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Antiviral Activity of Gemcitabine Against Echovirus 30 Infectionin Vitro 吉西他滨体外抗埃可病毒30感染的活性研究
Q4 Immunology and Microbiology Pub Date : 2019-12-01 DOI: 10.4167/jbv.2019.49.4.203
H. Choi, Jae-Hyoung Song, Kyungah Yoon
Echovirus 30 is one of the major causes of meningitis in children and adults. The purpose of our current study was to investigate whether selected antiviral drugs could provide antiviral activity against echovirus 30. Using RD cells, we assessed the cytopathic effect of echovirus 30, including viral RNA levels as indicators of viral replication. The effects of gemcitabine were compared to rupintrivir, a well-known antiviral drug. To understand the activity gemcitabine exerts on the viral life cycle, time course and time-of-addition assays were implemented. The most effective compounds against echovirus 30 were gemcitabine and rupintrivir, as demonstrated by their concentration-dependent activity. Gemcitabine affects the early stages of echovirus 30 infection by disrupting viral replication. However, gemcitabine failed to directly inactivate echovirus 30 particles or impede viral uptake into the RD cells. Gemcitabine can be considered as a lead candidate in the development of echovirus 30 antiviral drugs, specifically in the early stages of echovirus 30 replication. Based on the results produced from the E30 in vitro assay, we conducted time course experiments to analyze the mechanism of action of gemcitabine. Viral RNA from E30 was detected using RT-PCR at various times points (4, 6, 8, 10, and 12 h post-infection) and after gemcitabine (10  M) and rupintrivir (2  M) treatment of E30-infected cells. We could find E30 viral RNA as early as 8 h post-infection. Interestingly, gemcitabine was seen to block the proliferation of E30 in resemblance to rupintrivir (inhibitor of picornavirus 3C protease, Fig. 2). Based on the results of the time course experiments, we hypothesized that the antiviral effect of gemcitabine occurs relatively early in the infection process. To observe which step is influenced by gemcitabine, we performed a time-of-addition experiment. Gemcitabine (10  M) and rupintrivir (2  M) were added to the culture medium at -1, 0, 1, 2, 4, 6, 8, 10 and 12 h after virus infection. E30 RNA replication was analyzed infection. Therefore, we concluded that the antiviral effect of gemcitabine occurs relatively early during viral infection. To realize the potential of gemcitabine as an antiviral candidate, its mechanism of activity must be understood. It is important to differentiate between viral inactivation (virucidal activity) from antiviral activity. Direct viral inactivation is an early event where the virus is inactivated before it infects the cells while antiviral activity involves killing the virus or the suppression of viral replication. It would be ideal for viral infection treatments to possess both virucidal and antiviral activities. In our study, gemcitabine did not directly interact with E30 particles as pre-exposure of the virus to gemcitabine did not alter the infectivity of E30 particles. Furthermore, addition of UTP and CTP significantly reduced the antiviral activity of gemcitabine by increasing the levels of pyrimidine
