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1.
Sci Transl Med ; 12(551)2020 07 08.
Article in English | MEDLINE | ID: mdl-32641488

ABSTRACT

Atopic dermatitis (AD) is commonly associated with colonization by Staphylococcus aureus in the affected skin. To understand the role of S. aureus in the development of AD, we performed whole-genome sequencing of S. aureus strains isolated from the cheek skin of 268 Japanese infants 1 and 6 months after birth. About 45% of infants were colonized with S. aureus at 1 month regardless of AD outcome. In contrast, skin colonization by S. aureus at 6 months of age increased the risk of developing AD. Acquisition of dysfunctional mutations in the S. aureus Agr quorum-sensing (QS) system was primarily observed in strains from 6-month-old infants who did not develop AD. Expression of a functional Agr system in S. aureus was required for epidermal colonization and the induction of AD-like inflammation in mice. Thus, retention of functional S. aureus agr virulence during infancy is associated with pathogen skin colonization and the development of AD.


Subject(s)
Dermatitis, Atopic , Eczema , Animals , Mice , Skin , Staphylococcus/genetics , Staphylococcus aureus , Virulence
2.
mSphere ; 4(4)2019 08 14.
Article in English | MEDLINE | ID: mdl-31413173

ABSTRACT

Individual foot-and-mouth disease virus (FMDV) strains reveal different degrees of infectivity and pathogenicity in host animals. The differences in severity among outbreaks might be ascribable to these differences in infectivity among FMDV strains. To investigate the molecular mechanisms underlying these differences, we estimated the infectivity of O/JPN/2000 and O/JPN/2010, which caused outbreaks of markedly different scales, in cell lines, Holstein cattle, and suckling mice. Viral growth of the two strains in cells was not remarkably different; however, O/JPN/2000 showed apparently low transmissibility in cattle. Mortality rates of suckling mice inoculated intraperitoneally with a 50% tissue culture infective dose (TCID50) of 10 for O/JPN/2000 and O/JPN/2010 also differed, at 0% and 100%, respectively. To identify genes responsible for this difference in infectivity, genetic regions of the full-length cDNA of O/JPN/2010 were replaced with corresponding fragments of O/JPN/2000. A total of eight recombinant viruses were successfully recovered, and suckling mice were intraperitoneally inoculated. Strikingly, recombinants having either VP1 or 3D derived from O/JPN/2000 showed 0% mortality in suckling mice, whereas other recombinants showed 100% mortality. This finding indicates that VP1, the outermost component of the virus particle, and 3D, an RNA-dependent RNA polymerase, are individually involved in the virulence of O/JPN/2010. Three-dimensional structural analysis of VP1 confirmed that amino acid differences between the two strains were located mainly at the domain interacting with the cellular receptor. On the other hand, measurement of their mutation frequencies demonstrated that O/JPN/2000 had higher replication fidelity than O/JPN/2010.IMPORTANCE Efforts to understand the universal mechanism of foot-and-mouth disease virus (FMDV) infection may be aided by knowledge of the molecular mechanisms which underlie differences in virulence beyond multiple topotypes and serotypes of FMDV. Here, we demonstrated independent genetic determinants of two FMDV isolates which have different transmissibility in cattle, namely, VP1 and 3D protein. Findings suggested that the selectivity of VP1 for host cell receptors and replication fidelity during replication were important individual factors in the induction of differences in virulence in the host as well as in the severity of outbreaks in the field. These findings will aid the development of safe live vaccines and antivirals which obstruct viral infection in natural hosts.


Subject(s)
Disease Outbreaks , Foot-and-Mouth Disease Virus/genetics , Foot-and-Mouth Disease Virus/pathogenicity , Foot-and-Mouth Disease/virology , Virulence Factors/genetics , Animals , Animals, Suckling , Capsid Proteins/chemistry , Capsid Proteins/genetics , Cattle , Cell Line , Foot-and-Mouth Disease/mortality , Mice , RNA, Viral/genetics , Virulence
3.
J Antimicrob Chemother ; 65(7): 1382-6, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20478990

