Evidence map›Paper›PMID 37270805›Full record

ArticleBiomolecules & biomedicine2023

Cytoplasmic amino acid profiles of clinical and ATCC 29213 strains of Staphylococcus aureus harvested at different growth phases.

Mousa Alreshidi, Hugh Dunstan, Tim Roberts, Fayez Alreshidi, Ashfaque Hossain, Fevzi Bardakci, Mejdi Snoussi, Riadh Badraoui, Mohd Adnan, Sultan Alouffi and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Biomolecules & biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

11 authors at 4 institutions in 4 countries.

Mousa AlreshidiDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Hugh DunstanInnovAAte Pty Ltd, Newcastle, NSW, Australia.
Tim RobertsMetabolic Research Group, Faculty of Science, School of Environmental and Life Sciences, University Drive, Callaghan, NSW, Australia.
Fayez AlreshidiDepartment of Family and Community Medicine, College of Medicine, University of Ha'il, Ha'il, Saudi Arabia.
Ashfaque HossainDepartment of Medical Microbiology and Immunology, RAK Medical and Health Sciences University, Ras Al Khaimah, United Arab Emirates.
Fevzi BardakciDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Mejdi SnoussiDepartment of Biology, College of Science, University of Ha'il, Ha'il, Saudi Arabia; Laboratory of Genetics, Biodiversity and Valorization of Bio-Resources (LR11ES41), Higher Institute of Biotechnology of Monastir, University of Monastir, Monastir, Tunisia.
Riadh BadraouiDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Mohd AdnanDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Sultan AlouffiDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, Hail, Saudi Arabia.
Mohd SaeedDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
University of Ha'il · SARas al-Khaimah Medical and Health Sciences University · AEUniversity of Monastir · TNUniversity of Newcastle Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus strains are a great contributor to both hospital acquired infections as well as community acquired infections. The objective of the present investigation was to compare potential differences in cytoplasmic amino acid levels between clinical and ATCC 29213 strains of S. aureus. The two strains were grown under ideal conditions to mid-exponential and stationary growth phases, after which they were harvested to analyze their amino acid profiles. Initially, the amino acid patterns of both strains were compared at the mid-exponential phase when grown in controlled conditions. At the mid-exponential phase, both strains shared common features in cytoplasmic amino acid levels, with glutamic acid, aspartic acid, proline, and alanine identified as key amino acids. However, the concentration profiles of seven amino acids exhibited major variances between the strains, even though the total cytoplasmic levels of amino acids did not alter significantly. At the stationary phase, the magnitudes of the amino acids abundant in the mid-exponential phase were altered. Aspartic acid became the most abundant amino acid in both strains accounting for 44% and 59% of the total amino acids in the clinical and ATCC 29213 strains, respectively. Lysine was the second most abundant amino acid in both strains, accounting for 16% of the total cytoplasmic amino acids, followed by glutamic acid, the concentration of which was significantly higher in the clinical strain than in the ATCC 29213 strain. Interestingly, histidine was clearly present in the clinical strain but was virtually lacking in the ATCC 29213 strain. This study reveals the dynamic diversity of amino acid levels among strains, which is an essential step toward illustrating the variability in S. aureus cytoplasmic amino acid profiles and could be significant in explaining variances among strains of S. aureus.

Indexed as

Amino AcidsStaphylococcal InfectionsAspartic AcidCytoplasmGlutamic AcidHumansStaphylococcus aureusAmino AcidsAspartic AcidGlutamic Acid

Identifiers

PMID37270805
PMCPMC10655876
OpenAlexW4379364669

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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.