Centrin-deficient Leishmania mexicana confers protection against New World cutaneous leishmaniasis

• Published in: npj vaccines Vol. 7; no. 1; p. 32
• Main Authors: Volpedo, Greta, Pacheco-Fernandez, Thalia, Holcomb, Erin A., Zhang, Wen-Wei, Lypaczewski, Patrick, Cox, Blake, Fultz, Rebecca, Mishan, Chelsea, Verma, Chaitenya, Huston, Ryan H., Wharton, Abigail R., Dey, Ranadhir, Karmakar, Subir, Oghumu, Steve, Hamano, Shinjiro, Gannavaram, Sreenivas, Nakhasi, Hira L., Matlashewski, Greg, Satoskar, Abhay R.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.03.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 631/250/590/1867; 631/326/590; Biomedical and Life Sciences; Biomedicine; Bone marrow; Cytokines; Immunization; Immunogenicity; Infectious Diseases; Lesions; Lymph nodes; Medical Microbiology; Parasites; Parasitic diseases; Public Health; Vaccine; Vaccines; Vector-borne diseases; Virology
• ISSN: 2059-0105; 2059-0105
• DOI: 10.1038/s41541-022-00449-1

Leishmaniasis is a neglected protozoan disease affecting over 12 million people globally with no approved vaccines for human use. New World cutaneous leishmaniasis (CL) caused by L. mexicana is characterized by the development of chronic non-healing skin lesions. Using the CRISPR/Cas9 technique, we have generated live attenuated centrin knockout L. mexicana (LmexCen −/− ) parasites. Centrin is a cytoskeletal protein important for cellular division in eukaryotes and, in Leishmania , is required only for intracellular amastigote replication. We have investigated the safety and immunogenicity characteristics of LmexCen −/− parasites by evaluating their survival and the cytokine production in bone-marrow-derived macrophages (BMDMs) and dendritic cells (BMDCs) in vitro. Our data shows that LmexCen −/− amastigotes present a growth defect, which results in significantly lower parasitic burdens and increased protective cytokine production in infected BMDMs and BMDCs, compared to the wild type (WT) parasites. We have also determined the safety and efficacy of LmexCen −/− in vivo using experimental murine models of L. mexicana . We demonstrate that LmexCen −/− parasites are safe and do not cause lesions in susceptible mouse models. Immunization with LmexCen −/− is also efficacious against challenge with WT L. mexicana parasites in genetically different BALB/c and C57BL/6 mouse models. Vaccinated mice did not develop cutaneous lesions, displayed protective immunity, and showed significantly lower parasitic burdens at the infection site and draining lymph nodes compared to the control group. Overall, we demonstrate that LmexCen −/− parasites are safe and efficacious against New World cutaneous leishmaniasis in pre-clinical models.