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Volume 22, Number 4—April 2016
Letter

Follow-up of Ebola Patient, 2014–2015

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To the Editor: The 2014–2015 epidemic of Ebola virus disease (EVD) in West Africa affected 23,666 persons and caused 14,603 deaths (1). The World Health Organization (WHO) declared the epidemic a public health emergency (2). Although Ebola virus is transmitted by unprotected physical contact with infected persons, published reports about which body fluids are infected or the risk for fomite transmission are few (3). For most cases, virus was detected by reverse transcription PCR (RT-PCR) of clinical (saliva, feces, semen, breast milk, tears, nasal blood, skin swab) and environmental specimens (4). Earlier reports of the follow-up of recovered patients stated that viral RNA was detected by RT-PCR for up to 33 days in vaginal, rectal, and conjunctival swab samples from 1 patient and up to 101 days in seminal fluid from 4 patients. Infectious virus was detected in 1 seminal fluid sample 82 days after disease onset (4,5).

Attendees at the Eighth Meeting of the WHO Advisory Group on the EVD Response (1) discussed potential risk factors, including hidden chains of transmission and sexual transmission, and determined the following criteria. A country can declare “interruption of transmission” when 42 days have elapsed since the last diagnosis of a case. A country can declare that the “outbreak has stopped” when test results from the last case are negative twice or after another 90-day interval. For determining a cutoff for finally declaring the strategy and criteria for elimination, extensive follow-up on infectivity of semen in Ebola survivors is needed.

We report follow-up of a man who recovered from EVD and was monitored for 165 days after he was declared Ebola-free. The 26-year-old man from India returned to New Delhi, India, from Liberia on November 10, 2014, with a certificate from the government of Liberia stating that he was “cured” of Ebola. Because EVD is considered an exotic disease in India, he was placed in isolation at the Airport Health Organization quarantine center at Indira Gandhi International Airport, New Delhi (6). Serum and semen samples were collected and sent to the National Centre for Disease Control (NCDC), New Delhi, and the National Institute of Virology (NIV), Pune, India. The serum was negative by real-time RT- PCR ([7]; http://www.cdc.gov/vhf/ebola/diagnosis/index.htm) and positive (titer 1:400) by IgG ELISA (8). However, the semen was positive for Ebola viral RNA by real-time RT-PCR. A viral RNA extraction kit (QIAGEN, Valencia, CA, USA) was used to extract RNA from samples. Real-time RT-PCRs were set up in a Bio-Rad real-time PCR machine (Model C1000 Touch CFX96; Hercules, CA, USA) by using a SuperScript III Platinum One-Step qRT-PCR kit with ROX (Invitrogen, Carlsbad, CA, USA).

As a confirmatory measure, partial nucleoprotein gene (1216 nt), partial viral protein (VP) gene (337 nt), and the intergenic region near the VP gene along with VP polyA tail (383 nt) from the semen sample were amplified by RT-PCR (9). These sequences (GenBank accession nos. KT191140–KT191142) showed 100% similarity with Zaire ebolavirus isolate EBOV/DML14077/SLe/WesternUrban/20150630. To avoid cross-contamination, we used a γ-inactivated Ebola Reston virus strain as a positive control. The RT-PCRs were set up in a Bio-Rad thermal cycler (C1000) by using SuperScript III One-Step RT-PCR System with Platinum-Taq-DNA-Polymerase (Invitrogen).

Ebola virus isolation attempts were made from the semen sample in VeroE6 cells, Vero CCL81, Pipistrellus bat embryo, and BHK-21 cell lines at NIV. No isolate was obtained. Cycle thresholds of 28.5 and 31.5 were observed in Vero CCL81 and Vero E6 cells, respectively, in the first passage by real time RT-PCR, but no virus or cytopathic effect was detected in the subsequent 2 passages (Table).

According to WHO guidelines, the semen sample was transported from NCDC to a Biosafety Level 4 laboratory at NIV (for virus isolation). At the time of inoculation in cell culture, the sample had been subjected to a single freeze–thaw cycle. The sensitive nature of the virus may be why Ebola virus was not isolated. PCR positivity alone is not sufficient for considering a patient infectious for Ebola; however, because EVD is considered an exotic disease in India, we depended on real-time RT-PCR–based data for establishing EVD positivity.

Follow-up semen samples were positive by real time RT-PCR for up to 165 days after the patient was declared Ebola-free and were negative thereafter. Cycle thresholds of samples tested at NIV were 22.5 on day 45 after being declared Ebola-free, 24 on day 64, 34 on day 125, 38 on day 141, and 35.0 on day 165 (Table).

