News Release

A big step for fish herpesvirus diagnostics and treatment

Peer-Reviewed Publication

KeAi Communications Co., Ltd.

Gibel carp that potentially carried CaHV can be detected by the droplet digital PCR based method. Then the virus can be propagated in the GiCS cell line, and further research or treatment could be developed

image: 

Gibel carp that potentially carried CaHV can be detected by the droplet digital PCR based method. Then the virus can be propagated in the GiCS cell line, and further research or treatment could be developed

view more 

Credit: Lang Gui and Fei Ke

Researchers at the Institute of Hydrobiology, Chinese Academy of Sciences, have established a highly permissive cell line GiCS derived from the skin tissue of gibel carp (Carassius gibelio). This cell line, along with a novel diagnostic method, offers robust tools for the early detection and study of Carassius auratus herpesvirus (CaHV), according to two studies by the authors published in the KeAi journal Water Biology and Security.

 Gibel carp, a popular aquaculture species in China with an annual production exceeding 2.5 million tons, faces significant threats from infectious diseases, particularly those of viral origins. CaHV is known to cause severe gill hemorrhages and high mortality rates in gibel carp. Despite the virus being isolated and sequenced nearly a decade ago, knowledge on its pathogenesis has been limited due to the absence of a suitable cell line for in vitro virus propagation.

 To that end, the researchers analyzed the pathway for viruses’ entry into a fish. “Understanding the importance of the skin as the primary contact point with pathogens in aquatic environments, we focused on developing a cell line from this tissue, explains Ke Fei, lead authors of the two studies.

The GiCS cell line, characterized by a modal chromosome number of 156, exhibits high susceptibility to CaHV and several other aquatic animal viruses. This marks the first time that CaHV can be stably cultured in vitro.

In addition, a detection method utilizing droplet digital PCR was developed. This method allows for the sensitive detection of CaHV in infected fish on the first day post-infection, with a detection limit of less than 1 copy per microliter.

"The newly established in vitro infection model will significantly benefit and expedite our research on the pathogenesis mechanism of CaHV. It also opens up avenues for developing cell-based vaccines against the virus,” adds Ke. “With the droplet digital PCR method, we can now identify infected fish before clinical symptoms appear, enabling early intervention to prevent disease spread and reduce economic losses."

###

Contact the author: Contact author name: Fei Ke,Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China,Email: kefei@ihb.ac.cn

The publisher KeAi was established by Elsevier and China Science Publishing & Media Ltd to unfold quality research globally. In 2013, our focus shifted to open access publishing. We now proudly publish more than 100 world-class, open access, English language journals, spanning all scientific disciplines. Many of these are titles we publish in partnership with prestigious societies and academic institutions, such as the National Natural Science Foundation of China (NSFC).


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.