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Genetic Susceptibility to Norovirus GII.4 Sydney Strain Infections in Taiwanese Children

Tu, Li-Tzu BS; Liu, Fu-Ping BS; Huang, Yhu-Chering MD, PhD; Huang, Chung-Guei MS; Yang, Shuan BS; Tsao, Kuo-Chien BS; Lai, Ming-Wei MD, PhD; Chen, Chih-Jung MD, PhD

Pediatric Infectious Disease Journal: April 2017 - Volume 36 - Issue 4 - p 353–357
doi: 10.1097/INF.0000000000001446
Original Studies

Background: A comprehensive evaluation of associations between the susceptibility to norovirus infections and histo–blood group antigens is not available in the Taiwanese population, in which the nonsecretor phenotype is absent.

Methods: A 1:1 matched case–control study was conducted in northern Taiwan from February 2013 to December 2014 when an epidemic of norovirus infection occurred. Cases were children <18 years old who were hospitalized because of diarrhea and were found to have laboratory-confirmed norovirus infections. Controls were healthy children matched to the cases by age and gender. The norovirus genotype was determined by polymerase chain reaction sequencing of the VP1 gene. The secretor status, Lewis antigen and ABO type were determined by characterization of genetic polymorphisms in the FUT2, FUT3 and ABO genes, respectively.

Results: A total of 147 case–control pairs were included. GII.4 Sydney strain was the major genotype and identified in 78.3% of the cases. The weak-secretor and Lewis-positive genotypes were less commonly identified in cases than in controls (5.4% vs. 23.1% and 79.6% vs. 89.8%, respectively). Multivariate analysis revealed that the secretor and Lewis-negative genotypes were both independent factors associated with increased risk of norovirus infections [matched odds ratio: 6.766, 95% confidence interval (CI): 2.649–17.285, P < 0.0001 and matched odds ratio: 3.071, 95% confidence interval [CI]: 1.322–7.084, P = 0.0085, respectively]. The ABO types were not significantly related to norovirus infections (P > 0.05).

Conclusion: The weak-secretor genotype and the Lewis antigen–positive genotype were both protective factors against severe norovirus gastroenteritis during the GII.4 Sydney strain epidemic in Taiwan.

From the *School of Medicine, College of Medicine, Chang Gung University, Division of Pediatric Infectious Diseases, Department of Pediatrics, Chang Gung Memorial and Children’s Hospital, Department of Laboratory Medicine, Chang Gung Memorial Hospital, and §Division of Pediatric Gastroenterology, Department of Pediatrics, Chang Gung Memorial and Children’s Hospital, Taoyuan, Taiwan.

Accepted for publication August 24, 2016.

L-T.T. and F-P.L. contributed equally to this work.

This study was supported by grants from Chang Gung Memorial Hospital (CMRPG4C0051, CMRPG4C0052) and partly supported by a grant from Medical Foundation in Memory of Dr. Deh-Lin Cheng. The authors have no conflicts of interest to disclose.

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Address for correspondence: Chih-Jung Chen, MD, PhD, Division of Pediatric Infectious diseases, Department of Pediatrics, Chang Gung Children’s Hospital, No. 5, Fu-Shin Street, Kweishan 333, Taoyuan, Taiwan. E-mail: chinjung@adm.cgmh.org.tw.

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