phylogenetic tree

系统发育树
  • 文章类型: Journal Article
    背景:Santalum专辑L.是一种常绿树,主要分布在整个热带和温带地区。具有很年夜的药用和经济价值。
    结果:在这项研究中,组装并注释了完整的DNA基因组,可以用由三个重叠群组成的复杂分支结构来描述。这三个重叠群的长度是165,122bp,93,430bp和92,491bp。我们注释了34个编码蛋白质(PCGs)的基因,26个tRNA基因,和4个rRNA基因。对重复元件的分析表明,S.balog线粒体基因组中存在89个SSR和242对分散重复序列。我们还在叶绿体和线粒体中发现了20种MTPT。20个MTPTs序列的合并长度为22,353bp,占质体的15.52%,6.37%的线粒体基因组。此外,通过使用Deepred-mt工具,我们在34个PCGs中发现628个RNA编辑位点。此外,在S.alum及其相关的线粒体基因组之间观察到显着的基因组重排。最后,基于线粒体基因组PCGs,我们推断了S.alum和其他被子植物之间的系统发育联系。
    结论:我们首次报道了来自Santalales的线粒体基因组,这为我们研究线粒体基因组的进化提供了重要的遗传资源。
    BACKGROUND: Santalum album L. is an evergreen tree which is mainly distributes throughout tropical and temperate regions. And it has a great medicinal and economic value.
    RESULTS: In this study, the complete mitochondrial genome of S. album were assembled and annotated, which could be described by a complex branched structure consisting of three contigs. The lengths of these three contigs are 165,122 bp, 93,430 bp and 92,491 bp. We annotated 34 genes coding for proteins (PCGs), 26 tRNA genes, and 4 rRNA genes. The analysis of repeated elements shows that there are 89 SSRs and 242 pairs of dispersed repeats in S. album mitochondrial genome. Also we found 20 MTPTs among the chloroplast and mitochondria. The 20 MTPTs sequences span a combined length of 22,353 bp, making up 15.52 % of the plastome, 6.37 % of the mitochondrial genome. Additionally, by using the Deepred-mt tool, we found 628 RNA editing sites in 34 PCGs. Moreover, significant genomic rearrangement is observed between S. album and its associated mitochondrial genomes. Finally, based on mitochondrial genome PCGs, we deduced the phylogenetic ties between S. album and other angiosperms.
    CONCLUSIONS: We reported the mitochondrial genome from Santalales for the first time, which provides a crucial genetic resource for our study of the evolution of mitochondrial genome.
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  • 文章类型: Journal Article
    系统发育关联分析在研究微生物组成与微生物组研究中感兴趣的特定结果之间的相关性中起着至关重要的作用。然而,现有的测试这种关联的方法在高维环境中的线性关联假设和混杂效应的处理方面存在局限性.因此,需要能够表征复杂关联的方法,包括非单调关系。本文介绍了一种新颖的系统发育关联分析框架和相关测试,以通过采用条件等级相关性作为关联度量来解决这些挑战。拟议的测试以完全非参数的方式考虑了混杂因素,确保对异常值的鲁棒性和检测不同依赖关系的能力。所提出的框架使用加权求和和最大方法来捕获密集和稀疏信号,从而聚合子树的条件秩相关性。检验统计量的显著性水平通过最近邻自举方法进行校准来确定,这很容易实现,并且可以在其他数据集可用时容纳这些数据集。通过使用模拟和真实微生物组数据集的数值实验证明了所提出的框架的实际优势。
    Phylogenetic association analysis plays a crucial role in investigating the correlation between microbial compositions and specific outcomes of interest in microbiome studies. However, existing methods for testing such associations have limitations related to the assumption of a linear association in high-dimensional settings and the handling of confounding effects. Hence, there is a need for methods capable of characterizing complex associations, including nonmonotonic relationships. This article introduces a novel phylogenetic association analysis framework and associated tests to address these challenges by employing conditional rank correlation as a measure of association. The proposed tests account for confounders in a fully nonparametric manner, ensuring robustness against outliers and the ability to detect diverse dependencies. The proposed framework aggregates conditional rank correlations for subtrees using weighted sum and maximum approaches to capture both dense and sparse signals. The significance level of the test statistics is determined by calibration through a nearest-neighbour bootstrapping method, which is straightforward to implement and can accommodate additional datasets when these are available. The practical advantages of the proposed framework are demonstrated through numerical experiments using both simulated and real microbiome datasets.
