Evidence map›Paper›PMID 31337784›Full record

ArticleScientific reports2019

Genomic and molecular characterisation of Escherichia marmotae from wild rodents in Qinghai-Tibet plateau as a potential pathogen.

Sha Liu, Jie Feng, Ji Pu, Xuefang Xu, Shan Lu, Jing Yang, Yiting Wang, Dong Jin, Xiaochen Du, Xiangli Meng and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. New diagnostic methods forFrontiers in microbiology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. A novel phytopathogenFrontiers in cellular and infection microbiology · 2023
    Article
  12. Article
  13. EnteroBase: hierarchical clustering of 100 000s of bacterial genomes into species/subspecies and populations.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  14. mSphere · 2022
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. International journal of systematic and evolutionary microbiology · 2021
    Article
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

16 authors.

Sha LiuState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Jie FengInstitute of Microbiology, Chinese Academy of Sciences, No. 1 Beichen West Road, Beijing, 100101, China.
Ji PuState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Xuefang XuState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Shan LuState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Jing YangState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Yiting WangState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Dong JinState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Xiaochen DuInstitute of Microbiology, Chinese Academy of Sciences, No. 1 Beichen West Road, Beijing, 100101, China.
Xiangli MengState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Xia LuoState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Hui SunState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Yanwen XiongState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Changyun YeState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China.
Ruiting LanSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, New South Wales, Australia. r.lan@unsw.edu.au.
Jianguo XuState Key Laboratory of Infectious Disease Prevention and Control, Collaborative Innovation Center of Diagnosis and Treatment of Infectious Diseases, National Institute of Communicable Disease Control and Prevention, Chinese Center of Disease Control and Prevention, Beijing, 102206, China. xujianguo1@icdc.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wildlife is a reservoir of emerging infectious diseases of humans and domestic animals. Marmota himalayana mainly resides 2800-4000 m above sea level in the Qinghai-Tibetan Plateau, and is the primary animal reservoir of plague pathogen Yersinia pestis. Recently we isolated a new species, Escherichia marmotae from the faeces of M. himalayana. In this study we characterised E. marmotae by genomic analysis and in vitro virulence testing to determine its potential as a human pathogen. We sequenced the genomes of the seven E. marmotae strains and found that they contained a plasmid that carried a Shigella-like type III secretion system (T3SS) and their effectors, and shared the same O antigen gene cluster as Shigella dysenterae 8 and E. coli O38. We also showed that E. marmotae was invasive to HEp-2 cells although it was much less invasive than Shigella. Thus E. marmotae is likely to be an invasive pathogen. However, E. marmotae has a truncated IpaA invasin, and lacks the environmental response regulator VirF and the IcsA-actin based intracellular motility, rendering it far less invasive in comparison to Shigella. E. marmotae also carried a diverse set of virulence factors in addition to the T3SS, including an IS1414 encoded enterotoxin gene astA with 37 copies, E. coli virulence genes lifA/efa, cif, and epeA, and the sfp gene cluster, Yersinia T3SS effector yopJ, one Type II secretion system and two Type VI secretion systems. Therefore, E. marmotae is a potential invasive pathogen.

Indexed as

AnimalsChinaDisease ReservoirsEnterobacteriaceae InfectionsEscherichiaGenome, BacterialHumansMarmotaPhylogenySequence Analysis, DNAShiga-Toxigenic Escherichia coliTibetVirulence FactorsVirulence Factors

Identifiers

PMID31337784
PMCPMC6650469

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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.