Evidence map›Paper›PMID 38879505›Full record

ArticleAnnals of clinical microbiology and antimicrobials2024

Microbial metagenomic shifts in children with acute lymphoblastic leukaemia during induction therapy and predictive biomarkers for infection.

Huidi Wang, Yajie Zhang, Qianyi Zhou, Lihua Yu, Jingxiang Fu, Danna Lin, Lulu Huang, Xiaorong Lai, Li Wu, Jingxin Zhang and 6 more

Abstract read
In one paragraph

Article in Annals of clinical microbiology and antimicrobials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

16 authors.

Huidi Wang *Microbiome Medicine Center, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Yajie Zhang *Department of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Qianyi Zhou *Microbiome Medicine Center, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Lihua YuDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Jingxiang FuMicrobiome Medicine Center, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Danna LinDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Lulu HuangDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Xiaorong LaiDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Li WuDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Jingxin ZhangDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Juan ZiDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Xu LiaoDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Siying HuangDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China.
Yugu XieDepartment of Laboratory Medicine, Clinical Biobank Centre, Microbiome Medicine Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Yan HeMicrobiome Medicine Center, Department of Laboratory Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China. yanhe@smu.edu.cn.
Lihua YangDepartment of Paediatric Hematology, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, Guangdong, China. dryanglihua@163.com.

Funding

National Key Research and Development Program of China 2019YFA0802300National Natural Science Foundation of China 82022044
6 · The paper itself

Abstract

backgroundEmerging evidence has indicated a link between the gut microbiota and acute lymphoblastic leukaemia (ALL). However, the acute changes in gut microbiota during chemotherapy and the predictive value of baseline gut microbiota in infectious complication remain largely unknown.

methodsFaecal samples (n = 126) from children with ALL (n = 49) undergoing induction chemotherapy were collected at three timepoints, i.e., initiation of chemotherapy (baseline, T0), 7 days (T1) and 33 days (T2) after initiation of chemotherapy. Gut microbiome profile was performed via metagenomic shotgun sequencing. The bioBakery3 pipeline (Kneaddata, Metaphlan 3 and HUMAnN) was performed to assign taxonomy and functional annotations. Gut microbiome at T0 were used to predict infection during chemotherapy.

resultsThe microbial diversities and composition changed significantly during chemotherapy, with Escherichia coli, Klebsiella pneumoniae and Bifidobacterium longum being the most prominent species. The microbial metabolic pathways were also significantly altered during chemotherapy, including the pathway of pyruvate fermentation to acetate and lactate, and assimilatory sulfate reduction pathway. The receiver operating characteristic (ROC) models based on Bifidobacterium longum at T0 could predict infectious complications during the first month of chemotherapy with the area under the curve (AUC) of 0.720.

conclusionsOur study provides new insights into the acute changes in microbial and functional characteristics in children with ALL during chemotherapy. The baseline gut microbiota could be potential biomarkers for infections during chemotherapy.

trial registrationThe study was approved by the Ethics Committee of Zhujiang Hospital, Southern Medical University (2021-KY-171-01) and registered on http://www.chictr.org.cn (ChiCTR2200065406, Registration Date: November 4, 2022).

Indexed as

FecesGastrointestinal MicrobiomeMetagenomicsPrecursor Cell Lymphoblastic Leukemia-LymphomaBacteriaBiomarkersChildChild, PreschoolEscherichia coliFemaleHumansInduction ChemotherapyKlebsiella pneumoniaeMaleMetagenomeBiomarkersAcute lymphoblastic leukaemiaBiomarkerChildrenGut microbiotaInfection

Identifiers

PMID38879505
PMCPMC11180392

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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.