ABSTRACT

OBJECTIVES: To develop an easy-to-use method for the rapid detection of antibiotic-resistant bacteria. Here, a new immunochromatographic assay specific for aminoglycoside 6'-N-acetyltransferase AAC(6')-Iae was designed. AAC(6')-Iae is a significant marker molecule for multidrug-resistant (MDR) Pseudomonas aeruginosa isolates in Japan. METHODS: Monoclonal antibodies specific for AAC(6')-Iae were used to construct the assay. The assessment of the assay was performed using 116 P. aeruginosa clinical isolates obtained from hospitals in the Kanto area of Japan where little was known about AAC(6')-Iae producers. PCR analyses of the aac(6')-Iae and class 1 integron, antimicrobial susceptibility testing and PFGE analysis were performed to characterize positive strains. RESULTS: The detection limit of the assay was 1.0 x 10(5) cfu. Of 116 clinical isolates, 60 were positive for AAC(6')-Iae using the assay. The results of assessment with clinical isolates were fully consistent with those of aac(6')-Iae PCR analyses, showing no false positives or negatives. All positive strains detected by the assay showed MDR phenotypes that were resistant to several classes of antibiotic. PFGE analysis showed that 59 of 60 positive strains tightly clustered, and these included clonal expansions. CONCLUSIONS: The developed assay is an easy-to-use and reliable detection method for AAC(6')-Iae-producing MDR P. aeruginosa. This approach may be applicable for screening and investigation of antibiotic-resistant bacteria as an alternative to PCR analysis.


Subject(s)
Acetyltransferases/analysis , Bacteriological Techniques/methods , Chromatography/methods , Drug Resistance, Multiple, Bacterial , Pseudomonas aeruginosa/enzymology , Antibodies, Bacterial , Antibodies, Monoclonal , Bacterial Proteins/analysis , Bacterial Typing Techniques , Cluster Analysis , Cross Infection/microbiology , DNA Fingerprinting , DNA, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Genotype , Humans , Immunoassay/methods , Integrons , Japan , Polymerase Chain Reaction , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/isolation & purification , Sensitivity and Specificity
4.
Exp Anim ; 57(4): 377-84, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18633160

ABSTRACT

The h current (Ih) is an inwardly mixed cationic conductance activated by membrane hyperpolarization. We previously demonstrated that the Ih blockers CsCl and ZD7288 can significantly increase the threshold of electrically induced paroxysmal discharge in the rabbit hippocampus. In the present study, we examined the effects of these Ih blockers on inherited epilepsy in Mongolian gerbils. Seizure-sensitive Mongolian gerbils (n=29) underwent a series of seizure induction tests (including gentle handling for 1-2 min and being dropped from a height of 50 cm) before, during and after oral administration of 10 mM CsCl or 0.1 mM ZD7288. Their behavioral responses were classified into 3 grades corresponding to no seizure (score: 0), partial seizure (score: 1), and generalized seizure (score: 2). In the CsCl experiments (n=10), the average scores were 1.09 +/- 0.10 before administration, 0.82 +/- 0.10 during administration, and 0.96 +/- 0.10 after administration. CsCl significantly increased the ratio of grade 0 behavioral responses (P<0.01, compared with the value before administration), and decreased the ratio of grade 1 responses (P<0.01). In the ZD7288 experiments (n=19), the average scores were 0.99 +/- 0.07 before administration, 0.52 +/- 0.06 (P<0.01) during administration, and 0.76 +/- 0.07 (P<0.05) after administration. ZD7288 significantly increased the ratio of grade 0 behavioral responses (P<0.01), and decreased the ratio of grade 1 responses (P<0.05) and grade 2 responses (P<0.01). We conclude that both CsCl and ZD7288 have an anti-epileptic effect on inherited epilepsy in Mongolian gerbils.


