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      Epidemiological and Evolutionary Analysis of Dengue-1 Virus Detected in Guangdong during 2014: Recycling of Old and Formation of New Lineages

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          Abstract.

          The incidence of dengue is increasing in Guangdong, China, with the largest outbreak to date in 2014. Widespread awareness of epidemiological and molecular characteristics of the dengue virus (DENV) is required. In 2014, we isolated the virus from patients and sequenced its genome. The sequences of DENV isolated from Guangdong and other countries screened since 2005 were studied to establish molecular evolutionary databases along with epidemiological data to explore its epidemiological, phylogenetic, and molecular characteristics. Causes underlying the occurrence of the dengue epidemic included importation and localization of the virus. The number of indigenous cases significantly exceeded that of imported cases. Dengue virus 1 is the most important serotype and caused the long-term epidemic locally. Based on the data available since 2005, DENV1 was divided into three genotypes (I, IV, and V). Only genotypes I and V were detected in 2014. In 2014, an epidemic involving old lineages of DENV1 genotype V occurred after 2 years of silence. The genotype was previously detected from 2009 to 2011. Genotype I, which caused recent epidemics, demonstrated a continuation of new lineages, and a predictive pattern of molecular evolution since 2005 among the four lineages was present. The DENV isolated from Guangdong was closely related to those causing large-scale epidemics in neighboring countries, suggesting the possibility of its import from these countries. The lack of sufficient epidemiological data and evidence on the local mosquito-borne DENV emphasizes the importance of studying the molecular evolutionary features and establishing a well-established phylogenetic tree for dengue prevention and control in Guangdong.

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          Most cited references53

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          DNASTAR's Lasergene sequence analysis software.

          Lasergene's eight modules provide tools that enable users to accomplish each step of sequence analysis, from trimming and assembly of sequence data, to gene discovery, annotation, gene product analysis, sequence similarity searches, sequence alignment, phylogenetic analysis, oligonucleotide primer design, cloning strategies, and publication of the results. The Lasergene software suite provides the functions and customization tools needed so that users can perform analyses the software writers never imagined.
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            MEGA: Molecular Evolutionary Genetics Analysis software for microcomputers.

            A computer program package called MEGA has been developed for estimating evolutionary distances, reconstructing phylogenetic trees and computing basic statistical quantities from molecular data. It is written in C++ and is intended to be used on IBM and IBM-compatible personal computers. In this program, various methods for estimating evolutionary distances from nucleotide and amino acid sequence data, three different methods of phylogenetic inference (UPGMA, neighbor-joining and maximum parsimony) and two statistical tests of topological differences are included. For the maximum parsimony method, new algorithms of branch-and-bound and heuristic searches are implemented. In addition, MEGA computes statistical quantities such as nucleotide and amino acid frequencies, transition/transversion biases, codon frequencies (codon usage tables), and the number of variable sites in specified segments in nucleotide and amino acid sequences. Advanced on-screen sequence data and phylogenetic-tree editors facilitate publication-quality outputs with a wide range of printers. Integrated and interactive designs, on-line context-sensitive helps, and a text-file editor make MEGA easy to use.
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              Association between nasal shedding and fever that influenza A (H3N2) induces in dogs

              Background Avian origin canine influenza virus was reported in Korea. The dog to dog contact transmission of the avian origin canine influenza virus (CIV) H3N2 and CIV H3N8 was shown by experimental contact transmission. This study was focused on viral excretion and fever in order to elucidate the epidemiological associations which might be helpful to control the disease transmissions in CIV outbreak in dogs. Methods An influenza seronegative 10-week-old Beagle dog was experimentally inoculated with the canine influenza virus A/canine/01/2007, subtype H3N2. Eight hours after inoculation, the infected dog was cohoused with seven uninfected Beagle dogs. Clinical signs including fever were recorded for 14 days post inoculation. Results The infected dog and four of seven contact dogs in the study showed clinical signs (sneezing, nasal discharge and coughing) during the study. Viral shedding occurred in all of the animals tested and began on 1 to 6 DPI in dogs with clinical signs. Elevated body temperatures above 39.5°C (geometric mean temperature of 39.86°C±0.49) were observed in all symptomatic dogs. The mean viral titer during fever was 2.99 log EID50/ml, which was significantly higher than the viral titer detected in the non fever. Conclusions The data show that contact dogs with a canine influenza infected dog shed different levels of virus in their nasal excretions and demonstrate that clinical signs, including fever, significantly correlate with the viral shedding.
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                Author and article information

                Journal
                Am J Trop Med Hyg
                Am. J. Trop. Med. Hyg
                tpmd
                tropmed
                The American Journal of Tropical Medicine and Hygiene
                The American Society of Tropical Medicine and Hygiene
                0002-9637
                1476-1645
                October 2019
                05 August 2019
                05 August 2019
                : 101
                : 4
                : 870-883
                Affiliations
                [1 ]Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, China;
                [2 ]Guangdong Women and Children’s Hospital, Guangzhou Medical University, Guangzhou, China;
                [3 ]Department of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China;
                [4 ]Guangzhou Key Laboratory of Drug Research for Emerging Virus Prevention and Treatment, School of Pharmacy, Southern Medical University, Guangzhou, China;
                [5 ]School of Public Health, Guangdong Medical University, Dongguan, China
                Author notes
                [* ]Address correspondence to Wei Zhao or Weiwei Xiao, School of Public Health, Southern Medical University, Guangzhou, China. E-mails: zhaowei@ 123456smu.edu.cn or xweiwei74@ 123456126.com

                Authors’ addresses: Jianhai Yu, Xujuan Li, Xiaoen He, Xuling Liu, Qian Xie, Li Zhu, Fengyun Jia, Yingxue Mao, Zongqiu Chen, Ying Wen, and Bao Zhang, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, China, E-mails: chienhai@ 123456163.com , murong816@ 123456outlook.com , hexiaoen24@ 123456163.com , maiblume@ 123456163.com , xiyuxie89@ 123456126.com , zhuli89@ 123456126.com , 13078431254@ 123456163.com , milyx117@ 123456163.com , harpul@ 123456sina.com , wenying@ 123456gdciq.gov.cn , and zhangb@ 123456smu.edu.cn . Zhicheng Zhong, and Danjuan Ma, Guangzhou Medical University, Guangdong Women and Children’s Hospital Guangzhou, China, E-mails: zhongyan6291@ 123456163.com and mdj0702@ 123456163.com . Linzhong Yu, Department of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China, E-mail: yulzh@ 123456smu.edu.cn . Wei Zhao, School of Public Health, Southern Medical University, Guangzhou, China, E-mail: zhaowei@ 123456smu.edu.cn . Weiwei Xiao, School of Public Health, Southern Medical University, Guangzhou, China, E-mail: xweiwei74@ 123456126.com .

                [†]

                These authors contributed equally to this work.

                Article
                tpmd180951
                10.4269/ajtmh.18-0951
                6779206
                31392945
                80759532-6491-42a6-8886-03c5d79eb936
                © The American Society of Tropical Medicine and Hygiene

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 29 November 2018
                : 26 June 2019
                Page count
                Pages: 14
                Categories
                Articles

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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