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1.
Materials (Basel) ; 16(12)2023 Jun 08.
Artículo en Inglés | MEDLINE | ID: mdl-37374428

RESUMEN

To address the poor characteristics of low strength and poor toughness in phosphogypsum-based construction material, this study investigates the influence of different diameters, lengths, and dosages of polyvinyl alcohol (abbreviated as PVA) fibers on the workability and mechanical properties of phosphogypsum-based construction material. The results show that as the length and dosage of PVA fibers increase, the flowability of the slurry gradually decreases, and the setting time also shortens. With an increase in the diameter of PVA fibers, the rate of decrease in flowability slows down, and the rate of shortening of setting time also gradually slows down. Moreover, the inclusion of PVA fibers significantly improves the mechanical strength of the specimens. When PVA fibers with a diameter of 15 µm, length of 12 mm, and dosage of 1.6% are used, the phosphogypsum-based construction material reinforced with PVA fibers exhibits optimal performance. Under this mixing ratio, the strength values of the specimens for flexural strength, bending strength, compressive strength, and tensile strength are 10.07 MPa, 10.73 MPa, 13.25 MPa, and 2.89 MPa, respectively. Compared to the control group, the strength enhancements are 273.00%, 164.29%, 15.32%, and 99.31%, respectively. SEM scanning of the microstructure provides a preliminary explanation for the mechanism of how PVA fibers affect the workability and mechanical properties of phosphogypsum-based construction material. The findings of this study can provide a reference for the research and application of fiber-reinforced phosphogypsum-based construction material.

2.
Nat Microbiol ; 7(8): 1312-1323, 2022 08.
Artículo en Inglés | MEDLINE | ID: mdl-35902778

RESUMEN

Environmental RNA viruses are ubiquitous and diverse, and probably have important ecological and biogeochemical impacts. Understanding the global diversity of RNA viruses is limited by sampling biases, dependence on cell culture and PCR for virus discovery, and a focus on viruses pathogenic to humans or economically important animals and plants. To address this knowledge gap, we generated metatranscriptomic sequence data from 32 diverse environments in 16 provinces and regions of China. We identified 6,624 putatively novel virus operational taxonomic units from soil, sediment and faecal samples, greatly expanding known diversity of the RNA virosphere. These newly identified viruses included positive-sense, negative-sense and double-strand RNA viruses from at least 62 families. Sediments and animal faeces were rich sources of viruses. Virome compositions were affected by local environmental factors, including organic content and eukaryote species abundance. Notably, environmental factors had a greater impact on the abundance and diversity of plant, fungal and bacterial viruses than of animal viromes. Our data confirm that RNA viruses are an integral part of both terrestrial and aquatic ecosystems.


Asunto(s)
Virus ARN , Virus , Animales , China , Ecosistema , Genoma Viral , Humanos , Filogenia , Plantas , ARN , Virus ARN/genética , Viroma , Virus/genética
3.
Adv Sci (Weinh) ; 7(13): 1903661, 2020 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-32670752

RESUMEN

MicroRNAs (miRNAs) have been widely investigated as potential biomarkers for early clinical diagnosis of cancer. Developing an miRNA detection platform with high specificity, sensitivity, and exploitability is always necessary. Electrochemiluminescence (ECL) is an electrogenerated chemiluminescence technology that greatly decreases background noise and improves detection sensitivity. The development of a paper-based ECL biosensor further makes ECL suitable for point-of-care detection. Recently, clustered regularly interspaced short palindromic repeats (CRISPR)/Cas13a as high-fidelity, efficient, and programmable CRISPR RNA (crRNA) guided RNase has brought a next-generation biosensing technology. However, existing CRISPR/Cas13a based detection often faces a trade-off between sensitivity and specificity. In this research, a CRISPR/Cas13a powered portable ECL chip (PECL-CRISPR) is constructed. Wherein target miRNA activates Cas13a to cleave a well-designed preprimer, and triggers the subsequent exponential amplification and ECL detection. Under optimized conditions, a limit-of-detection of 1 × 10-15 m for miR-17 is achieved. Through rationally designing the crRNA, the platform can provide single nucleotide resolution to dramatically distinguish miRNA target from its highly homologous family members. Moreover, the introduction of "light-switch" molecule [Ru(phen)2dppz]2+ allows the platform to avoid tedious electrode modification and washing processes, thereby simplifying the experimental procedure and lower testing cost. Analysis results of miRNA from tumor cells also demonstrate the PECL-CRISPR platform holds a promising potential for molecular diagnosis.