Subject(s)
Cardiotonic Agents/pharmacology , Cesium/pharmacology , Chlorides/pharmacology , Cyclic Nucleotide-Gated Cation Channels/drug effects , Epilepsy/veterinary , Gerbillinae , Potassium Channels/drug effects , Pyrimidines/pharmacology , Rodent Diseases/physiopathology , Animals , Epilepsy/genetics , Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
5.
Nippon Ganka Gakkai Zasshi ; 108(1): 29-37, 2004 Jan.
Article in Japanese | MEDLINE | ID: mdl-14969091

ABSTRACT

BACKGROUND: We report two rare cases of Senior-Loken syndrome, one with fundus lesions simulating Coats disease. CASE 1: A 14-year-old boy had juvenile nephronophthisis and bilateral retinitis pigmentosa with retionochoroidal atrophy and salt and pepper fundus. Electroretinogram (ERG) showed non-recordable changes and the Goldmann perimeter showed ring scotomas. CASE 2: A 14-year-old boy had bilateral retinitis pigmentosa and juvenile nephronophthisis with continuous ambulatory peritoneal dialysis. Additionally, both eyes showed massive exudates seen in Coats disease in the entire periphery, exudative retinal detachment, proliferative changes in the inferior periphery, yellow opacitas corporis vitrei, keratoconus, and cataract. The left eye had vitreous hemorrhages. Both eyes received vitreous surgery and endophotocoagulation. After the surgery the left eye showed neovascular glaucoma and a cyclophotcoagulation was performed. The massive edema in the superior retina of both eyes disappeared and intra-ocular pressure in the left eye was normalized. However, despite these treatments, both eyes finally had no light perception. CONCLUSION: Case 1 was a typical SLS, and case 2 was a rare one with fundus lesions simulating Coats disease, keratoconus, and cataract. We suspect the exudative changes resulted from various vessel changes and choroidal circulatory disturbance of renal retinopathy, retinal vascular damage, and destruction of blood-retinal barrier with retinitis pigmentosa, the inflammatory changes of vessels, and other things.


Subject(s)
Polycystic Kidney, Autosomal Recessive/genetics , Retinitis Pigmentosa/genetics , Adolescent , Electroretinography , Fundus Oculi , Humans , Keratoconus/complications , Kidney Failure, Chronic/etiology , Male , Polycystic Kidney, Autosomal Recessive/complications , Retinitis Pigmentosa/complications , Syndrome
6.
Epilepsia ; 44(1): 20-4, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12581225

ABSTRACT

PURPOSE: The h current (Ih) is an inwardly mixed cationic conductance activated by membrane hyperpolarization and distributed predominantly in the apical dendrites of hippocampal pyramidal neurons. To verify a hypothesis that an anomalous hyperpolarization generates an abnormal excitation by way of Ih channels, we examined the effects of Ih blockers (CsCl and ZD7288) on electrically induced paroxysmal discharges (PADs). METHODS: Fifty-three adult male rabbits were used. We measured the PAD threshold elicited by stimulation to the apical dendritic layer of the hippocampal CA1 region before and after injecting 50 microl of each Ih blocker or saline extracellularly into the same region. RESULTS: In Ih blocker injection groups (n = 26), we obtained a significant increase in PAD threshold (1 mM CsCl: 163%, p < 0.01; 10 mM CsCl: 265%, p < 0.01; 100 mM CsCl: 199%, p < 0.01; 100 microM ZD7288: 192%, p < 0.05; 1 mM ZD7288: 246%, p < 0.05). Conversely, we did not obtain the increase in PAD threshold in a saline injection group (n = 10, 107%). The magnitude as well as duration of the effect had a tendency to depend on concentration of Ih blockers, although a saturated or declining tendency was observed with the 100 mM CsCl injection. CONCLUSIONS: We concluded that Ih channels might contribute to hippocampal epileptiform discharges in vivo. Our hypothesis for epileptogenesis demonstrated in the present experiment offers an idea to develop a new type of antiepileptic drug based on Ih blockers for the treatment of epileptic disorders refractory to current medications.


Subject(s)
Anticonvulsants/pharmacology , Calcium Channels/drug effects , Cesium/pharmacology , Chlorides/pharmacology , Epilepsy/physiopathology , Hippocampus/drug effects , Membrane Potentials/drug effects , Pyramidal Cells/drug effects , Pyrimidines/pharmacology , Sodium Channels/drug effects , Synaptic Transmission/drug effects , Animals , Calcium Channels/physiology , Dose-Response Relationship, Drug , Electroencephalography/drug effects , Hippocampus/physiopathology , Male , Membrane Potentials/physiology , Pyramidal Cells/physiology , Rabbits , Sodium Channels/physiology , Synaptic Transmission/physiology
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