Detection of Rickettsia lusitaniae Among Ornithodoros sawaii Soft Ticks Collected From Japanese Murrelet Seabird Nest Material From Gugul Island, Republic of Korea

Author:

Kim Heung-Chul1ORCID,Jiang Ju23,Hang Jun4,Kim Su Yeon5,Yun Seok-Min6,Park Chang-uk7,Kim Miran7,Chong Sung-Tae1,Farris Christina M2,Richards Allen L8,Klein Terry A1ORCID

Affiliation:

1. Force Health Protection & Preventive Medicine, US Army Medical Activity-Korea, Unit #15281, APO AP, USA

2. Viral and Rickettsial Diseases Department, Naval Medical Research Center, Silver Spring, MD, USA

3. The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, USA

4. Viral Diseases Branch, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, MD, USA

5. Pathogen Resource Management TF, National Research Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju-si, Chungbuk Province, Republic of Korea

6. Division of Arboviruses, National Institute of Health, Korea Centers for Diseases Control and Prevention, Cheongju-si, Chungbuk Province, Republic of Korea

7. Migratory Birds Research Center, Korea National Park Research Institute, Korea National Park Service, Shinan-gun, Jeonnam Province, Republic of Korea

8. Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, MD 20814, USA

Abstract

Abstract In a follow-up to the investigations of soft ticks identified from seabird nest soil and litter collected from coastal islands of the Republic of Korea (ROK), Ornithodoros sawaii and Ornithodoros capensis were assessed for the presence and identification of rickettsiae. Ticks collected from samples of 50–100 g of nest litter and soil from seabird nests were identified individually by morphological techniques, and species confirmed by sequencing of the mt-rrs gene. Subsequently, tick DNA preparations were screened for the presence of rickettsiae using a genus-specific nested PCR (nPCR) assay targeting the 17 kDa antigen gene. The amplicons from the 17 kDa assay and two additional nPCR assays targeting the gltA and ompB gene fragments were sequenced and used to identify the rickettsiae. A total of 134 soft ticks belonging to two species, O. sawaii Kitaoka & Suzuki 1973 (n = 125) and O. capensis Neumann 1901 (n = 9), were collected. Rickettsia lusitaniae DNA was detected and identified among O. sawaii ticks (n = 11, 8.8%) collected from nest litter and soil of the Japanese murrelet (Synthliboramphus wumizusume Temminck 1836) at Gugul Island along the western coastal area of the ROK. This study confirmed for the first time the presence of R. lusitaniae associated with O. sawaii collected from migratory seabird nests in the ROK.

Funder

Armed Forces Health Surveillance Division

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Insect Science,General Veterinary,Parasitology

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