回声病毒30是导致儿童和成人脑膜炎的主要原因之一。我们目前研究的目的是调查所选的抗病毒药物是否能提供对抗回声病毒30的抗病毒活性。使用RD细胞,我们评估了回声病毒30的细胞病变效应,包括作为病毒复制指标的病毒RNA水平。将吉西他滨的效果与著名的抗病毒药物鲁匹利韦进行了比较。为了了解吉西他滨对病毒生命周期的作用,进行了时间过程和添加时间测定。对抗回声病毒30最有效的化合物是吉西他滨和鲁平替韦,其浓度依赖性活性证明了这一点。吉西他滨通过破坏病毒复制影响回声病毒30感染的早期阶段。然而,吉西他滨未能直接灭活回声病毒30颗粒或阻碍病毒摄入RD细胞。吉西他滨可以被认为是开发回声病毒30抗病毒药物的主要候选药物,特别是在回声病毒30复制的早期阶段。基于E30体外试验的结果,我们进行了时间过程实验来分析吉西他滨的作用机制。在不同时间点(感染后4、6、8、10和12小时)和吉西他滨(10 M) 和rupintrivir(2 M) E30感染细胞的处理。我们最早可以在感染后8小时发现E30病毒RNA。有趣的是,吉西他滨可以阻断E30的增殖,类似于rupintrivir(小核糖核酸病毒3C蛋白酶抑制剂,图2)。根据时间进程实验的结果,我们假设吉西他滨的抗病毒作用在感染过程中相对较早发生。为了观察哪一步受到吉西他滨的影响,我们进行了一次添加时间实验。吉西他滨(10 M) 和rupintrivir(2 M) 在病毒感染后的-1、0、1、2、4、6、8、10和12小时加入培养基中。E30 RNA复制分析感染。因此,我们得出结论,吉西他滨的抗病毒作用在病毒感染期间相对较早发生。为了实现吉西他滨作为抗病毒候选药物的潜力,必须了解其活性机制。区分病毒灭活(杀病毒活性)和抗病毒活性是很重要的。直接病毒灭活是一种早期事件,病毒在感染细胞之前被灭活,而抗病毒活性涉及杀死病毒或抑制病毒复制。同时具有杀病毒和抗病毒活性将是病毒感染治疗的理想选择。在我们的研究中,吉西他滨不直接与E30颗粒相互作用,因为病毒预暴露于吉西他宾不会改变E30颗粒的传染性。此外,UTP和CTP的添加通过增加嘧啶核苷酸的水平显著降低了吉西他滨的抗病毒活性。吉西他滨的抗回声病毒活性可以通过在转化为吉西他宾三磷酸后降低CTP和UTP的水平来改变。因此,本研究表明吉西他滨可能具有抗E30的抗病毒活性。它不会直接灭活E30颗粒,但通过干扰病毒复制影响E30感染的初始阶段。吉西他滨治疗诱导的抗病毒活性可以通过在转化为吉西他宾三磷酸后降低CTP和UTP的水平来调节。这些结果可用于设计用作抗病毒药物的新抑制剂。
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引用次数: 0
Aralia cordataExtract Activates NF-κB and MAPK Signaling Pathways and Induces Pro-inflammatory Changes in RAW264.7 Macrophages 木耳提取物激活NF-κB和MAPK信号通路,诱导RAW264.7巨噬细胞促炎改变
Q4 Immunology and Microbiology Pub Date : 2019-12-01 DOI: 10.4167/jbv.2019.49.4.153
D. Seo, Yong-il Cho, Y. Yi, Sang-Myeong Lee
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引用次数: 0
Identification of Candida Species Using 26S Ribosomal RNA Gene Sequencing in Patients with Periodontitis 应用26S核糖体RNA基因测序技术鉴定牙周炎患者念珠菌属
Q4 Immunology and Microbiology Pub Date : 2019-12-01 DOI: 10.4167/jbv.2019.49.4.212
N. N. Al-Dabbagh, Wissam Hamid Al-janabi, M. Al-Shuhaib
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). The infection with Candida spp. for oral cavity is being increasingly reported. However, its variations have not yet been specifically described in periodontitis. The present study was conducted to use an uniplex 26S rRNAbased amplicons to detect and discriminate Candida using only one pair of ribosomal primers. A total of 50 patients with chronic periodontitis was involved in the study. Pure Candida colonies were isolated from 23 patients and genomic DNA was extracted, and PCR was conducted. Direct DNA sequencing followed by comprehensive phylogenetic analyses were performed to confirm the identity of Candida colonies. Results indicated that the ration of Candida-infected patients was 46%, with a high prevalence of C. albicans, followed by remarkably lower ratios of C. parapsilosis, C. glabrata, C. kefyr, and C. dubliniensis respectively. Phylogenetic analyses indicated obvious discrimination amongst the analyzed Candida species as each observed species occupied a distinctive phylogenetic position. The current results reported a simple, efficient, and low-cost detection of five species of Candida without the need for other costly techniques of molecular screening. The current findings may help dentists to easily take a snapshot of the patterns of Candida infection in periodontitis cases to assess the nature and grade of infection.