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  • 文章类型: Journal Article
    假伯克霍尔德菌是一种革兰氏阴性杆菌,是人类和动物的类骨病的病因。该病在澳大利亚北部和东南亚高度流行。全面的基因组数据对于了解细菌的传播和来自不同地理区域的菌株之间的遗传关系至关重要。在这项研究中,我们在2011年至2018年间对泰国南部的54株环境和动物来源的假单胞菌分离株进行了抗菌药物敏感性试验和全基因组测序.他们的基因组学确定了抗生素抗性基因(ARGs),毒力相关基因,移动遗传元件(MGEs),序列类型(ST),和单核苷酸多态性(SNP)来评估其流行病学相关性。值得注意的是,所有54个分离株对通常用于类鼻窦病治疗的抗微生物药物均表现出敏感性.我们鉴定了9种不同的序列类型:ST392、ST51、ST409、ST508、ST376、ST1721、ST389、ST395和ST289。Oxacillinase基因和外排泵(RND)的抗性结瘤家族被确定为抗生素耐药性的贡献者。系统发育分析表明与东南亚分离的其他菌株有密切的遗传关系。此外,在分离株中鉴定出172个毒力相关基因,提示临床表现的变化。这些发现强调了持续的假单胞菌分子遗传监测对于有效的医疗保健管理和降低类鼻窦炎死亡率的重要性。
    Burkholderia pseudomallei is a Gram-negative bacillus and the etiological agent of melioidosis in humans and animals. The disease is highly endemic in northern Australia and Southeast Asia. Comprehensive genomic data are essential for understanding the bacteria\'s dissemination and genetic relationships among strains from different geographical regions. In this study, we conducted antimicrobial susceptibility testing and whole-genome sequencing of 54 B. pseudomallei isolates obtained from environmental and animal sources in southern Thailand between 2011 and 2018. Their genomics were determined of antibiotic-resistant genes (ARGs), virulence-associated genes, mobile genetic elements (MGEs), sequence types (STs), and single nucleotide polymorphisms (SNPs) to evaluate their epidemiological relatedness. Remarkably, all 54 isolates displayed sensitivity to antimicrobial agents typically used for melioidosis treatment. We identified nine distinct sequence types: ST392, ST51, ST409, ST508, ST376, ST1721, ST389, ST395, and ST289. Oxacillinase genes and the resistance nodulation family of efflux pumps (RND) were identified as contributors to antimicrobial resistance. Phylogenetic analysis demonstrated close genetic relations with other strains isolated from Southeast Asia. Furthermore, 172 virulence-associated genes were identified among the isolates, suggesting variations in clinical presentations. These findings underscore the importance of ongoing molecular genetic surveillance of B. pseudomallei for effective healthcare management and reducing melioidosis mortality.
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  • 文章类型: Journal Article
    在这项研究中,通过生物信息学分析和基因组数据鉴定了菲律宾蛤仔的Fox基因家族。结果表明,在菲律宾R。中共鉴定出21个Fox基因,分为16个亚科,包括Foxa亚家族的两个成员(Foxa1,Foxa2),Foxl亚家族的三个成员(Foxl1b,Foxl1a,FOXL2),Foxn亚家族的三个成员(FOXN3,FOX4A,Foxn4b)和其他家庭的一名成员。染色体分布,域,保守的图案,内含子,预测了这21个Fox基因的外显子和蛋白质三级结构。通过分析菲律宾念珠菌的RNA-seq数据,发现Fox基因家族在不同组织中差异表达,不同的发育阶段和热和冷胁迫下。大多数Fox基因在四个组织中高表达:唇瓣,性腺,刺和脚。大多数Fox基因在囊胚期高度表达。年夜多半Fox基因在两个群体的高温组中高表达,还有Foxo,FOXG1在低温组中高表达。此外,qPCR结果显示,在急性冷应激下,Foxo和Foxj1b基因的表达水平显著升高。因此,我们推测Fox基因可能在菲律宾R.philippinarum的胚胎发育和温度胁迫中起重要作用,本研究为进一步探索Fox介导低温耐受的分子机制提供了依据。
    In this study, the Fox gene family of Ruditapes philippinarum was identified by bioinformatics analysis and genome data. The results showed that a total of 21 Fox genes were identified in R. philippinarum, which were divided into 16 subfamilies, including two members of Foxa subfamily (Foxa1, Foxa2), three members of Foxl subfamily (Foxl1b, Foxl1a, FOXL2), three members of Foxn subfamily (FOXN3, FOX4A, Foxn4b) and one member of other families. The chromosome distribution, domains, conserved motifs, introns, exons and protein tertiary structures of these 21 Fox genes were predicted. By analyzing the RNA-seq data of R. philippinarum, it was found that the Fox gene family was differentially expressed in different tissues, different developmental stages and under heat and cold stress. Most of Fox genes were highly expressed in four tissues: labial palp, gonad, gill and foot. Most of the Fox genes were highly expressed in blastula stage. Most of the Fox genes were highly expressed in high temperature group of two populations, and Foxo, FOXG1 were highly expressed in low temperature group. In addition, qPCR showed that the expression levels of Foxo and Foxj1b genes increased significantly under acute cold stress. Therefore, we speculate that Fox genes may play important roles in embryo development and the temperature stress of R. philippinarum, and this study provides a basis for further exploring the molecular mechanism of low temperature tolerance mediated by Fox.
