A suspected case of sexual transmission of Ebola virus disease (EVD) in Liberia was confirmed using genomic analysis, thanks to in-country laboratory capabilities¹ established by U.S. Army scientists in collaboration² with the Liberian Institute for Biomedical Research (LIBR). The work, described in today's edition of the New England Journal of Medicine, provides molecular³ evidence of Ebola virus (EBOV) transmission between an EVD survivor⁴ and his female partner. It also demonstrates the value of real-time genomic surveillance during an outbreak, according to senior author Gustavo Palacios, Ph.D., of the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID). 

 

CPT Suzanne Mate, Ph.D., of USAMRIID, said scientists working at the LIBR earlier this year analyzed⁵ blood samples from a female patient who tested positive for EBOV in March 2015 when there had been no new documented cases for 30 days. The patient was reported to have had recent sexual intercourse⁶ with a male partner who had survived EVD and had been declared EBOV negative in early October 2014.

 

Following the patient's death on March 27, Mate said, public health officials were able to secure the consent of the male survivor to obtain and test a semen sample from him. The semen sample tested EBOV positive by quantitative⁷ RT-PCR, but the assay⁸ indicated that the level of viral RNA was low and required a different sample preparation method than the one originally deployed⁹ to sequence EBOV RNA from acute samples. 

 

"We implemented¹⁰ a new enrichment strategy in collaboration with scientists from Illumina, Inc. that was pivotal in obtaining the required coverage¹¹ to complete downstream genomic analysis," said Michael Wiley, Ph.D, of USAMRIID. Next-generation sequencing of the enriched EBOV RNA extracted from the male survivor's semen was used to compare the genome for similarity to the virus RNA extracted from the female patient's blood sample.

 

 "Ebola virus genomes assembled from the patient's blood and the survivor's semen were consistent with direct transmission," commented Jason Ladner, Ph.D., of USAMRIID. "The samples shared three genetic¹² substitutions that have not been found in any other Ebola virus sequences in Western Africa."

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