A novel real-time PCR approach for detection of infectious hypodermal and haematopoietic necrosis virus (IHHNV) in the freshwater crayfish Procambarus clarkii

2018 ◽  
Vol 157 ◽  
pp. 100-103 ◽  
Author(s):  
Bo-Kun Chen ◽  
Zhen Dong ◽  
Neng-Yuan Pang ◽  
Yan-Ying Nian ◽  
Dong-Chun Yan
Aquaculture ◽  
2017 ◽  
Vol 477 ◽  
pp. 76-79 ◽  
Author(s):  
Bo-Kun Chen ◽  
Zhen Dong ◽  
Da-Peng Liu ◽  
Yong-Bin Yan ◽  
Neng-Yuan Pang ◽  
...  

2005 ◽  
Vol 110 (3-4) ◽  
pp. 167-179 ◽  
Author(s):  
L DALLAVALLE ◽  
V TOFFOLO ◽  
M LAMPRECHT ◽  
C MALTESE ◽  
G BOVO ◽  
...  

2021 ◽  
Vol 9 (8) ◽  
pp. 856
Author(s):  
Chorong Lee ◽  
Seong-Kyoon Choi ◽  
Hye Jin Jeon ◽  
Seung Ho Lee ◽  
Young Kyoon Kim ◽  
...  

Freshwater crayfish, which are cultivated in aquaculture, are economically important for food and ornamental purposes. However, relatively few studies have focused on potentially pathogenic viruses in crayfish compared to in penaeid shrimp. Commodity red claw crayfish (Cherax quadricarinatus; 400 crayfish in 10 batches) and red swamp crayfish (Procambarus clarkii; 40 crayfish in 2 batches) imported into South Korea from Indonesia and China were screened by PCR to detect infectious hypodermal and hematopoietic necrosis virus (IHHNV or Decapod penstylhamaparvovirus 1). IHHNV was detected in tissue samples pooled from nine out of ten batches of red claw crayfish imported from Indonesia. Phylogenetic analysis of PCR amplicons from representative pools clustered the IHHNV strain with infectious-type II sequences commonly detected in Southeast Asian countries rather than with type III strains detected previously in whiteleg shrimp (Penaeus vannamei) cultured in South Korea. IHHNV DNA was detected most frequently in the muscle (eight batches, 66.7% samples), followed by in the hepatopancreas (five batches, 41.7% samples) and gills tissue (three batches, 25.0% samples). These data suggest that red claw crayfish could be a potential carrier of the virus and that quarantine procedures must be strengthened in South Korea to avoid importing infectious types of IHHNV in commodity crustaceans such as red claw crayfish.


2017 ◽  
Vol 107 ◽  
pp. 98-105 ◽  
Author(s):  
Qiang Lin ◽  
Xiaozhe Fu ◽  
Lihui Liu ◽  
Hongru Liang ◽  
Huizhi Guo ◽  
...  

2016 ◽  
Vol 28 (4) ◽  
pp. 382-391 ◽  
Author(s):  
Maureen K. Purcell ◽  
Schuyler Pearman-Gillman ◽  
Rachel L. Thompson ◽  
Jacob L. Gregg ◽  
Lucas M. Hart ◽  
...  

2013 ◽  
Vol 106 (2) ◽  
pp. 103-115 ◽  
Author(s):  
MK Purcell ◽  
RL Thompson ◽  
KA Garver ◽  
LM Hawley ◽  
WN Batts ◽  
...  

2015 ◽  
Vol 1 (1) ◽  
Author(s):  
Nefi Andriana ◽  
Muhamad Ali ◽  
Sulaiman N. Depamede

Serangan virus White Spot Syndrome (WSSV) telah memberikan dampak finansial yang cukup besar sejak tahun 1992. Tingkat mortalitas yang mencapai 100% menyebabkan banyak pembudidaya udang dan lobster menderita kerugian. Untuk mengatasi permasalahan tersebut sangat diperlukan informasi tentang cara penyebaran virus WSSV sehingga dapat diketahui solusi yang tepat untuk menghentikan penyebarannya pada tambak-tambak udang maupun lobster. Pada penelitian ini, Lobster Air Tawar yang dibudidayakan di BBI Aik Bukak dijadikan kontrol negatif (belum terinfeksi virus WSSV). Hasil penelitian ini menunjukkan bahwa penularan virus WSSV pada lobster air tawar dapat berlangsung melalui konsumsi udang yang telah terinfeksi virus WSSV serta melalui aliran air. Pleopod atau kaki renang yang dideteksi dengan teknologi Real Time Polimerase Chain Reaction (RT-PCR) mengandung virus WSSV yang lebih dominan dibandingkan insangKata kunci: White Spot Syndrome Virus, Lobster Air Tawar, RT-PCR


2006 ◽  
Vol 89 (1) ◽  
pp. 240-244 ◽  
Author(s):  
Zhi-Qin Yue ◽  
Hong Liu ◽  
Wei-Ji Wang ◽  
Zhi-Wen Lei ◽  
Cheng-Zhu Liang ◽  
...  

Abstract An assay was developed for the detection of infectious hypodermal and hematopoietic necrosis virus (IHHNV) based on real-time quantitative polymerase chain reaction (PCR). A pair of primers and a TaqMan probe were designed that are specific for the recognition of a conservative region in the IHHNV genome. The IHHNV real-time PCR assay had a detection limit of 9 DNA copies,with a dynamic range of detection between 9 106 and 9 DNA copies. The primer pairs and probe were specific to IHHNV and did not cross-reactwith shrimp genomic DNAor other shrimp viruses such as White Spot Syndrome Virus (WSSV), Monodon Baculovirus (MBV), and hepatopancreatic parvovirus (HPV). This assay has a broad application for basic and clinical investigations. For clinical samples, the real-time PCR assay detected all the positive samples screened by conventional PCR, which indicated the sensitivity of the real-time assay. The IHHNV real-time PCR assay with high sensitivity, specificity, wide range of detection ability, and simplicity is particularly useful for screening large numbers of specimens and measuring viral loads to monitor the broodstock.


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