genotypes

基因型
  • 文章类型: Journal Article
    小反刍动物慢病毒(SRLV)引起多系统,绵羊和山羊的变性和慢性疾病。有五种基因型(A,B,C,D和E),其中A和B是最普遍的。这项研究的目的是评估EradkitSRLV基因分型ELISA的血清分型效率和新开发的巢式实时PCR的分子分型效率,该PCR靶向长末端重复序列gag(LTR-gag)区域,使用感染了已知在波兰流通的SRLV亚型的动物样品。
    对34只绵羊和63只山羊的97份血清样本进行了免疫测定,用PCR检测了31只绵羊和55只山羊的86份DNA样本。所有反刍动物均被A1,A5,A12,A13,A16,A17,A18,A23,A24,A27,B1和B2亚型的已知SRLV菌株感染。
    总共69(80.2%,86个测试样品中的95%置信区间71.6%-88.8%)在PCR中给出了阳性结果。在86个样本中的17个(19.8%)中,未检测到SRLV的前病毒DNA。通过PCR进行的MVV(基因型A)和CAEV(基因型B)之间的区别总是与预先的系统发育分析相匹配。没有观察到交叉反应性。另一方面,通过较早的系统发育分析和EradikitSRLV基因分型ELISA进行基因分型的样本比例为42.3%.该测试无法对40.2%的样本进行分类,17.5%的血清分类不正确。
    我们的结果表明,EradikitSRLV基因分型试剂盒不是预测SRLV基因型的可靠方法,虽然基于LTR-gag区域的嵌套实时PCR确实被证明是,至少对于基因型A和B。
    UNASSIGNED: Small ruminant lentiviruses (SRLV) cause multisystemic, degenerative and chronic disease in sheep and goats. There are five genotypes (A, B, C, D and E), of which A and B are the most widespread. The purpose of this study was to evaluate the serotyping efficiency of the Eradikit SRLV Genotyping ELISA and the molecular typing efficiency of a newly developed nested real-time PCR targeting the long terminal repeat-gag (LTR-gag) region using samples from animals infected with subtypes of SRLV known to circulate in Poland.
    UNASSIGNED: A total of 97 sera samples taken from 34 sheep and 63 goats were immunoassayed, and 86 DNA samples from 31 sheep and 55 goats were tested with the PCR. All ruminants were infected with known SRLV strains of the A1, A5, A12, A13, A16, A17, A18, A23, A24, A27, B1 and B2 subtypes.
    UNASSIGNED: A total of 69 (80.2%, 95% confidence interval 71.6%-88.8%) out of 86 tested samples gave positive results in the PCR. In 17 out of the 86 (19.8%) samples, no proviral DNA of SRLV was detected. The differentiation between MVV (genotype A) and CAEV (genotype B) by PCR matched the predating phylogenetic analysis invariably. No cross-reactivity was observed. On the other hand, the proportion of samples genotyped the same by the older phylogenetic analysis and the Eradikit SRLV Genotyping ELISA was 42.3%. The test was unable to classify 40.2% of samples, and 17.5% of sera were incorrectly classified.
    UNASSIGNED: Our results showed that the Eradikit SRLV genotyping kit is not a reliable method for predicting SRLV genotype, while the nested real-time PCR based on the LTR-gag region did prove to be, at least for genotypes A and B.
