Novel Camelid Antibody Fragments Targeting Recombinant Nucleoprotein of Araucaria hantavirus: A Prototype for an Early Diagnosis of Hantavirus Pulmonary Syndrome |
| |
Authors: | Soraya S. Pereira Leandro S. Moreira-Dill Michelle S. S. Morais Nidiane D. R. Prado Marcos L. Barros Andrea C. Koishi Giovanny A. C. A. Mazarrotto Giselle M. Gon?alves Juliana P. Zuliani Leonardo A. Calderon Andreimar M. Soares Luiz H. Pereira da Silva Claudia N. Duarte dos Santos Carla F. C. Fernandes Rodrigo G. Stabeli |
| |
Affiliation: | 1. Fundação Oswaldo Cruz, Fiocruz Rondônia, Porto Velho, RO, Brazil.; 2. Instituto Carlos Chagas, Fiocruz Paraná, Curitiba, PA, Brazil.; 3. Departamento de Medicina, Universidade Federal de Rondônia, UNIR, Porto Velho, RO, Brazil.; 4. Centro de Pesquisa em Medicina Tropical, CEPEM, Porto Velho, RO, Brazil.; Division of Clinical Research, United States of America, |
| |
Abstract: | In addition to conventional antibodies, camelids produce immunoglobulins G composed exclusively of heavy chains in which the antigen binding site is formed only by single domains called VHH. Their particular characteristics make VHHs interesting tools for drug-delivery, passive immunotherapy and high-throughput diagnosis. Hantaviruses are rodent-borne viruses of the Bunyaviridae family. Two clinical forms of the infection are known. Hemorrhagic Fever with Renal Syndrome (HFRS) is present in the Old World, while Hantavirus Pulmonary Syndrome (HPS) is found on the American continent. There is no specific treatment for HPS and its diagnosis is carried out by molecular or serological techniques, using mainly monoclonal antibodies or hantavirus nucleoprotein (N) to detect IgM and IgG in patient serum. This study proposes the use of camelid VHHs to develop alternative methods for diagnosing and confirming HPS. Phage display technology was employed to obtain VHHs. After immunizing one Lama glama against the recombinant N protein (prNΔ85) of a Brazilian hantavirus strain, VHH regions were isolated to construct an immune library. VHHs were displayed fused to the M13KO7 phage coat protein III and the selection steps were performed on immobilized prNΔ85. After selection, eighty clones recognized specifically the N protein. These were sequenced, grouped based mainly on the CDRs, and five clones were analyzed by western blot (WB), surface plasmon resonance (SPR) device, and ELISA. Besides the ability to recognize prNΔ85 by WB, all selected clones showed affinity constants in the nanomolar range. Additionaly, the clone {"type":"entrez-nucleotide","attrs":{"text":"KC329705","term_id":"468362168","term_text":"KC329705"}}KC329705 is able to detect prNΔ85 in solution, as well as the native viral antigen. Findings support the hypothesis that selected VHHs could be a powerful tool in the development of rapid and accurate HPS diagnostic assays, which are essential to provide supportive care to patients and reduce the high mortality rate associated with hantavirus infections. |
| |
Keywords: | |
|
|