dysf gene)
Spontaneous disease: high incidence of lung adenoma, predisposed to congenital malformations, amyloidosis
Hepatic tumors with H. hepaticus infection
AKR
Albino
Ecotropic retrovirus in all tissues, viremic from birth, high rate of T-cell lymphoma/leukemia
Paralysis with LDV
Males get urinary obstruction
129
16 substrains - white belly agouti (Aw) or albino.
Used for ES cell lines and to generated Tm strains
High incidence of testicular teratoma, arteritis, acidophilic macrophage pneumonia
BALB/c
Albino
Age-related hearing loss
Research use: monoclonal antibody production, plasmacytoma with injection of mineral oil
Spontaneous disease: cardiac calcinosis, hypocallosity, Reye’s-like syndrome, polycystic kidney disease
C3H
Agouti
Retinal degeneration
Spontaneous disease: cardiac calcinosis, liver tumors (hepatoma), mammary adenocarcinoma, alopecia areata
TLR4 - highly susceptible to gram negative infection
C57BL/6
Black
Hearing loss
Spontaneous disease: hydrocephaply, malocclusion, lymphoma, micropthalmia, amyloidosis, barbering/UD, postpartum ileus
Susceptible to diet-induced atherosclerosis/obesity/type 2 DM
DBA/2
Dilute brown nonagouti
Hearing loss
Spontaneous disease: cardiac + soft tissue mineralization, glaucoma, audiogenic seizures (young age)
Complement C5 deficient
Resistant to diet-induced atherosclerosis
FVB
Albino
Retinal degeneration
Research use: transgenic development due to large pronucleus, airway responsiveness/asthma, chemical-induced SCC
Spontaneous disease: epilepsy, auditory seizures
SJL
Albino
Retinal degeneration
Research use: EAE, muscular dystrophy (dysf gene)
Spontaneous disease: reticulum cell sarcoma, amyloidosis
SWR
Albino
Retinal degeneration
Research use: EAE
Spontaneous disease: lung tumors, mammary gland tumors, diabetes insipidus
Inbred mouse strains with retinal degeneration
SWR
SJL
FVB
C3H
CBA
Inbred mouse strains with age-related hearing loss
BALB/c
A
C57
129
NOD
DBA
Inbred mouse strains with dystrophic mineralization
BALB/c (epicardial)
C3H (cardiac)
DBA (cardiac + soft tissue)
Inbred mouse strains with audiogenic seizures
DBA/2 (at young ages, then hearing loss)
FVB
SJL
Inbred strains susceptible to primary amyloidosis
A
SJL
C57BL/6 (older)
Inbred strains resistant to primary amyloidosis
BALB/c
C3H
Inbred strains with dysf mutation
A
SJL
Inbred strains with high rates of male aggression
BALB/c
SJL
FVB
Nude mouse
Foxn1 gene
T cell deficient
Hairless
SCID mouse
Prkdc^scid mutation
T and B cell deficient
Susceptible to ionizing radiation
Rag1/Rag2 mouse
RAG1 or RAG2 gene
T and B cell deficient
“non-leaky”
NOD
Albino
Hearing loss
Type 1 DM
Defects in antigen presentation, T lymphocyte repertoire, NK cell function, macrophage cytokine production, and C5 complement
NSG
T and B cell deficient
NK cell deficient
Complement deficient
Impaired macrophage and dendritic cell function
XID
Burton’s tyrosine kinase gene defect
Decreased B cells, low IgM
Model of x-linked agammaglobulinemia
Moth-eaten
T and NK cell deficient
Autoimmune syndrome, hypergammaglobulinemia
Folliculitis leads to moth eaten coat
Beige
Lyst(bg) mutation
Model for Chediak-Higashi syndrome, lysosomal storage disease
Decreased NK activity, decreased neutrophil function
RFM mice
Atrial thrombosis
CBA
Research use: granulomatous experimental autoimmune thyroiditis,
Spontaneous disease: Exocrine pancreatic insufficiency, renal tubulointerstitial lesions
NZB
Autoimmune disease - hemolytic anemia, glomerulonephritis
Inbred strains with high rate of mammary tumors
C3H
A
DBA/2
Inbred strains with low rate of mammary tumors
BALB/c
C57BL
AKR
ACI rat
Black agouti with white belly and feet
Congenital genitourinary abnormalities (renal agenesis/hypoplasia, hydronephrosis)
Testicular and prostatic tumors
Susceptible to estrogen-induced mammary tumors
BB/Wor rat
Albino
Type 1 diabetes mellitus
BN (Brown Norway)
Brown
Airway hyperresponsiveness/asthma, eosinophilic granulomatous pulmonary inflammation
Bladder tumors, hydronephrosis, transplantable myeloid leukemia
BUF (Buffalo)
Albino
Autoimmune thyroiditis
COP (Copenhagen)
Hooded
Prostatic adenocarcinoma
F344
Albino
National Toxicology Program’s Carcinogen Bioassay Program and National Institute on Aging rat
Interstitial/leydig cell tumors, large granular lymphocytic leukemia, CPN, corneal mineralization, nephrocalcinosis
LEW (Lewis)
Albino
Autoimmune disease model, EAE, multiple sclerosis
LOU/C
Albino
Myeloma, Plasmacytoma, IgG autoantibody
SHR
Albino
Spontaneous hypertensive rat
Hypertension, polyarteritis nodosa
WF (Wistar-Furth)
Albino
Mononuclear cell leukemia
Fuzzy mutation - dermatology research
Inducible carcinoma of the mammary gland
Zucker
Hooded
Obesity, type 2 DM
Increased incidence of urinary tract infections and urolithiasis
Brattleboro
Hooded (?)