4.
Nat Commun ; 11(1): 267, 2020 01 14.
Artículo en Inglés | MEDLINE | ID: mdl-31937772

RESUMEN

The ability to detect low numbers of microbial cells in food and clinical samples is highly valuable but remains a challenge. Here we present a detection system (called 'APC-Cas') that can detect very low numbers of a bacterial pathogen without isolation, using a three-stage amplification to generate powerful fluorescence signals. APC-Cas involves a combination of nucleic acid-based allosteric probes and CRISPR-Cas13a components. It can selectively and sensitively quantify Salmonella Enteritidis cells (from 1 to 105 CFU) in various types of samples such as milk, showing similar or higher sensitivity and accuracy compared with conventional real-time PCR. Furthermore, APC-Cas can identify low numbers of S. Enteritidis cells in mouse serum, distinguishing mice with early- and late-stage infection from uninfected mice. Our method may have potential clinical applications for early diagnosis of pathogens.


Asunto(s)
Bacterias/aislamiento & purificación , Técnicas Microbiológicas/métodos , Regulación Alostérica , Animales , Aptámeros de Nucleótidos , Sistemas CRISPR-Cas , Catálisis , ADN Bacteriano/genética , Fluorescencia , Microbiología de Alimentos , Ratones , Leche/microbiología , Reacción en Cadena en Tiempo Real de la Polimerasa , Infecciones por Salmonella/sangre , Infecciones por Salmonella/diagnóstico , Salmonella enteritidis/aislamiento & purificación
5.
Sci Rep ; 9(1): 13176, 2019 Sep 11.
Artículo en Inglés | MEDLINE | ID: mdl-31511528

RESUMEN

Diseases caused by Rickettsiales bacteria are a global public health problem. To better understand the diversity and origins of Rickettsiales infection in humans and animals, we sampled 134 febrile patients, 173 rodents and 43 shrews, as well as 358 ticks, from two cities in Jiangsu and Jiangxi provinces, China. Our data revealed a relatively high prevalence of scrub typhus cases in both localities. In addition, both serological tests and genetic analysis identified three patients infected with Anaplasma bovis, Rickettsia monacensis, and Orientia tsutsugamushi bacteria. Molecular epidemiological investigation revealed the co-circulation of multiple species of Rickettsiales bacteria in small mammals and ticks in both provinces, potentially including novel bacterial species. In sum, these data demonstrate the ongoing importance of Rickettsiales infection in China and highlight the need for the regular surveillance of local arthropods, mammals and humans.


Asunto(s)
Anaplasma/genética , Variación Genética , Orientia tsutsugamushi/genética , Rickettsia/genética , Tifus por Ácaros/epidemiología , Anciano , Anciano de 80 o más Años , Anaplasma/fisiología , Animales , China/epidemiología , Femenino , Geografía , Humanos , Masculino , Orientia tsutsugamushi/fisiología , Filogenia , Prevalencia , Rickettsia/fisiología , Rickettsiales/clasificación , Rickettsiales/genética , Roedores/microbiología , Tifus por Ácaros/microbiología , Musarañas/microbiología , Garrapatas/microbiología
6.
Micromachines (Basel) ; 10(8)2019 Aug 13.
Artículo en Inglés | MEDLINE | ID: mdl-31412540

RESUMEN

Pathogenic bacterial contamination greatly threats human health and safety. Rapidly biosensing pathogens in the early stage of infection would be helpful to choose the correct drug treatment, prevent transmission of pathogens, as well as decrease mortality and economic losses. Traditional techniques, such as polymerase chain reaction and enzyme-linked immunosorbent assay, are accurate and effective, but are greatly limited because they are complex and time-consuming. Electrochemiluminescence (ECL) biosensors combine the advantages of both electrochemical and photoluminescence analysis and are suitable for high sensitivity and simple pathogenic bacteria detection. In this review, we summarize recent advances in ECL sensors for pathogenic bacteria detection and highlight the development of paper-based ECL platforms in point of care diagnosis of pathogens.