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    文章类型: Journal Article
    动脉粥样硬化性心血管疾病的主要可改变的危险因素是脂质和脂蛋白代谢异常,这在HIV及其治疗中很常见。Apo-E是一种在血浆脂质稳态中很重要的蛋白质,其遗传等位基因已被证明有助于脂质异常。我们研究了Apo-E基因多态性对蛋白酶抑制剂治疗PLHIV血浆脂质水平的影响。
    这是一项对感染艾滋病毒的成年人进行的横断面研究。脂质轮廓,在空腹血浆中测量Apo-B和Apo-A。使用SeeplexApo-EACE基因分型试剂盒测定Apo-E基因型的扩增和分析。将定量值的差异与非参数分析方法进行比较。
    招募了84人参加研究,75%的人被病毒抑制。3个纯合基因型的低密度脂蛋白胆固醇(LDL-C)水平差异显著,载脂蛋白B(Apo-B)和载脂蛋白A1(Apo-A1)。apoε2/ε2患者的LDL-C高于apoε3/ε3患者(3.26(3.61)mmol/Lvs.2.76(1.28)mmol/L,p=0.010)。与apoε3/ε3相比,apoε4/ε4的Apo-A1较低(0.84(0.48)g/dL与1.27(0.70)g/dL,p=0.009)。与同组相比,杂合基因型,载脂蛋白ε2/ε3的甘油三酯水平较低:1.33(0.65)mmol/Lvs.1.86(1.11)mmol/L,p=0.045。
    Apo-E基因的多态性可能对PI治疗的PLHIV中的血浆脂质和载脂蛋白水平有重大影响。这可能对评估心血管疾病的风险有影响。
    UNASSIGNED: A major modifiable risk factor for atherosclerotic cardiovascular disease is abnormalities in lipid and lipoprotein metabolism which are frequently seen in HIV as well as its treatment. Apo-E is a protein that is important in plasma lipid homeostasis and its genetic alleles have been shown to contribute to lipid abnormalities. We examined for the effect of Apo-E gene polymorphisms on plasma lipid levels in PLHIV on protease inhibitor therapy.
    UNASSIGNED: This was a cross-sectional study conducted among adult persons living with HIV. Lipid profile, Apo-B and Apo-A were measured in fasting plasma. Amplification and analysis of Apo-E genotypes were determined using the Seeplex Apo-E ACE genotyping kit. Differences in quantitative values were compared with non-parametric analysis methods.
    UNASSIGNED: Eighty-four persons were recruited into the study, 75% of whom were virally suppressed. The 3 homozygous genotypes had significantly different levels of low-density lipoprotein cholesterol (LDL-C), Apolipoprotein B (Apo-B) and Apolipoprotein A1 (Apo-A1). Persons with apo ε2/ε2 had higher LDL-C compared to those with apo ε3/ε3 (3.26 (3.61) mmol/L vs. 2.76 (1.28) mmol/L, p = 0.010). Those with apo ε4/ε4 had lower Apo-A1 compared to those with apo ε3/ε3 (0.84 (0.48) g/dL vs. 1.27 (0.70) g/dL, p =0.009). Compared with the same group, the heterozygous genotype, apo ε2/ε3 had lower triglyceride levels :1.33 (0.65) mmol/ L vs. 1.86 (1.11) mmol/L, p = 0.045.
    UNASSIGNED: Polymorphisms in the Apo-E gene may have significant influences on plasma lipid and apolipoprotein levels in PLHIV on PI therapy. This may have implications for the assessment of risk for cardiovascular disease.
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  • 文章类型: Journal Article
    腹泻,通常由轮状病毒(RV)和诺如病毒(NV)引起,是全球健康问题。本研究集中于济宁市2021年至2022年的RV和NV。在2021年至2022年之间,共收集了1052个腹泻样本。实时定量荧光逆转录酶-PCR检测RV-A,NVGI,和NVGII。对于RV-A阳性样本,VP7和VP4基因测序用于基因型分析,其次是进化树的建造。同样,对于NV-GII阳性样本,对VP1和RdRp基因进行测序以进行基因型分析,随后建造了进化树。在2021年至2022年之间,济宁市的检出率各不相同:仅RV-A(不包括RV-A和NVGII的合并感染)为7.03%,NVGI为0.10%,仅NVGII(不包括RV-A和NVGII的共感染)为5.42%,RV-A和NVGII共感染1.14%。最高的RV-A比率显示在≤1岁和2-5岁的儿童中。济宁,金乡县,和梁山县的RV-A比率明显较高,分别为24.37%(不包括RV-A和NVGII的合并感染)和18.33%(不包括RV-A和NVGII的合并感染),分别。济宁,曲阜市,微山没有RV-A阳性。微山的NVGII比率最高,为35.48%(不包括RV-A和NVGII的共感染)。基因型分析显示,2021年,G9P[8]和G2P[4]占主导地位,分别为94.44%和5.56%,分别。2022年,G8P[8],G9P[8],G1P[8]突出,为75.86%,13.79%,10.35%,分别。2021年,GII.3[P12],GII.4[P16],GII.4[P31]占71.42%,14.29%,和14.29%,分别。2022年,GII.3[P12]和GII.4[P16]分别占55.00%和45.00%,分别。RV-A和NV在不同的时间范围内显示出不同的模式,年龄组,和济宁市内的地区。从2021年到2022年,济宁市流行的RV-A和NVGII菌株也发生了基因型变化。建议对RV-A和NV进行持续监测,以进行有效的预防和控制。