Diabetes insipidus (autosomal recessive)
Vasopressin deficiency
Gunn
Albino (?)
Jaundice, unconjugated hyperbilirubinemia (autosomal recessive defect of bilirubin glucuronidation, UGT); Crigler-Najjar syndrome
Hydronephrosis (single dominant gene)
Obese SHR
Type 4 hyperlipoproteinemia (autosomal recessive)
Nude rat
Hooded
Foxn1 - rnu
Autosomal recessive
Sprague Dawley
Outbred stock; albino
Spontaneous disease: polyarteritis nodosa, pituitary adenoma (chromophobe adenoma most common), mammary fibroadenoma, CPN, chronic myocardial disease
Larger than Wistar
Wistar
Outbred stock; Albino
Seizures
Smaller than Sprague-Dawley
Long Evans
Outbred stock; hooded
Royal college of surgeons rat (RCS)
Tan hooded
Retinal degeneration
Long-evans Cinnamon rat
“Cinnamon-like”, kinda looks tan hooded but with more tan
Copper accumulation in liver; Wilson’s disease
Dahl rat
Albino
Hypertension and renal failure on high-salt diet; hyperlipidemia, insulin resistance
FHR (Fawn-Hooded Rat)
Fawn hooded
Hypertension
Substrain designation occurs if two colonies of inbred mice are…
Separated before F40
Separate for 100 generations
If genetic differences arise
Wistar-Kyoto
Normotensive control for SHR
High rates of cardiac septal defects, resulting in right ventricular hypertrophy
KHC Rabbit
Kurosawa and Kusanagi Hypercholesterolemic rabbit
Autosomal recessive - LDL receptor gene has a 12bp deletion
Elevated serum cholesterol, triglyceride, phospholipid; decreased HDL
WHHL rabbit
Watanabe heritable hyperlipidemia
Marked deficiency of LDL receptors
Increased incidence of athersclerosis
St Thomas Hospital strain rabbits
Normal functioning LDL receptor
Hypercholesterolemic
IAF guinea pig
Hairless
Derm tox
Abyssinian guinea pig
Long hair in whorls
Peruvian guinea pig
Long straight hair
Yucatan minipig
Grey-ish/black color
Mini and micro sizes
Lineage with VSD
Lineage that is white/hairless for derm studies
Hanford minipig
Largest minipig
White
Device implant studies, dermal studies
Sinclair minipig
White (lots of hair)
Malignant, spontaneously regressing, melanoma
Slow growers
Gottingen
Smallest minipig
White color
Used in pharma/tox
Prone to type III hypersensitivity - thrombocytopenic purpura
Ossabaw swine
Black or black/tan spotted
Diabetes and metabolic syndrome
Rapacz familial hypercholesterolemia pigs
Atherosclerosis
Norwegian yorkshire swine
Inherited form of autoimmune glomerulonephritis
Gal-KO pig
Knockout of the gene that encodes for alpha1,3Gal
Background breed - MGH, SLAdd line (most inbred)
MGH swine
Massachusetts general hospital
Homozygous for defined SLA/MHC
SLAaa, SLAcc, SLAdd
SLAdd further inbred
Swine breeds susceptible to porcine stress syndrome
Landrace
Yorkshire
Duroc
Pietrain
Poland China
Landrace pig
Big and white
Ears point down, long snout
Yorkshire pig
Big and white
Ears point up, shorter snout
Duroc pig
Big and brown
Pietrain pig
White with black spots
1.50 syrian hamster
Cardiomyopathy
Defect in the sarcoglycan gene
APA hamster
“Albino-panda-albino” hamster
Diabetric nephropathy after STZ administration
Develop atrial thrombosis more commonly (maybe due to cardiac hypertrophy)
Gray collies
Cyclic hematopoiesis
Periodic fluctuations in neutrophil population
Golden retrievers
Duchenne muscular dystrophy
X-linked recessive
Doberman pinscher
Narcolepsy
Bedlington terrier
Copper storage (Wilson’s) disease
Abyssinian cat
Retinal degeneration
rdAc
Corriedale sheep
Dubin-Johnson syndrome (congenital hyperbilirubinemia)
Conjugated
Hepatic anion excretory defect
Big white and very puffy
Southdown sheep
Gilbert’s syndrome (congenital hyperbilirubinemia)
Unconjugated
Hepatic anion uptake defect
Little white and only a little puffy
Rambouillet sheep
Gamma-glutamyl carboxylase deficiency
Yellow-white with big horns
Holstein cattle
Inherited cardiomyopathy
Leukocyte adhesion deficiency
Chediak-Higashi
Fainting goats
Myotonia congenita
Quiver quail
Neurofilament deficient mutant quail
Wide-spread tremors
Complement 4 deficient guinea pig
Partially dominant mode of inheritence (Heterozyogtes are intermediate)
Susceptible to syphylis
Wz guinea pig
Waltzing
Spontaneous
Autosomal dominant, full penetrance