Mixture Effects of Polystyrene Microplastics on the Gut Microbiota in C57BL/6 Mice

被引:0
作者
Gao, Bei [1 ,2 ]
Shi, Xiaochun [3 ]
Zhao, Meng [3 ]
Ren, Fangfang [4 ]
Xu, Weichen [5 ]
Gao, Nan [4 ]
Shan, Jinjun [5 ]
Shen, Weishou [3 ,6 ]
机构
[1] Nanjing Univ Informat Sci & Technol, Sch Marine Sci, Nanjing 210044, Peoples R China
[2] Nanjing Univ Informat Sci & Technol, Key Lab Hydrometeorol Disaster Mech & Warning, Minist Water Resources, Nanjing 210044, Peoples R China
[3] Nanjing Univ Informat Sci & Technol, Sch Environm Sci & Engn, Nanjing 210044, Peoples R China
[4] Nanjing Tech Univ, Sch Biol & Pharmaceut Engn, Nanjing 211816, Peoples R China
[5] Nanjing Univ Chinese Med, Inst Pediat, Med Metabol Ctr, Jiangsu Key Lab Pediat Resp Dis, Nanjing 210023, Peoples R China
[6] Collaborat Innovat Ctr Atmospher Environm & Equipm, Jiangsu Key Lab Atmospher Environm Monitoring & Po, Nanjing 210044, Peoples R China
来源
ACS OMEGA | 2025年 / 10卷 / 08期
基金
中国国家自然科学基金;
关键词
LIPID-METABOLISM; GENE; RESISTANCE; DYSBIOSIS; DISORDER; FUNGI;
D O I
10.1021/acsomega.4c00645
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Microplastics are plastic particles with sizes of less than 5 mm. The ubiquity of microplastics in the environment has raised serious public health concerns. Microplastics could disturb the composition of the gut microbiota due to both chemical composition and physical interactions, which might further influence the metabolism and immune function of the host. However, most of the exposure studies chose microplastics of specific sizes. In the natural environment, living organisms are exposed to a mixture of microplastics of various sizes. In this study, male C57BL/6 mice were exposed to polystyrene (PS) microplastics with different sizes, including microplastics with diameters of 0.05-0.1 mu m (PS0.1 group, 100 ppb), 9-10 mu m (PS10 group, 100 ppb), and microplastic mixtures of both 0.05-0.1 and 9-10 mu m (PSMix group) at a total concentration of 100 ppb (50 ppb for each size). Mixture effects of microplastics were investigated on the composition of bacteria and fungi as well as functional metagenome and microbial genes encoding antibiotic resistance and virulence factors. We found that some bacteria, fungi, and microbial metabolic pathways were only altered in the PSMix group, not in the PS0.1 or PS10 group, suggesting the toxic effects of the microplastic mixture on the composition of fungi and bacteria, and the functional metagenome is different from the effects of microplastics at specific sizes. Meanwhile, altered genes encoding antibiotic resistance and virulence factors in the PSMix group were shared with the PS0.1 and PS10 groups, possibly due to functional redundancy. Our findings help improve the understanding of the toxic effects of the microplastic mixture on the gut microbiome.
引用
收藏
页码:7597 / 7608
页数:12
相关论文
共 96 条
[1]   New lnu(C) gene conferring resistance to lincomycin by nucleotidylation in Streptococcus agalactiae UCN36 [J].
Achard, A ;
Villers, C ;
Pichereau, V ;
Leclercq, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (07) :2716-2719
[2]  
Arthur C., 2009, P THEINTERNATIONAL R
[3]  
Bastian M., 2009, P INT AAAI C WEB SOC, V3, P361
[4]   Integrating taxonomic, functional, and strain-level profiling of diverse microbial communities with bioBakery 3 [J].
