Evidence map›Paper›PMID 39700217›Full record

ArticlePloS one2024

Preliminary analyses of tryptophan, kynurenine, and the kynurenine: Tryptophan ratio in plasma, as potential biomarkers for systemic chlamydial infections in koalas.

Chien-Jung Chen, Benjamin Kimble, Astrid Van Aggelen, Shalini Fischer, Cheyne Flanagan, Amber Gillett, Jackie Reed, Jodie Wakeman, Merran Govendir

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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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

3 citing papers in PubMed.

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4 · The record

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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.

Chien-Jung ChenSydney School of Veterinary Science, The University of Sydney, Sydney, New South Wales, Australia.ORCID 0000-0002-6757-9323
Benjamin KimbleSydney School of Veterinary Science, The University of Sydney, Sydney, New South Wales, Australia.
Astrid Van AggelenPort Macquarie Koala Hospital, Koala Conservation Australia, Port Macquarie, New South Wales, Australia.
Shalini FischerPort Macquarie Koala Hospital, Koala Conservation Australia, Port Macquarie, New South Wales, Australia.
Cheyne FlanaganPort Macquarie Koala Hospital, Koala Conservation Australia, Port Macquarie, New South Wales, Australia.
Amber GillettAustralia Zoo Wildlife Hospital, Wildlife Warriors, Beerwah, Queensland, Australia.
Jackie ReedNorthern Rivers Koala Hospital, Friends of the Koala, East Lismore, New South Wales, Australia.
Jodie WakemanNorthern Rivers Koala Hospital, Friends of the Koala, East Lismore, New South Wales, Australia.ORCID 0009-0007-2343-250X
Merran GovendirSydney School of Veterinary Science, The University of Sydney, Sydney, New South Wales, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chlamydiosis is the major infectious disease responsible for significant morbidity and mortality in free-living koalas. Recently, it was reported that 28.5% of koalas infected with chlamydiosis were presented with no overt clinical signs. Identification and quantification of changes in plasma biomarkers' fluctuations have the potential to enhance C. pecorum detection and facilitate the monitoring of therapeutic efficacy of antibiotics to treat this disease in koalas. Therefore, concentrations of the essential amino acid tryptophan, tryptophan's metabolite kynurenine, and the kynurenine:tryptophan ratio were quantified by high-performance liquid chromatography in the plasma of clinically normal koalas (n = 35), koalas identified with chlamydial disease (n = 35) and koalas that had other non-chlamydial co-morbidities (n = 10). Results showed that there was a significant difference between the clinically normal versus diseased, and clinically normal versus 'other' (both p < 0.001) in kynurenine plasma concentrations and kynurenine:tryptophan ratio; and also between the clinically normal and diseased in tryptophan plasma concentrations (p = 0.001). Proposed reference ranges of tryptophan, kynurenine, and kynurenine:tryptophan ratio in koalas are: 4.27-10.4 μg/mL, 0.34-1.23 μg/mL, and 0.05-0.22, respectively. Proposed optimal cut-off points to differentiate between clinically normal and diseased are: ≤ 4.75 μg/mL (tryptophan), ≥ 0.88 μg/mL (kynurenine), and ≥ 0.12 (kynurenine:tryptophan); and ≤ 7.67 μg/mL (tryptophan), ≥ 1.18 μg/mL (kynurenine), and ≥ 0.16 (kynurenine:tryptophan) to differentiate between released/recovered and euthanised of the diseased/'other' koalas. Significant differences in haematological and biochemical analytes were in the plasma globulins between the clinically normal and diseased koalas (p = 0.01), and in alkaline phosphatase between the clinically normal and 'other' koalas (p = 0.03). Although these potential biomarkers, especially tryptophan, may not be specific for detecting C. pecorum from the rest of the population, kynurenine and the kynurenine:tryptophan ratio may have a role in identifying unhealthy koalas from the clinically normal ones, irrespective of the underlying cause.

Indexed as

BiomarkersChlamydia InfectionsKynureninePhascolarctidaeTryptophanAnimalsChromatography, High Pressure LiquidFemaleMaleBiomarkersKynurenineTryptophan

Identifiers

PMID39700217
PMCPMC11658483

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