©这是一篇根据知识共享署名非商业许可条款分发的开放获取文章(http://creativecommons.org/license/by-nc/3.0/)。口腔念珠菌感染的报道越来越多。然而,其变异尚未在牙周炎中得到具体描述。本研究仅使用一对核糖体引物,使用基于单联26S rRNA的扩增子来检测和区分念珠菌。共有50名慢性牙周炎患者参与了这项研究。从23名患者中分离出纯念珠菌菌落,提取基因组DNA,并进行PCR。进行直接DNA测序,然后进行全面的系统发育分析,以确认念珠菌菌落的身份。结果表明,念珠菌感染患者的比例为46%,白色念珠菌的患病率较高,其次是副psilosis念珠菌、光滑念珠菌、kefyr念珠菌和都柏林念珠菌。系统发育分析表明,所分析的念珠菌物种之间存在明显的差异,因为每个观察到的物种都占据着独特的系统发育位置。目前的结果报告了一种简单、高效、低成本的五种念珠菌检测方法,而不需要其他昂贵的分子筛选技术。目前的研究结果可能有助于牙医轻松掌握牙周炎患者念珠菌感染的模式,以评估感染的性质和级别。
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引用次数: 0
Analysis of Integrons and Antimicrobial Resistances of Multidrug ResistantEscherichia coliIsolated in Korea 韩国多药耐药大肠杆菌的整合子及耐药性分析
Q4 Immunology and Microbiology Pub Date : 2019-12-01 DOI: 10.4167/jbv.2019.49.4.176
Yun-Yi Yang, M. Suh
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Antibacterial drugs are one of the most important therapeutic agents of bacterial infections but multidrug resistant Escherichia coli (MDREC) is an increasing problem worldwide. Major resistance mechanism of MDREC is horizontal gene transfer of R plasmids harboring integrons, which the integron integrase (IntI) catalyzes gene cassette insertion and excision through site specific recombination. In this study, resistance profiles of integron harboring E. coli isolated in Korea and the genetic environments of integron gene cassettes were analyzed by PCR and direct sequencing to clarify the mechanisms of spread of integron harboring E. coli. Resistance rates of integron harboring E. coli, including β-lactams, aminoglycosides, and fluoroquinolones and MDR frequencies were significantly higher than that of E. coli without integron (p<0.01). Majority (80%) of integron harboring E. coli showed resistance transfer by conjugation. Most (80%) of E. coli had dfrA17-aadA5 cassette array and PcH1 hybrid promoter; 16.7% of E. coli had dfrA12-orfF-aadA2 cassette array and PcW promoter. The higher prevalence of weak Pc variants among most (96.7%) of integron harboring MDREC suggests that a flexible cassette array is more important than enhanced expression. All the integrons had LexA binding motif suggests that SOS responses control the expression of these integrons. In conclusion, the genetic bases of integrons were diverse, and the spread and the expression of prevalent gene cassette arrays may be deeply related with strengths of Pc promoters in integrons. These informations will provide important knowledge to control the increase of integron harboring MDREC.
