Rapid differential detection of genotype I and III Japanese encephalitis virus from clinical samples by a novel duplex TaqMan probe-based RT-qPCR assay

2020 ◽  
Vol 279 ◽  
pp. 113841 ◽  
Author(s):  
Xin Wang ◽  
Shuang Guo ◽  
Muddassar Hameed ◽  
Junjie Zhang ◽  
Linlin Pang ◽  
...  
Viruses ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 357
Author(s):  
Muddassar Hameed ◽  
Abdul Wahaab ◽  
Mohsin Nawaz ◽  
Sawar Khan ◽  
Jawad Nazir ◽  
...  

Japanese encephalitis (JE) is a vaccine-preventable disease caused by the Japanese encephalitis virus (JEV), which is primarily prevalent in Asia. JEV is a Flavivirus, classified into a single serotype with five genetically distinct genotypes (I, II, III, IV, and V). JEV genotype III (GIII) had been the most dominant strain and caused numerous outbreaks in the JEV endemic countries until 1990. However, recent data shows the emergence of JEV genotype I (GI) as a dominant genotype and it is gradually displacing GIII. The exact mechanism of this genotype displacement is still unclear. The virus can replicate in mosquito vectors and vertebrate hosts to maintain its zoonotic life cycle; pigs and aquatic wading birds act as an amplifying/reservoir hosts, and the humans and equines are dead-end hosts. The important role of pigs as an amplifying host for the JEV is well known. However, the influence of other domestic animals, especially birds, that live in high abundance and close proximity to the human is not well studied. Here, we strive to briefly highlight the role of birds in the JEV zoonotic transmission, discovery of birds as a natural reservoirs and amplifying host for JEV, species of birds susceptible to the JEV infection, and the proposed effect of JEV on the poultry industry in the future, a perspective that has been neglected for a long time. We also discuss the recent in vitro and in vivo studies that show that the newly emerged GI viruses replicated more efficiently in bird-derived cells and ducklings/chicks than GIII, and an important role of birds in the JEV genotype shift from GIII to GI.


2011 ◽  
Vol 85 (19) ◽  
pp. 9847-9853 ◽  
Author(s):  
X.-L. Pan ◽  
H. Liu ◽  
H.-Y. Wang ◽  
S.-H. Fu ◽  
H.-Z. Liu ◽  
...  

Viruses ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 552 ◽  
Author(s):  
Muhammad Naveed Anwar ◽  
Xin Wang ◽  
Muddassar Hameed ◽  
Abdul Wahaab ◽  
Chenxi Li ◽  
...  

The phenotypic and genotypic characteristics of a live-attenuated genotype I (GI) strain (SD12-F120) of Japanese encephalitis virus (JEV) were compared with its virulent parental SD12 strain to gain an insight into the genetic changes acquired during the attenuation process. SD12-F120 formed smaller plaque on BHK-21 cells and showed reduced replication in mouse brains compared with SD12. Mice inoculated with SD12-F120 via either intraperitoneal or intracerebral route showed no clinical symptoms, indicating a highly attenuated phenotype in terms of both neuroinvasiveness and neurovirulence. SD12-F120 harbored 29 nucleotide variations compared with SD12, of which 20 were considered silent nucleotide mutations, while nine resulted in eight amino acid substitutions. Comparison of the amino acid variations of SD12-F120 vs. SD12 pair with those from other four isogenic pairs of the attenuated and their virulent parental strains revealed that the variations at E138 and E176 positions of E protein were identified in four and three pairs, respectively, while the remaining amino acid variations were almost unique to their respective strain pairs. These observations suggest that the genetic changes acquired during the attenuation process were likely to be strain-specific and that the mechanisms associated with JEV attenuation/virulence are complicated.


2019 ◽  
Vol 13 (9) ◽  
pp. e0007716 ◽  
Author(s):  
Muddassar Hameed ◽  
Ke Liu ◽  
Muhammad Naveed Anwar ◽  
Abdul Wahaab ◽  
Anum Safdar ◽  
...  

2013 ◽  
Vol 1 (1) ◽  
Author(s):  
F. Aubry ◽  
M. Vongsouvath ◽  
A. Nougairede ◽  
R. Phetsouvanh ◽  
B. Sibounheuang ◽  
...  

2011 ◽  
Vol 17 (2) ◽  
pp. 319-321 ◽  
Author(s):  
Pradip V. Fulmali ◽  
Gajanan N. Sapkal ◽  
Sulabha Athawale ◽  
Milind M. Gore ◽  
Akhilesh C. Mishra ◽  
...  

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