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  • 文章类型: Journal Article
    树图是生物分类和系统遗传学中可视化的主要形式。从1960年代中期到1980年代,在所谓的系统论战争期间,系统主义者发表的大多数期刊文章和教科书都包含树形图。尽管这一集系统学已经被历史学家和生物学哲学家充分研究,大多数分析将科学理论优先于实践,并倾向于强调相互冲突的理论假设。在这篇文章中,我通过代表性实践的视角来观察冲突,并以数值分类学家(物候图)和分支(分支图)使用的树形图为例进行了研究,从而提供了另一种观点。我认为,分子系统发育学的当前状态不应被解释为系统学内部观点竞争的结果。相反,分子系统发育学独立于系统学而产生,分类和物候的元素被整合到分子系统发育学的框架中,通过物候和分类实践与分子系统发育的定量方法的相容性促进。我的研究表明,科学变革的这一插曲比关于战斗、胜利者或冲突和妥协的常见叙述更为复杂。今天,分支图仍被使用并解释为特定类型的分子系统发育树。虽然在系统论战争时期,物象图和分支图代表了不同形式的知识,今天,它们都被用来代表进化关系。这表明图表是科学实践的通用元素,可以改变其含义,取决于理论框架内的使用背景。
    Tree diagrams are the prevailing form of visualization in biological classification and phylogenetics. Already during the time of the so-called Systematist Wars from the mid-1960s until the 1980s most journal articles and textbooks published by systematists contained tree diagrams. Although this episode of systematics is well studied by historians and philosophers of biology, most analyses prioritize scientific theories over practices and tend to emphasize conflicting theoretical assumptions. In this article, I offer an alternative perspective by viewing the conflict through the lens of representational practices with a case study on tree diagrams that were used by numerical taxonomists (phenograms) and cladists (cladograms). I argue that the current state of molecular phylogenetics should not be interpreted as the result of a competition of views within systematics. Instead, molecular phylogenetics arose independently of systematics and elements of cladistics and phenetics were integrated into the framework of molecular phylogenetics, facilitated by the compatibility of phenetic and cladistic practices with the quantitative approach of molecular phylogenetics. My study suggests that this episode of scientific change is more complex than common narratives of battles and winners or conflicts and compromises. Today, cladograms are still used and interpreted as specific types of molecular phylogenetic trees. While phenograms and cladograms represented different forms of knowledge during the time of the Systematist Wars, today they are both used to represent evolutionary relationships. This indicates that diagrams are versatile elements of scientific practice that can change their meaning, depending on the context of use within theoretical frameworks.
