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...
Autores principales: | , , , , |
---|---|
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 |