Evidence map›Paper›PMID 37495972›Full record

ArticleBMC genomics2023

Non-coding RNAs identification and regulatory networks in pathogen-host interaction in the microsporidia congenital infection.

Zigang Shen, Qiong Yang, Lie Luo, Tangxin Li, Zhuojun Ke, Tian Li, Jie Chen, Xianzhi Meng, Heng Xiang, Chunfeng Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 18 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

13 authors at 3 institutions in 1 country.

Zigang ShenState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Qiong YangSericulture and Agri-Food Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, People's Republic of China.
Lie LuoState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Tangxin LiState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Zhuojun KeState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Tian LiState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Jie ChenState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Xianzhi MengState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Heng XiangCollege of Animal Science and Technology, Southwest University, Chongqing, People's Republic of China.
Chunfeng LiState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Zeyang ZhouState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China.
Ping ChenState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China. chenping1918@swu.edu.cn.
Guoqing PanState Key Laboratory of Resource Insects, Southwest University, Tiansheng Street, Chongqing, 400715, People's Republic of China. gqpan@swu.edu.cn.
Southwest University · CNChongqing Normal University · CNGuangdong Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe interaction networks between coding and non-coding RNAs (ncRNAs) including long non-coding RNA (lncRNA), covalently closed circular RNA (circRNA) and miRNA are significant to elucidate molecular processes of biological activities and interactions between host and pathogen. Congenital infection caused by vertical transmission of microsporidia N. bombycis can result in severe economic losses in the silkworm-feeding industry. However, little is known about ncRNAs that take place in the microsporidia congenital infection. Here we conducted whole-transcriptome RNA-Seq analyses to identify ncRNAs and regulatory networks for both N. bombycis and host including silkworm embryos and larvae during the microsporidia congenital infection.

resultsA total of 4,171 mRNAs, 403 lncRNA, 62 circRNAs, and 284 miRNAs encoded by N. bombycis were identified, among which some differentially expressed genes formed cross-talk and are involved in N. bombycis proliferation and infection. For instance, a lncRNA/circRNA competing endogenous RNA (ceRNA) network including 18 lncRNAs, one circRNA, and 20 miRNAs was constructed to describe 14 key parasites genes regulation, such as polar tube protein 3 (PTP3), ricin-B-lectin, spore wall protein 4 (SWP4), and heat shock protein 90 (HSP90). Regarding host silkworm upon N. bombycis congenital infection, a total of 14,889 mRNAs, 3,038 lncRNAs, 19,039 circRNAs, and 3,413 miRNAs were predicted based on silkworm genome with many differentially expressed coding and non-coding genes during distinct developmental stages. Different species of RNAs form interacting network to modulate silkworm biological processes, such as growth, metamorphosis and immune responses. Furthermore, a lncRNA/circRNA ceRNA network consisting of 140 lncRNAs, five circRNA, and seven miRNAs are constructed hypothetically to describe eight key host genes regulation, such as Toll-6, Serpin-6, inducible nitric oxide synthase (iNOS) and Caspase-8. Notably, cross-species analyses indicate that parasite and host miRNAs play a vital role in pathogen-host interaction in the microsporidia congenital infection.

conclusionThis is the first comprehensive pan-transcriptome study inclusive of both N. bombycis and its host silkworm with a specific focus on the microsporidia congenital infection, and show that ncRNA-mediated regulation plays a vital role in the microsporidia congenital infection, which provides a new insight into understanding the basic biology of microsporidia and pathogen-host interaction.

Indexed as

MicroRNAsMicrosporidiosisNosemaRNA, Long NoncodingGene Regulatory NetworksHost-Pathogen InteractionsRNA, CircularRNA, MessengerMicroRNAsRNA, CircularRNA, Long NoncodingRNA, MessengerCongenital infectionHost–pathogen interactionMicrosporidiaNon-coding RNAsNosema bombycisRegulatory networks

Identifiers

PMID37495972
PMCPMC10373312
OpenAlexW4385261052

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.