sábado, 18 de agosto de 2018

Case of Microcephaly after Congenital Infection with Asian Lineage Zika Virus, Thailand - Volume 24, Number 9—September 2018 - Emerging Infectious Diseases journal - CDC

Case of Microcephaly after Congenital Infection with Asian Lineage Zika Virus, Thailand - Volume 24, Number 9—September 2018 - Emerging Infectious Diseases journal - CDC





Volume 24, Number 9—September 2018

Research Letter

Case of Microcephaly after Congenital Infection with Asian Lineage Zika Virus, Thailand

Thidathip Wongsurawat1, Niracha Athipanyasilp1, Piroon Jenjaroenpun, Se-Ran Jun, Bualan Kaewnapan, Trudy M. Wassenaar, Nattawat Leelahakorn, Nasikarn Angkasekwinai, Wannee Kantakamalakul, David W. Ussery, Ruengpung Sutthent, Intawat Nookaew2Comments to Author , and Navin Horthongkham2Comments to Author 
Author affiliations: University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA (T. Wongsurawat, P. Jenjaroenpun, S.-R. Jun, D.W. Ussery, I. Nookaew)Siriraj Hospital, Mahidol University, Bangkok, Thailand (N. Athipanyasilp, B. Kaewnapan, N. Leelahakorn, N. Angkasekwinai, W. Kantakamalakul, R. Sutthent, N. Horthongkham)Molecular Microbiology and Genomics Consultants, Zotzenheim, Germany (T.M. Wassenaar)