7.
Open Forum Infect Dis ; 6(6): ofz209, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-31211156

RESUMEN

BACKGROUND: Severe fever with thrombocytopenia syndrome (SFTS) is a typical tick-borne, natural focal disease. The natural foci of SFTS were considered to exist in hilly and mountainous areas before 2015. A cluster of 3 patients exposed to a patient with a fulminant disease consistent with SFTS occurred from July to August 2015 in Dongtai County, which is characterized by alluvial plains; this prompted investigation. METHODS: The epidemiological, clinical, and laboratory features of 4 patients in the cluster were analyzed. Serum samples from the indigenous healthy population and native domesticated animals were collected to conduct laboratory tests, along with small wild animals and ticks. RESULTS: In 3 secondary case patients, high fever, thrombocytopenia and leukopenia developed within 8-13 days after contact with blood or bloody secretions from the index patient; SFTS was then diagnosed by means of reverse-transcription polymerase chain reaction. Genomic sequencing and analysis of S and L segments of 2 viral strains isolated from 2 secondary case patients showed that they shared 99.8%-99.9% homology in nucleotide sequence. The seroprevalences among indigenous healthy population, native livestock, native poultry, and small wild animals was 0.74%, 17.54%, 6.67%, and 1.12%, respectively. Three questing ticks, 61 feeding ticks, and 178 small wild animals were collected in August 2015. Survey on tick density and seasonal fluctuation in 2016 showed that ticks were active from March to October. All ticks were identified as Haemaphysalis longicornis. Severe fever with thrombocytopenia bunyavirus (SFTSV)-specific RNA was detected in the ticks collected in 2016, and the minimum SFTSV infection rate in these ticks was 0.54% (1 of 185).Wild mammals and ticks collected in August 2015 tested negative for SFTSV-specific RNA. CONCLUSIONS: Aside from hilly or mountainous area, a coastal plain was identified as the natural foci of SFTSV in Dongtai County, China. The involvement of migration in the evolution of SFTSV might lead to a transregional transmission event of SFTSV.

8.
Nature ; 561(7722): E6, 2018 09.
Artículo en Inglés | MEDLINE | ID: mdl-29946168

RESUMEN

Change history: In this Article, author Li Liu should be associated with affiliation number 5 (College of Marine Sciences, South China Agricultural University, Guangzhou, Guangdong, China), rather than affiliation number 4 (Wenzhou Center for Disease Control and Prevention, Wenzhou, Zhejiang, China). This has been corrected online.

9.
Nature ; 556(7700): 197-202, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29618816

RESUMEN

Our understanding of the diversity and evolution of vertebrate RNA viruses is largely limited to those found in mammalian and avian hosts and associated with overt disease. Here, using a large-scale meta-transcriptomic approach, we discover 214 vertebrate-associated viruses in reptiles, amphibians, lungfish, ray-finned fish, cartilaginous fish and jawless fish. The newly discovered viruses appear in every family or genus of RNA virus associated with vertebrate infection, including those containing human pathogens such as influenza virus, the Arenaviridae and Filoviridae families, and have branching orders that broadly reflected the phylogenetic history of their hosts. We establish a long evolutionary history for most groups of vertebrate RNA virus, and support this by evaluating evolutionary timescales using dated orthologous endogenous virus elements. We also identify new vertebrate-specific RNA viruses and genome architectures, and re-evaluate the evolution of vector-borne RNA viruses. In summary, this study reveals diverse virus-host associations across the entire evolutionary history of the vertebrates.


Asunto(s)
Evolución Molecular , Filogenia , Virus ARN/clasificación , Virus ARN/aislamiento & purificación , Vertebrados/clasificación , Vertebrados/virología , Anfibios/virología , Animales , Biodiversidad , Peces/virología , Genoma Viral/genética , Interacciones Huésped-Patógeno , Virus ARN/genética , Reptiles/virología , Transcriptoma
10.
BMJ Open ; 7(10): e017503, 2017 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-29092901

RESUMEN

PURPOSE: This study was established to provide direct evidence on the incidence of laboratory-confirmed influenza virus and respiratory syncytial virus (RSV) infections in older adults in two cities in Jiangsu Province, China, and the potential impact of acute respiratory infections on frailty. PARTICIPANTS: The cohort was enrolled in Suzhou and Yancheng, two cities in Jiangsu Province in Eastern China. Between November 2015 and March 2016, we enrolled 1532 adults who were 60-89 years of age, and collected blood samples along with baseline data on demographics, general health, chronic diseases, functional status and cognitive function through face-to-face interviews using a standardised questionnaire. Participants are being followed weekly throughout the year to identify acute respiratory illnesses. We schedule home visits to ill participants to collect mid-turbinate nasal and oropharyngeal swabs for laboratory testing and detailed symptom information for the acute illness. Regular follow-up including face-to-face interviews and further blood draws will take place every 6-12 months. FINDINGS TO DATE: As of 3 September 2016, we had identified 339 qualifying acute respiratory illness events and 1463 (95%) participants remained in the study. Laboratory testing is ongoing. FUTURE PLANS: We plan to conduct laboratory testing to estimate the incidence of influenza virus and RSV infections in older adults. We plan to investigate the impact of these infections on frailty and functional status to determine the association of pre-existing immune status with protection against influenza and RSV infection in unvaccinated older adults, and to assess the exposure to avian influenza viruses in this population.