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  • 文章类型: Journal Article
    没有一项研究在越南成功分离出细小病毒。这项研究旨在分离和鉴定越南本地的细小病毒株,以开发针对猪细小病毒(PPV)的疫苗。
    我们收集了越南六个省的血清和死胎样本,和PPV阳性样品使用聚合酶链反应鉴定。尝试使用维持在补充有5%胎牛血清和1%抗生素(青霉素-链霉素)的最低必需培养基中的PK-15细胞分离细小病毒。将细胞在37°C和5%CO2下孵育。对白色初产母猪进行毒力实验,通过血凝抑制(HI)滴度和胎儿病变评价PPV毒株的毒力。
    我们分析了360份血清和32份死胎(肝脏和肺)样本,显示其中32/392(8.2%)为PPV阳性,全部属于PPV1。成功分离出32份PPV阳性样本,与VP2序列具有100%同一性。系统发育树显示与Kresse菌株(1996年从加拿大分离)和PPV1-0225-L-SD菌株(2022年从中国分离)密切相关。选择两种表现出高50%组织培养感染剂量滴度的PPV分离株(来自Dongnai的VC5和来自Thanhhoa的TX7)进行毒力实验。第21天,注射后,HI抗体滴度范围为10log2至12log2.在第90天,71%-80%的胎儿被木乃伊化。
    这项研究表明,越南的PPV感染率为8.2%。32个分离株属于PPV1。两个PPV菌株,通过注射到小母猪后的HI滴度的结果确定VC5和TX7具有高毒力。VC5和TX7被确定为进一步研究PPV疫苗的良好候选者。
    UNASSIGNED: No study has successfully isolated parvovirus in Vietnam. This study aimed to isolate and characterize parvovirus strains indigenous in Vietnam for vaccine development against porcine parvovirus (PPV).
    UNASSIGNED: We collected serum and stillbirth samples from six provinces in Vietnam, and PPV-positive samples were identified using a polymerase chain reaction. Parvovirus isolation was attempted using the PK-15 cells maintained in a minimum essential medium supplemented with 5% fetal bovine serum and 1% antibiotics (Penicillin-streptomycin). The cells were incubated at 37°C with 5% CO2. Virulence experiments were conducted on white primiparous sows to evaluate the virulence of the PPV strain through hemagglutination inhibition (HI) titers and fetus lesions.
    UNASSIGNED: We analyzed 360 serum and 32 stillbirth (liver and lungs) samples, revealing that 32/392 (8.2% ) of them were PPV-positive, all belonging to PPV1. Thirty-two PPV-positive samples were successfully isolated, with 100% identity as VP2 sequences. The phylogenetic tree revealed a close relationship with the Kresse strain (isolated from Canada in 1996) and the PPV1-0225-L-SD strain (isolated from China in 2022). Two PPV isolates (VC5 from Dongnai and TX7 from Thanhhoa) that exhibited high 50% tissue culture infectious dose titers were selected for the virulence experiment. On day 21, after injection, the HI antibody titers ranged from 10log2 to 12log2. On day 90, 71%-80% of fetuses were mummified.
    UNASSIGNED: This study showed that the PPV infection rate in Vietnam was 8.2%. Thirty-two isolates belonged to PPV1. Two PPV strains, VC5 and TX7, were determined to be highly virulent by the results of HI titers after injection into gilts. VC5 and TX7 were determined to be good candidates for further research on PPV vaccines.
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  • 文章类型: Journal Article
    完整的Nekemiasgrossedentata(N.grossedentata)是一种药用和食用植物。嫩叶和嫩茎专门用于制造藤茶,传统上用于治疗普通感冒热等疾病,喉咙痛,黄疸性肝炎,和其他疾病。根茎的形态类似于加拿大的Nekemias(N。广东)和猕猴桃(N.巨叶藻),这导致了混乱的市场供应。大量研究证实,叶绿体基因组和色谱在植物分类中起着重要作用。这里,在Illumina测序平台中对三种Nekemias物种的整个叶绿体(cp)基因组进行测序。同时,使用高效液相色谱(HPLC)构建了其色谱指纹图谱。成果注解,三个叶绿体基因组均为典范的四方构造,长度为162,147bp(N.grossedentata),161,981bp(N.巨叶藻),和162,500bp(N.cantoniensis),分别。共89(N.grossedentata)/86(N.巨叶病和山竹)蛋白质编码基因,37个tRNA基因和8个rRNA基因的注释。在这三个物种中,IR/SC边界区域相对保守,虽然有三个区域(rps19-rpl2,rpl32-trnL-UAG,ccsA-ndhD)表现出高于1%的可变位点的核苷酸多样性值(Pi)。系统发育分析表明,与广角菜的亲缘关系比广角菜的亲缘关系更密切。此外,色谱指纹图谱显示,三个物种的主要功能成分和遗传亲缘性与形态学结果高度相似。总之,藤茶的起源植物可以被认为是藤茶的起源植物。这项研究为物种鉴定提供了适当的信息,系统发育,对三种属的药用植物进行质量评估,并将有助于藤茶原料的标准化。