    Diarrhea, often caused by viruses like rotavirus (RV) and norovirus (NV), is a global health concern. This study focuses on RV and NV in Jining City from 2021 to 2022. Between 2021 and 2022, a total of 1052 diarrhea samples were collected. Real-Time Quantitative Fluorescent Reverse Transcriptase-PCR was used to detect RV-A, NV GI, and NV GII. For RV-A-positive samples, VP7 and VP4 genes were sequenced for genotype analysis, followed by the construction of evolutionary trees. Likewise, for NV-GII-positive samples, VP1 and RdRp genes were sequenced for genotypic analysis, and evolutionary trees were subsequently constructed. Between 2021 and 2022, Jining City showed varying detection ratios: RV-A alone (excluding co-infection of RV-A and NV GII) at 7.03%, NV GI at 0.10%, NV GII alone (excluding co-infection of RV-A and NV GII) at 5.42%, and co-infection of RV-A and NV GII at 1.14%. The highest RV-A ratios were shown in children ≤1 year and 2-5 years. Jining, Jinxiang County, and Liangshan County had notably high RV-A ratios at 24.37% (excluding co-infection of RV-A and NV GII) and 18.33% (excluding co-infection of RV-A and NV GII), respectively. Jining, Qufu, and Weishan had no RV-A positives. Weishan showed the highest NV GII ratios at 35.48% (excluding co-infection of RV-A and NV GII). Genotype analysis showed that, in 2021, G9P[8] and G2P[4] were dominant at 94.44% and 5.56%, respectively. In 2022, G8P[8], G9P[8], and G1P[8] were prominent at 75.86%, 13.79%, and 10.35%, respectively. In 2021, GII.3[P12], GII.4[P16], and GII.4[P31] constituted 71.42%, 14.29%, and 14.29%, respectively. In 2022, GII.3[P12] and GII.4[P16] accounted for 55.00% and 45.00%, respectively. RV-A and NV showed varying patterns for different time frames, age groups, and regions within Jining. Genotypic shifts were also observed in prevalent RV-A and NV GII strains in Jining City from 2021 to 2022. Ongoing monitoring of RV-A and NV is recommended for effective prevention and control.
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  • 文章类型: Journal Article
    (1)背景:我们确定了在博茨瓦纳农村和城市周边地区没有人类免疫缺陷病毒(HIV)的人群中乙型肝炎病毒(HBV)的患病率。(2)方法:我们从博茨瓦纳联合预防计划(BCPP)(2013-2018)随机选择的无HIV人群(n=2135)的存档血浆样本中筛选了乙型肝炎表面抗原(HBsAg)。我们使用BigDye测序化学对415bp的表面区域进行了测序。(3)结果:参与者的中位年龄为31岁(IQR:24-46),女性占64%(1360/2135)。HBV患病率为4.0%(86/2135)[95%CI:3.3-4.9]),范围在0-9.2%之间。年龄较大的参与者(>35岁)HBV阳性的几率增加(OR:1.94;95%CI:[1.32-2.86];p=0.001)。对13个样本进行了测序,其中7个(53.8%)为基因型A,基因型D和基因型E各3例(23.1%)。在表面区域发现了临床上重要的突变,但没有发现经典的耐药突变。(4)结论:我们报告了在博茨瓦纳农村和城市周边社区没有艾滋病毒的人中HBV的患病率为4.0%(95%CI3.3-4.9),在不同的社区不同的比率。博茨瓦纳需要一个全面的国家HBV计划来指导HBV预防,测试和管理。
