The anal pore route is efficient to infect Amblyomma spp. ticks with Rickettsia rickettsii and allows the assessment of the role played by infection control targets

Adult Amblyomma sculptum and Amblyomma aureolatum ticks are partially refractory to Rickettsia rickettsii when fed on infected hosts, hindering the functional characterization of potentially protective targets in the bacterial acquisition. In the current study, we used the anal pore route to infect...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in cellular and infection microbiology Vol. 13; p. 1260390
Main Authors: Nassar, Marcelly Bastos, Pavanelo, Daniel B., Labruna, Marcelo B., Daffre, Sirlei, Esteves, Eliane, Fogaça, Andréa C.
Format: Journal Article
Language:English
Published: Frontiers Media S.A 12-10-2023
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Adult Amblyomma sculptum and Amblyomma aureolatum ticks are partially refractory to Rickettsia rickettsii when fed on infected hosts, hindering the functional characterization of potentially protective targets in the bacterial acquisition. In the current study, we used the anal pore route to infect adult A. sculptum and A. aureolatum ticks with R. rickettsii and to assess the effects of the knockdown of microplusin in infection control. The anal pore route was efficient to infect both species, resulting in a prevalence of around 100% of infected ticks. Higher loads of R. rickettsii were detected in microplusin-silenced A. aureolatum in relation to the control, as previously obtained when microplusin-silenced ticks were fed on R. rickettsii -infected rabbits. This is the first report showing R . rickettsii infection through the anal pore in Amblyomma ticks, highlighting this route as a powerful tool to assess the role played by additional targets in the control of pathogens.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Reviewed by: Benjamin Cull, University of Minnesota Twin Cities, United States; Girish Neelakanta, University of Tennessee, United States
Edited by: Isaura Simões, University of Coimbra, Portugal
These authors have contributed equally to this work
These authors have contributed equally to this work and share senior authorship
Present addresses: Eliane Esteves, Department of Microbiology and Immunology, College of Medicine, University of South Alabama, Mobile, AL, United States; Daniel B. Pavanelo, Laboratório Central do Rio Grande do Sul, Centro Estadual de Vigilância em Saúde, Secretaria da Saúde, Porto Alegre, Brazil
ISSN:2235-2988
2235-2988
DOI:10.3389/fcimb.2023.1260390