Multihospital Outbreak of a Middle East Respiratory Syndrome Coronavirus Deletion Variant, Jordan: A Molecular, Serologic, and Epidemiologic Investigation

Author:

Payne Daniel C1,Biggs Holly M1,Al-Abdallat Mohammad Mousa2,Alqasrawi Sultan2,Lu Xiaoyan1,Abedi Glen R1,Haddadin Aktham3,Iblan Ibrahim4,Alsanouri Tarek5,Al Nsour Mohannad5,Sheikh Ali Sami2,Rha Brian1,Trivedi Suvang U6,Rasheed Mohammed Ata Ur6,Tamin Azaibi1,Lamers Mart M7,Haagmans Bart L7,Erdman Dean D1,Thornburg Natalie J1,Gerber Susan I1

Affiliation:

1. Division of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia

2. Communicable Diseases Directorate, Amman, Jordan

3. Laboratory Directorate, Amman, Jordan

4. Field Epidemiology Training Program, Jordan Ministry of Health, Amman, Jordan

5. Eastern Mediterranean Public Health Network, Amman, Jordan

6. IHRC, Inc, contracting agency for the Centers for Disease Control and Prevention, Atlanta, Georgia

7. Viroscience Department, Erasmus University Medical Center, Rotterdam, the Netherlands

Abstract

Abstract Background An outbreak of Middle East respiratory syndrome coronavirus (MERS-CoV) in Jordan in 2015 involved a variant virus that acquired distinctive deletions in the accessory open reading frames. We conducted a molecular and seroepidemiologic investigation to describe the deletion variant’s transmission patterns and epidemiology. Methods We reviewed epidemiologic and medical chart data and analyzed viral genome sequences from respiratory specimens of MERS-CoV cases. In early 2016, sera and standardized interviews were obtained from MERS-CoV cases and their contacts. Sera were evaluated by nucleocapsid and spike protein enzyme immunoassays and microneutralization. Results Among 16 cases, 11 (69%) had health care exposure and 5 (31%) were relatives of a known case; 13 (81%) were symptomatic, and 7 (44%) died. Genome sequencing of MERS-CoV from 13 cases revealed 3 transmissible deletions associated with clinical illness during the outbreak. Deletion variant sequences were epidemiologically clustered and linked to a common transmission chain. Interviews and sera were collected from 2 surviving cases, 23 household contacts, and 278 health care contacts; 1 (50%) case, 2 (9%) household contacts, and 3 (1%) health care contacts tested seropositive. Conclusions The MERS-CoV deletion variants retained human-to-human transmissibility and caused clinical illness in infected persons despite accumulated mutations. Serology suggested limited transmission beyond that detected during the initial outbreak investigation.

Funder

Erasmus Graduate Program Infection & Immunity

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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