scholarly journals Determination of Avian Influenza A Viruses in Some Avian Species in Van Lake Basin by Real Time-PCR, Isolation and Subtyping

2011 ◽  
Vol 10 (4) ◽  
pp. 502-510
Author(s):  
Banur Boynukara ◽  
Timur Gulhan ◽  
Ozdemir Adizel ◽  
Ziya Ilhan ◽  
Abdulbaki Aksakal ◽  
...  
2021 ◽  
Author(s):  
Hong Bo ◽  
Ye Zhang ◽  
Libo Dong ◽  
Jie Dong ◽  
Xiyan Li ◽  
...  

Abstract Background Avian influenza viruses persist in animal hosts and continue to cause human infections in China. It is important to analyse the geographic and seasonal distributions of avian influenza viruses and compare the subtypes and their prevalence among sample sites in environment.MethodsA total of 329,276 environmental samples were collected from locations associated with poultry and wild birds from 2014 to 2017. Viral RNA was extracted from the environmental samples. Real-time PCR assays for influenza A, and the H5, H7, and H9 subtypes were performed on all the samples. Virus isolation was performed on the influenza A-positive samples detected by real-time PCR. Whole-genome sequencing was then performed on an Illumina sequencer.ResultsThe proportions of samples that tested positive for total influenza A and the H5, H9 and H7 subtypes varied among different geographical regions and seasons. Significantly higher proportions of influenza A- and H5-, H9-, and H7-positive samples were collected from live poultry markets and poultry slaughtering locations. Influenza A positivity rates in sewage and chopping board swab samples were higher than those in other sample types. Multiple subtypes related to avian influenza viruses, including 9 HA and 7 NA subtypes, were detected in environmental samples.ConclusionsThese findings indicate that multiple subtypes of avian influenza A viruses continuously coexist in environments associated with poultry and increase the risk of reassortment and transmission, highlighting the need for environmental surveillance in China.


2021 ◽  
pp. 104063872199481
Author(s):  
Yixin Xiao ◽  
Fan Yang ◽  
Fumin Liu ◽  
Hangping Yao ◽  
Nanping Wu ◽  
...  

The H2 subtypes of avian influenza A viruses (avian IAVs) have been circulating in poultry, and they have the potential to infect humans. Therefore, establishing a method to quickly detect this subtype is pivotal. We developed a TaqMan minor groove binder real-time RT-PCR assay that involved probes and primers based on conserved sequences of the matrix and hemagglutinin genes. The detection limit of this assay was as low as one 50% egg infectious dose (EID50)/mL per reaction. This assay is specific, sensitive, and rapid for detecting avian IAV H2 subtypes.


2014 ◽  
Vol 9 (6) ◽  
pp. 628-633
Author(s):  
Dawid Nidzworski ◽  
Joanna Dobkowska ◽  
Marcin Hołysz ◽  
Beata Gromadzka ◽  
Bogusław Szewczyk

AbstractInfluenza is a contagious disease of humans and animals caused by viruses belonging to the Orthomyxoviridae family. The influenza A virus genome consists of negative sense, single-stranded, segmented RNA. Influenza viruses are classified into subtypes based on two surface antigens known as hemagglutinin (H) and neuraminidase (N). The main problem with influenza A viruses infecting humans is drug resistance, which is caused by antigenic changes. A few antiviral drugs are available, but the most popular is the neuraminidase inhibitor — oseltamivir. The resistance against this drug has probably developed through antigenic drift by a point mutation in one amino acid at position 275 (H275Y). In order to prevent a possible influenza pandemic it is necessary to develop fast diagnostic tests. The aim of this project was to develop a new test for detection of influenza A virus and determination of oseltamivir resistance/sensitivity in humans. Detection and differentiation of oseltamivir resistance/sensitivity of influenza A virus was based on real-time PCR. This test contains two TaqMan probes, which work at different wavelengths. Application of techniques like multiplex real-time PCR has greatly enhanced the capability for surveillance and characterization of influenza viruses. After its potential validation, this test can be used for diagnosis before treatment.


2004 ◽  
Vol 117 (2) ◽  
pp. 103-112 ◽  
Author(s):  
Belinda Stone ◽  
Julie Burrows ◽  
Sonia Schepetiuk ◽  
Geoff Higgins ◽  
Alan Hampson ◽  
...  

2012 ◽  
Vol 181 (2) ◽  
pp. 188-191 ◽  
Author(s):  
Markos Mölsä ◽  
Katja A. Koskela ◽  
Esa Rönkkö ◽  
Niina Ikonen ◽  
Thedi Ziegler ◽  
...  

2014 ◽  
Vol 8 (09) ◽  
pp. 1169-1175 ◽  
Author(s):  
Ahmed Ashshi ◽  
Esam Azhar ◽  
Ayman Johargy ◽  
Atif Asghar ◽  
Aiman Momenah ◽  
...  

Introduction: The World Health Organization’s persistent reporting of global outbreaks of influenza A viruses, including the 2009 pandemic swine A H1N1 strain (H1N1pdm09), justified the targeted surveillance of pilgrims during their annual congregation that pools more than two million people from around 165 nations in a confined area of Makkah city in the Kingdom of Saudi Arabia (KSA). Methodology: A total of 1,600 pilgrims were included in the targeted surveillance of influenza A and the 2009 pandemic swine H1N1 strain in the Hajj (pilgrimage) season of 2010. Each pilgrim responded to a demographic and health questionnaire. Collected oropharyngeal swabs were analyzed by real-time PCR for influenza A viruses, and positive samples were further analyzed for the presence of H1N1pdm09. Fisher’s exact test was applied in the analysis of the significance of the distribution of influenza-positive pilgrims according to demographic characters. Results: A total of 120 pilgrims (7.5%) tested positive for influenza A viruses by real-time PCR. Nine out of the 120 influenza-A-positive pilgrims (7.5%) were positive for H1N1pdm09. Demographics played a significant role in those pilgrims who tested positive for influenza A. Conclusions: The detection of H1N1pdm09 in pilgrims at their port of entry to the KSA was alarming, due to the high potential of trans-boundary transmission. This situation necessitates the implementation of specific prevention and control programs to limit infection by influenza A viruses.


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