Development of a Recombinase Polymerase Amplification (RPA) assay for Acute Hepatopancreatic Necrosis Disease (AHPND) detection in Pacific white shrimp (Penaeus vannamei)

2021 ◽  
pp. 101710
Author(s):  
Hung Nam Mai ◽  
Luis F. Aranguren Caro ◽  
Roberto Cruz-Flores ◽  
Arun K. Dhar
2018 ◽  
Vol 6 (25) ◽  
Author(s):  
Siddhartha Kanrar ◽  
Arun K. Dhar

ABSTRACT Vibrio parahaemolyticus carrying the toxin genes pirA and pirB causes acute hepatopancreatic necrosis disease in shrimp. A genome sequence of V. parahaemolyticus strain R13 was determined that showed deletions of the entire pirA gene and the 5ʹ end of the pirB gene and does not cause the disease in experimental challenge.


2021 ◽  
Author(s):  
Ge Li ◽  
Guosi Xie ◽  
Hailiang Wang ◽  
Xiaoyuan Wan ◽  
Xinshu Li ◽  
...  

Aquaculture ◽  
2021 ◽  
pp. 736905
Author(s):  
Aya S. Hussain ◽  
Deyaaedin A. Mohammad ◽  
Wafaa S. Sallam ◽  
Nahla M. Shoukry ◽  
D. Allen Davis

Author(s):  
Thomas Caceci ◽  
Kay F. Neck ◽  
Donal D H. Lewis ◽  
Raymond F. Sis

Fourteen specimens of the hepatopancreas of the Pacific white shrimp, Penaeus vannamei, were prepared for examination with the transmission and scanning electron microscopes and with the light microscope. The histology and ultrastructure of this organ is similar to that seen in other Decapoda. At the ultrastructural level, it was observed that B-cells rupture at approximately the level of gap junctions located on the lateral plasma membranes of the cells, and discharge the contents of their large vacuoles into the intercellular space. This efflux of enzymatic material may be the mechanism by which cells are released from the wall of the tubule at the proximal end: the rupture and collapse of a B-cell may be analagous to the removal of the keystone which supports an arch. Deprived of support, and lacking structural adaptations for cohesion (there are no desmosomes or interdigitations in the epithelium) and with the intercellular material digested, the remaining intact cells collapse into the lumen of the tubule. The lysis of individual cells of all types - R-, F-, and B-cells - may contribute to the tubules’ total complement of digestive enzymes.


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