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Review
. 2020 Apr 1;5(2):49.
doi: 10.3390/tropicalmed5020049.

Scrub Typhus: Historic Perspective and Current Status of the Worldwide Presence of Orientia Species

Affiliations
Review

Scrub Typhus: Historic Perspective and Current Status of the Worldwide Presence of Orientia Species

Allen L Richards et al. Trop Med Infect Dis. .

Abstract

Scrub typhus and its etiological agents, Orientia species, have been around for a very long time. Historical reference to the rickettsial disease scrub typhus was first described in China (313 AD) by Hong Ge in a clinical manual (Zhouhofang) and in Japan (1810 AD) when Hakuju Hashimoto described tsutsuga, a noxious harmful disease in the Niigata prefecture. Other clinicians and scientists in Indonesia, Philippines, Taiwan, Australia, Vietnam, Malaysia, and India reported on diseases most likely to have been scrub typhus in the early 1900s. All of these initial reports about scrub typhus were from an area later designated as the Tsutsugamushi Triangle-an area encompassing Pakistan to the northwest, Japan to the northeast and northern Australia to the south. It was not until the 21st century that endemic scrub typhus occurring outside of the Tsutsugamushi Triangle was considered acceptable. This report describes the early history of scrub typhus, its distribution in and outside the Tsutsugamushi Triangle, and current knowledge of the causative agents, Orientia species.

Keywords: Orientia species; Tsutsugamushi Triangle; scrub typhus.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
The Tsutsugamushi Triangle: Geographical Distribution of Scrub Typhus Caused by Orientia tsutsugamushi.
Figure 2
Figure 2
Geographical Distribution of Orientia spp. and the Scrub Typhus: A Worldwide Disease.
Figure 3
Figure 3
Phylogenetic Tree. The evolutionary relationships of Orientia species detected outside of the Tsutsugamushi Triangle were compared with Orientia tsutsugamushi strains, Rickettsia species and other bacteria. The tree was constructed with the 560 bp rrs gene fragments using the Maximum Likelihood method and the Tamura–Nei model in MEGAX. The values of the bootstrap test (1000 replicates) were shown next to the branches.

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