    (1) Background: we determined the prevalence of the hepatitis B virus (HBV) amongst people without human immunodeficiency virus (HIV) in rural and peri-urban areas in Botswana. (2) Methods: We screened for the hepatitis B surface antigen (HBsAg) from archived plasma samples of people without HIV (n = 2135) randomly selected from the Botswana Combination Prevention Program (BCPP) (2013-2018). We sequenced 415 bp of the surface region using BigDye sequencing chemistry. (3) Results: The median age of participants was 31 (IQR: 24-46) and 64% (1360/2135) were female. HBV prevalence was 4.0% (86/2135) [95% CI: 3.3-4.9]) and ranged between 0-9.2%. Older participants (>35 years) had increased odds of HBV positivity (OR: 1.94; 95% CI: [1.32-2.86]; p = 0.001). Thirteen samples were sequenced and seven (53.8%) were genotype A, three (23.1%) were genotype D and genotype E each. Clinically significant mutations were identified in the surface region, but no classic drug resistance mutations were identified. (4) Conclusions: We report an HBV prevalence of 4.0% (95% CI 3.3-4.9) among people without HIV in rural and peri-urban communities in Botswana with varying rates in different communities. A comprehensive national HBV program is required in Botswana to guide HBV prevention, testing and management.
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  • 文章类型: Journal Article
    全球范围内,A组轮状病毒(RVA)是5岁以下儿童急性胃肠炎的主要原因,巴基斯坦的RVA相关发病率和死亡率最高。本研究旨在确定轮状病毒的遗传多样性,并评估Rotarix疫苗引入对巴基斯坦疾病流行病学的影响。共有4749名儿童,2018年至2020年期间因急性胃肠炎住院,在拉合尔和卡拉奇的四家医院进行了测试。在总数中,19.3%(918/4749)例RVA抗原检测呈阳性,阳性率每年变化(2018年=22.7%,2019年=14.4%,2020年=20.9%)。在RVA阳性儿童中,66.3%的人年龄在1岁以下。662个酶联免疫吸附试验阳性样本的基因分型显示主要基因型为G9P[4](21.4%),其次是G1P[8](18.9%),G3P[8](11.4%),G12P[6](8.7%),G2P[4](5.7%),G2P[6](4.8%),10.8%为混合基因型。在接种疫苗的儿童中,基因型G9P[4]和G12P[6]检测频率更高,而观察到G2P[4]下降。系统发育分析证实,除G9和P[6]菌株外,该国较早检测到的土著基因型持续循环。我们的发现突出了疫苗引入后G9P[4]基因型的优势,因此强调持续监测以监测疾病负担,病毒多样性,以及它们对控制儿童轮状病毒胃肠炎的影响。
    Globally, Group A rotavirus (RVA) is the leading cause of acute gastroenteritis in children under 5 years old, with Pakistan having the highest rates of RVA-related morbidity and mortality. The current study aims to determine the genetic diversity of rotavirus and evaluate the impact of Rotarix-vaccine introduction on disease epidemiology in Pakistan. A total of 4749 children, hospitalized with acute gastroenteritis between 2018 and 2020, were tested at four hospitals in Lahore and Karachi. Of the total, 19.3% (918/4749) cases were tested positive for RVA antigen, with the positivity rate varying annually (2018 = 22.7%, 2019 = 14.4%, 2020 = 20.9%). Among RVA-positive children, 66.3% were under 1 year of age. Genotyping of 662 enzyme-linked immuno sorbent assay-positive samples revealed the predominant genotype as G9P[4] (21.4%), followed by G1P[8] (18.9%), G3P[8] (11.4%), G12P[6] (8.7%), G2P[4] (5.7%), G2P[6] (4.8%), and 10.8% had mixed genotypes. Among vaccinated children, genotypes G9P[4] and G12P[6] were more frequently detected, whereas a decline in G2P[4] was observed. Phylogenetic analysis confirmed the continued circulation of indigenous genotypes detected earlier in the country except G9 and P[6] strains. Our findings highlight the predominance of G9P[4] genotype after the vaccine introduction thus emphasizing continual surveillance to monitor the disease burden, viral diversity, and their impact on control of rotavirus gastroenteritis in children.
