The immunological benefits
from the wild mice's gut bacteria may, in part, explain a persistent problem in disease research: Why disease experiments in lab mice, such as vaccine studies, turn out very differently in humans or other animals.
This is a visualization of the process of transferring gut microbiota
from wild mice to laboratory mice.
The researchers confirmed that C57BL / 6 mice had distinct gut microbiomes
from wild mice.
«Gut bacteria
from wild mice boost health in lab mice.»
Now, immunologists at the National Institute of Diabetes and Digestive and Kidney Diseases in Bethesda, Maryland, have contaminated lab mice in a different way: by giving them gut bacteria
from wild mice.
The gut bacteria
from the wild mice were fairly similar, but the microbiomes of the lab mice were significantly different, with fewer Bacteroidetes and Proteobacteria, for example.
Researchers aware of this reality have now shown that transplanting gut bacteria
from wild mice into «clean» lab mice has made those rodents less likely to die from the flu or develop cancer.
Not exact matches
The researchers then transplanted the gut bacteria
from healthy,
wild Maryland
mice (which were most similar genetically to the lab
mice) into the lab
mice.
Barbara Rehermann and Stephan Rosshart first collected 800
wild house
mice (Mus musculus domesticus) in the Washington, D.C., metro area, and compared their DNA and gut bacteria both with a lab
mouse strain and with
wild mice from all over the world.
Hur added, «To investigate whether Cpf1 had off - target effects, we performed whole genome sequencing using genomic DNA isolated
from one Foxn1 mutant
mouse and its
wild - type sibling.
Activated,
wild type B cells
from female
mice tightly localize Xist RNA at their inactive X chromosomes (left), whereas Xist RNA becomes dispersed throughout the entire nucleus when YY1 is deleted (right).
These organoids had more stem cells than those isolated
from wild - type
mice.
Probing the link between adiponectin deficiency and metabolic disorders like diabetes and obesity, researchers
from the Albert Einstein College of Medicine in New York City injected adiponectin into
wild - type
mice, diabetic
mice, and obese diabetic
mice.
In neurons of DIXDC1 mutant
mice (center) the dendrites — neural antennae that receive input
from other brain cells — have fewer of the dendritic spines (white with red arrows)-- the receiving half of most synaptic inputs — compared to dendrites in
wild type
mice (left).
(Left) Blood smears
from anemic
mice indicate irregular shapes of red blood cells; (right)
wild type
mice indicate normal shapes of red blood cells.
The researchers followed up with two experiments: in one, they injected vasopressin into the brains of
mouse parents
from both of the
wild species, and in the other, they genetically manipulated vasopressin neurons in the brains of house
mice (Mus musculus) to excite them.
Professor Mark Viney and colleagues
from the University of Bristol and the London School of Hygiene & Tropical Medicine studied the immune systems of 460
wild mice taken
from 12 sites in the UK and compared them with
mice bred in captivity.
He was part of a team that found that, in
mice with mitochondria
from both lab and distantly related
wild populations, one mitochondrial lineage tended to dominate.
No significant differences in bone growth were seen in
wild type
mice that received rosuvastatin or vehicle (right and second
from right).
All clones with the
wild type Tyr302, including the Envs
from the viral innoculum and two Envs
from X4 - ZFN
mice utilized CXCR4 approximately 1000-fold more efficiently than CCR5 and comparably to the X4 - tropic control TYBE (Figure 6C).
It suggests that the early hunter - gatherer settlements transformed ecological interactions and food webs, allowing house
mice that benefited
from human settlements to out - compete
wild mice and establish themselves as the dominant population.
Numbers represent percent increases relative to
wild type
mice and were calculated
from the data shown in Table 1.
Moreover, loss of myostatin activity resulting either
from postnatal inactivation of the Mstn gene [3], [4] or following administration of various myostatin inhibitors to
wild type adult
mice [5]--[7] can also lead to significant muscle growth.
Finally,
from about 11,500 years ago, when people in the region began farming and became sedentary, the
wild mice were displaced again (PNAS, doi.org/b4wn).
The researchers trapped more than 800
wild mice from eight locations across Maryland and the District of Columbia to find healthy, suitable candidates for a gut microbiota donation.
Four generations later, the
mice still carried either the
wild microbiomes or the control laboratory microbiomes passed down
from their foremothers.
In the most extreme case, muscle weights in F66 / Mstn − / −
mice were increased by 250 — 350 %
from those seen in
wild type
mice (Figures 2b and 3).
They observed a significant decrease in the number of proliferating stem cells in the brains of HIV / gp120 -
mice compared with similar tissue
from normal,
wild - type
mice.
