Changes in gut microbiome following anti-tuberculosis treatment: a prospective cohort from eastern China

被引:0
作者
Zhang, Simin [1 ,2 ]
Xu, Zhipeng [3 ]
Wang, Zhan [1 ]
Fei, Xinru [1 ,4 ]
Li, Zhongqi [4 ]
Zhu, Limei [4 ]
Martinez, Leonardo [5 ]
Wang, Jianming [1 ]
Liu, Qiao [1 ,4 ]
机构
[1] Nanjing Med Univ, Ctr Global Hlth, Key Lab Publ Hlth Safety & Emergency Prevent & Con, Dept Epidemiol,Sch Publ Hlth, Nanjing, Peoples R China
[2] Nanjing Med Univ, Sch Publ Hlth, Dept Social Med & Hlth Educ, Natl Vaccine Innovat Platform, Nanjing, Peoples R China
[3] Nanjing Med Univ, Sch Basic Med Sci, Dept Pathogen Biol, Natl Vaccine Innovat Platform, Nanjing, Peoples R China
[4] Ctr Dis Control & Prevent Jiangsu Prov, Dept Chron Communicable Dis, Nanjing, Peoples R China
[5] Boston Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
关键词
Tuberculosis; Gut Microbiome; Anti-tuberculosis treatment; Dysbiosis; Diversity; PULMONARY TUBERCULOSIS; CONTRIBUTES; DYSBIOSIS; SYMPTOMS; DISEASE;
D O I
10.1186/s12879-025-10800-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
BackgroundThe treatment of people with tuberculosis necessitates the administration of both broad-spectrum and narrow-spectrum antibiotics for a minimum duration of six months. Prolonged antibiotic therapy may result in dysregulation of the gut microbiota, potentially influencing the onset and progression of tuberculosis. There is a paucity of studies focus on the characteristics of gut microbiota changes at various time points during tuberculosis treatment. This study aims to elucidate the relationship between the composition of gut microbiota and their stage within anti-tuberculosis therapy.MethodsA multi-center, observational prospective cohort study was conducted at four designated hospitals in Jiangsu Province in eastern China. The Gastrointestinal Symptom Rating Scale was employed to evaluate the gastrointestinal discomfort experienced during anti-tuberculosis treatment. Fecal samples were collected at baseline before initiating anti-tuberculosis therapy and at the end of 2 months and 6 months during treatment. Total microbial genomic DNA was extracted and sequenced. Rarefaction curves and alpha diversity indices including observed operational taxonomic units, Chao1 richness and Shannon index were calculated.ResultsFrom October 2020 to December 2022, a total of 204 people with tuberculosis were diagnosed. Among these, 85 people with tuberculosis provided baseline, 2-month, and 6-month fecal samples. The average age was 41.8 +/- 15.193 years, with a gender ratio of 77 males to 8 females. Only 28.2% of the cohort reported being free of gastrointestinal symptoms during anti-tuberculosis treatment. Anti-tuberculosis treatment significantly reduced gut microbiota diversity, with a transient decrease in alpha diversity indices observed after two months. A higher alpha diversity in baseline (Shannon index with mean +/- standard deviation (SD) 2.92 +/- 0.93 vs. 2.50 +/- 0.84, P = 0.0014, inverse Simpson's index with 11.9 +/- 8.66 vs. 7.87 +/- 6.42, P = 0.0012), compared with people with tuberculosis after 2 months of treatment. No significant differences were identified between 2 months of treatment and at the end of treatment microbiota diversity (Shannon index 2.50 +/- 0.84 vs 2.58 +/- 0.81, P = 0.55, inverse Simpson's index 7.87 +/- 6.42 vs 11.90 +/- 8.66, P = 0.43).ConclusionsFindings from our study show that anti-tuberculosis treatment has profound effects on people with tuberculosis gastrointestinal function and the gut microbiota, particularly during the intensive phase of therapy. After the intensive treatment phase, the gut microbiota has partially recovered, but it is an extremely slow process.
引用
收藏
页数:12
相关论文
共 54 条
  • [1] Host-bacterial mutualism in the human intestine
    Bäckhed, F
    Ley, RE
    Sonnenburg, JL
    Peterson, DA
    Gordon, JI
    [J]. SCIENCE, 2005, 307 (5717) : 1915 - 1920
  • [2] Disease-associated gut microbiome and metabolome changes in patients with chronic obstructive pulmonary disease
    Bowerman, Kate L.
    Rehman, Saima Firdous
    Vaughan, Annalicia
    Lachner, Nancy
    Budden, Kurtis F.
    Kim, Richard Y.
    Wood, David L. A.
    Gellatly, Shaan L.
    Shukla, Shakti D.
    Wood, Lisa G.
    Yang, Ian A.
    Wark, Peter A.
    Hugenholtz, Philip
    Hansbro, Philip M.
    [J]. NATURE COMMUNICATIONS, 2020, 11 (01)
  • [3] Distribution of pathogens and antimicrobial resistance in bacteraemia according to hospitalization duration: a nationwide surveillance study in Switzerland
    Buetti, Niccolo
    Marschall, Jonas
    Timsit, Jean-Francois
    Atkinson, Andrew
    Kronenberg, Andreas
    Sommerstein, Rami
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2021, 27 (12) : 1820 - 1825
  • [4] Cao DM, 2021, MICROBIOL SPECTR, V9, DOI [10.1128/Spectrum.00615-21, 10.1128/spectrum.00615-21]
  • [5] Chen L., 2022, Ifnar gene variants influence gut microbial production of palmitoleic acid and host immune responses to tuberculosis, V4, P359
  • [6] Airway microbial dysbiosis in asthmatic patients: A target for prevention and treatment?
    Chung, Kian Fan
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 139 (04) : 1071 - 1083
  • [7] The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism
    den Besten, Gijs
    van Eunen, Karen
    Groen, Albert K.
    Venema, Koen
    Reijngoud, Dirk-Jan
    Bakker, Barbara M.
    [J]. JOURNAL OF LIPID RESEARCH, 2013, 54 (09) : 2325 - 2340
  • [8] The Long-Term Stability of the Human Gut Microbiota
    Faith, Jeremiah J.
    Guruge, Janaki L.
    Charbonneau, Mark
    Subramanian, Sathish
    Seedorf, Henning
    Goodman, Andrew L.
    Clemente, Jose C.
    Knight, Rob
    Heath, Andrew C.
    Leibel, Rudolph L.
    Rosenbaum, Michael
    Gordon, Jeffrey I.
    [J]. SCIENCE, 2013, 341 (6141) : 44 - +
  • [9] HOST-MICROBE INTERACTION Rules of the game for microbiota
    Faust, Karoline
    Raes, Jeroen
    [J]. NATURE, 2016, 534 (7606) : 182 - 183
  • [10] Giorgia M., 2021, PLoS Pathog, V17, P4