Asunto(s)
Gripe Humana/epidemiología , Orthomyxoviridae , Infecciones por Virus Sincitial Respiratorio/epidemiología , Virus Sincitiales Respiratorios , Infecciones del Sistema Respiratorio/epidemiología , Factores de Edad , Anciano , Anciano de 80 o más Años , Envejecimiento , Animales , China/epidemiología , Femenino , Fragilidad , Humanos , Incidencia , Gripe Humana/virología , Masculino , Persona de Mediana Edad , Nariz/virología , Orofaringe/virología , Orthomyxoviridae/crecimiento & desarrollo , Estudios Prospectivos , Infecciones por Virus Sincitial Respiratorio/virología , Virus Sincitiales Respiratorios/crecimiento & desarrollo , Infecciones del Sistema Respiratorio/virología , Encuestas y Cuestionarios , Población Urbana
11.
Gen Comp Endocrinol ; 246: 63-70, 2017 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-28263817

RESUMEN

Type 2 diabetes (T2DM) has been considered to be associated with a higher likelihood of hearing impairment (HI). However, the molecular mechanisms underlying the association between diabetes and HI are poorly understood. MicroRNAs have recently been demonstrated to be closely associated with hearing loss and considered as promising therapeutic targets. Herein, we investigated whether miR-34a contributes to diabetes-related cochlear hair cell apoptosis and sought to identify the underlying mechanism. The results showed that miR-34a was up-regulated in the cochleas of db/db mice, accompanied by significant hearing threshold elevation and hair cell loss. However, the expression of SIRT1 was significantly down-regulated, while hypoxia-inducible factor-1alpha (HIF-1α) levels were dramatically increased in the cochleas of db/db mice. In addition, in the high-glucose cultured House Ear Institute-Organ of Corti 1 (HEI-OC1) cell line, miR-34a overexpression inhibited sirtuin1 (SIRT1) expression, increased HIF-1α levels and promoted apoptosis. MiR-34a knockdown exerted effects that were diametrically opposed to those observed with overexpression. Interestingly, HIF-1α knockdown almost eliminated the cell apoptosis induced by high glucose levels. We also examined the modulation of HIF-1α expression by SIRT1. The results showed that SIRT1 knockdown further promoted high-glucose-induced HIF-1α expression, while SIRT1 overexpression significantly inhibited HIF-1α level induced by high glucose. These findings point to a new mechanism by which miR-34a exerts its detrimental effects by negatively regulating SIRT1/HIF-1α signaling and provide new therapeutic targets for treating hearing impairment during diabetes.


Asunto(s)
Apoptosis/genética , Diabetes Mellitus Experimental/patología , Células Ciliadas Auditivas/patología , Pérdida Auditiva/patología , Subunidad alfa del Factor 1 Inducible por Hipoxia/metabolismo , MicroARNs/genética , Sirtuina 1/metabolismo , Animales , Western Blotting , Células Cultivadas , Diabetes Mellitus Experimental/genética , Diabetes Mellitus Experimental/metabolismo , Modelos Animales de Enfermedad , Regulación de la Expresión Génica , Células Ciliadas Auditivas/metabolismo , Pérdida Auditiva/etiología , Pérdida Auditiva/metabolismo , Subunidad alfa del Factor 1 Inducible por Hipoxia/genética , Masculino , Ratones , Ratones Endogámicos C57BL , ARN Mensajero/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Transducción de Señal , Sirtuina 1/genética
12.
Artículo en Chino | MEDLINE | ID: mdl-27192899

RESUMEN

OBJECTIVE: To investigate the clinical and pathological features of solitary pterygoid benign lesions, as well as the treatment and outcome of endoscopic surgery. METHOD: We retrospectively analyzed clinical data of 4 patients with pterygoid benign lesions in our department. High resolution CT and enhanced MRI were performed before the operations, then endoscopic surgeries were carried out under the circumstance of general anesthesia. After a follow-up in 12 months to 48 months, nasal endoscopy and MRI examination were performed. Therefore we are able to understand the situation of operations and postoperative recurrences, and to inquire about the changes of symptoms and the relief of symptoms before and after surgery. RESULT: From the Pathological diagnosis, it showed 2 cases of cystic lesions, 1 case of spindle cell lipoma, 1 case of inflammatory lesion. Postoperative follow up showed scar formation, smooth surface, no recurrence, and no new symptom. Nasal obstruction is relieved after the surgery, and no changes in the sympotoms of headache were observed. CONCLUSION: The combination of high resolution CT with enhanced MRI isimportant for ascertaining the location, extent and nature of the pterygoid lesions. Endoscopic surgery is a minimally invasive, safe, and effective method for the treatment of solitary pterygoid benign lesions.


