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Bioinformatic challenges in metagenomic next generation sequencing data analysis while unravelling a case of uncommon campylobacteriosis
ID
Kogoj, Rok
(
Author
),
ID
Bosilj, Martin
(
Author
),
ID
Celar Šturm, Andraž
(
Author
),
ID
Korva, Miša
(
Author
),
ID
Strašek Smrdel, Katja
(
Author
),
ID
Kvas, Eva
(
Author
),
ID
Pirš, Mateja
(
Author
),
ID
Lepen, Lidija
(
Author
),
ID
Triglav, Tina
(
Author
)
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https://www.sciencedirect.com/science/article/pii/S153204642500070X
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Abstract
Objective: This study aimed to employ advanced bioinformatics and modern sequencing approaches to solve a diagnostic problem of persistent Campylobacter spp. molecular detection yet negative culture results from four consecutive stool samples of a previously healthy patient with newly diagnosed selective IgA deficiency and prolonged diarrhoea. Methods: Metagenomic next-generation sequencing (mNGS) based on short-paired end reads with basic bioinformatic read classification analysis was used at first. Due to ambiguous results, advanced bioinformatics involving contigs construction and classification, reference genome mappings and reads filtering with BBSplit, additionally coupled with metagenomic long-reads sequencing and Full-length 16S rRNA metabarcoding were employed to further elucidate the results. Virulence factors were analysed using the Prokka Genome Annotation tool. Modified classical bacteriology methods were finally used for further clarification. Results: Short-pair end reads analysis identified several Campylobacter species in all four samples. After advanced bioinformatic approaches were applied, candidatus C. infans was suspected as the putative pathogen. This result was further supported by metagenomic long-reads sequencing and Full-length 16S rRNA metabarcoding. Nevertheless, after modifying the culture conditions based on mNGS results, a mixed culture of candidatus C. infans and C. ureolyticus was obtained. Sequencing of the mixed culture resulted in an 87.48% and 73.47% genome coverage of candidatus C. infans and C. ureolyticus, respectively. In the candidatus C. infans genome more virulence factors hits were found than in the C. ureolyticus genome thus supporting the first as the most probable cause of symptoms. Conclusion: This study shows the pivotal role and strengths of mNGS in unravelling an unusual case of diarrhoea and demonstrates how mNGS can guide established microbiological methods to improve on current limitations. However, it also emphasises the need for careful interpretation of sequencing data, particularly for closely related bacterial species from clinical samples that are known to support complex microbial communities.
Language:
English
Keywords:
16S rRNA metabarcoding
,
bioinformatics
,
Campylobacter
,
metagenomics
,
NGS
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2025
Number of pages:
7 str.
Numbering:
Vol. 166, art. 104841
PID:
20.500.12556/RUL-169442
UDC:
659.2:004
ISSN on article:
1532-0480
DOI:
10.1016/j.jbi.2025.104841
COBISS.SI-ID:
237243395
Publication date in RUL:
28.05.2025
Views:
534
Downloads:
158
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Record is a part of a journal
Title:
Journal of biomedical informatics
Publisher:
Elsevier
ISSN:
1532-0480
COBISS.SI-ID:
23743783
Licences
License:
CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:
http://creativecommons.org/licenses/by-nc/4.0/
Description:
A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.
Secondary language
Language:
Slovenian
Keywords:
metačrtno kodiranje 16S rRNA
,
bioinformatika
,
kampilobakter
,
metagenomika
Projects
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P3-0083
Name:
Odnosi parazitskega obstajanja
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