    Nekemias grossedentata (N. grossedentata) is a medicinal and edible plant. The young leaves and tender stems are specifically utilized to manufacture vine tea, which is traditionally employed in the treatment of conditions such as the common cold fever, sore throat, jaundice hepatitis, and other ailments. The morphologically of N. grossedentata similar to Nekemias cantoniensis (N. cantoniensis) and Nekemias megalophylla (N. megalophylla), which lead to a chaotic market supply. Numerious studies have confirmed that chloroplast genomes and chromatography play important role in plant classification. Here, the whole chloroplast (cp) genomes of the three Nekemias species were sequenced in Illumina sequencing platform. Meanwhile, their chromatographic fingerprints have constructed using high-performance liquid chromatography (HPLC). The annotation results demonstrated that the three chloroplast genomes were typical quadripartite structures, with lengths of 162,147 bp (N. grossedentata), 161,981 bp (N. megalophylla), and 162,500 bp (N. cantoniensis), respectively. A total of 89 (N. grossedentata) /86 (N. megalophylla and N. cantoniensis) protein-coding genes, 37 tRNA gene and 8 rRNA genes were annotated. The IR/SC boundary regions were relatively conserved across the three species, although three regions (rps19-rpl2, rpl32-trnL-UAG, ccsA-ndhD) exhibited nucleotide diversity values (Pi) of variable sites higher than 1%. Phylogenetic analysis indicated that N. grossedentata had a closer genetic relationship with N. megalophylla than that of N. cantoniensis. Moreover, the chromatographic fingerprints revealed that the main functional components and genetic relatedness of three species were highly similar with their morphological results. In conclusion, N. grossedentata and N. megalophylla can be consider as the origin plants of vine tea. This study provides appropriate information for species identification, phylogeny, quality assessment of three medicinal plants of the genus Nekemias and will contribute to the standardization of vine tea raw materials.
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  • 文章类型: Journal Article
    Heptathelakimurai(岸田,1920)是属于七叶科的蜘蛛,七叶科是蜘蛛的基底谱系。与衍生家族的蜘蛛物种相比,属于七叶科等家族的祖先物种的分子信息相对有限。在这里,我们介绍了H.kimurai的完整线粒体基因组序列(mtDNA)。使用大规模平行测序技术获得序列。环状基因组长度为14224bp,AT含量为69.53%。H.kimurai线粒体基因组包含13个蛋白质编码基因(PCGs),21个tRNA基因,和2个rRNA基因。在重链中发现了大多数PCG。
    Heptathela kimurai (Kishida, 1920) is a spider that belongs to the family Heptathelidae which is a basial lineage of spiders. The molecular information of ancestral species belonging to families like Heptathelidae is comparatively limited when compared to spider species from derived families. Here we present the complete mitochondrial genome sequence (mtDNA) of H. kimurai. The sequence was obtained using massively parallel sequencing technology. The circular genome was 14,224 bp in length, and the AT content was 69.53%. The H. kimurai mitochondrial genome contains 13 protein-coding genes (PCGs), 21 tRNA genes, and 2 rRNA genes. The majority of PCGs were found in the heavy strand.
