Evidence map›Paper›PMID 19332815›Full record

ArticleMicrobiology (Reading, England)2009

Localization and assembly of proteins comprising the outer structures of the Bacillus anthracis spore.

Rebecca Giorno, Michael Mallozzi, Joel Bozue, Krishna-Sulayman Moody, Alex Slack, Dengli Qiu, Rong Wang, Arthur Friedlander, Susan Welkos, Adam Driks

Open access · greenAbstract read
In one paragraph

Article in Microbiology (Reading, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  10. TheMicrobiology spectrum · 2019
    Review
  11. Development of dual reporter imaging system forClinical and experimental vaccine research · 2018
    Article
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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.

Rebecca GiornoDepartment of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA.
Michael MallozziDepartment of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA.
Joel BozueBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.
Krishna-Sulayman MoodyBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.
Alex SlackDepartment of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA.
Dengli QiuDepartment of Biological, Chemical, and Physical Sciences, Illinois Institute of Technology, Chicago, IL 60616, USA.
Rong WangDepartment of Biological, Chemical, and Physical Sciences, Illinois Institute of Technology, Chicago, IL 60616, USA.
Arthur FriedlanderHeadquarters, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.
Susan WelkosBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.
Adam DriksDepartment of Microbiology and Immunology, Loyola University Medical Center, Maywood, IL 60153, USA.
Loyola University Medical Center · USUnited States Army Medical Research Institute of Infectious Diseases · USIllinois Institute of Technology · US

Funding

IDENTIFICATION OF B. ANTRACIS SPORE-SURFACE PROTEINSR21AI053365 · NIAID · LOYOLA UNIVERSITY CHICAGO · PI DRIKS, ADAM · 2002 to 2003
$444k
NIAID NIH HHS AI53365NIAID NIH HHS R21 AI053365
6 · The paper itself

Abstract

Bacterial spores possess a series of concentrically arranged protective structures that contribute to dormancy, survival and, ultimately, germination. One of these structures, the coat, is present in all spores. In Bacillus anthracis, however, the spore is surrounded by an additional, poorly understood, morphologically complex structure called the exosporium. Here, we characterize three previously discovered exosporium proteins called ExsFA (also known as BxpB), ExsFB (a highly related paralogue of exsFA/bxpB) and IunH (similar to an inosine-uridine-preferring nucleoside hydrolase). We show that in the absence of ExsFA/BxpB, the exosporium protein BclA accumulates asymmetrically to the forespore pole closest to the midpoint of the sporangium (i.e. the mother-cell-proximal pole of the forespore), instead of uniformly encircling the exosporium. ExsFA/BxpB may also have a role in coat assembly, as mutant spore surfaces lack ridges seen in wild-type spores and have a bumpy appearance. ExsFA/BxpB also has a modest but readily detected effect on germination. Nonetheless, an exsFA/bxpB mutant strain is fully virulent in both intramuscular and aerosol challenge models in Guinea pigs. We show that the pattern of localization of ExsFA/BxpB-GFP is a ring, consistent with a location for this protein in the basal layer of the exosporium. In contrast, ExsFB-GFP fluorescence is a solid oval, suggesting a distinct subcellular location for ExsFB-GFP. We also used these fusion proteins to monitor changes in the subcellular locations of these proteins during sporulation. Early in sporulation, both fusions were present throughout the mother cell cytoplasm. As sporulation progressed, GFP fluorescence moved from the mother cell cytoplasm to the forespore surface and formed either a ring of fluorescence, in the case of ExsFA/BxpB, or a solid oval of fluorescence, in the case of ExsFB. IunH-GFP also resulted in a solid oval of fluorescence. We suggest the interpretation that at least some ExsFB-GFP and IunH-GFP resides in the region between the coat and the exosporium, called the interspace.

Indexed as

AnimalsAnthraxBacillus anthracisBacterial ProteinsFemaleGreen Fluorescent ProteinsGuinea PigsHumansMembrane GlycoproteinsMicroscopy, Atomic ForceMicroscopy, Electron, TransmissionMicroscopy, FluorescenceMutationRecombinant Fusion ProteinsSpores, BacterialSubcellular FractionsBacterial ProteinsBclA protein, Bacillus anthracisGreen Fluorescent ProteinsMembrane GlycoproteinsRecombinant Fusion Proteins

Identifiers

PMID19332815
PMCPMC2895233
OpenAlexW2115869936

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.