Kevin Debatisse, Théophile Niault, Sarah Peeters, Amandine Maire, Busra Toktas, Baptiste Darracq, Zeynep Baharoglu, David Bikard, Didier Mazel, Céline Loot
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引用次数: 0
摘要
背景:霍乱弧菌 O1 El Tor 是导致上一次霍乱大流行的病原体,它已成为一种成熟的模式生物,有一些遗传工具可用。虽然CRISPRi技术已被应用于霍乱弧菌,但仍需加以改进以扩大其应用范围,并通过高通量测序对该细菌进行集中筛选:在本研究中,我们提出了一种全基因组 CRISPR-dCas9 筛选方法,该方法专门针对霍乱弧菌 N16961 El Tor 模式菌株进行了优化。这种方法的特点是严格控制 dCas9 的表达和活性,以及简化实验设置。我们的文库可以删除霍乱弧菌基因组中的 3,674 个(98.9%)注释基因。为了证实它的有效性,我们筛选了在富培养基中指数生长过程中必不可少的基因,并确定了 369 个基因,这些基因的向导在文库中被显著删除(log2FC < -2)。值得注意的是,这些基因中有 82% 以前曾被描述为霍乱弧菌或近缘细菌纳氏霍乱弧菌中的假定必需基因:因此,我们验证了基于 CRISPRi 的方法在特定条件下评估基因适应性的稳健性和准确性。我们的研究结果凸显了所开发的 CRISPRi 平台作为霍乱弧菌高通量功能基因组学研究的强大工具的功效。
Fine-tuning of a CRISPRi screen in the seventh pandemic Vibrio cholerae.
Background: Vibrio cholerae O1 El Tor, the etiological agent responsible for the last cholera pandemic, has become a well-established model organism for which some genetic tools are available. While CRISPRi technology has been applied to V. cholerae, improvements were necessary to upscale it and enable pooled screening by high-throughput sequencing in this bacterium.
Results: In this study, we present a genome-wide CRISPR-dCas9 screen specifically optimized for the N16961 El Tor model strain of V. cholerae. This approach is characterized by a tight control of dCas9 expression and activity, as well as a streamlined experimental setup. Our library allows the depletion of 3,674 (98.9%) annotated genes from the V. cholerae genome. To confirm its effectiveness, we screened for genes that are essential during exponential growth in rich medium and identified 369 genes for which guides were significantly depleted from the library (log2FC < -2). Remarkably, 82% of these genes had previously been described as hypothetical essential genes in V. cholerae or in a closely related bacterium, V. natriegens.
Conclusion: We thus validated the robustness and accuracy of our CRISPRi-based approach for assessing gene fitness in a given condition. Our findings highlight the efficacy of the developed CRISPRi platform as a powerful tool for high-throughput functional genomics studies of V. cholerae.
期刊介绍:
BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics.
BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.