Genome-wide CRISPR knockout cell screening platform for the disease vector tick species Ixodes scapularis

Publication information:

Matthew Butnaru, William McKenna, Srishti Goswami, Alejandra Wu-Chuang, Enzo Mameli, Abigail Wilcox, Leopoldine Quennesson, Ah-Ram Kim, Austin Veal, Weihang Chen, Hugo Verzone, Elizabeth A Lane, Hanna J Laukaitis-Yousey, Chad Araneo, Nisha Singh, Joao Pedra, Yanhui Hu, Raghuvir Viswanatha, Norbert Perrimon, and Stephanie E Mohr. 2026. “Genome-Wide CRISPR Knockout Cell Screening Platform for the Disease Vector Tick Species Ixodes Scapularis”. BioRxiv. doi:10.64898/2026.05.05.721418

Abstract

The black legged tick, Ixodes scapularis, is a vector of the bacterium that causes Lyme disease and several other illnesses, including anaplasmosis, babesiosis, and tick-borne encephalitis. Although high-quality genome annotations are available for I. scapularis, functional understanding of I. scapularis genes is limited. To address this, we developed a platform for genome-wide CRISPR-Cas9 knockout screening in I. scapularis cells. To evaluate the platform, we performed a screen to identify genes associated with cellular fitness, and screens for resistance to treatment with copper chloride, Antimycin A, or Destruxin A (DA), a cyclic hexadepsipeptide produced by the pathogenic fungus Metarhizium anisopliae. In each case, the screens implicate specific sets of conserved and non-conserved I. scapularis genes in relevant cellular functions, providing the first experimental evidence of function for a large set of I. scapularis genes. Altogether, in this first-of-its-kind effort for the arthropod subclass Acari, we present an unbiased genome-wide CRISPR-Cas9 knockout cell screening platform, related resources, and datasets that will be broadly useful to efficiently uncover cellular functions of I. scapularis genes.Competing Interest StatementThe authors have declared no competing interest.Fairbairn Foundation HMS Lyme InitiativeNational Institute of Allergy and Infectious Diseases, R21AI168592, R01AI186279, R01AI116523, P01AI138949Howard Hughes Medical Institute, https://ror.org/006w34k90