Evidence map›Paper›PMID 27375581›Full record

ArticleFrontiers in microbiology2016

Identification and Characterization of Novel Small RNAs in Rickettsia prowazekii.

Casey L C Schroeder, Hema P Narra, Abha Sahni, Mark Rojas, Kamil Khanipov, Jignesh Patel, Riya Shah, Yuriy Fofanov, Sanjeev K Sahni

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Hybrid capture RNA-seq defines temporal gene expression inbioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Prevalence of small base-pairing RNAs derived from diverse genomic loci.Biochimica et biophysica acta. Gene regulatory mechanisms · 2020
    Review
  7. Review
  8. Review
  9. New approaches in the systematics of rickettsiae.New microbes and new infections · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

9 authors.

Casey L C SchroederDepartment of Pathology, University of Texas Medical Branch Galveston, TX, USA.
Hema P NarraDepartment of Pathology, University of Texas Medical Branch Galveston, TX, USA.
Abha SahniDepartment of Pathology, University of Texas Medical Branch Galveston, TX, USA.
Mark RojasDepartment of Pharmacology, University of Texas Medical Branch Galveston, TX, USA.
Kamil KhanipovDepartment of Pharmacology, University of Texas Medical Branch Galveston, TX, USA.
Jignesh PatelDepartment of Pathology, University of Texas Medical Branch Galveston, TX, USA.
Riya ShahDepartment of Neuroscience, University of Texas at Dallas Dallas, TX, USA.
Yuriy FofanovDepartment of Pharmacology, University of Texas Medical Branch Galveston, TX, USA.
Sanjeev K SahniDepartment of Pathology, University of Texas Medical Branch Galveston, TX, USA.

Funding

Riboregulation in Pathogenic RickettsiaeR21AI115231 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SAHNI, SANJEEV K. · 2015 to 2016
$426k
NIAID NIH HHS R21 AI115231
6 · The paper itself

Abstract

Emerging evidence implicates a critically important role for bacterial small RNAs (sRNAs) as post-transcriptional regulators of physiology, metabolism, stress/adaptive responses, and virulence, but the roles of sRNAs in pathogenic Rickettsia species remain poorly understood. Here, we report on the identification of both novel and well-known bacterial sRNAs in Rickettsia prowazekii, known to cause epidemic typhus in humans. RNA sequencing of human microvascular endothelial cells (HMECs), the preferred targets during human rickettsioses, infected with R. prowazekii revealed the presence of 35 trans-acting and 23 cis-acting sRNAs, respectively. Of these, expression of two trans-acting (Rp_sR17 and Rp_sR60) and one cis-acting (Rp_sR47) novel sRNAs and four well-characterized bacterial sRNAs (RNaseP_bact_a, α-tmRNA, 4.5S RNA, 6S RNA) was further confirmed by Northern blot or RT-PCR analyses. The transcriptional start sites of five novel rickettsial sRNAs and 6S RNA were next determined using 5' RLM-RACE yielding evidence for their independent biogenesis in R. prowazekii. Finally, computational approaches were employed to determine the secondary structures and potential mRNA targets of novel sRNAs. Together, these results establish the presence and expression of sRNAs in R. prowazekii during host cell infection and suggest potential functional roles for these important post-transcriptional regulators in rickettsial biology and pathogenesis.

Indexed as

epidemic typhusRickettsia prowazekiiRNA sequencingsmall RNAsvascular endothelium

Identifiers

PMID27375581
PMCPMC4896933

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Registered trials

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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.