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  • 文章类型: Journal Article
    牛冠状病毒(BCoV),牛轮状病毒,牛病毒性腹泻病毒,牛星状病毒是引起牛腹泻的最常见的肠道病原病毒。我们从2020年1月至2023年8月收集了1646份牛粪便样本。BCoV是检测到的主要病原体,阳性率为34.02%(560/1646)。在670份腹泻样本和976份无症状样本中,209和351为BCoV阳性,分别。研究与BCoV相关的腹泻的相关性表明,感染后腹泻症状的发作与牛的年龄密切相关,也可能与品种有关。我们扩增并测序了血凝素酯酶(HE),刺突蛋白,和部分阳性样本的整个基因组,并获得了六个完整的HE序列,七个完整的尖峰序列,和六个完整的基因组。分子鉴定表明,有6个菌株是分枝的中国菌株,日本菌株,和来自GⅡb亚组的部分美国菌株。菌株HBSJZ2202和JSYZ2209在HE上有四个氨基酸插入。我们还分析了ORF1a,发现GIIb中各个地区的差异,它们位于系统发育树中的不同分支上。这项工作为进一步调查BCoV的流行病学以及了解和分析BCoV的分布和动态提供了数据。
    Bovine coronavirus (BCoV), bovine rotavirus, bovine viral diarrhea virus, and bovine astrovirus are the most common intestinal pathogenic viruses causing diarrhea in cattle. We collected 1646 bovine fecal samples from January 2020 to August 2023. BCoV was the major pathogen detected, with a positive rate of 34.02% (560/1646). Of the 670 diarrheal samples and 976 asymptomatic samples, 209 and 351 were BCoV-positive, respectively. Studying the relevance of diarrhea associated with BCoV has shown that the onset of diarrheal symptoms post-infection is strongly correlated with the cattle\'s age and may also be related to the breed. We amplified and sequenced the hemagglutinin esterase (HE), spike protein, and whole genomes of the partially positive samples and obtained six complete HE sequences, seven complete spike sequences, and six whole genomes. Molecular characterization revealed that six strains were branched Chinese strains, Japanese strains, and partial American strains from the GⅡb subgroup. Strains HBSJZ2202 and JSYZ2209 had four amino acid insertions on HE. We also analyzed ORF1a and found disparities across various regions within GIIb, which were positioned on separate branches within the phylogenetic tree. This work provides data for further investigating the epidemiology of BCoV and for understanding and analyzing BCoV distribution and dynamics.
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  • 文章类型: Journal Article
    全球范围内,轮状病毒仍然是严重小儿胃肠炎的主要病因,通过环境水库传播该疾病已成为发展中国家新出现的问题。从2021年8月到10月,共有69个样本,包括48个未经处理的污水,和21个地表水,从四个德班污水处理厂(DWWTP)收集,和污水接收河流,分别。对从样品中回收和鉴定的轮状病毒进行测序,基因分型,和系统发育分析。在65份(94.2%)轮状病毒阳性样本中,33.3%来自原污水,16%来自活性污泥,15.9%来自最终流出物,29.0%来自接收河流样本。在污水中检测到49个G和41个P基因型,而在河流样品中检测到15个G和22个P基因型。G1基因型在污水中占主导地位(24.5%),其次是G3(22.4%),G2(14.3%),G4(12.2%),G12(10.2%),G9(8.2%),和八国集团(6.1%)。同样,G1在河水样品中占主导地位(33.3%),其次是G2,G4(各20.0%),G3和G12(各13.3%)。轮状病毒VP4基因型P[4],P[6],P[8]占36.6%,29.3%,9.8%,分别,在污水中。相应地,45.5%,31.8%,在河流样本中检出13.6%。对于污水和河水样品,未通过所用方法鉴定的G和P基因型分别为2.1%对24.3%和0.1%对9.1%,分别。序列比较研究表明G1,G2,G3,G4,G8VP7和P[4]中的核苷酸同一性很高,P[6],来自环境的菌株和来自该地区患者的菌株之间的P[8]VP4基因序列。这是该地理区域城市废水及其接收河流中轮状病毒G和P基因型多样性的首次基于环境的研究。环境和临床轮状病毒毒株之间的高度相似性表明该病毒的局部循环和潜在的暴露风险。此外,它强调了污水监测作为流行病学调查的额外工具的有用性,特别是在包括亚临床或无症状感染的人群中,这些感染在基于病例的研究中被排除。
    Globally, rotavirus continues to be the leading etiology of severe pediatric gastroenteritis, and transmission of the disease via environmental reservoirs has become an emerging concern in developing countries. From August to October 2021, a total of 69 samples comprising 48 of raw and treated sewage, and 21 surface waters, were collected from four Durban wastewater treatment plants (DWWTP), and effluent receiving rivers, respectively. Rotaviruses recovered and identified from the samples were subjected to sequencing, genotyping, and phylogenetic analysis. Of the 65 (94.2%) rotavirus-positive samples, 33.3% were from raw sewage, 16% from activated sludge, 15.9% from final effluents, and 29.0% were from the receiving river