©这是一篇基于知识共享署名非商业许可协议(http://creativecommons.org/ License /by-nc/3.0/)的开放获取文章。抗菌药物是治疗细菌感染最重要的药物之一,但耐多药大肠杆菌(MDREC)是一个日益严重的世界性问题。MDREC的主要耐药机制是携带整合子的R质粒的水平基因转移,整合子整合酶(IntI)通过位点特异性重组催化基因盒的插入和切除。本研究采用PCR和直接测序的方法,分析了韩国分离的含整合子大肠杆菌的耐药谱和整合子基因盒的遗传环境,以阐明含整合子大肠杆菌的传播机制。含整合子的大肠杆菌对β-内酰胺类、氨基糖苷类、氟喹诺酮类药物的耐药率和耐多药频次均显著高于未含整合子的大肠杆菌(p<0.01)。大多数(80%)携带整合子的大肠杆菌通过偶联转移抗性。大多数(80%)大肠杆菌具有dfrA17-aadA5盒式阵列和PcH1杂交启动子;16.7%的大肠杆菌含有dfrA12-orfF-aadA2盒式阵列和PcW启动子。在大多数(96.7%)携带MDREC的整合子中,弱Pc变体的患病率较高,这表明灵活的盒式阵列比增强表达更重要。所有整合子都含有LexA结合基序,表明SOS应答控制了这些整合子的表达。综上所述,整合子的遗传基础是多样的,普遍基因盒阵列的传播和表达可能与整合子中Pc启动子的强度密切相关。这些信息将为控制携带MDREC的整合子的增加提供重要的知识。
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引用次数: 1
p90RSK Activation Promotes Epithelial-Mesenchymal Transition in Cisplatin-Treated Triple-Negative Breast Cancer Cells p90RSK激活促进顺铂治疗的三阴性乳腺癌症细胞的上皮-间充质转化
Q4 Immunology and Microbiology Pub Date : 2019-12-01 DOI: 10.4167/jbv.2019.49.4.221
Yujin Jin, K. Heo
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). p90 ribosomal S6 kinase (p90RSK), one of the downstream effectors in ERK1/2 pathways, shows high expression in human breast cancer tissues. However, its role in breast cancer development and drug resistance is not fully understood. Here, we demonstrate that Cis-DDP treatment failed to increase cytotoxicity in MDA-MB-231 cells compared to MCF-7 cells and p90RSK activation was involved in Cis-DDP-resistance to MDA-MB-231 cells. In the study, we found that inhibition of p90RSK expression or activation using a small interfering RNA (siRNA) or dominant-negative kinase mutant (DN-p90RSK) plasmid overexpression increased Cis-DDP-induced cytotoxicity of MDA-MB-231 cells, respectively. Mechanistically, we found that Cis-DDP resistance was associated with up-regulation of epithelial growth factor (EGF) expression and EGF treatment induced cancer survival signaling pathway including activation of ERK1/2, p90RSK, and Akt. We also examined the expression of epithelial-mesenchymal transition (EMT)-associated proteins using a reverse transition-quantitative PCR analysis. Cis-DDP treatment induced EMT by increasing the expression levels of N-cadherin, Snail, and Twist, while decreasing the expression levels of E-cadherin. Furthermore, we examined the epithelial marker, Zonula occludens-1 (ZO-1) using immunofluorescence analysis and found that Cis-DDP-inhibited ZO-1 expression was recovered by p90RSK deactivated condition. Therefore, we conclude that Cis-DDP resistance is involved in EMT via regulating the EGF-mediated p90RSK signaling pathway in MDA-MB-231 cells.
©这是一篇根据知识共享署名非商业许可条款分发的开放获取文章(http://creativecommons.org/license/by-nc/3.0/)。p90核糖体S6激酶(p90RSK)是ERK1/2通路的下游效应物之一,在人类癌症组织中显示高表达。然而,它在癌症发展和耐药性中的作用尚不完全清楚。在这里,我们证明了与MCF-7细胞相比,Cis-DDP处理未能增加MDA-MB-231细胞的细胞毒性,并且p90RSK激活参与了Cis-DDP-对MDA-MB/231细胞的耐药性。在该研究中,我们发现使用小干扰RNA(siRNA)或显性阴性激酶突变体(DN-p90RSK)质粒过表达抑制p90RSK的表达或激活分别增加了Cis-DDP诱导的MDA-MB-231细胞的细胞毒性。从机制上讲,我们发现Cis-DDP耐药性与上皮生长因子(EGF)表达的上调和EGF治疗诱导的癌症生存信号通路有关,包括ERK1/2、p90RSK和Akt的激活。我们还使用反向转化定量PCR分析检测了上皮-间充质转化(EMT)相关蛋白的表达。顺铂通过增加N-钙粘蛋白、Snail和Twist的表达水平,同时降低E-钙粘蛋白的表达水平来诱导EMT。此外,我们使用免疫荧光分析检测了上皮标记物闭塞带蛋白-1(ZO-1),发现Cis-DDP抑制的ZO-1表达通过p90RSK失活条件恢复。因此,我们得出结论,顺铂耐药性通过调节MDA-MB-231细胞中EGF介导的p90RSK信号通路参与EMT。
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引用次数: 1
World Outbreak Trend of Infectious Diseases with Surveillance 世界传染病暴发趋势及监测
Q4 Immunology and Microbiology Pub Date : 2019-09-01 DOI: 10.4167/jbv.2019.49.3.141
S. Choi, J. H. Kim, Ji Yeon Kim, E. Hwang
