Articles Vol. 67 No. CĐ4-HN Ký sinh trùng-HN Hóa sinh 2026 14/04/2026

ALTERATIONS OF GUT MICROBIOTA AND SHORT-CHAIN FATTY ACID IN PATIENTS INFECTED WITH HEAVY STRONGYLOIDES STERCORALIS

Nguyen Thi Hai1,2, Nong Phuc Thang1,2, Nguyen Thi Quynh Trang1,2, Doan Thuy Dung1,2
1 Thai Nguyen University of Medicine and Pharmacy
2 Đại học Y Dược Thái Nguyên
DOI: 10.52163/yhc.v67iCD4.4677
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Abstract

Objective: To evaluate the changes of gut microbiota and acetic acid in patients with different levels of Strongyloides stercoralis- infected.

Methods: This study was conducted on the farmers in the Northeastern region of Thailand. Fifty patients infected with S. stercoralis were divided into two groups, SA and SF.

The SA group included patients in whom S. stercoralis was detected only by the agar plate culture method, whereas the SF group included patients in whom the parasite was detected by both agar plate culture and the formalin–ether concentration technique. Bacterial DNA was extracted from individual faecal samples and was then pooled into two groups (SA and SF) for amplification and sequencing of the V3-V4 region of the 16S gene with next-generation technology. Acetic acid in blood was determined by gas chromatography-mass spectrometry GC-MS.

Results: The results showed that the intensity of S. stercoralis infection was associated with alterations in the gut microbiota and acetic acid levels. Compared with the mildly infected group (SA), the severely infected group (SF) exhibited a significant reduction in acetic acid levels, accompanied by a marked decrease in beneficial bacterial genera, including Bifidobacterium, Lactobacillus, and Blautia. In contrast, potentially pathogenic genera such as Escherichia–Shigella, Proteus, and Bacteroides were significantly increased in the SF group. Notably, several beneficial short-chain fatty acid–producing bacterial species, including Coprococcus eutactus, Lactobacillus salivarius, and Lactobacillus reuteri, were markedly reduced in severely infected patients, indicating gut microbiota dysbiosis associated with infection intensity.

Conclusion: Heavy S. stercoralis infection reduced beneficial intestinal bacteria and acetic acid in patients.

References
[1]
Buonfrate D, Bisanzio D, Giorli G, et al. The global prevalence of Strongyloides stercoralis infection. Pathogens. 2020;9(6):468. doi:10.3390/pathogens9060468 Google Scholar
[2]
Marcos LA, Terashima A, Canales M, Gotuzzo E. Update on strongyloidiasis in the immunocompromised host. Curr Infect Dis Rep. 2011;13(1):35–46. doi:10.1007/s11908-010-0150-z Google Scholar
[3]
Figueira CF, Gaspar MT, Cos LD, Ussami EY, Otoch JP, Felipe-Silva A. Strongyloides stercoralis hyperinfection associated with impaired intestinal motility disorder. Autops Case Rep. 2015;5(2):27–34. doi:10.4322/acr.2015.005 Google Scholar
[4]
Qu TT, Yang Q, Yu MH, Wang J. A fatal Strongyloides stercoralis hyperinfection syndrome in a patient with chronic kidney disease: a case report and literature review. Medicine (Baltimore). 2016;95(19):e3638. doi:10.1097/MD.0000000000003638 Google Scholar
[5]
Viney ME, Lok JB. The biology of Strongyloides spp. WormBook. 2015:1–17. doi:10.1895/wormbook.1.141.2 Google Scholar
[6]
Tamboli CP, Neut C, Desreumaux P, Colombel JF. Dysbiosis in inflammatory bowel disease. Gut. 2004;53(1):1–4. doi:10.1136/gut.53.1.1 Google Scholar
[7]
Sekirov I, Russell SL, Antunes LCM, Finlay BB. Gut microbiota in health and disease. Physiol Rev. 2010;90(3):859–904. doi:10.1152/physrev.00045.2009 Google Scholar
[8]
Hasan N, Yang H. Factors affecting the composition of the gut microbiota, and its modulation. PeerJ. 2019;7:e7502. doi:10.7717/peerj.7502 Google Scholar
[9]
Su C, Su L, Li Y, et al. Helminth-induced alterations of the gut microbiota exacerbate bacterial colitis. Mucosal Immunol. 2018;11(1):144–157. doi:10.1038/mi.2017.20 Google Scholar
[10]
Kaewrat W, Sengthong C, Yingklang M, et al. Improved agar plate culture conditions for diagnosis of Strongyloides stercoralis. Acta Trop. 2020;203:105291. doi:10.1016/j.actatropica.2019.105291 Google Scholar
[11]
Fellows R, Denizot J, Stellato C, et al. Microbiota-derived short-chain fatty acids promote histone crotonylation in the colon through histone deacetylases. Nat Commun. 2018;9:105. doi:10.1038/s41467-017-02651-5 Google Scholar
[12]
Hou K, Wu ZX, Chen XY, et al. Microbiota in health and diseases. Signal Transduct Target Ther. 2022;7(1):135. doi:10.1038/s41392-022-00974-4 Google Scholar
[13]
Nogal A, Louca P, Zhang X, et al. Circulating levels of the short-chain fatty acid acetate mediate the effect of the gut microbiome on visceral fat. Front Microbiol. 2021;12:711359. doi:10.3389/fmicb.2021.711359 Google Scholar
[14]
Yang R, Shan S, Shi J, et al. Coprococcus eutactus, a potent probiotic, alleviates colitis via acetate-mediated IgA response and microbiota restoration. J Agric Food Chem. 2023;71(7):3273–3284. doi:10.1021/acs.jafc.2c06697 Google Scholar