Maestre-Carballa Lucia, Navarro-López Vicente, Martinez-Garcia Manuel
Department of Physiology, Genetics and Microbiology, University of Alicante, Alicante, Spain.
Clinical Microbiology and Infectious Disease Unit, Hospital Universitario Vinalopó, Elche, Spain.
Front Microbiol. 2022 May 11;13:858831. doi: 10.3389/fmicb.2022.858831. eCollection 2022.
A comprehensive characterization of the human body resistome [sets of antibiotic resistance genes (ARGs)] is yet to be done and paramount for addressing the antibiotic microbial resistance threat. Here, we study the resistome of 771 samples from five major body parts (skin, nares, vagina, gut, and oral cavity) of healthy subjects from the Human Microbiome Project (HMP) and addressed the potential dispersion of ARGs in pristine environments. A total of 28,714 ARGs belonging to 235 different ARG types were found in the HMP proteome dataset ( = 9.1 × 10 proteins analyzed). Our study reveals a distinct resistome profile (ARG type and abundance) between body sites and high interindividual variability. Nares had the highest ARG load (≈5.4 genes/genome) followed by the oral cavity, whereas the gut showed one of the highest ARG richness (shared with nares) but the lowest abundance (≈1.3 genes/genome). The fluroquinolone resistance genes were the most abundant in the human body, followed by macrolide-lincosamide-streptogramin (MLS) or tetracycline. Most ARGs belonged to common bacterial commensals and multidrug resistance trait were predominant in the nares and vagina. Many ARGs detected here were considered as low risk for human health, whereas only a few of them, such as , 14, 17, or , were classified as high-risk ARG. Our data also provide hope, since the spread of common ARG from the human body to pristine environments ( = 271 samples; 77 Gb of sequencing data and 2.1 × 10 proteins analyzed) thus far remains very unlikely (only one case found in an autochthonous bacterium from a pristine environment). These findings broaden our understanding of ARG in the context of the human microbiome and the One-Health Initiative of WHO uniting human host-microbes and environments as a whole.
对人类机体耐药基因组(抗生素抗性基因[ARGs]集)进行全面表征的工作尚未完成,而这对于应对抗生素微生物耐药性威胁至关重要。在此,我们研究了来自人类微生物组计划(HMP)健康受试者五个主要身体部位(皮肤、鼻腔、阴道、肠道和口腔)的771份样本的耐药基因组,并探讨了ARGs在原始环境中的潜在扩散情况。在HMP蛋白质组数据集中(分析了9.1×10⁶个蛋白质)共发现了属于235种不同ARG类型的28714个ARGs。我们的研究揭示了不同身体部位之间独特的耐药基因组图谱(ARG类型和丰度)以及较高的个体间变异性。鼻腔的ARG负荷最高(约5.4个基因/基因组),其次是口腔,而肠道显示出最高的ARG丰富度之一(与鼻腔相同)但丰度最低(约1.3个基因/基因组)。氟喹诺酮抗性基因在人体中最为丰富,其次是大环内酯-林可酰胺-链阳霉素(MLS)或四环素。大多数ARGs属于常见的共生细菌,多重耐药性状在鼻腔和阴道中占主导地位。此处检测到的许多ARGs被认为对人类健康风险较低,而其中只有少数,如blaCTX-M-14、blaNDM-17或mcr-1,被归类为高风险ARG。我们的数据也带来了希望,因为到目前为止,常见ARGs从人体传播到原始环境(271份样本;77Gb测序数据和2.1×10⁶个蛋白质分析)的可能性仍然非常小(仅在一个来自原始环境土壤的本地细菌中发现一例)。这些发现拓宽了我们在人类微生物组背景下对ARGs的理解,以及世界卫生组织将人类宿主-微生物和环境作为一个整体的“同一健康”倡议的理解。