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). The diverse infectious diseases can occur everywhere in the world, but high-risk infectious diseases should be monitored immediately after the occurrence, and be controlled not to spread to the public. Other highly contagious ones also should be screened with the surveillance system and made to be prevented from a serious effect on public health. The outbreak information, articles and news reports concerning global infectious disease outbreaks were collected from known web-based resources and deposited in Global Center for Infectious Diseases since 2016. The number of reports collected from various sources was analyzed on the respect of Blueprint priority diseases and vaccine-preventable diseases, and the characteristic outbreak trend was shown in the geographic distribution and the so-called socio-economic level of countries. The WHO R&D Blueprint priority diseases are being reported especially in the region of Africa and Asia. The vaccine-preventable and other infectious diseases also are reported continuously and world-widely. They threaten the safety of life continuously in public. Therefore, keeping close observation and strengthening infectious disease surveillance is needed, and more effort to expand the collecting resources to get more outbreak information is warranted.
©这是一篇基于知识共享署名非商业许可协议(http://creativecommons.org/ License /by-nc/3.0/)的开放获取文章。世界上任何地方都可能发生各种各样的传染病,但高风险传染病发生后应立即进行监测,控制不向公众传播。其他高传染性疾病也应通过监测系统进行筛查,防止对公共卫生造成严重影响。自2016年以来,从已知的网络资源中收集有关全球传染病暴发的疫情信息、文章和新闻报道,并存入全球传染病中心。就蓝图重点疾病和疫苗可预防疾病方面,分析了从各种来源收集的报告数量,并在地理分布和所谓的国家社会经济水平上显示了特有的爆发趋势。世卫组织研发蓝图的重点疾病正在报告中,特别是在非洲和亚洲区域。疫苗可预防的疾病和其他传染病也在世界范围内不断得到报告。他们在公共场合不断威胁着生命安全。因此,需要密切观察和加强传染病监测,并进一步努力扩大收集资源,以获得更多的疫情信息。
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引用次数: 3
Rapid Whole-genome Sequencing of Zika Viruses using Direct RNA Sequencing 利用直接RNA测序技术对寨卡病毒进行快速全基因组测序
Q4 Immunology and Microbiology Pub Date : 2019-09-01 DOI: 10.4167/jbv.2019.49.3.115
J. H. Kim, Ji Yeon Kim, Bon-Sang Koo, H. Oh, J. Hong, E. Hwang
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Zika virus (ZIKV) is one of the pathogens which is transmitted world widely, but there are no effective drugs and vaccines. Whole genome sequencing (WGS) of viruses could be applied to viral pathogen characterization, diagnosis, molecular surveillance, and even finding novel pathogens. We established an improved method using direct RNA sequencing with Nanopore technology to obtain WGS of ZIKV, after adding poly (A) tails to viral RNA. This established method does not require specific primers, complimentary DNA (cDNA) synthesis, and polymerase chain reaction (PCR)-based enrichment, resulting in the reduction of biases as well as of the ability to find novel RNA viruses. Nanopore technology also allows to read long sequences. It makes WGS easier and faster with long-read assembly. In this study, we obtained WGS of two strains of ZIKV following the established protocol. The sequenced reads resulted in 99% and 100% genome coverage with 63.5X and 21,136X, for the ZIKV PRVABC59 and MR 766 strains, respectively. The sequence identities of the ZIKV PRVABC59 and MR 766 strains for each reference genomes were 98.76% and 99.72%, respectively. We also found that the maximum length of reads was 10,311 bp which is almost the whole genome size of ZIKV. These long-reads could make overall structure of whole genome easily, and WGS faster and easier. The protocol in this study could provide rapid and efficient WGS that could be applied to study the biology of RNA viruses including identification, characterization, and global surveillance.
