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Immun Inflamm Dis . Molecular epidemiology of SARS-CoV-2 in Mongolia, first experience with nanopore sequencing in lower- and middle-income countri

tetano

Editor, Senior Moderator
Immun Inflamm Dis


. 2023 Dec;11(12):e1095.
doi: 10.1002/iid3.1095. Molecular epidemiology of SARS-CoV-2 in Mongolia, first experience with nanopore sequencing in lower- and middle-income countries setting

Munkhtuya Erendereg[SUP] 1 2 [/SUP], Suvd Tumurbaatar[SUP] 3 [/SUP], Otgonjargal Byambaa[SUP] 1 [/SUP], Gerelmaa Enebish[SUP] 1 [/SUP], Natsagdorj Burged[SUP] 4 [/SUP], Tungalag Khurelsukh[SUP] 4 [/SUP], Nomin-Erdene Baatar[SUP] 5 [/SUP], Badmaarag Munkhjin[SUP] 6 [/SUP], Jargaltulga Ulziijargal[SUP] 7 [/SUP], Anuujin Gantumur[SUP] 1 [/SUP], Oyunbaatar Altanbayar[SUP] 1 [/SUP], Ochbadrakh Batjargal[SUP] 3 [/SUP], Delgermurun Altangerel[SUP] 2 [/SUP], Khosbayar Tulgaa[SUP] 3 [/SUP], Sarangua Ganbold[SUP] 8 [/SUP], Odgerel Tundev[SUP] 8 [/SUP], Sarantsetseg Jigjidsuren[SUP] 9 [/SUP], Tsogbadrakh Nyamdorj[SUP] 4 [/SUP], Naranzul Tsedenbal[SUP] 8 [/SUP], Bumdelger Batmunkh[SUP] 8 [/SUP], Baigalmaa Jantsansengee[SUP] 8 [/SUP], Battur Lkhagvaa[SUP] 8 [/SUP], Bilegtsaikhan Tsolmon[SUP] 3 8 [/SUP], Oyunsuren Enebish[SUP] 10 [/SUP], Erdembileg Tsevegmid[SUP] 10 [/SUP], Enkhbold Sereejav[SUP] 10 [/SUP], Khurelbaatar Nyamdavaa[SUP] 11 [/SUP], Ryenchindorj Erkhembayar[SUP] 12 13 [/SUP], Battogtokh Chimeddorj[SUP] 1 3 [/SUP]



Affiliations
Free PMC article Abstract

Background: Coronavirus disease (COVID-19) has had a significant impact globally, and extensive genomic research has been conducted on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineage patterns and its variants. Mongolia's effective response resulted in low prevalence until vaccinations became available. However, due to the lack of systematically collected data and absence of whole genome sequencing capabilities, we conducted a two-stepped, nationally representative molecular epidemiologic study of SARS-CoV-2 in Mongolia for 2020 and 2021.
Methods: We used retrospective analysis of stored biological samples from November 2020 to October 2021 and a variant-specific real-time reverse transcription polymerase chain reaction (RT-PCR) test to detect SARS-CoV-2 variants, followed by whole genome sequencing by Nanopore technology. Samples were retrieved from different sites and stored at -70°C deep freezer, and tests were performed on samples with cycle threshold <30.
Results: Out of 4879 nucleic acid tests, 799 whole genome sequencing had been carried out. Among the stored samples of earlier local transmission, we found the 20B (B.1.1.46) variant predominated in the earlier local transmission period. A slower introduction and circulation of alpha and delta variants were observed compared to global dynamics in 2020 and 2021. Beta or Gamma variants were not detected between November 2020 and September 2021 in Mongolia.
Conclusions: SARS-CoV-2 variants of concerns including alpha and delta were delayed in circulation potentially due to public health stringencies in Mongolia. We are sharing our initial experience with whole genome sequencing of SARS-CoV-2 from Mongolia, where sequencing data is sparse.

Keywords: COVID-19; SARS-CoV-2; molecular epidemiology; mongolia; whole genome sequencing.

 
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