Evidence map›Paper›PMID 41910145›Full record

ArticleMicrobiology spectrum2026

SPCS2 serves as a critical host factor for JEV replication by regulating viral protein stability and virion assembly.

Bei Niu, Shi-Meng Liu, Shu-Jian Zhang, Yu-Ting Huang, Jian-Hui Zhang, Sen Hu, Zhi-Gao Bu, Rong-Hong Hua

Abstract read
In one paragraph

Article in Microbiology spectrum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Bei Niu *State Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Shi-Meng Liu *State Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Shu-Jian ZhangState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Yu-Ting HuangState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Jian-Hui ZhangState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Sen HuState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Zhi-Gao BuState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.ORCID 0000-0001-9242-4211
Rong-Hong HuaState Key Laboratory of Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.ORCID 0000-0001-7034-5766

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-structural protein 2B (NS2B) of flaviviruses plays multiple versatile roles in viral replication through interacting with viral proteins and cellular factors. Identification of NS2B-interacting host factors is essential for a detailed understanding of the viral life cycle, as well as for the development of antiviral therapeutics. To identify the cellular factors that interact with NS2B and are important for JEV replication, JEV-infected cell lysates were co-immunoprecipitated and analyzed by mass spectrometry. Signal peptidase complex subunit 2 (SPCS2) was identified as a novel host factor that interacts with JEV NS2B. SPCS2 was also found to interact with JEV NS5. We revealed that SPCS2 is a host factor required for the replication of JEV by silencing and knocking out endogenous SPCS2. Knockout of SPCS2 markedly impaired intracellular virion assembly and production of infectious JEV particles. Furthermore, we found that SPCS2 depletion promoted the degradation of viral prM, E, and NS1 proteins, but not NS2B protein. Functional loss of SPCS2 does not influence viral attachment, cell entry, RNA replication, protein translation and processing, or even the formation of endoplasmic reticulum membrane-invaginated vesicles during the life cycle of JEV replication. Our findings suggest that SPCS2, a novel host factor that interacts with NS2B and NS5, plays a crucial role in maintaining viral protein stability and in the assembly of JEV virions.IMPORTANCEThe flavivirus non-structural protein, NS2B, participates in viral replication and assembly by interacting with viral proteins and host cellular factors. However, the currently known viral replication, which requires host factors that interact with NS2B, is still very limited. In this study, we identified SPCS2 as a novel NS2B-interacting host factor required for JEV replication using co-immunoprecipitation and mass spectrometry analyses. We revealed that SPCS2 plays essential roles in maintaining the stability of the viral proteins prM, E, and NS1, and in the assembly of infectious JEV particles. This study enriches our understanding of the molecular details underlying host factor involvement in the JEV replication life cycle.

Indexed as

flavivirushost factorNS2Bprotein-protein interactionsSPCS2viral replication

Identifiers

PMID41910145
PMCPMC13141937

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.