Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.

Pathogenic Leptospira is the etiological cause of the zoonotic life‐threatening infection called leptospirosis. The disease is spread worldwide with higher risk in tropical regions. Although leptospirosis represents a burden to the health of humans and animals, the pathogenic mechanisms of Leptospir...

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Main Authors: Igor R. M. Silva, Maria B. Takahashi, Aline F. Teixeira, Ana L. T. O. Nascimento
Format: Article
Language:English
Published: Wiley 2025-03-01
Series:FEBS Open Bio
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Online Access:https://doi.org/10.1002/2211-5463.13942
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author Igor R. M. Silva
Maria B. Takahashi
Aline F. Teixeira
Ana L. T. O. Nascimento
author_facet Igor R. M. Silva
Maria B. Takahashi
Aline F. Teixeira
Ana L. T. O. Nascimento
author_sort Igor R. M. Silva
collection DOAJ
description Pathogenic Leptospira is the etiological cause of the zoonotic life‐threatening infection called leptospirosis. The disease is spread worldwide with higher risk in tropical regions. Although leptospirosis represents a burden to the health of humans and animals, the pathogenic mechanisms of Leptospira infection are yet to be clarified. Leptospirosis infection is multifactorial, involving functionally redundant proteins with the capability to invade, disseminate, and escape the host's immune response. In this work, we describe a putative lipoprotein encoded by the gene LIC_13355, genome annotated as hypothetical of unknown function. The coding sequence is conserved among pathogenic Leptospira spp. with high percentage of coverage and identity. The recombinant protein, rLIC_13355, was expressed in Escherichia coli host system in its insoluble form. The circular dichroism spectrum of the refolded protein showed it containing a mixture of secondary structures. rLIC_13355 interacts with extracellular matrix (ECM) component laminin and binds plasminogen (PLG), generating plasmin (PLA), thus possibly participating during the adhesion and dissemination processes. The rLIC_13355 has the ability to interact with Ea.hy926 and HMEC‐1 endothelial cells either in monolayer or suspension. The binding of rLIC_13355 with monolayer cells is dose‐dependent on protein concentration. Taken together, our data suggest that this is presumably an adhesion lipoprotein that may play diverse roles in host–Leptospira interactions by mediating the interaction with host components and with endothelial cell.
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spelling doaj-art-c72c9ea698fb42009ff4e36699b636b72025-08-20T02:46:51ZengWileyFEBS Open Bio2211-54632025-03-0115344746110.1002/2211-5463.13942Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.Igor R. M. Silva0Maria B. Takahashi1Aline F. Teixeira2Ana L. T. O. Nascimento3Laboratório de Desenvolvimento de Vacinas Instituto Butantan São Paulo BrazilLaboratório de Desenvolvimento de Vacinas Instituto Butantan São Paulo BrazilLaboratório de Desenvolvimento de Vacinas Instituto Butantan São Paulo BrazilLaboratório de Desenvolvimento de Vacinas Instituto Butantan São Paulo BrazilPathogenic Leptospira is the etiological cause of the zoonotic life‐threatening infection called leptospirosis. The disease is spread worldwide with higher risk in tropical regions. Although leptospirosis represents a burden to the health of humans and animals, the pathogenic mechanisms of Leptospira infection are yet to be clarified. Leptospirosis infection is multifactorial, involving functionally redundant proteins with the capability to invade, disseminate, and escape the host's immune response. In this work, we describe a putative lipoprotein encoded by the gene LIC_13355, genome annotated as hypothetical of unknown function. The coding sequence is conserved among pathogenic Leptospira spp. with high percentage of coverage and identity. The recombinant protein, rLIC_13355, was expressed in Escherichia coli host system in its insoluble form. The circular dichroism spectrum of the refolded protein showed it containing a mixture of secondary structures. rLIC_13355 interacts with extracellular matrix (ECM) component laminin and binds plasminogen (PLG), generating plasmin (PLA), thus possibly participating during the adhesion and dissemination processes. The rLIC_13355 has the ability to interact with Ea.hy926 and HMEC‐1 endothelial cells either in monolayer or suspension. The binding of rLIC_13355 with monolayer cells is dose‐dependent on protein concentration. Taken together, our data suggest that this is presumably an adhesion lipoprotein that may play diverse roles in host–Leptospira interactions by mediating the interaction with host components and with endothelial cell.https://doi.org/10.1002/2211-5463.13942Leptospiraleptospirosispathogenesisrecombinant protein
spellingShingle Igor R. M. Silva
Maria B. Takahashi
Aline F. Teixeira
Ana L. T. O. Nascimento
Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
FEBS Open Bio
Leptospira
leptospirosis
pathogenesis
recombinant protein
title Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
title_full Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
title_fullStr Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
title_full_unstemmed Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
title_short Evaluation of binding activities of a putative lipoprotein LIC_13355 of Leptospira spp.
title_sort evaluation of binding activities of a putative lipoprotein lic 13355 of leptospira spp
topic Leptospira
leptospirosis
pathogenesis
recombinant protein
url https://doi.org/10.1002/2211-5463.13942
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