Asunto(s)
Endoscopía , Obstrucción Nasal/diagnóstico , Obstrucción Nasal/cirugía , Procedimientos Quírurgicos Nasales , Quistes/diagnóstico , Quistes/cirugía , Cefalea , Humanos , Lipoma/diagnóstico , Lipoma/cirugía , Imagen por Resonancia Magnética , Recurrencia Local de Neoplasia , Nariz , Periodo Posoperatorio , Estudios Retrospectivos , Tomografía Computarizada por Rayos X
13.
Circ Cardiovasc Genet ; 9(1): 37-44, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26582766

RESUMEN

BACKGROUND: Multiple genetic loci associated with lipid levels have been identified predominantly in Europeans, and the issue of to what extent these genetic loci can predict blood lipid levels increases over time and the incidence of future hyperlipidemia remains largely unknown. METHODS AND RESULTS: We conducted a meta-analysis of genome-wide association studies of lipid levels in 8344 subjects followed by replication studies including 14 739 additional individuals. We replicated 17 previously reported loci. We also newly identified 3 Chinese-specific variants in previous regions (HLA-C, LIPG, and LDLR) with genome-wide significance. Almost all the variants contributed to lipid levels change and incident hyperlipidemia >8.1-year follow-up among 6428 individuals of a prospective cohort study. The strongest associations for lipid levels change were detected at LPL, TRIB1, APOA1-C3-A4-A5, LIPC, CETP, and LDLR (P range from 4.84×10(-4) to 4.62×10(-18)), whereas LPL, TRIB1, ABCA1, APOA1-C3-A4-A5, CETP, and APOE displayed significant strongest associations for incident hyperlipidemia (P range from 1.20×10(-3) to 4.67×10(-16)). The 4 lipids genetic risk scores were independently associated with linear increases in their corresponding lipid levels and risk of incident hyperlipidemia. A C-statistics analysis showed significant improvement in the prediction of incident hyperlipidemia on top of traditional risk factors including the baseline lipid levels. CONCLUSIONS: These findings identified some evidence for allelic heterogeneity in Chinese when compared with Europeans in relation to lipid associations. The individual variants and those cumulative effects were independent risk factors for lipids increase and incident hyperlipidemia.


Asunto(s)
Predisposición Genética a la Enfermedad , Hiperlipidemias/genética , Lípidos/genética , Polimorfismo de Nucleótido Simple , Adulto , Pueblo Asiatico , China/epidemiología , Femenino , Estudio de Asociación del Genoma Completo , Humanos , Hiperlipidemias/sangre , Hiperlipidemias/epidemiología , Incidencia , Lípidos/sangre , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Factores de Riesgo
14.
Hypertension ; 66(4): 786-92, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26283040

RESUMEN

Although multiple genetic markers associated with blood pressure have been identified by genome-wide association studies, their aggregate effect on risk of incident hypertension and cardiovascular disease is uncertain, particularly among East Asian who may have different genetic and environmental exposures from Europeans. We aimed to examine the association between genetic predisposition to higher blood pressure and risk of incident hypertension and cardiovascular disease in 26 262 individuals in 2 Chinese population-based prospective cohorts. A genetic risk score was calculated based on 22 established variants for blood pressure in East Asian. We found the genetic risk score was significantly and independently associated with linear increases in blood pressure and risk of incident hypertension and cardiovascular disease (P range from 4.57×10(-3) to 3.10×10(-6)). In analyses adjusted for traditional risk factors including blood pressure, individuals carrying most blood pressure-related risk alleles (top quintile of genetic score distribution) had 40% (95% confidence interval, 18-66) and 26% (6-45) increased risk for incident hypertension and cardiovascular disease, respectively, when compared with individuals in the bottom quintile. The genetic risk score also significantly improved discrimination for incident hypertension and cardiovascular disease and led to modest improvements in risk reclassification for cardiovascular disease (all the P<0.05). Our data indicate that genetic predisposition to higher blood pressure is an independent risk factor for blood pressure increase and incident hypertension and cardiovascular disease and provides modest incremental information to cardiovascular disease risk prediction. The potential clinical use of this panel of blood pressure-associated polymorphisms remains to be determined.


