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141.
Microorganisms typically adapt to environmental cues by turning on and off the expression of virulence genes which, in turn, allows for optimal growth and survival within different environmental niches. This adaptation strategy includes sensing and responding to changes in nutrients, pH, temperature, oxygen tension, redox potential, microbial flora, and osmolarity. For a bacterium to adhere to, penetrate, replicate in, and colonize host cells, it is critical that virulence genes are expressed during certain periods of the infection process. Thus, throughout the different stages of an infection, different sets of virulence factors are turned on and off in response to different environmental signals, allowing the bacterium to effectively adapt to its varying niche. In this review, we focus on the regulation of virulence gene expression in two pathogens which have been implicated as major etiological agents in adult and juvenile periodontal diseases: Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans. Understanding the mechanisms of virulence gene expression in response to the local environment of the host will provide crucial information in the development of effective treatments targeted at eradication of these periodontal disease pathogens. 相似文献
142.
The Rubella Virus Putative Replicase Interacts with the Retinoblastoma Tumor Suppressor Protein 总被引:6,自引:0,他引:6
Atreya Chintamani D. Lee Nancy S. Forng Ren-Yo Hofmann Jorg Washington Glennelle Marti Gerald Nakhasi Hira L. 《Virus genes》1998,16(2):177-183
In utero fetal infection of rubella virus (RV), a positive-stranded RNA virus, frequently induces birth defects if contracted in the
first trimester of pregnancy. The underlying mechanism of RV-induced birth defects is not known. Birth defects are also common
in certain DNA viral infections such as human cytomegalovirus (HCMV). During HCMV infection, one of its proteins interacts
with a cell growth regulatory protein, the retinoblastoma protein (Rb) and stimulates DNA synthesis which is associated with
chromosomal damage and cellular mitotic arrest. These affects have been implicated in HCMV induced teratogenesis. Since RV
and HCMV both cause teratogenesis, we postulated that during RV infection, a virus-encoded protein might interact with Rb
and affect fetal cell growth. In the present study, we have identified a known Rb-binding motif, L×C×E (LPCAE) in the carboxy-terminal
half of the putative replicase (NSP90) of RV and demonstrated that the C-terminal region specifically binds to GST-Rb in vitro. Further, by coimmunoprecipitating NSP90 and Rb using specific antibodies to respective proteins, we have confirmed that
NSP90 specifically binds to Rb in vivo as well. In addition, RV replication was shown to be less in null-mutant (Rb−/−) mouse embryonic fibroblast cells than in wild-type (Rb+/+) cells, suggesting a possible physiological role for this interaction. Thus, in facilitating RV replication, binding of NSP90
to Rb potentially alters the cell growth regulatory property of Rb, and this could be one of the initial steps in RV-induced
teratogenesis.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
143.
Walder RY; Shalev H; Brennan TM; Carmi R; Elbedour K; Scott DA; Hanauer A; Mark AL; Patil S; Stone EM; Sheffield VC 《Human molecular genetics》1997,6(9):1491-1497
Familial hypomagnesemia with secondary hypocalcemia (HSH) (MIM 307600) was
studied in three inbred Bedouin kindreds from Israel. The three kindreds,
one extended and two nuclear families, contained 13 affected individuals,
11 males and two females. Assuming that the individuals affected with
hypomagnesemia shared a chromosomal region inherited from a common
ancestor, we used a DNA pooling strategy in a genome-wide search for loci
which show homozygosity for shared alleles in affected individuals. DNA
samples from affected individuals within a single kindred were pooled and
used as the template for PCR amplification of short tandem repeat
polymorphic markers (STRPs). Pooled DNA from unaffected siblings and
parents were used as controls. A shift towards homozygosity was observed in
the affected DNA pool compared with the control pools with D9S301
(GATA7D12). Genotyping of individual DNA samples with D9S301 and several
flanking markers confirmed linkage to chromosome 9 with maximum LOD scores
of 3.4 (theta = 0.05), 3.7 (theta = 0) and 2.3 (theta = 0) for the three
families. We have identified a 14 cM interval on chromosome 9
(9q12-9q22.2), flanked by proximal marker D9S1874 and distal marker
D9S1807, within which all affected individuals from the three kindreds are
homozygous for a shared haplotype. The disease segregates with a common
affected haplotype in the three families, suggesting that hypomagnesemia is
caused by a common ancestral mutation in these families. Although HSH has
been previously reported to be X linked, these linkage data demonstrate
that the disorder is an autosomal recessive disease in these kindreds.