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  • 文章类型: Journal Article
    系统发育树代表了各种物种或生物群体的进化关系和祖先。通过测量它们之间的距离来比较这些树对于诸如树聚类和生命之树项目之类的应用至关重要。系统发育树的许多距离度量都集中在同一组分类单元上定义的树上。然而,有些问题需要计算不同但重叠的分类群集合的树之间的距离。这项研究回顾了这种树木的最先进的距离测量,涵盖六种主要方法,包括基于约束的罗宾逊-福尔德(RF)距离RF(-),基于完成的RF(+),广义射频(GRF),差异度量,矢量树距离,以及扩展的Billera-Holmes-Vogtmann树空间中的测地距离。其中,三种基于RF的方法,RF(-),RF(+),和GRF,详细检查了在不同但相互重叠的分类单元集合上定义的系统发育树的生成簇。此外,我们回顾了九种相关技术,包括叶子插补方法,树编辑距离,视觉比较相关距离度量的比较,突出它们的主要优点和缺点,提供。这篇综述提供了对它们的适用性和性能的宝贵见解,根据树类型(有根或无根)和信息类型(拓扑或分支长度)指导这些指标的适当使用。
    Phylogenetic trees represent the evolutionary relationships and ancestry of various species or groups of organisms. Comparing these trees by measuring the distance between them is essential for applications such as tree clustering and the Tree of Life project. Many distance metrics for phylogenetic trees focus on trees defined on the same set of taxa. However, some problems require calculating distances between trees with different but overlapping sets of taxa. This study reviews state-of-the-art distance measures for such trees, covering six major approaches, including the constraint-based Robinson-Foulds (RF) distance RF(-), the completion-based RF(+), the generalized RF (GRF), the dissimilarity measure, the vectorial tree distance, and the geodesic distance in the extended Billera-Holmes-Vogtmann tree space. Among these, three RF-based methods, RF(-), RF(+), and GRF, were examined in detail on generated clusters of phylogenetic trees defined on different but mutually overlapping sets of taxa. Additionally, we reviewed nine related techniques, including leaf imputation methods, the tree edit distance, and visual comparison. A comparison of the related distance measures, highlighting their principal advantages and shortcomings, is provided. This review offers valuable insights into their applicability and performance, guiding the appropriate use of these metrics based on tree type (rooted or unrooted) and information type (topological or branch lengths).
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  • 文章类型: Journal Article
    近年来,登革热病例的数量急剧增加。在拉丁美洲,2023年的病例和死亡人数是有记录以来最高的.我们报道了一名患者,他于2023年9月在哥斯达黎加逗留期间感染了登革热病毒,并在返回日本后患上了这种疾病。从患者获得的血浆用于诊断和通过实时PCR进行登革热病毒血清分型。然后用直接测序法测定登革热病毒包膜区的核苷酸序列,该序列用于系统发育分析。发现患者感染了3型基因型III的登革热病毒。本案的序列与佛罗里达州注册的序列更同源,美国,与2022年前往古巴的旅行相比,与10年前在哥斯达黎加注册的序列有关。泛美卫生组织报告说,2019-2021年哥斯达黎加仅报告了1型和2型登革热病毒病例,而2022年开始报告3型和4型登革热病毒病例。2023年,报告的3型和4型登革热病毒病例数超过1型和2型登革热病毒病例数。此外,在哥斯达黎加观察到特有菌株的区域差异。我们的研究结果表明,感染患者的3型登革热病毒更有可能是近年来在古巴等加勒比国家流行的一种病毒的涌入,而不是哥斯达黎加本土病毒的重新出现。自2022年以来,哥斯达黎加流行的登革热病毒血清型一直在变化。所有四种血清型均在2023年流行,登革热3型和4型病毒的病例数特别急剧增加。未来的监测和监测是必不可少的,因为地方性血清型的变化可以导致抗体依赖性增强,这可能导致严重的登革热表现。
    The number of dengue cases has increased dramatically in recent years. In Latin America, the number of cases and deaths in 2023 was the highest ever recorded. We report on a patient who had been infected with dengue virus during his stay in Costa Rica in September 2023, and developed the disease after returning to Japan. Plasma obtained from the patient was used for diagnosis and dengue virus serotyping by real-time PCR. The nucleotide sequence of the envelope region of dengue virus was then determined by the direct sequencing method, and this sequence was used for phylogenetic analyses. The patient was found to be infected with dengue virus type 3 genotype III. The sequence from the present case was more homologous with sequences registered in Florida, USA, associated with travel to Cuba in 2022 than with sequences registered in Costa Rica 10 years ago. The Pan American Health Organization reported that only dengue virus type 1 and 2 cases were reported in Costa Rica in 2019-2021, whereas dengue virus type 3 and 4 cases started being reported in 2022. In 2023, the reported numbers of cases with dengue virus types 3 and 4 exceeded those of dengue virus types 1 and 2. In addition, regional differences in endemic strains have been observed in Costa Rica. Our findings suggest that the dengue virus type 3 that infected the patient was more likely an influx of a strain that had been circulating in Caribbean countries such as Cuba in recent years, rather than a re-emergence of an indigenous virus in Costa Rica. The serotypes of dengue virus prevalent in Costa Rica have been changing since 2022. All four serotypes were prevalent in 2023, with a particularly sharp increase in the number of cases of dengue virus types 3 and 4. Future monitoring and surveillance are essential because changes in endemic serotypes can cause antibody-dependent enhancement, which can lead to severe dengue disease presentations.
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