Asunto(s)
Presión Sanguínea/fisiología , Predisposición Genética a la Enfermedad , Hipertensión/genética , Polimorfismo Genético , Medición de Riesgo/métodos , Adulto , Anciano , Determinación de la Presión Sanguínea , Enfermedades Cardiovasculares/epidemiología , Enfermedades Cardiovasculares/genética , Enfermedades Cardiovasculares/fisiopatología , China/epidemiología , Femenino , Estudios de Seguimiento , Estudio de Asociación del Genoma Completo , Humanos , Hipertensión/epidemiología , Hipertensión/fisiopatología , Masculino , Persona de Mediana Edad , Morbilidad/tendencias , Estudios Prospectivos , Factores de Riesgo
15.
Am J Hypertens ; 27(1): 72-80, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24004934

RESUMEN

BACKGROUND: In the Genetic Epidemiology Network of Salt Sensitivity (GenSalt) study, we observed that blood pressure (BP) responses to dietary sodium and potassium interventions and the cold pressor test (CPT) varied greatly among individuals. We conducted a replication study to confirm our previous findings among 695 study participants. METHODS: The dietary intervention included a 7-day low sodium (51.3 mmol/day), a 7-day high sodium (307.8 mmol/day), and a 7-day high sodium with potassium supplementation (307.8 mmol sodium and 60 mmol potassium/day). BP measurements were obtained during the baseline and each intervention phase. During the CPT, BP was measured before and at 0, 1, 2, and 4 minutes after the participants immersed their right hand in ice water for 1 minute. RESULTS: Systolic and diastolic BP responses (mean ± SD (range), mm Hg) were 8.1±8.4 (-39.1 to 18.2) and -3.5±5.1 (-25.1 to 11.1) to low sodium, 9.1±8.4 (-13.3 to 33.1) and 4.0±5.4 (-16.0 to 20.7) to high sodium, and -4.6±5.8 (-31.8 to 11.6) and -1.9±4.3 (-16.9 to 14.2) to potassium supplementation, respectively (all P < 0.0001 for comparison with each former phase). The mean maximum systolic and diastolic BP responses to the CPT were 16.5±10.5 (-15.3 to 63.3) and 7.6±6.1 (-8.7 to 39.3), respectively (all P < 0.0001). CONCLUSIONS: Our study indicates that there are large variations in BP responses to dietary sodium and potassium interventions and to the CPT among individuals.


Asunto(s)
Presión Sanguínea , Frío , Dieta Hiposódica , Suplementos Dietéticos , Hipertensión/dietoterapia , Potasio en la Dieta/efectos adversos , Salud Rural , Cloruro de Sodio Dietético/efectos adversos , Vasoconstricción , Adulto , Determinación de la Presión Sanguínea , China/epidemiología , Femenino , Humanos , Hipertensión/diagnóstico , Hipertensión/epidemiología , Hipertensión/fisiopatología , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Factores de Tiempo , Resultado del Tratamiento
16.
Dalton Trans ; 43(3): 1460-70, 2014 Jan 21.
Artículo en Inglés | MEDLINE | ID: mdl-24212126

RESUMEN

Seven coordination polymers, namely [Mn(4-cptpy)2]n (1), [Co(4-cptpy)2]n (2), [Mn3(4-cptpy)6(H2O)]n·2nH2O (3), [Co(4-cptpy)(HCOO)(H2O)]n·nDMF (4), [Zn2(4-Hcptpy)2Cl4]n·2nC2H5OH·nH2O (5), [Co4(3-cptpy)4(HCOO)4(H2O)2]n (6), and [Mn(3-cptpy)2]n (7) (4-Hcptpy = 4-(4-carboxyphenyl)-4,2':6',4''-terpyridine; 3-Hcptpy = 4-(4-carboxyphenyl)-3,2':6',3''-terpyridine), have been synthesized under hydro(solvo)thermal conditions and structurally characterized. A general solvothermal method is proposed for preparing carboxylate complexes in DMF solution without any basic additive. 1 and 2 possess isostructural 3D metal-organic frameworks containing nanosized cavities. 3 is a beautiful 2D coordination polymer assembled by flower-like Mn3(4-cptpy)6(H2O) subunits. 4 and 6 both display 2D polymeric networks constructed from 4/3-cptpy(-) ligands, in which the formate ligands originate from the hydrolysis of DMF. 5 is a 1D 2(1) helical chain polymer. 7 shows a 2D network with a (3.6) two-nodal kgd topology. 4/3-Hcptpy ligands display seven types of coordination modes. The zinc complex 5 emits strong violet luminescence. 1 and 2 are both thermally stable below 440 °C and exhibit antiferromagnetic interactions.