Mapping of a chromosomal breakpoint in a somatic cell line established from
a patient with HSH and a balanced X;9 translocation placed the chromosomal
breakpoint in a 500 kb region flanked by D9S1844 and D9S273. Identification
of the gene responsible for hypomagnesemia will provide insight into the
regulation of this essential cation.
相似文献
144.
Resistance of a Tn4351-generated polysaccharide mutant of Porphyromonas gingivalis to polymorphonuclear leukocyte killing. 总被引:1,自引:2,他引:1 下载免费PDF全文
In this study, we describe the development of an efficient transpositional mutagenesis system for Porphyromonas gingivalis using the Bacteroides fragilis transposon Tn4351. Using this system, we have isolated and characterized a Tn4351-generated mutant of P. gingivalis A7436, designated MSM-1, which exhibits enhanced resistance to polymorphonuclear leukocyte (PMN) phagocytosis and killing. P. gingivalis MSM-1 was initially selected based on its colony morphology; MSM-1 appeared as a mucoid, beige-pigmented colony. Analysis of P. gingivalis MSM-1 by electron microscopy and staining with ruthenium red revealed the presence of a thick ruthenium red-staining layer that was twice the thickness of this layer observed in the parent strain. P. gingivalis MSM-1 was found to be more hydrophilic than strain A7436 by hydrocarbon partitioning. Analysis of phenol-water extracts prepared from P. gingivalis A7436 and MSM-1 by Western (immunoblot) analysis and immunodiffusion with hyperimmune sera raised against A7436 and MSM-1 revealed the loss of a high-molecular-weight anionic polysaccharide component in extracts prepared from MSM-1. P. gingivalis MSM-1 was also found to be more resistant to PMN phagocytosis and intracellular killing than the parent strain, as assessed in a fluorochrome phagocytosis microassay. These differences were statistically significant (P < 0.05) when comparing PMN phagocytosis in nonimmune serum and intracellular killing in nonimmune and immune sera. P. gingivalis MSM-1 was also more resistant to killing by crude granule extracts from PMNs than was P. gingivalis A7436. These results indicate that the increased evasion of PMN phagocytosis and killing exhibited by P. gingivalis MSM-1 may result from alterations in polysaccharide-containing antigens. 相似文献
145.
Mammalian genotoxicity assessment of methylene blue in plasma: implications for virus inactivation 总被引:7,自引:1,他引:7
BACKGROUND: The risk of adverse consequences of virus-inactivation procedures for plasma and cellular blood components must be less than the risk of transfusion-associated viral disease. Previous studies demonstrated that methylene blue, which is currently used in Europe for virus inactivation in fresh-frozen plasma, can elicit mutations in bacterial test systems. This study investigates the potential for methylene blue genotoxicity in two mammalian test systems. STUDY DESIGN AND METHODS: Different concentrations of methylene blue were prepared in plasma (heat-treated at 56 degrees C for 1 hour to reduce cytotoxicity) and used, without illumination, in an in vitro mouse lymphoma cell assay designed to detect forward mutations in the gene encoding thymidine kinase. The assay was performed in the presence or absence of rat liver S9 microsomal fraction. Similarly prepared samples of methylene blue in heat-treated plasma were used in an in vivo mouse micronucleus assay. Each system included a negative vehicle control (heat-treated plasma without methylene blue) and a positive control consisting of a known genotoxic agent. RESULTS: Intravenous administration to mice of 62 mg per kg of methylene blue did not increase the frequency of micronuclei in polychromatic red cells harvested from bone marrow. However, methylene blue concentrations of 10 micrograms per mL (with S9 activation) and 30 micrograms per mL (without S9 activation) significantly increased the thymidine kinase mutation frequency of mouse lymphoma cells to approximately 110 × 10(- 6), from a spontaneous frequency of 28 × 10(-6). CONCLUSION: Methylene blue is mutagenic in cultured mammalian cells. In contrast, results from the mouse micronucleus assay suggest that the genotoxicity is not expressed in vivo. Considerably more investigation will be required to assess the genotoxic potential of intravenously administered methylene blue used in virus-inactivation procedures, because of the likelihood of the formation of methylene blue photoproducts or the impact of metabolic conversion of methylene blue to leukomethylene blue in vivo. 相似文献