Pathogenic Rickettsia spp. as emerging models for bacterial biology

Our understanding of free-living bacterial models like Escherichia coli far outpaces that of obligate intracellular bacteria, which cannot be cultured axenically. All obligate intracellular bacteria are host-associated, and many cause serious human diseases. Their constant exposure to the distinct biochemical niche of the host has driven the evolution of numerous specialized bacteriological and genetic adaptations, as well as innovative molecular mechanisms of infection. Here, we review the history and use of pathogenic Rickettsia species, which cause an array of vector-borne vascular illnesses, as model systems to probe microbial biology. Although many challenges remain in our studies of these organisms, the rich pathogenic and biological diversity of Rickettsia spp. constitutes a unique backdrop to investigate how microbes survive and thrive in host and vector cells. We take a bacterial-focused perspective and highlight emerging insights that relate to new host-pathogen interactions, bacterial physiology, and evolution. The transformation of Rickettsia spp. from pathogens to models demonstrates how recalcitrant microbes may be leveraged in the lab to tap unmined bacterial diversity for new discoveries. Rickettsia spp. hold great promise as model systems not only to understand other obligate intracellular pathogens but also to discover new biology across and beyond bacteria.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:206

Enthalten in:

Journal of bacteriology - 206(2024), 2 vom: 22. Feb., Seite e0040423

Sprache:

Englisch

Beteiligte Personen:

Sit, Brandon [VerfasserIn]
Lamason, Rebecca L [VerfasserIn]

Links:

Volltext

Themen:

Bacterial pathogen
Journal Article
Model organism
Obligate intracellular bacteria
Research Support, N.I.H., Extramural
Research Support, U.S. Gov't, Non-P.H.S.
Review
Rickettsia

Anmerkungen:

Date Completed 23.02.2024

Date Revised 08.03.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1128/jb.00404-23

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM368042898