samples. A total of 49 G and 41 P genotypes were detected in sewage while 15 G and 22 P genotypes were detected in river samples. G1 genotype predominated in sewage (24.5%) followed by G3 (22.4%), G2 (14.3%), G4 (12.2%), G12 (10.2%), G9 (8.2%), and G8 (6.1%). Similarly, G1 predominated in river water samples (33.3%) and was followed by G2, G4 (20.0% each), G3, and G12 (13.3% each). Rotavirus VP4 genotypes P[4], P[6], and P[8] accounted for 36.6%, 29.3%, and 9.8%, respectively, in sewage. Correspondingly, 45.5%, 31.8%, and 13.6% were detected in river samples. The G and P genotypes not identified by the methods used were 2.1% versus 24.3% and 0.1% versus 9.1% for sewage and river water samples, respectively. Sequence comparison studies indicated a high level of nucleotide identity in the G1, G2, G3, G4, G8 VP7, and P[4], P[6], and P[8] VP4 gene sequences between strains from the environment and those from patients in the region. This is the first environmental-based study on the G and P genotypes diversity of rotavirus in municipal wastewater and their receiving rivers in this geographical region. The high similarity between environmental and clinical rotavirus strains suggests both local circulation of the virus and potential exposure risks. In addition, it highlights the usefulness of sewage surveillance as an additional tool for an epidemiological investigation, especially in populations that include individuals with subclinical or asymptomatic infections that are precluded in case-based studies.
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  • 文章类型: Journal Article
    弓形虫是一种对人类和兽医健康至关重要的细胞内寄生虫。弓形虫基因型种群的结构和多样性在地理上有很大差异,但是三个血统,I型,II和III,分布在全球。谱系III基因型在生物学方面特征最差,宿主免疫力和毒力。一旦宿主感染了T.gondii,参与先天免疫机制以减少组织中的寄生虫负担,并创造促炎环境,在该环境中,TH1应答发展以确保存活.这项研究调查了Swiss-Webster小鼠腹膜内感染后的早期细胞免疫反应,该小鼠具有四种不同的非克隆基因型III和局部分离株ToxoDB#1的10个速殖子。毒力表型,ROP5,ROP16,ROP18和GRA15的累积死亡率(CM)和等位基因谱先前已发表。
    通过实时PCR和IFNγ的相对表达水平分析寄生虫在不同组织中的传播,颈淋巴结(CLN)中的IL12-p40,IL-10和TBX21,使用ΔΔCt方法计算脑和脾。通过检测脑中的BAG1转录物确定阶段转化。
    组织播散取决于毒力表型,但不取决于CM,而TBX21和细胞因子水平和动力学与CM的相关性比毒力表型更好。BAG1的最早检测是感染后7天。只有高CM基因型(69.4%)的感染与CLN24h中的高T-bet水平和在第一周内持续的高全身IFNγ表达有关,而感染基因型较低的CM(38.8%,10.7%和6.8%)的特征在于IFNγ的下调和/或系统水平低。响应强度,通过细胞因子水平评估,随着时间的推移,高CM的基因型逐渐减弱,而逐渐增加到低CM的基因型。
    结果表明,免疫应答与毒力表型和/或等位基因谱无关,但是早期发作,强烈的促炎反应是高CM基因型的特征。此外,大脑中的高IFNγ水平可能会阻碍阶段转换。
    UNASSIGNED: Toxoplasma gondii is an intracellular parasite of importance to human and veterinary health. The structure and diversity of the genotype population of T. gondii varies considerably with respect to geography, but three lineages, type I, II and III, are distributed globally. Lineage III genotypes are the least well characterized in terms of biology, host immunity and virulence. Once a host is infected with T.gondii, innate immune mechanisms are engaged to reduce the parasite burden in tissues and create a pro-inflammatory environment in which the TH1 response develops to ensure survival. This study investigated the early cellular immune response of Swiss-Webster mice post intraperitoneal infection with 10 tachyzoites of four distinct non-clonal genotypes of lineage III and a local isolate of ToxoDB#1. The virulence phenotype, cumulative mortality (CM) and allele profiles of ROP5, ROP16, ROP18 and GRA15 were published previously.
    UNASSIGNED: Parasite dissemination in different tissues was analyzed by real-time PCR and relative expression levels of IFNγ, IL12-p40, IL-10 and TBX21 in the cervical lymph nodes (CLN), brain and spleen were calculated using the ΔΔCt method. Stage conversion was determined by detection of the BAG1 transcript in the brain.
