Thwe Myat N, Moné Yves, Sen Bhaswati, Czerski Samuel, Azad Ahmed, Earl Joshua P, Hall Donald C, Ehrlich Garth D
School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104, USA.
Department of Microbiology and Immunology, Drexel University College of Medicine, Drexel University, Philadelphia, PA 19102, USA.
Microorganisms. 2025 Apr 1;13(4):807. doi: 10.3390/microorganisms13040807.
The discovery of profound differences in the brain microbiota of Alzheimer's disease (AD) patients and age-matched controls (AMCs) raised questions of postmortem contamination and bacterial transport processes which could be informed by microspatial heterogeneities. We performed semiquantitative species-specific bacterial analyses on multiple micro biopsies from each of the 30 brain specimens (AD and controls). We trimmed ~1 mm of each specimen's edges for surface contaminants and made multiple sterile biopsy punches of the resultant core of each specimen. To identify species-specific abundances, we used our validated, semiquantitative, full-length 16S rRNA gene pan-domain amplification protocol followed by high-fidelity circular consensus sequencing performed on a Pacific Biosciences Sequel IIe instrument. Statistical analyses showed no significant increase in bacterial abundance on trimmed surfaces compared to core specimens, including , the most abundant species previously identified in AD. We did find evidence of substantial bacterial species abundance differences among micro-biopsies obtained from within individual tissue blocks supporting our hypothesis of microspatial heterogeneities. The autopsy brain specimens used in our analyses in this study and our previous publication were not contaminated prior to or postharvesting but we suggest that future microbiological analyses of brain specimens include similar types of edge-core comparison analyses. Further, the species-level bacterial abundance heterogeneities among specimens of the same tissue suggest that multiple symbiotic processes may be occurring.
阿尔茨海默病(AD)患者与年龄匹配的对照者(AMC)大脑微生物群存在显著差异,这一发现引发了关于死后污染和细菌传播过程的问题,而微观空间异质性可能为这些问题提供线索。我们对30个脑标本(AD组和对照组)中的每一个进行了多次微量活检,进行了半定量的物种特异性细菌分析。我们将每个标本的边缘修剪约1毫米以去除表面污染物,并对每个标本剩余的核心部分进行多次无菌活检取样。为了确定物种特异性丰度,我们使用了经过验证的半定量全长16S rRNA基因全结构域扩增方案,随后在PacBio Sequel IIe仪器上进行高保真环形一致测序。统计分析表明,与核心标本相比,修剪后的表面细菌丰度没有显著增加,包括之前在AD中鉴定出的最丰富的物种。我们确实发现,从单个组织块内获取的微量活检样本中,细菌物种丰度存在显著差异,这支持了我们关于微观空间异质性的假设。我们在本研究及之前发表的文章中分析所使用的尸检脑标本在收获前和收获后均未受到污染,但我们建议未来对脑标本进行微生物分析时应包括类似的边缘 - 核心比较分析。此外,同一组织标本之间的物种水平细菌丰度异质性表明可能正在发生多种共生过程。