scholarly journals Identification of Molecular Markers Associated with Alteration of Receptor-Binding Specificity in a Novel Genotype of Highly Pathogenic Avian Influenza A(H5N1) Viruses Detected in Cambodia in 2013

2014 ◽  
Vol 88 (23) ◽  
pp. 13897-13909 ◽  
Author(s):  
S. Rith ◽  
C. T. Davis ◽  
V. Duong ◽  
B. Sar ◽  
S. V. Horm ◽  
...  
2015 ◽  
Vol 89 (10) ◽  
pp. 5395-5405 ◽  
Author(s):  
Alla Heider ◽  
Larisa Mochalova ◽  
Timm Harder ◽  
Alexander Tuzikov ◽  
Nicolai Bovin ◽  
...  

ABSTRACTHighly pathogenic avian influenza viruses (HPAIVs) of hemagglutinin H5 and H7 subtypes emerge after introduction of low-pathogenic avian influenza viruses (LPAIVs) from wild birds into poultry flocks, followed by subsequent circulation and evolution. The acquisition of multiple basic amino acids at the endoproteolytical cleavage site of the hemagglutinin (HA) is a molecular indicator for high pathogenicity, at least for infections of gallinaceous poultry. Apart from the well-studied significance of the multibasic HA cleavage site, there is only limited knowledge on other alterations in the HA and neuraminidase (NA) molecules associated with changes in tropism during the emergence of HPAIVs from LPAIVs. We hypothesized that changes in tropism may require alterations of the sialyloligosaccharide specificities of HA and NA. To test this hypothesis, we compared a number of LPAIVs and HPAIVs for their HA-mediated binding and NA-mediated desialylation of a set of synthetic receptor analogs, namely, α2-3-sialylated oligosaccharides. NA substrate specificity correlated with structural groups of NAs and did not correlate with pathogenic potential of the virus. In contrast, all HPAIVs differed from LPAIVs by a higher HA receptor-binding affinity toward the trisaccharides Neu5Acα2-3Galβ1-4GlcNAcβ (3′SLN) and Neu5Acα2-3Galβ1-3GlcNAcβ (SiaLec) and by the ability to discriminate between the nonfucosylated and fucosylated sialyloligosaccharides 3′SLN and Neu5Acα2-3Galβ1-4(Fucα1-3)GlcNAcβ (SiaLex), respectively. These results suggest that alteration of the receptor-binding specificity accompanies emergence of the HPAIVs from their low-pathogenic precursors.IMPORTANCEHere, we have found for the first time correlations of receptor-binding properties of the HA with a highly pathogenic phenotype of poultry viruses. Our study suggests that enhanced receptor-binding affinity of HPAIVs for a typical “poultry-like” receptor, 3′SLN, is provided by substitutions in the receptor-binding site of HA which appeared in HA of LPAIVs in the course of transmission of LPAIVs from wild waterfowl into poultry flocks, with subsequent adaptation in poultry. The identification of LPAIVs with receptor characteristics of HPAIVs argues that the sialic acid-binding specificity of the HA may be used as a novel phenotypic marker of HPAIVs.


2011 ◽  
Vol 6 (4) ◽  
pp. 398-403
Author(s):  
Yasuo Suzuki ◽  

The highly pathogenic avian influenza, H5N1 subtype, has been transmitted to humans in 15 countries in the world, with a significantly high fatality rate. The transmission to humans has been expanded. Since the virus was transmitted to humans for the first time in Hong Kong in 1997, the transmission of the virus from human to human has been limited. One of the reasons of the limitation can be found in the fact that the sialoglycoconjugates receptor-binding specificity of H5N1 virus is avian-type, and a mutation of the virus for acquiring receptor-binding specificity exclusively to humans has not occurred. However, it is concerned that if such a mutation of the virus occurred, a pandemic of highly pathogenic avian influenza would break out with a scale far exceeding that of the disastrous Spanish influenza in the past. This paper deals with the present condition of the highly pathogenic avian influenza virus, the mechanism of the virus to acquire the propensity of transmissibility to humans, and the measures against such a mutation.


2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Knut Madslien ◽  
Torfinn Moldal ◽  
Britt Gjerset ◽  
Sveinn Gudmundsson ◽  
Arne Follestad ◽  
...  

Abstract Background Several outbreaks of highly pathogenic avian influenza (HPAI) caused by influenza A virus of subtype H5N8 have been reported in wild birds and poultry in Europe during autumn 2020. Norway is one of the few countries in Europe that had not previously detected HPAI virus, despite widespread active monitoring of both domestic and wild birds since 2005. Results We report detection of HPAI virus subtype H5N8 in a wild pink-footed goose (Anser brachyrhynchus), and several other geese, ducks and a gull, from south-western Norway in November and December 2020. Despite previous reports of low pathogenic avian influenza (LPAI), this constitutes the first detections of HPAI in Norway. Conclusions The mode of introduction is unclear, but a northward migration of infected geese or gulls from Denmark or the Netherlands during the autumn of 2020 is currently our main hypothesis for the introduction of HPAI to Norway. The presence of HPAI in wild birds constitutes a new, and ongoing, threat to the Norwegian poultry industry, and compliance with the improved biosecurity measures on poultry farms should therefore be ensured. [MK1]Finally, although HPAI of subtype H5N8 has been reported to have very low zoonotic potential, this is a reminder that HPAI with greater zoonotic potential in wild birds may pose a threat in the future. [MK1]Updated with a sentence emphasizing the risk HPAI pose to poultry farms, both in the Abstract and in the Conclusion-section in main text, as suggested by Reviewer 1 (#7).


2015 ◽  
Vol 64 (1) ◽  
pp. 144-156 ◽  
Author(s):  
N. Haider ◽  
K. Sturm-Ramirez ◽  
S. U. Khan ◽  
M. Z. Rahman ◽  
S. Sarkar ◽  
...  

2015 ◽  
Vol 21 (5) ◽  
pp. 775-780 ◽  
Author(s):  
Hye-Ryoung Kim ◽  
Yong-Kuk Kwon ◽  
Il Jang ◽  
Youn-Jeong Lee ◽  
Hyun-Mi Kang ◽  
...  

2017 ◽  
Vol 22 (19) ◽  
Author(s):  
Wenfei Zhu ◽  
Jianfang Zhou ◽  
Zi Li ◽  
Lei Yang ◽  
Xiyan Li ◽  
...  

With no or low virulence in poultry, avian influenza A(H7N9) virus has caused severe infections in humans. In the current fifth epidemic wave, a highly pathogenic avian influenza (HPAI) H7N9 virus emerged. The insertion of four amino acids (KRTA) at the haemagglutinin (HA) cleavage site enabled trypsin-independent infectivity of this virus. Although maintaining dual receptor-binding preference, its HA antigenicity was distinct from low-pathogenic avian influenza A(H7N9). The neuraminidase substitution R292K conferred a multidrug resistance phenotype.


2017 ◽  
Vol 23 (2) ◽  
pp. 220-231 ◽  
Author(s):  
Hongbo Guo ◽  
Erik de Vries ◽  
Ryan McBride ◽  
Jojanneke Dekkers ◽  
Wenjie Peng ◽  
...  

2015 ◽  
Vol 21 (12) ◽  
pp. 2135-2140 ◽  
Author(s):  
Carmen S. Arriola ◽  
Deborah I. Nelson ◽  
Thomas J. Deliberto ◽  
Lenee Blanton ◽  
Krista Kniss ◽  
...  

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