Enteric pathogens relationship with small bowel histologic features of environmental enteric dysfunction in a multicountry cohort study.
LMIC
TAC
enteropathogens
environmental enteric dysfunction
qPCR
virulence loci
Journal
The American journal of clinical nutrition
ISSN: 1938-3207
Titre abrégé: Am J Clin Nutr
Pays: United States
ID NLM: 0376027
Informations de publication
Date de publication:
Sep 2024
Sep 2024
Historique:
received:
05
09
2023
revised:
14
02
2024
accepted:
22
02
2024
medline:
20
9
2024
pubmed:
20
9
2024
entrez:
20
9
2024
Statut:
ppublish
Résumé
Environmental Enteric Dysfunction (EED) is an acquired disorder of asymptomatic altered gut function, the etiology of which is unknown. EED is postulated to be a major contributor to growth faltering in early childhood in regions where early-life enteropathogenic carriage is prevalent. Few studies have examined the critical organ (the upper small bowel) with enteropathogens in the evolution of small bowel disease. The objective of this study was to determine if fecal enteropathogenic detection predicts subsequent EED histology. Fecal samples were obtained from undernourished children aged <2 y without diarrhea enrolled in 3 cohort studies, who failed nutritional intervention and subsequently underwent endoscopy. Duodenal biopsies from 245 (Bangladesh n = 120, Pakistan n = 57, and Zambia n = 68) children were scored using a semiquantitative histologic grading protocol. Thirteen enteropathogens were sought in common across the 3 centers using TaqMan array cards (TAC) (Bangladesh and Pakistan) and the Luminex platform (Zambia). An additional 18 pathogens and 32 virulence loci were sought by TAC and included in sensitivity analyses restricted to TAC data. Multivariable linear regressions adjusting for study center, age at stool collection, and stool-to-biopsy interval demonstrated the following: 1) an association of norovirus and Shigella detection with subsequent enterocyte injury [β 0.2 (95% CI: 0.1, 0.3); P = 0.002 and β 0.2 (95% CI: 0.0, 0.3); P = 0.008, respectively], 2) association of Campylobacter with intraepithelial lymphocytes [β 0.2 (95% CI: 0.0, 0.4); P = 0.046], and 3) association of Campylobacter and enterotoxigenic Escherichia coli with a summative EED histopathology index score [β 4.2 (95% CI: 0.8, 7.7); P = 0.017 and β 3.9 (95% CI: 0.5, 7.3); P = 0.027, respectively]. All but 2 of these associations (Shigella-enterocyte injury and Campylobacter-index score) were also demonstrated in TAC-only sensitivity analyses, which identified additional associations between other pathogens, pathogen burden, or virulence loci primarily with the same histologic parameters. The detection of some enteropathogens in asymptomatic infections is associated with subsequent EED histopathology. These novel findings offer a basis for future EED etiology and pathogenesis studies.
Sections du résumé
BACKGROUND
BACKGROUND
Environmental Enteric Dysfunction (EED) is an acquired disorder of asymptomatic altered gut function, the etiology of which is unknown. EED is postulated to be a major contributor to growth faltering in early childhood in regions where early-life enteropathogenic carriage is prevalent. Few studies have examined the critical organ (the upper small bowel) with enteropathogens in the evolution of small bowel disease.
OBJECTIVES
OBJECTIVE
The objective of this study was to determine if fecal enteropathogenic detection predicts subsequent EED histology.
METHODS
METHODS
Fecal samples were obtained from undernourished children aged <2 y without diarrhea enrolled in 3 cohort studies, who failed nutritional intervention and subsequently underwent endoscopy. Duodenal biopsies from 245 (Bangladesh n = 120, Pakistan n = 57, and Zambia n = 68) children were scored using a semiquantitative histologic grading protocol. Thirteen enteropathogens were sought in common across the 3 centers using TaqMan array cards (TAC) (Bangladesh and Pakistan) and the Luminex platform (Zambia). An additional 18 pathogens and 32 virulence loci were sought by TAC and included in sensitivity analyses restricted to TAC data.
RESULTS
RESULTS
Multivariable linear regressions adjusting for study center, age at stool collection, and stool-to-biopsy interval demonstrated the following: 1) an association of norovirus and Shigella detection with subsequent enterocyte injury [β 0.2 (95% CI: 0.1, 0.3); P = 0.002 and β 0.2 (95% CI: 0.0, 0.3); P = 0.008, respectively], 2) association of Campylobacter with intraepithelial lymphocytes [β 0.2 (95% CI: 0.0, 0.4); P = 0.046], and 3) association of Campylobacter and enterotoxigenic Escherichia coli with a summative EED histopathology index score [β 4.2 (95% CI: 0.8, 7.7); P = 0.017 and β 3.9 (95% CI: 0.5, 7.3); P = 0.027, respectively]. All but 2 of these associations (Shigella-enterocyte injury and Campylobacter-index score) were also demonstrated in TAC-only sensitivity analyses, which identified additional associations between other pathogens, pathogen burden, or virulence loci primarily with the same histologic parameters.
CONCLUSIONS
CONCLUSIONS
The detection of some enteropathogens in asymptomatic infections is associated with subsequent EED histopathology. These novel findings offer a basis for future EED etiology and pathogenesis studies.
Identifiants
pubmed: 39300666
pii: S0002-9165(24)00273-9
doi: 10.1016/j.ajcnut.2024.02.026
pii:
doi:
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
S84-S93Investigateurs
Kumail Ahmed
(K)
Sheraz Ahmed
(S)
Md Ashraful Alam
(MA)
S Asad Ali
(SA)
Beatrice Amadi
(B)
Subhasish Das
(S)
Md Amran Gazi
(MA)
Rashidul Haque
(R)
Md Mehedi Hasan
(MM)
Md Shabab Hossain
(MS)
Aneeta Hotwani
(A)
Shahneel Hussain
(S)
Junaid Iqbal
(J)
Sadaf Jakhro
(S)
Ta-Chiang Liu
(TC)
Ramendra Nath Mazumder
(RN)
Christopher A Moskaluk
(CA)
Abdul Khalique Qureshi
(AK)
Shyam S Raghavan
(SS)
Masudur Rahman
(M)
Najeeb Rahman
(N)
Kamran Sadiq
(K)
Shafiqul Alam Sarker
(SA)
Peter B Sullivan
(PB)
Guillermo J Tearney
(GJ)
Fayaz Umrani
(F)
Omer H Yilmaz
(OH)
Kanekwa Zyambo
(K)
Informations de copyright
Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.