17.
Circ Cardiovasc Genet ; 6(6): 598-607, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-24165912

RESUMEN

BACKGROUND: Blood pressure (BP) responses to dietary sodium and potassium intervention and cold pressor test vary considerably among individuals. We aimed to identify novel genetic variants influencing individuals' BP responses to dietary intervention and cold pressor test. METHODS AND RESULTS: We conducted a genome-wide association study of BP responses in 1881 Han Chinese and de novo genotyped top findings in 698 Han Chinese. Diet-feeding study included a 7-day low-sodium (51.3 mmol/d), a 7-day high-sodium (307.8 mmol/d), and a 7-day high-sodium plus potassium supplementation (60 mmol/d). Nine BP measurements were obtained during baseline observation and each intervention period. The meta-analyses identified 8 novel loci for BP phenotypes, which physically mapped in or near PRMT6 (P=7.29 × 10(-9)), CDCA7 (P=3.57 × 10(-8)), PIBF1 (P=1.78 × 10(-9)), ARL4C (P=1.86 × 10(-8)), IRAK1BP1 (P=1.44 × 10(-10)), SALL1 (P=7.01 × 10(-13)), TRPM8 (P=2.68 × 10(-8)), and FBXL13 (P=3.74 × 10(-9)). There was a strong dose-response relationship between the number of risk alleles of these independent single-nucleotide polymorphisms and the risk of developing hypertension during the 7.5-year follow-up in the study participants. Compared with those in the lowest quartile of risk alleles, odds ratios (95% confidence intervals) for those in the second, third, and fourth quartiles were 1.39 (0.97, 1.99), 1.72 (1.19, 2.47), and 1.84 (1.29, 2.62), respectively (P=0.0003 for trend). CONCLUSIONS: Our study identified 8 novel loci for BP responses to dietary sodium and potassium intervention and cold pressor test. The effect size of these novel loci on BP phenotypes is much larger than those reported by the previously published studies. Furthermore, these variants predict the risk of developing hypertension among individuals with normal BP at baseline.


Asunto(s)
Presión Sanguínea/genética , Predisposición Genética a la Enfermedad/genética , Estudio de Asociación del Genoma Completo/métodos , Polimorfismo de Nucleótido Simple , Factores de Ribosilacion-ADP/genética , Adulto , Alelos , Pueblo Asiatico/genética , China , Proteínas F-Box/genética , Femenino , Frecuencia de los Genes , Predisposición Genética a la Enfermedad/etnología , Genotipo , Humanos , Hipertensión/etnología , Hipertensión/genética , Masculino , Persona de Mediana Edad , Proteínas Nucleares/genética , Oportunidad Relativa , Potasio en la Dieta/administración & dosificación , Proteínas Gestacionales/genética , Proteína-Arginina N-Metiltransferasas/genética , Sodio en la Dieta/administración & dosificación , Factores Supresores Inmunológicos/genética , Canales Catiónicos TRPM/genética , Factores de Transcripción/genética
18.
Zhonghua Liu Xing Bing Xue Za Zhi ; 31(3): 300-3, 2010 Mar.
Artículo en Chino | MEDLINE | ID: mdl-20510058

RESUMEN

OBJECTIVE: To better understand the epidemiology of rabies during the past ten years in Yancheng city, Jiangsu province. METHODS: Data was collected and analyzed on rabies cases in Yancheng. Density and vaccination rate on Canine, Rate of injured people bit by dogs, and the information of post-exposure prophylaxis were studied. Rabies virus in the dog brains, collected around the epidemic areas of Yancheng, were detected and analyzed. RESULTS: A total of 135 human rabies cases occurred from 1999 through 2008, and formed the second epidemic peak since 1958. Of these victims, 84% (114) were farmers. In general, the rate of people having dogs were 3% - 6% per 100 people, and the injured person-times of 100 dogs were 6.37 per year. Notably, the vaccination rate of dogs was only 20%. Of those people injured by dogs and other animals, 77% had received post-exposure treatment, and only 5% - 10% had been administered anti-rabies serum. Rabies virus antigen was found in 4 (3.6%) of 111 brain specimens among dogs collected from epidemic areas. Genetic analysis of N and G genes, which were amplified from brain specimens, indicated that these viruses belong to genotype I rabies and expressing a close relationship with the Chinese vaccine strain CTN. CONCLUSION: The large number of dogs with low vaccination rate among them, together with the incorrect and low post-exposure treatment in rural areas seemed to be responsible for the outbreak of rabies in Yancheng city.


