Evidence map›Paper›PMID 38400087›Full record

ArticleViruses2024

Generation of High-Quality African Swine Fever Virus Complete Genome from Field Samples by Next-Generation Sequencing.

Chuan Shi, Qinghua Wang, Yutian Liu, Shujuan Wang, Yongqiang Zhang, Chunju Liu, Yongxin Hu, Dongxia Zheng, Chengyou Sun, Fangfang Song and 4 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.8field-weighted citation impact, top 11% of its field
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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

14 authors at 1 institution in 1 country.

Chuan ShiChina Animal Health and Epidemiology Center, Qingdao 266032, China.ORCID 0009-0001-8449-2385
Qinghua WangChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Yutian LiuChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Shujuan WangChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Yongqiang ZhangChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Chunju LiuChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Yongxin HuChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Dongxia ZhengChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Chengyou SunChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Fangfang SongChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Xiaojing YuChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Yunling ZhaoChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Jingyue BaoChina Animal Health and Epidemiology Center, Qingdao 266032, China.
Zhiliang WangChina Animal Health and Epidemiology Center, Qingdao 266032, China.
China Animal Health and Epidemiology Center · CN

Funding

National Key Research and Development Program 2022YFD1800503
6 · The paper itself

Abstract

African swine fever (ASF) is a lethal contagious viral disease of domestic pigs and wild boars caused by the African swine fever virus (ASFV). The pandemic spread of ASF has caused severe effects on the global pig industry. Whole-genome sequencing provides crucial information for virus strain characterization, epidemiology analysis and vaccine development. Here, we evaluated the performance of next-generation sequencing (NGS) in generating ASFV genome sequences from clinical samples. Thirty-four ASFV-positive field samples including spleen, lymph node, lung, liver and blood with a range of Ct values from 14.73 to 25.95 were sequenced. For different tissue samples collected from the same sick pigs, the proportion of ASFV reads obtained from the spleen samples was 3.69-9.86 times higher than other tissues. For the high-viral-load spleen samples (Ct < 20), a minimum of a 99.8% breadth of ≥10× coverage was revealed for all the samples. For the spleen samples with Ct ≥ 20, 6/12 samples had a minimum of a 99.8% breadth of ≥10× coverage. A high average depth of sequencing coverage was also achieved from the blood samples. According to our results, high-quality ASFV whole-genome sequences could be obtained from the spleen or blood samples with Ct < 20. The high-quality ASFV genome sequence generated in this study was further used for the high-resolution phylogenetic analysis of the ASFV genomes in the early stage of the ASF epidemic in China. Our study demonstrates that NGS may act as a useful tool for efficient ASFV genome characterization, providing valuable information for disease control.

Indexed as

African Swine FeverAfrican Swine Fever VirusAnimalsHigh-Throughput Nucleotide SequencingPhylogenySus scrofaSwineAfrican swine fever virusclinical samplesgenome characterizationnext-generation sequencing

Identifiers

PMID38400087
PMCPMC10891787
OpenAlexW4391930789

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.