Clear criteria for elimination and declaration of the end of an outbreak are needed because any misinterpretation or miscommunication among the countries could negatively affect community confidence (10). Although we monitored the patient for 165 days, monitoring began ≈10 days after the patient had recovered. Ebola viral RNA persistence has been documented in a human semen sample for up to 10 months after the patient was declared Ebola-free (11). According to the data from this study, the current elimination period may need to be extended, and further studies on the infectivity of semen samples from recovered EVD patients are warranted.

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Acknowledgments

We gratefully acknowledge the encouragement and support extended by the Secretary, Government of India, Department of Health Research; Director General, Indian Council of Medical Research, New Delhi; and Rashmi Arora, for support in conducting this study. We extend our thanks and gratitude toward workers of the integrated diseases surveillance program for their cooperation with this study. We also thank Rajen Lakra, Prasad Sarkale, Prasad Kokate, Deepak Patil, Yosman Rajendran, and Anila Rajendran for technical support.

Financial support was provided by Indian Government Ministry of Health and Family Welfare.

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Venkatesh Srinivas, Pragya D. Yadav, Veena Mittal, Gouri Chaubal, Mala Chhabra, Sanjay Mattoo, Arvind Rai, and Devendra T. MouryaComments to Author 

Author affiliations: National Centre for Disease Control, New Delhi, India (S. Venkatesh, V. Mittal, M. Chhabra, A. Rai); National Institute of Virology, Pune, India (P. Yadav, G. Chaubal, D.T. Mourya); Airport Authority of India, New Delhi (S. Matto)

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References

  1. World Health Organization. Eighth Meeting of the WHO Advisory Group on the EVD Response; 2015 Mar 20; Geneva. Geneva: The Organization; 2015 [cited 2015 Mar 25]. http://www.who.int/csr/disease/ebola/advisory-groups/8th-meeting-report.pdf?ua=1
  2. World Health Organization. WHO Statement on the Meeting of the International Health Regulations Emergency Committee Regarding the 2014 Ebola Outbreak in West Africa; 2014 Aug 8; Geneva. Geneva: The Organization; 2014 [cited 2014 Nov 3]. http://www.who.int/mediacentre/news/statements/2014/ebola-20140808/en/
  3. Osterholm  MT, Moore  KA, Kelley  NS, Brosseau  LM, Wong  G, Murphy  FA, Transmission of Ebola viruses: what we know and what we do not know. mBiol. 2015;6 [cited 2016 Jan 19]. http://dx.doi: DOI
  4. Bausch  DG, Towner  JS, Dowell  SF, Kaducu  F, Lukwiya  M, Sanchez  A, Assessment of the risk of Ebola virus transmission from bodily fluids and fomites. J Infect Dis. 2007;196(Suppl 2):S1427. DOIPubMed
  5. Rodriguez  LL, De Roo  A, Guimard  Y, Trappier  SG, Sanchez  A, Bressler  D, Persistence and genetic stability of Ebola virus during the outbreak in Kikwit, Democratic Republic of the Congo, 1995. J Infect Dis. 1999;179(Suppl 1):S1706. DOIPubMed
  6. ProMEDmail. Ebola virus disease—ex Africa (39): India, worldwide susp. or quarantined. 2014 Nov 18 [cited 2015 Dec 23]. http://www.promedmail.org, archive no. 20141118.2966874.
  7. Towner  JS, Sealy  TK, Ksiazek  TG, Nichol  ST. High-throughput molecular detection of hemorrhagic fever virus threats with applications for outbreak settings. J Infect Dis. 2007;196(Suppl 2):S20512. DOIPubMed
  8. Ksiazek  TG, Rollin  PE, Williams  AJ, Bressler  DS, Martin  ML, Swanepoel  M, Clinical virology of Ebola hemorrhagic fever (EHF): virus, virus antigen, and IgG and IgM antibody findings among EHF patients in Kikwit, Democratic Republic of the Congo, 1995. J Infect Dis. 1999;179(Suppl 1):S17787. DOIPubMed
  9. Drosten  C, Göttig  S, Schilling  S, Asper  M, Panning  M, Schmitz  H, Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR. J Clin Microbiol. 2002;40:232330. DOIPubMed
  10. O'Dempsey  T, Khan  SH, Bausch  DG. Rethinking the discharge policy for Ebola convalescents in an accelerating epidemic. Am J Trop Med Hyg. 2015;92:2389. DOIPubMed
  11. Deen  GF, Knust  B, Broutet  N, Sesay  FR, Formenty  P. Ross  C Ebola RNA persistence in semen of Ebola virus disease survivors—preliminary report. N Engl J Med. 2015 Oct 14 [cited 2015 Oct 20]. DOI

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Cite This Article

DOI: 10.3201/eid2204.151405

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Table of Contents – Volume 22, Number 4—April 2016

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Devendra T. Mourya, National Institute of Virology, Pune, 20-A, Dr. Ambedkar Rd, Pune (Maharashtra), Pin 411001, India; ,

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Page created: March 16, 2016
Page updated: March 16, 2016
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The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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