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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lypd8tm2Ktak
targeted mutation 2, Kiyoshi Takeda
MGI:6508395
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lypd8tm2Ktak/Lypd8tm2Ktak B6.Cg-Lypd8tm2Ktak MGI:6514260


Genotype
MGI:6514260
hm1
Allelic
Composition
Lypd8tm2Ktak/Lypd8tm2Ktak
Genetic
Background
B6.Cg-Lypd8tm2Ktak
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lypd8tm2Ktak mutation (0 available); any Lypd8 mutation (22 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• vancomycin treatment results in increased numbers of fecal Lactobacillus, Proteus, Escherichia and Helicobacter
• following oral gentamicin treatment, feces show decreased numbers of Proteus, Escherichia and Helicobacter
• although mucin production is normal, intestinal bacteria such as Proteus, Helicobacter and Escherichia (i.e. flagellated Gram-negative rod bacteria) are detected in close proximity to the epithelial cell layers in the large intestine, unlike in wild-type controls
• intestinal bacteria penetrate the inner mucus layer in the large intestine that normally is free of commensal microbiota
• intestinal bacteria such as Proteus, Helicobacter and Escherichia penetrate the inner mucus layer and further into the crypts in the large intestine, unlike in wild-type controls
• under SPF conditions, colonic epithelial are invaded by commensal bacteria, unlike in wild-type controls
• bacterial DNA is significantly amplified in colonic tissues, but not in luminal contents; numbers of several bacterial genera are increased in colonic tissues, esp. Proteus, Helicobacter and Escherichia
• upon culture of colonic tissues on agar plates, Proteus mirabilis forms an unusual colony with a swarming migration pattern
• FISH analysis using a Proteus-specific 16S rRNA probe revealed that Proteus spp. were present just above the epithelial cell layer and in the crypts
• after transanal inoculation, carboxyfluorescein succinimidyl ester (CFSE)-labelled Proteus mirabilis is present in closer proximity to the epithelial cell layers, unlike in wild-type controls
• after oral gentamicin treatment, no bacteria are detected just above the epithelial layers; in contrast, vancomycin treatment does not induce changes in the inner layers
• despite penetration of colonic epithelia by flagellated bacteria, no inflammatory response is noted in the colon under SPF conditions, as determined by inflammatory cytokine and chemokine expression
• at day 8 of 2% DSS administration, mice exhibit more severe weight loss and intestinal inflammation in colonic tissues than DSS-treated wild-type controls
• oral treatment with gentamicin (active against Gram-negative bacteria including P. mirabilis) ameliorates the weight loss and intestinal inflammation in DSS-treated mice
• oral treatment with vancomycin (active against Gram-positive cocci) exacerbates the weight loss and intestinal inflammation in DSS-treated mice
• after 2% DSS administration, mice exhibit higher mortality than DSS-treated wild-type controls
• oral treatment with gentamicin ameliorates the survival rate in DSS-treated mice, whereas vancomycin treatment has the opposite effect

immune system
• at day 8 of 2% DSS administration, mice exhibit more severe weight loss and intestinal inflammation in colonic tissues than DSS-treated wild-type controls
• oral treatment with gentamicin (active against Gram-negative bacteria including P. mirabilis) ameliorates the weight loss and intestinal inflammation in DSS-treated mice
• oral treatment with vancomycin (active against Gram-positive cocci) exacerbates the weight loss and intestinal inflammation in DSS-treated mice
• after 2% DSS administration, mice exhibit higher mortality than DSS-treated wild-type controls
• oral treatment with gentamicin ameliorates the survival rate in DSS-treated mice, whereas vancomycin treatment has the opposite effect

endocrine/exocrine glands
• intestinal bacteria such as Proteus, Helicobacter and Escherichia penetrate the inner mucus layer and further into the crypts in the large intestine, unlike in wild-type controls

mortality/aging
• after 2% DSS administration, mice exhibit higher mortality than DSS-treated wild-type controls
• oral treatment with gentamicin ameliorates the survival rate in DSS-treated mice, whereas vancomycin treatment has the opposite effect





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory