Evidence map›Paper›PMID 28691659›Full record

ArticleMicrobiology (Reading, England)2017

Proline utilization system is required for infection by the pathogenic α-proteobacterium Brucella abortus.

Mitchell T Caudill, James A Budnick, Lauren M Sheehan, Christian R Lehman, Endang Purwantini, Biswarup Mukhopadhyay, Clayton C Caswell

Abstract read
In one paragraph

Article in Microbiology (Reading, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Role of Proline in Pathogen and Host Interactions.Antioxidants & redox signaling · 2019
    Review
  3. Article
  4. Article
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Mitchell T CaudillDepartment of Biomedical Sciences and Pathobiology, Center for Molecular Medicine and Infectious Diseases, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA.
James A BudnickDepartment of Biomedical Sciences and Pathobiology, Center for Molecular Medicine and Infectious Diseases, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA.
Lauren M SheehanDepartment of Biomedical Sciences and Pathobiology, Center for Molecular Medicine and Infectious Diseases, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA.
Christian R LehmanDepartment of Biomedical Sciences and Pathobiology, Center for Molecular Medicine and Infectious Diseases, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA.
Endang PurwantiniDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Biswarup MukhopadhyayDepartment of Biochemistry, Virginia Tech, Blacksburg, VA 24061, USA.
Clayton C CaswellDepartment of Biomedical Sciences and Pathobiology, Center for Molecular Medicine and Infectious Diseases, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24060, USA.
Virginia Tech · USVirginia–Maryland College of Veterinary Medicine · US

Funding

Characterization of a novel genetic pathway required for Brucella virulenceR15AI117648 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CASWELL, CLAYTON C · 2015 to 2015
$459k
NIAID NIH HHS R15 AI117648
6 · The paper itself

Abstract

Proline utilization (Put) systems have been described in a number of bacteria; however, the importance and functionality of the Put system in the intracellular pathogen Brucellaabortus has not been explored. Generally, bacterial Put systems are composed of the bifunctional enzyme proline dehydrogenase PutA and its transcriptional activator PutR. Here, we demonstrate that the genes putA (bab2_0518) and putR (bab2_0517) are critical for the chronic infection of mice by B. abortus, but putA and putR are not required for the survival and replication of the bacteria in naive macrophages. Additionally, in vitro experiments revealed that putR is necessary for the ability of the bacteria to withstand oxidative stress, as a ΔputR deletion strain is hypersensitive to hydrogen peroxide exposure. Quantitative reverse transcription-PCR and putA-lacZ transcriptional reporter studies revealed that PutR acts as a transcriptional activator of putA in Brucella, and electrophoretic mobility shift assays confirmed that PutR binds directly to the putA promoter region. Biochemical analyses demonstrated that a purified recombinant B. abortus PutA protein possesses quintessential proline dehydrogenase activity, as PutA is capable of catalysing the conversion of proline to glutamate. Altogether, these data are the first to reveal that the Put system plays a significant role in the ability of B. abortus to replicate and survive within its host, as well as to describe the genetic regulation and biochemical activity of the Put system in Brucella.

Indexed as

AnimalsBacterial ProteinsBrucella abortusBrucellosisGene Expression Regulation, BacterialGlutamic AcidHumansMiceMice, Inbred BALB CProlineProline OxidaseTrans-ActivatorsVirulenceBacterial ProteinsGlutamic AcidProlineProline OxidaseTrans-Activators

Identifiers

PMID28691659
PMCPMC5737144
OpenAlexW2730987564

What OpenQuestion holds

Textmetadata
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.