©这是一篇根据知识共享署名非商业许可条款分发的开放获取文章(http://creativecommons.org/寨卡病毒是世界范围内广泛传播的病原体之一,但目前尚无有效的药物和疫苗。病毒全基因组测序(WGS)可用于病毒病原体的鉴定、诊断、分子监测,甚至寻找新的病原体。我们建立了一种改进的方法,使用纳米孔技术直接测序,在病毒RNA中添加poly(A)尾后,获得ZIKV的WGS。这种已建立的方法不需要特异性引物、互补DNA(cDNA)合成和基于聚合酶链式反应(PCR)的富集,从而减少了偏差以及发现新RNA病毒的能力。纳米孔技术还允许读取长序列。它使WGS更容易和更快的长读汇编。在本研究中,我们按照既定方案获得了两株ZIKV的WGS。ZIKV PRVABC59和MR 766菌株的测序读数分别导致99%和100%的基因组覆盖率,分别为63.5X和21136X。ZIKV PRVABC59和MR 766菌株对每个参考基因组的序列同源性分别为98.76%和99.72%。我们还发现,读取的最大长度为10311bp,几乎是ZIKV的整个基因组大小。这些长的读数可以使整个基因组的整体结构变得容易,并且WGS更快更容易。本研究中的方案可以提供快速有效的WGS,可用于研究RNA病毒的生物学,包括鉴定、表征和全球监测。
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引用次数: 1
Recharacterization of the Canine Adenovirus Type 1 Vaccine Strain based on the Biological and Molecular Properties 基于生物学和分子特性的犬腺病毒1型疫苗株的再鉴定
Q4 Immunology and Microbiology Pub Date : 2019-09-01 DOI: 10.4167/jbv.2019.49.3.124
Dong-Kun Yang, Ha-Hyun Kim, Eunjung Lee, J. Yoo, Soon-Seek Yoon, Jungwon Park, C. Kim, Ho Kim
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Canine adenovirus type 1 (CAV-1) infection results in hepatitis in dogs. In this study, we investigated the biologic and genetic characteristics of the CAV-1 vaccine strain (CAV1V) to improve quality control about CAV vaccine. The identity of CAV1V as CAV-1 was confirmed based on its cytopathic effects and the results of hemagglutination (HA) and immunofluorescence assays, and electron microscopy. The CAV1V strain reached 10 7.5 TCID50/mL in MDCK cells at 4 days post-inoculation and exhibited hemmagglutination activity of 256 U using guinea pig erythrocytes. Intranuclear fluorescence in the infected cells was observed and typical adenoviruses were observed in electon microscope. CAV1V strain was identified as a CAV-1 strain by nucleotide sequence analysis. In a comparison of the nucleotide sequences of the fiber genes of several CAV strains, CAV1V showed the highest similarity (99.8%) with the GLAXO strain, which was isolated in Canada. Our biological characterization of CAV1V will facilitate quality control of the canine hepatitis vaccine.
