Evidence map›Paper›PMID 16861648›Full record

ArticleInfection and immunity2006

Maltodextrin utilization plays a key role in the ability of group A Streptococcus to colonize the oropharynx.

Samuel A Shelburne, Paul Sumby, Izabela Sitkiewicz, Nnaja Okorafor, Chanel Granville, Payal Patel, Jovanka Voyich, Richard Hull, Frank R DeLeo, James M Musser

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.4field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 67 citations in OpenAlex.

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  9. ModelingFrontiers in cellular and infection microbiology · 2019
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  12. Specific Imaging of Bacterial Infection Using 6″-Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2017
    Article
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  15. Review
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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

10 authors at 3 institutions in 1 country.

Samuel A ShelburneSection of Infectious Diseases, Department of Medicine, Baylor College of Medicine, Houston, Texas 77030, USA.
Paul Sumby
Izabela Sitkiewicz
Nnaja Okorafor
Chanel Granville
Payal Patel
Jovanka Voyich
Richard Hull
Frank R DeLeo
James M Musser
Houston Methodist · USBaylor College of Medicine · USNational Institutes of Health · US

Funding

Interaction Of Pathogenic Bacteria With LeukocytesZ01AI000900 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI DELEO, FRANK R · 2001 to 2008
$2.8M
NCRR NIH HHS K12 RR 17655-04
6 · The paper itself

Abstract

Analysis of multiple group A Streptococcus (GAS) genomes shows that genes encoding proteins involved in carbohydrate utilization comprise some 15% of the core GAS genome. Yet there is a limited understanding of how carbohydrate utilization contributes to GAS pathogenesis. Previous genome-wide GAS studies led us to a focused investigation of MalE, a putative maltodextrin-binding protein. Analysis of 28 strains of 22 distinct M protein serotypes showed that MalE is highly conserved among diverse GAS strains. malE transcript levels were significantly increased during growth in human saliva compared to growth in a chemically defined glucose-containing medium or a nutrient-rich medium. MalE was accessible to antibody binding, indicating that it is expressed on the GAS cell surface. Moreover, growth in human saliva appeared to increase MalE surface expression compared to growth in a nutrient-rich medium. Analysis of a delta malE isogenic mutant strain revealed decreased growth in human saliva compared to wild-type GAS. Radiolabeled carbohydrate binding assays showed that MalE was required for the binding of maltose but not glucose. The delta malE isogenic mutant strain colonized a lower percentage of GAS-challenged mice compared to wild-type and genetically complemented strains. Furthermore, decreased numbers of CFU were recovered from mice infected with the delta malE strain compared to those infected with wild-type GAS. These data demonstrate that maltodextrin acquisition is likely to be a key factor in the ability of GAS to successfully infect the oropharynx. Further investigation into carbohydrate transport and metabolism pathways may yield novel insights into GAS pathogenesis.

Indexed as

AnimalsBacterial ProteinsCarrier ProteinsCulture MediaFemaleGene Expression Regulation, BacterialHumansMiceMutationOropharynxPolysaccharidesSalivaStreptococcus pyogenesBacterial ProteinsCarrier ProteinsCulture MediamaltodextrinPolysaccharides

Identifiers

PMID16861648
PMCPMC1539623
OpenAlexW2099039960

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.