Insights into tick-pathogen interactions – a single cell RNA sequencing approach of transcriptional changes during ehrlichial infection

This study provides a single-cell resolution framework for interpreting tick cell line biology during infection with a medically relevant ehrlichial pathogen. Using scRNA-seq, we show that the <i>I. scapularis</i> embryonic-derived ISE6 cell line comprises multiple transcriptionally distinct cell states, yet these states do not map cleanly onto canonical tick tissue signatures, even when compared against a curated reference tissue atlas. Despite this heterogeneity, EME broadly infects ISE6 cell population, indicating that susceptibility is not restricted to a specific cell type. We further define a time-dependent arthropod vector response in which early infection is marked by activation of stress and metabolic adaptation response, followed by late-stage inhibition of key signaling, transcriptional, and proliferative pathways as bacterial burden increases. Together, these findings strengthen the biological interpretation of ISE6 as an in vitro model for tick-pathogen interactions and provide a resource for future mechanistic studies of ehrlichial persistence, replication, and vector competence.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-03-20
DOI
https://doi.org/10.64898/2026.03.19.712879
Primary Topic
Vector-borne infectious diseases
Type
article
Field-Weighted Citation Impact
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article

Insights into tick-pathogen interactions – a single cell RNA sequencing approach of transcriptional changes during ehrlichial infection

Joseph A. Aspinwall, Forrest Hoyt, Abdulsalam Adegoke, Adam X. Miranda et al.
bioRxiv (Cold Spring Harbor Laboratory)
Vector-borne infectious diseases
article

Insights into tick-pathogen interactions – a single cell RNA sequencing approach of transcriptional changes during ehrlichial infection

Joseph A. Aspinwall, Forrest Hoyt, Abdulsalam Adegoke, Adam X. Miranda, Taís B. Saito, Margaret Ho, Vinod Nair, Justin Lack, Colton McNinch
article en

Abstract

This study provides a single-cell resolution framework for interpreting tick cell line biology during infection with a medically relevant ehrlichial pathogen. Using scRNA-seq, we show that the <i>I. scapularis</i> embryonic-derived ISE6 cell line comprises multiple transcriptionally distinct cell states, yet these states do not map cleanly onto canonical tick tissue signatures, even when compared against a curated reference tissue atlas. Despite this heterogeneity, EME broadly infects ISE6 cell population, indicating that susceptibility is not restricted to a specific cell type. We further define a time-dependent arthropod vector response in which early infection is marked by activation of stress and metabolic adaptation response, followed by late-stage inhibition of key signaling, transcriptional, and proliferative pathways as bacterial burden increases. Together, these findings strengthen the biological interpretation of ISE6 as an in vitro model for tick-pathogen interactions and provide a resource for future mechanistic studies of ehrlichial persistence, replication, and vector competence.

bioRxiv (Cold Spring Harbor Laboratory)
National Institutes of Health (US), National Institute of Health Sciences (LK), National Institute of Health (AM), Frederick National Laboratory for Cancer Research (US), National Institute of Health of Thailand (TH), National Institute of Allergy and Infectious Diseases (US)
Openalex Percentile: Top 12%
Vector-borne infectious diseases
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