    UNASSIGNED: Tissue dissemination depends on the virulence phenotype but not CM, while the TBX21 and cytokine levels and kinetics correlate better with CM than virulence phenotype. The earliest detection of BAG1 was seven days post infection. Only infection with the genotype of high CM (69.4%) was associated with high T-bet levels in the CLN 24 h and high systemic IFNγ expression which was sustained over the first week, while infection with genotypes of lower CM (38.8%, 10.7% and 6.8%) is characterized by down-regulation and/or low systemic levels of IFNγ. The response intensity, as assessed by cytokine levels, to the genotype of high CM wanes over time, while it increases gradually to genotypes of lower CM.
    UNASSIGNED: The results point to the conclusion that the immune response is not correlated with the virulence phenotype and/or allele profile, but an early onset, intense pro-inflammatory response is characteristic of genotypes with high CM. Additionally, high IFNγ level in the brain may hamper stage conversion.
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  • 文章类型: Journal Article
    多枝苔藓种的两种种质,即德国和塞尔维亚基因型,受到盐胁迫,旨在研究该物种的发育和生理特征。将各种浓度的氯化钠应用于两种苔藓基因型的无菌体外培养物中,并跟踪生长参数和生理特征变化。根据形态发育参数和生存指数推断,与德国基因型相比,塞尔维亚基因型对盐胁迫的抵抗力更高。然而,两种苔藓基因型均在最高浓度(500mM)下存活。不出所料,短时间接触盐很容易克服。在胁迫期间没有观察到糖含量和变化的清晰模式,但它们肯定包括在Formosum的盐应激反应和耐受性中。更长的胁迫增加了两种基因型的总叶绿素含量。在短期施加的盐胁迫中,塞尔维亚基因型具有较高的总叶绿素浓度来控制未受胁迫的植物,而德国基因型降低了叶绿素的总量。同样,类胡萝卜素在塞尔维亚基因型中显示明显更高,在无应力和经过处理的植物中,与德国相比。与德国登录名相比,塞尔维亚基因型的生育酚含量更高,在受控的无胁迫和随后的短期和长期胁迫的小植株中。总的来说,我们可以假设Formosum对盐胁迫具有出乎意料的耐受性,并且在整个欧洲人口的各种种质中存在差异,由两个随机选择的基因型,这很可能是不同遗传结构的结果。
    The two accessions of the polytrichaceous moss species Polytrichum formosum, namely German and Serbian genotypes, were subjected to salt stress, aiming to study the species\' developmental and physiological features. Various concentrations of sodium chloride were applied to an axenic in vitro culture of the two moss genotypes, and the growth parameters as well as physiological feature changes were followed. As inferred by the morpho-developmental parameters and survival index, the Serbian genotype showed higher resistance to salt stress as compared to the German one. However, both moss genotypes survived the highest applied concentration (500 mM). As expected, short exposures to salt were rather easily overcome. No clear patterns in sugar content and changes were observed during the stress, but they are surely included in salt stress response and tolerance in P. formosum. Longer stress increased total chlorophyll content in both genotypes. In short-term applied salt stress, the Serbian genotype had a higher total chlorophyll concentration to control unstressed plants, while the German genotype decreased the total amount of chlorophyll. Similarly, carotenoids were shown to be significantly higher in the Serbian genotype, both in unstressed and treated plants, compared to the German one. The contents of tocopherols were higher in the Serbian genotype in controlled unstressed and subsequently short- and long-stressed plantlets compared to the German accession. In general, we can assume that P. formosum is unexpectedly tolerant to salt stress and that there are differences within various accessions of overall European populations, as referred by two randomly selected genotypes, which is most probably a consequence of different genetic structure.