©这是一篇基于知识共享署名非商业许可协议(http://creativecommons.org/ License /by-nc/3.0/)的开放获取文章。犬腺病毒1型(CAV-1)感染导致犬肝炎。本研究对CAV-1疫苗株(CAV1V)的生物学和遗传特性进行了研究,旨在提高CAV疫苗的质量控制水平。根据其细胞病变作用、血凝(HA)和免疫荧光检测以及电镜检查结果,证实了CAV1V为CAV-1。接种4天后,CAV1V菌株在MDCK细胞中达到10 7.5 TCID50/mL,在豚鼠红细胞中表现出256 U的血凝活性。电镜下观察感染细胞核内荧光和典型腺病毒。经核苷酸序列分析,鉴定为CAV-1型毒株。对几种CAV菌株纤维基因的核苷酸序列进行比较,CAV1V与加拿大分离的GLAXO株的相似性最高(99.8%)。CAV1V的生物学特性将为犬肝炎疫苗的质量控制提供依据。
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引用次数: 6
Histopathological Evaluation of the Efficacy for Plant-produced E2 Protein Vaccine against Classical Swine Fever Virus (CSFV) in Piglets 猪经典猪瘟病毒(CSFV)植物E2蛋白疫苗免疫效果的组织病理学评价
Q4 Immunology and Microbiology Pub Date : 2019-09-01 DOI: 10.4167/jbv.2019.49.3.133
Sun Young Kim, Bo-Kyoung Jung, G. Park, Hye-Ran Kim, D. An, Eun-Ju Shon, Kyung-Soo Chang
Sun-Young Kim, Bo-Kyoung Jung, Gyu-Nam Park, Hye-Ran Kim, Dong-Jun An, Eun-Ju Shon and Kyung-Soo Chang 1Department of Pathology, Dongnam Institute of Radiological and Medical Sciences, Busan 46033, Republic of Korea; 2Department of Clinical Laboratory Science, College of Health Sciences, Catholic University of Pusan, Busan 46252, Republic of Korea; 3Animal and Plant Quarantine and Inspection Agency (QIA), 177, Hyeoksin 8-ro, Gimcheon-si, Gyengsangbuk-do 39660 Republic of Korea; 4Department of Clinical Laboratory Science, College of Medical Sciences, Daegu Haany University, Gyeongsan 38610, Republic of Korea; 5BioApplications Inc., Pohang Techno Park Complex, 394 Jigok-ro Nam-gu, Pohang 37668, Korea; 6Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang 37673, Korea
金善英、郑宝景、朴圭南、金惠兰、安东俊、顺恩柱、张敬洙1韩国东南放射医学研究所病理学系,釜山46033;2釜山天主教大学卫生科学学院临床检验学系,釜山46252;3韩国庆尚北道金川市赫新8路177号动植物检疫检验局(QIA) 39660;4大邱哈尔滨大学医学部临床检验学系,韩国庆山38610;5韩国浦项南区志谷路394号浦项科技园园区生物应用公司;6浦项理工大学综合生物科学与生物技术学院,浦项37673
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引用次数: 0
Role of Particulate Matter in Skin Inflammation 颗粒物在皮肤炎症中的作用
Q4 Immunology and Microbiology Pub Date : 2019-06-01 DOI: 10.4167/JBV.2019.49.2.89
Madeeha Arooj, Y. Koh
©This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Environmental pollution is a major global problem that affects human health. Among different types of environmental pollution, particulate matter (PM) has a key role. As PM spreads in the air so it causes different bronchial and skin inflammatory conditions. PM increases oxidative stress by ROS production and pro-inflammatory cytokines. As a result, matrix metalloproteinase is also produced, such as MMP1, MMP9 and MMP2 that is a known major cause of skin collagen degradation. Recently it has been shown that the PM worsens allergic conditions like dermatitis, psoriasis, and skin cancer. Different extensive efforts have been made across the globe to control this PM.
©这是一篇根据知识共享署名非商业许可条款分发的开放获取文章(http://creativecommons.org/license/bync/3.0/)。环境污染是影响人类健康的一个重大全球问题。在不同类型的环境污染中,颗粒物(PM)起着关键作用。当PM在空气中传播时,它会引起不同的支气管和皮肤炎症。PM通过产生ROS和促炎细胞因子增加氧化应激。结果,还产生基质金属蛋白酶,如MMP1、MMP9和MMP2,这是已知的皮肤胶原降解的主要原因。最近有研究表明,PM会加重过敏性疾病,如皮炎、牛皮癣和皮肤癌症。为了控制这一PM,全球范围内已经做出了不同的广泛努力。
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引用次数: 1
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Journal of Bacteriology and Virology
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