Male or female (5 - 6 wks old)
wild type and genetically modified
mice (as required for individual investigator's protocols) will be fed a high fat high sucrose diet (
from Research Diets ranging in fat
from 45 - 58 % of calories as fat, 26 - 39 % carbohydrate (sucrose) and 16 % protein or control diets (10 % fat, 73 % carbohydrate, 16.4 % protein or rodent chow) for up to 16 weeks.
The goal of this protocol (written in French) is to describe the steps and quality controls to prepare new stable murine embryonic stem cells lines: ① either
from wild type
mouse embryos to introduce a mutation by genetic targeting or homologous recombination to get a genetically modified
mouse line ② or
from genetically modified
mouse embryos with two aims:
The present findings are derived
from studies using CD4KO
mice and thus, raise the question as to whether the CD4 + T cell - independent immune mechanisms in CD4 KO
mice differ
from those involved in corneal allograft rejection in
wild - type
mice whose CD4 + T cells population have been depleted with monoclonal antibodies.
Histopathological examination of rejected corneal allografts in CD4 KO
mice revealed a mixed inflammatory infiltrate containing large numbers of neutrophils and mononuclear cells, which was indistinguishable
from the infiltrate seen in rejected corneal allografts in
wild - type
mice (data not shown).
Their content is optimized for genetic mapping in the Collaborative Cross and Diveristy Outbred populations; for discriminating haplotypes
from common laboratory strains and substrains; and for evaluating the ancestry of
wild - caught
mice.
Membrane resistance and rheobase in both dSPN and iSPNs
from 2 - month old Q175
mice did not significantly differ
from Wild - type (WT) dSPN and iSPNs respectively, suggesting that deficits in SPN excitability emerged largely in parallel in each subtype.
Radiation - induced thymic lymphomas
from a
wild - type
mouse (A) and
from a p21 - deficient
mouse (B).
Overexpression of Galgt2 in skeletal muscle prevents injury resulting
from eccentric contractions in both mdx and
wild - type
mice.
In striking contrast,
wild - type LCMV Armstrong,
from which these variants were generated, induces a potent CTL response in immunocompetent
mice and the LCMV infection is rapidly cleared.
C57BL / 6 (
wild type) and perforin - deficient (C57BL / 6 - Prf 1tm1Sdz / J, Prf1 − / −)
mice were obtained
from the Jackson Laboratory and bred in the Abramson Research Center Animal Facility at The Children's Hospital of Philadelphia.
Isolated right and left atria and small mesenteric arteries
from wild type and tau deficient (KO)...
mice of two age groups (13 and 23 months old) were used to assess cardiovascular phenotypes.
Given that our
wild type B. burgdorferi acquired by xenodiagnostic ticks retain the ability to express ospC (also shown by RT - PCR in Fig 4), we can not rule out the possibility that a tick midgut - adapted phenotype, in the absence of salivation and feeding, contributed to the failure of the B. burgdorferi acquired
from XT to infect SCID
mice.
Brain, eyes, and optic nerves were taken
from transgenic and
wild - type
mice of 3 to 12 months of age and processed for immunohistochemistry, qPCR, or western immunoblotting.
(A) Demonstration of Slc6a14 mRNA up - regulation in PyMT - driven mammary tumours in
mice; N, mammary tissue
from wild - type
mice; T, mammary tumour tissue
from PyMT - Tg
mice.
«What this might suggest is that transfer of some of the «good» microbiota
from wild - type
mice to replace the «bad» microbiota
from mice lacking AIM2 offers increased protection against colorectal cancer,» Man said.
Analysis of transcriptomes in tumour tissues
from wild - type
mice and Slc6a14 - null
mice indicated no compensatory changes in the expression of any other amino acid transporter mRNA.
The next slide actually shows you one of the slides
from this publication, showing you that this is the
wild - type
mice; males on the left and females on the right.
(A) Genotype documentation of - / y hemizygous males and - / - homozygous females; evidence of Slc6a14 deletion in colon and lung tissues
from - / y hemizygous males and - / - homozygous females; expression of Slc6a14 in colon (C) and lung (L) but not in mammary gland (M) in
wild - type (WT) female
mice.
We examined the expression of Slc6a14 in breast tumours obtained
from 4 - month - old PyMT - Tg female
mice and in mammary glands obtained
from age - matched
wild - type female
mice.
Because the SD of brain progranulin in
wild - type
mice was about 10 % of the mean level, progranulin levels in Grn + / −
mice would need to increase
from 50 % of normal to 80 % of normal, i.e. by 30 % of the normal value, to reach the lower limit of normal.
Frozen sections of lung and colon tissues
from wild - type
mice and Slc6a14 − / −
mice were also used for immunofluorescence analysis of Slc6a14 protein expression with an antibody raised against a
mouse peptide sequence [17].
(A) Knockout
mice are indistinguishable
from those of
wild type in morphology and size.