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  • 文章类型: Journal Article
    背景:高危型人乳头瘤病毒(HPV)的持续感染被认为是宫颈上皮内瘤变和宫颈癌的主要原因。但HPV感染引起的各种宫颈病变可通过及时接种疫苗得到适当预防。然而,HPV基因型的分布在地理上有所不同.
    方法:回顾性分析2020-2022年中国咸宁市16,150例女性高危型HPV流行情况。HPV基因分型使用PCR-RDB试剂盒进行,该试剂盒可检测中国国家药品监督管理局推荐的18种高危型HPV基因型。分析18种高危型HPV基因型的患病率及其与宫颈病变的关系以及疫苗的疗效。
    结果:共有2431名女性被证实患有不同类型的高危型HPV感染。总阳性率达15.05%(2431/16,150)。最普遍的高危型HPV基因型是HPV52、16、58、53和51。高危型HPV的患病率在≤20岁(20.95%)和≥61岁(20.56%)达到峰值。宫颈癌病例中最常见的高危型HPV基因型是HPV16、58、18、33和52。HPV16、52、58、33和18inCIN2/3例,和HPV52、58、16、53和18在CIN1病例中,分别。
    结论:HPV16、58和18是咸宁最危险和致癌的基因型,中国。开展高危型HPV流行病学调查对指导HPV疫苗接种工作具有重要的临床价值。
    BACKGROUND: The persistent infection of high-risk Human papillomavirus(HPV) is considered the main cause of cervical intraepithelial neoplasia and cervical cancer. But various cervical lesions caused by HPV infection can be properly prevented by timely vaccination. However, the distribution of HPV genotypes varies geographically.
    METHODS: Retrospective analysis of high-risk HPV prevalence of 16,150 women from 2020 to 2022 in xianning of China. HPV genotyping was performed using a PCR-RDB Kit that can detect 18 high-risk HPV genotypes recommended by China\'s National Medical Products Administration. The prevalence of 18 high-risk HPV genotypes and their relationship with cervical lesions as well as vaccine efficacy were analyzed.
    RESULTS: A total of 2431 women were confirmed to have different types of high-risk HPV infections. The overall positive rate reached 15.05%(2431/16,150). The most prevalent high-risk HPV genotypes were HPV52, 16, 58, 53, and 51. The prevalence of high-risk HPV reached peak at age ≤ 20(20.95%) and age ≥ 61(20.56%). The most prevalent high-risk HPV genotypes were HPV16, 58, 18, 33 and 52 in cervical cancer cases, HPV16, 52, 58, 33 and 18 in CIN2/3 cases, and HPV52, 58, 16, 53 and 18 in CIN1 cases, respectively.
    CONCLUSIONS: HPV16, 58 and 18 are the most dangerous and carcinogenic genotypes in xianning, China. Conducting epidemiological investigations on high-risk HPV has significant clinical value in guiding HPV vaccination work.
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