Beghini, Francesco ;
McIver, Lauren J. ;
Blanco-Miguez, Aitor ;
Dubois, Leonard ;
Asnicar, Francesco ;
Maharjan, Sagun ;
Mailyan, Ana ;
Manghi, Paolo ;
Scholz, Matthias ;
Thomas, Andrew Maltez ;
Valles-Colomer, Mireia ;
Weingart, George ;
Zhang, Yancong ;
Zolfo, Moreno ;
Huttenhower, Curtis ;
Franzosa, Eric A. ;
Segata, Nicola .
ELIFE, 2021, 10
[5]   Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2 [J].
Bolyen, Evan ;
Rideout, Jai Ram ;
Dillon, Matthew R. ;
Bokulich, NicholasA. ;
Abnet, Christian C. ;
Al-Ghalith, Gabriel A. ;
Alexander, Harriet ;
Alm, Eric J. ;
Arumugam, Manimozhiyan ;
Asnicar, Francesco ;
Bai, Yang ;
Bisanz, Jordan E. ;
Bittinger, Kyle ;
Brejnrod, Asker ;
Brislawn, Colin J. ;
Brown, C. Titus ;
Callahan, Benjamin J. ;
Caraballo-Rodriguez, Andres Mauricio ;
Chase, John ;
Cope, Emily K. ;
Da Silva, Ricardo ;
Diener, Christian ;
Dorrestein, Pieter C. ;
Douglas, Gavin M. ;
Durall, Daniel M. ;
Duvallet, Claire ;
Edwardson, Christian F. ;
Ernst, Madeleine ;
Estaki, Mehrbod ;
Fouquier, Jennifer ;
Gauglitz, Julia M. ;
Gibbons, Sean M. ;
Gibson, Deanna L. ;
Gonzalez, Antonio ;
Gorlick, Kestrel ;
Guo, Jiarong ;
Hillmann, Benjamin ;
Holmes, Susan ;
Holste, Hannes ;
Huttenhower, Curtis ;
Huttley, Gavin A. ;
Janssen, Stefan ;
Jarmusch, Alan K. ;
Jiang, Lingjing ;
Kaehler, Benjamin D. ;
Bin Kang, Kyo ;
Keefe, Christopher R. ;
Keim, Paul ;
Kelley, Scott T. ;
Knights, Dan .
NATURE BIOTECHNOLOGY, 2019, 37 (08) :852-857
[6]   Gut microbiome lipid metabolism and its impact on host physiology [J].
Brown, Eric M. ;
Clardy, Jon ;
Xavier, Ramnik J. .
CELL HOST & MICROBE, 2023, 31 (02) :173-186
[7]   Invasive Curvularia Infection in Pediatric Patients With Hematologic Malignancy Identified by Fungal Sequencing [J].
Chang, Yeh-Chung ;
Graf, Erin ;
Green, Abby M. .
JOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY, 2019, 8 (01) :87-91
[8]   Isolation of DiNP-Degrading Microbes from the Mouse Colon and the Influence DiNP Exposure Has on the Microbiota, Intestinal Integrity, and Immune Status of the Colon [J].
Chiu, Karen K. ;
Bashir, Shah Tauseef ;
Abdel-Hamid, Ahmed M. ;
Clark, Lindsay V. ;
Laws, Mary J. ;
Cann, Isaac ;
Nowak, Romana A. ;
Flaws, Jodi A. .
TOXICS, 2022, 10 (02)
[9]   Minireview: Gut Microbiota: The Neglected Endocrine Organ [J].
Clarke, Gerard ;
Stilling, Roman M. ;
Kennedy, Paul J. ;
Stanton, Catherine ;
Cryan, John F. ;
Dinan, Timothy G. .
MOLECULAR ENDOCRINOLOGY, 2014, 28 (08) :1221-1238
[10]   Periodontal pathogens and tetracycline resistance genes in subgingival biofilm of periodontally healthy and diseased Dominican adults [J].
Collins, James R. ;
Arredondo, Alexandre ;
Roa, Alma ;
Valdez, Yleana ;
Leon, Ruben ;
Blanc, Vanessa .
CLINICAL ORAL INVESTIGATIONS, 2016, 20 (02) :349-356