Cargando…

Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host

Ixodes scapularis is a medically important tick that transmits several microbes to humans, including rickettsial pathogen Anaplasma phagocytophilum. In nature, these ticks encounter several abiotic factors including changes in temperature, humidity, and light. Many organisms use endogenously generat...

Descripción completa

Detalles Bibliográficos
Autores principales: Khanal, Supreet, Taank, Vikas, Anderson, John F., Sultana, Hameeda, Neelakanta, Girish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998576/
https://www.ncbi.nlm.nih.gov/pubmed/35408905
http://dx.doi.org/10.3390/ijms23073545
_version_ 1784684976054206464
author Khanal, Supreet
Taank, Vikas
Anderson, John F.
Sultana, Hameeda
Neelakanta, Girish
author_facet Khanal, Supreet
Taank, Vikas
Anderson, John F.
Sultana, Hameeda
Neelakanta, Girish
author_sort Khanal, Supreet
collection PubMed
description Ixodes scapularis is a medically important tick that transmits several microbes to humans, including rickettsial pathogen Anaplasma phagocytophilum. In nature, these ticks encounter several abiotic factors including changes in temperature, humidity, and light. Many organisms use endogenously generated circadian pathways to encounter abiotic factors. In this study, we provide evidence for the first time to show that A. phagocytophilum modulates the arthropod circadian gene for its transmission to the vertebrate host. We noted a circadian oscillation in the expression of arthropod clock, bmal1, period and timeless genes when ticks or tick cells were exposed to alternate 12 h light: 12 h dark conditions. Moreover, A. phagocytophilum significantly modulates the oscillation pattern of expression of these genes. In addition, increased levels of clock and bmal1 and decreased expression of Toll and JAK/STAT pathway immune genes such as pelle and jak, respectively, were noted during A. phagocytophilum transmission from ticks to the vertebrate host. RNAi-mediated knockdown of clock gene expression in ticks resulted in the reduced expression of jak and pelle that increased bacterial transmission from ticks to the murine host. Furthermore, clock-deficient ticks fed late and had less engorgement weights. These results indicate an important role for circadian modulation of tick gene expression that is critical for arthropod blood feeding and transmission of pathogens from vector to the vertebrate host.
format Online
Article
Text
id pubmed-8998576
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-89985762022-04-12 Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host Khanal, Supreet Taank, Vikas Anderson, John F. Sultana, Hameeda Neelakanta, Girish Int J Mol Sci Article Ixodes scapularis is a medically important tick that transmits several microbes to humans, including rickettsial pathogen Anaplasma phagocytophilum. In nature, these ticks encounter several abiotic factors including changes in temperature, humidity, and light. Many organisms use endogenously generated circadian pathways to encounter abiotic factors. In this study, we provide evidence for the first time to show that A. phagocytophilum modulates the arthropod circadian gene for its transmission to the vertebrate host. We noted a circadian oscillation in the expression of arthropod clock, bmal1, period and timeless genes when ticks or tick cells were exposed to alternate 12 h light: 12 h dark conditions. Moreover, A. phagocytophilum significantly modulates the oscillation pattern of expression of these genes. In addition, increased levels of clock and bmal1 and decreased expression of Toll and JAK/STAT pathway immune genes such as pelle and jak, respectively, were noted during A. phagocytophilum transmission from ticks to the vertebrate host. RNAi-mediated knockdown of clock gene expression in ticks resulted in the reduced expression of jak and pelle that increased bacterial transmission from ticks to the murine host. Furthermore, clock-deficient ticks fed late and had less engorgement weights. These results indicate an important role for circadian modulation of tick gene expression that is critical for arthropod blood feeding and transmission of pathogens from vector to the vertebrate host. MDPI 2022-03-24 /pmc/articles/PMC8998576/ /pubmed/35408905 http://dx.doi.org/10.3390/ijms23073545 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Khanal, Supreet
Taank, Vikas
Anderson, John F.
Sultana, Hameeda
Neelakanta, Girish
Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title_full Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title_fullStr Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title_full_unstemmed Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title_short Rickettsial Pathogen Perturbs Tick Circadian Gene to Infect the Vertebrate Host
title_sort rickettsial pathogen perturbs tick circadian gene to infect the vertebrate host
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998576/
https://www.ncbi.nlm.nih.gov/pubmed/35408905
http://dx.doi.org/10.3390/ijms23073545
work_keys_str_mv AT khanalsupreet rickettsialpathogenperturbstickcircadiangenetoinfectthevertebratehost
AT taankvikas rickettsialpathogenperturbstickcircadiangenetoinfectthevertebratehost
AT andersonjohnf rickettsialpathogenperturbstickcircadiangenetoinfectthevertebratehost
AT sultanahameeda rickettsialpathogenperturbstickcircadiangenetoinfectthevertebratehost
AT neelakantagirish rickettsialpathogenperturbstickcircadiangenetoinfectthevertebratehost