Asunto(s)
Mordeduras y Picaduras/epidemiología , Rabia/epidemiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Animales , Niño , China/epidemiología , Enfermedades de los Perros/epidemiología , Perros , Femenino , Humanos , Masculino , Persona de Mediana Edad , Profilaxis Posexposición , Virus de la Rabia/genética , Virus de la Rabia/inmunología , Adulto Joven
19.
Wei Sheng Wu Xue Bao ; 48(7): 911-6, 2008 Jul.
Artículo en Chino | MEDLINE | ID: mdl-18837369

RESUMEN

OBJECTIVE: Tetrodotoxin and its analogues (TTXs) were responsible for the poisoning incidents associated with snail Nassarius spp. We studied bacteria isolated from toxic snails as well as their habitat to probe into the relationship between bacteria and toxicity of nassariid gastropod. METHODS: Two snail samples were collected from Sheyang, Jiangsu Province on June 13 and 19, 2006, and the toxicity of the snail samples was tested with mouse bioassay method. Bacteria were isolated from the snail samples and from their habitat. A part of isolated bacteria were then cultured in the lab, and TTX in bacteria were screened with an ELISA method. RESULTS: The snails collected were identified as Nassarius semiplicatus, and the toxicity of the 2 samples were 247 mouse unit (MU) and 270 MU / 100 g tissue (wet weight), respectively. TTX was detected in 9 strains among the 14 strains of bacteria isolated from the snail samples and their habitat. TTX content in the toxic strains was very low, which ranged from 15 ng/g to 96 ng/g. Partial of the 16S ribosomal DNA (rDNA) of the toxic strains were then sequenced after PCR amplification, and the toxic strains of bacteria were tentatively identified based on the alignment of these sequences with published data. Toxic strains were closely affiliated with Vibrio, Shewanella, Planococcus, Marinomonas, Photobacterium. CONCLUSION: These findings suggested that TTX-producing bacteria may play an important role in TTX production or accumulation in nassariid gastropod.


Asunto(s)
Bacterias/aislamiento & purificación , Bacterias/metabolismo , Ecosistema , Caracoles/microbiología , Tetrodotoxina/biosíntesis , Tetrodotoxina/toxicidad , Animales , Bacterias/clasificación , Calibración , ADN Ribosómico/genética , Ratones , Filogenia , Análisis de Secuencia de ADN , Tetrodotoxina/metabolismo
20.
Zhonghua Liu Xing Bing Xue Za Zhi ; 26(4): 282-5, 2005 Apr.
Artículo en Chino | MEDLINE | ID: mdl-15941539

RESUMEN

OBJECTIVE: To determine the partial sequence of virus strains causing an aseptic meningitis outbreak in northern part of Jiangsu province in 2003 and to compare them with the same serotype strains isolated in other countries to better understand its genetic characteristics and hereditary trend of development. METHODS: Virus RNA was amplified using two sets of specific enteroviral 3' half of VP1 primers 012/011 and 040/011. Polymerase chain reaction (PCR) products were purified and sequenced. BLAST program was then used to perform on nucleotide and amino acid pairwise-alignment with all available sequences in NCBI database. Phylogenetic trees were drawed to compare with other enteroviral sequences using PHYLIP software. RESULTS: Under BLAST program, three sequences we submitted to GenBank were identically inferred as echovirus type 30, which had been identified by neutralization test in previous study. Phylogenetic analysis demonstrated that strains isolated from this outbreak were aggregated into a cluster, and the closest relationships with them were those isolated in 1999 and 2000. This phenomenon indicated that Echo30 from this outbreak was different from other strains in different epidemic area. CONCLUSION: 3' half of VP1 sequence could be used to quickly identify the serotype of isolated enterovirus. Strains isolated from this outbreak had the similar hereditary developing trend comparing with Echo30 strains isolated from other countries.


Asunto(s)
ADN Viral/genética , Brotes de Enfermedades , Enterovirus Humano B/aislamiento & purificación , Meningitis Aséptica/epidemiología , Meningitis Aséptica/virología , Secuencia de Bases , China/epidemiología , Enterovirus Humano B/genética , Femenino , Humanos , Masculino , Datos de Secuencia Molecular , Análisis de Secuencia de ADN
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