Abstract

We sequenced the virus genomes from 3 pregnant women in Thailand with Zika virus diagnoses. All had infections with the Asian lineage. The woman infected at gestational week 9, and not those infected at weeks 20 and 24, had a fetus with microcephaly. Asian lineage Zika viruses can cause microcephaly.
Although Zika virus has circulated in Asia longer than in the Americas, only 3 confirmed cases of congenital Zika virus infection with microcephaly have been reported in Asia (2 Thailand, 1 Vietnam) (1). As of June 2018, the genomic sequences of the viruses from these 3 cases have not been reported; thus, whether these cases were caused by an Asian lineage or an imported American lineage is unknown.
Several mechanisms involving virus genome sequences have been proposed to explain how Zika virus might cause microcephaly (2). Liang et al. (3) showed in vitro that replication of both the African (strains MR766 and IbH30656) and American (strain H/PF/2013) lineage viruses suppress Akt phosphorylation; this suppression is caused by an accumulation of mutations in the Zika virus genome that increase the number of phosphorylation sites on virus proteins that compete with host proteins for phosphorylation. Yuan et al. proposed that a serine to asparagine substitution (S17N) in the premembrane protein (stably conserved in the American lineage but not in the Asian) contributes to the onset of microcephaly (4). An increased frequency of retinoic acid response elements in the American lineage genome versus the Asian lineage genome has also been observed (2). We question these explanations because we report a confirmed case of congenital Zika virus infection with microcephaly in Thailand caused by an Asian lineage virus.
We sequenced 7 Zika virus genomes obtained from 5 patients, including 3 pregnant women (PW1–3), in 2016 and 2017. PW1 had fever, maculopapular rash, and mild conjunctivitis at 24 weeks of gestation. Her urine sample was positive for Zika virus (BKK05, GenBank accession no. MG807647), and she gave birth to an infant without birth defects at full term. PW2 had a suspected Zika virus infection at 9 weeks’ gestation with high fever, maculopapular rash, and mild conjunctivitis. At 16 weeks, a sample of the amniotic fluid was positive for Zika virus (BKK03, GenBank accession no. MG548660). The pregnancy was terminated at 17 weeks. Autopsy of the fetus demonstrated a head circumference of 12.5 cm (less than the third percentile for this gestational age); Zika virus was detected in the brain (BKK02, GenBank accession no. MF996804) and placenta (BKK04, GenBank accession no. MG548661). No other etiologic agents associated with birth defects (cytomegalovirus, herpes simplex virus types 1 and 2, rubella virus, syphilis virus, Toxoplasma gondiiTreponema pallidum) were detectable by real-time PCR. PW2 had detectable hepatitis B viral surface antigen but no concurrent medical conditions. These findings suggest that Zika virus was the causative agent of this case of microcephaly. PW3 had a maculopapular rash without fever or conjunctivitis and received a Zika virus diagnosis at 20 weeks’ gestation. Her urine sample was positive for Zika virus (BKK07, GenBank accession no. MH013290), and she gave birth to a healthy infant at full term. The last 2 samples were from a 6-year-old child with mild fever and maculopapular rash (BKK06, GenBank accession no. MG807647) and a 64-year-old man with fever and maculopapular rash (BKK01, GenBank accession no. KY272987).
Thumbnail of Maximum-likelihood phylogenetic analysis of nonredundant Zika virus genomes including 7 isolates from patients in Thailand, 2016–2017, and amino acid changes corresponding with 3 evolutionary events (2). Circles indicate the Zika virus isolates from this report; the Zika virus strains used by Liang et al. (3) are indicated by asterisks and Yuan et al. (4) by squares. The key amino acid residue changes corresponding with the 3 evolutionary events (2) are shown, and the conserved amin
Figure. Maximum-likelihood phylogenetic analysis of nonredundant Zika virus genomes including 7 isolates from patients in Thailand, 2016–2017, and amino acid changes corresponding with 3 evolutionary events (2). Circles indicate the...
We retrieved 121 nonredundant Zika virus genomes (444 viruses, 99.9% nucleic acid identity cutoff) from GenBank to compare these isolates by phylogenetic analysis. All 7 BKK Zika virus isolates grouped within the Asian lineage (Figure). Virus from the amniotic fluid (BKK03), fetal brain (BKK02), and placenta (BKK04) of PW2 closely resembled each other (5 mismatches in BKK04 and 6 in BKK03, overall 99.898% identity). These 3 isolates were separated on the tree from their closest neighbor, a 2016 isolate from Singapore, by 40 mismatches. The number of retinoic acid response elements and predicted phosphorylation sites in BKK01–BKK07 was the same as the number in other Asian lineage Zika viruses (2). Also, the S17N substitution in premembrane was absent in all 7 isolates. Thus, all 3 proposed mechanisms failed to explain the case of congenital Zika virus infection with microcephaly in PW2. This case clinically resembled that of a woman in Finland infected during week 11 of pregnancy while traveling in Mexico, Guatemala, and Belize (5); in that case, Zika virus was detected in the brain of the aborted fetus at week 21.
The 3 cases in pregnant women described here support the hypothesis that the timing of Zika virus infection during pregnancy might be a key contributor to the development of microcephaly during congenital Zika virus infection. PW2 was infected around week 9 of gestation, during embryonic neurulation and cortical neurogenesis, which lay the foundation for the developing brain. Infection during week 20 (for PW3) and 24 (for PW1) of gestation did not led to microcephaly. Our observations are in agreement with reports involving American lineage Zika viruses that show a high risk for microcephaly when infection occurs before week 21 (6), during weeks 7–14 (7), or during the first trimester (810). Our findings show that Zika viruses circulating in Asia can cause microcephaly, just like American strains.
Dr. Wongsurawat is a postdoctoral research fellow at the Arkansas Center for Genomic Epidemiology & Medicine in Little Rock, Arkansas, USA. Her primary research interests are applying next-generation and third-generation sequencing technologies to perform DNA and RNA viral genome and metagenome sequencing.
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Acknowledgment

This work was funded in part by Siriraj Research (grant no. RO16034012), the Helen Adams & Arkansas Research Alliance Endowed Chair, and the National Institute of General Medical Sciences of the National Institutes of Health (award no. P20GM125503).
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Cite This Article

DOI: 10.3201/eid2409.180416
Original Publication Date: 7/31/2018
1These first authors contributed equally to this article.
2These senior authors contributed equally to this article.

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