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1.
Biosaf Health ; 1(3): 150-154, 2019 Dec.
Article in English | MEDLINE | ID: mdl-32501448

ABSTRACT

Here, we report the identification of Histoplasma causing an unexplained disease cluster in Matthews Ridge, Guyana. In March 2019, 14 employees of Chongqing Bosai Mining Company, China, working in a manganese mining of Guyana, had unexplained fever, and two of them died. We obtained lung and brain tissues as well as the blood samples from the two deceased cases (patient No. 1 and 2), and bronchoscopy lavages and cerebrospinal fluid samples from one severe case (patient No. 3), respectively. All samples were tested by pathological examination, high-throughput sequencing, and real-time PCR. Pathological detection showed the presence of spore-like structures in the lung tissue of patient No. 1, indicating a fungal infection in this patient. Nanopore sequencing identified the existing of H. capsulatum in the lung tissue sample within 13 h. Next-generation sequencing identified specific fragments of H. capsulatum in all of the samples tested (lung, brain and blood serum from the deceased cases, and plasma from the severe case). Real-time PCR assays did not reveal any viral infection related to transmission from bat feces. We conclude that H. capsulatum was the causative pathogen of this disease cluster based on epidemiologic, clinical, pathological and nucleic acid evidence.

2.
Cell Rep ; 23(3): 909-917, 2018 Apr 17.
Article in English | MEDLINE | ID: mdl-29669294

ABSTRACT

The 2016-2017 epidemic of influenza A (H7N9) virus in China prompted concern that a genetic change may underlie increased virulence. Based on an evolutionary analysis of H7N9 viruses from all five outbreak waves, we find that additional subclades of the H7 and N9 genes have emerged. Our analysis indicates that H7N9 viruses inherited NP genes from co-circulating H7N9 instead of H9N2 viruses. Genotypic diversity among H7N9 viruses increased following wave I, peaked during wave III, and rapidly deceased thereafter with minimal diversity in wave V, suggesting that the viruses entered a relatively stable evolutionary stage. The ZJ11 genotype caused the majority of human infections in wave V. We suggest that the largest outbreak of wave V may be due to a constellation of genes rather than a single mutation. Therefore, continuous surveillance is necessary to minimize the threat of H7N9 viruses.


Subject(s)
Influenza A Virus, H7N9 Subtype/genetics , Influenza, Human/pathology , Amino Acid Substitution , Antigens/genetics , Antigens/immunology , Antigens/metabolism , China/epidemiology , Disease Outbreaks , Evolution, Molecular , Genotype , Humans , Influenza A Virus, H7N9 Subtype/isolation & purification , Influenza A Virus, H7N9 Subtype/pathogenicity , Influenza, Human/epidemiology , Influenza, Human/virology , Nucleocapsid Proteins , Phylogeny , RNA-Binding Proteins/classification , RNA-Binding Proteins/genetics , RNA-Dependent RNA Polymerase/classification , RNA-Dependent RNA Polymerase/genetics , Viral Core Proteins/classification , Viral Core Proteins/genetics , Viral Proteins/classification , Viral Proteins/genetics
3.
Emerg Microbes Infect ; 5(7): e73, 2016 Jul 20.
Article in English | MEDLINE | ID: mdl-27436363

ABSTRACT

H6 avian influenza viruses (AIVs), which are prevalent in domestic and wild birds in Eurasian countries, have been isolated from pigs, a dog and a human. Routine virological surveillance at live poultry markets or poultry farms was conducted in southern China from 2009 to 2011. This study investigated the genetic and antigenic characteristics, analyzed the receptor-binding properties and evaluated the kinetics of infectivity of the AIVs in A549, MDCK and PK15 cells. A total of 14 H6N6 and 2 H6N2 isolates were obtained from four provinces in southern China. Genetic analysis indicated two distinct hemagglutinin lineages of the H6 strains cocirculating in southern China, and these strains facilitated active evolution and reassortment among multiple influenza virus subtypes from different avian species in nature. None of these isolates grouped with the novel Taiwan H6N1 virus responsible for human infection. Receptor-binding specificity assays showed that five H6 AIVs may have acquired the ability to recognize human receptors. Growth kinetics experiments showed that EV/HB-JZ/02/10(H6N2) and EV/JX/15/10(H6N6) initially reproduced faster and achieved higher titers than other viruses, suggesting that enhanced binding to α-2,6-linked sialic acids correlated with increased viral replication in mammalian cells. Overall, the results emphasize the need for continued surveillance of H6 outbreaks and extensive characterization of H6 isolates to better understand genetic changes and their implications.


Subject(s)
Influenza A virus/classification , Influenza A virus/genetics , Influenza in Birds/virology , Phylogeny , Virus Replication/genetics , Animals , Antigens, Viral/genetics , Birds/virology , Cell Line, Tumor , China/epidemiology , Disease Outbreaks , Epidemiological Monitoring , Genome, Viral , Hemagglutinin Glycoproteins, Influenza Virus/genetics , Humans , Influenza A virus/growth & development , Influenza A virus/isolation & purification , Influenza in Birds/epidemiology , Neuraminidase/genetics , RNA, Viral , Real-Time Polymerase Chain Reaction , Sequence Analysis, DNA , Taiwan/epidemiology , Virus Attachment , Virus Replication/physiology
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