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http://dx.doi.org/10.4014/jmb.1707.07058

Fecal Respiratory Viruses in Acute Viral Respiratory Infection and Nasopharyngeal Diarrheal Viruses in Acute Viral Gastroenteritis: Clinical Impact of Ectopic Viruses Is Questionable  

Kweon, Oh Joo (Department of Laboratory Medicine, Aerospace Medical Center)
Lim, Yong Kwan (Department of Laboratory Medicine, Chung-Ang University College of Medicine)
Kim, Hye Ryoun (Department of Laboratory Medicine, Chung-Ang University College of Medicine)
Kim, Tae-Hyoung (Department of Urology, Chung-Ang University College of Medicine)
Lee, Mi-Kyung (Department of Laboratory Medicine, Chung-Ang University College of Medicine)
Publication Information
Journal of Microbiology and Biotechnology / v.28, no.3, 2018 , pp. 465-472 More about this Journal
Abstract
Our aim was to determine the detection rate of respiratory viruses (RVs) in feces of patients with acute viral respiratory infection (AVRI) and the detection rate of diarrheal viruses (DVs) in nasopharyngeal samples from patients with acute viral gastroenteritis. The relationships between the presence of fecal RVs or nasopharyngeal DVs and their impacts on the clinical severity were also investigated. A total of 144 fecal specimens were collected from AVRI patients and 95 nasopharyngeal specimens were collected from acute viral gastroenteritis patients. Clinical characteristics and laboratory profiles were compared between subgroups on the basis of the presence or absence of virus in the specimens. The detection rate of RVs in feces was 17.4% (25/144), whereas the detection rate for viruses identical to the respiratory pathogen was 10.4% (identical group, 15/144). Within the identical group, adenovirus (86.7%, 13/15) was most commonly found. Patients in the identical group showed statistically higher values for C-reactive protein, mean age, increased frequency of vomiting, and decreased frequency of chest film involvement and cough (p < 0.05). The detection rate of nasopharyngeal DVs among acute viral gastroenteritis patients was 19.0% (18/95), and in the identical group it was 15.8% (15/95). Norovirus group II and enteric adenovirus were the major pathogens detected in the identical group. There were no significant differences in clinical characteristics and laboratory profiles between the subgroups. In conclusion, the major pathogens of fecal RV and nasopharyngeal DV were adenovirus and norovirus group II, respectively. However, their relationship with the clinical symptoms or disease severity is unclear.
Keywords
Respiratory virus; diarrheal virus; fecal virus detection; nasopharyngeal virus detection;
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1 van den Hoogen BG, Osterhaus DM, Fouchier RA. 2004. Clinical impact and diagnosis of human metapneumovirus infection. Pediatr. Infect. Dis. J. 23: S25-S32.   DOI
2 Park JS. 2009. Acute viral lower respiratory tract infections in children. Korean J. Pediatr. 52: 269-276.   DOI
3 Arena C, Amoros JP, Vaillant V, Balay K, Chikhi-Brachet R, Varesi L, et al. 2012. Simultaneous investigation of influenza and enteric viruses in the stools of adult patients consulting in general practice for acute diarrhea. Virol. J. 9: 116.   DOI
4 Chan MC, Lee N, Chan PK, Leung TF, Sung JJ. 2009. Fecal detection of influenza A virus in patients with concurrent respiratory and gastrointestinal symptoms. J. Clin. Virol. 45: 208-211.   DOI
5 Blomqvist S, Savolainen-Kopra C, Paananen A, Hovi T, Roivainen M. 2009. Molecular characterization of human rhinovirus field strains isolated during surveillance of enteroviruses. J. Gen. Virol. 90: 1371-1381.   DOI
6 Harvala H, McIntyre CL, McLeish NJ, Kondracka J, Palmer J, Molyneaux P, et al. 2012. High detection frequency and viral loads of human rhinovirus species A to C in fecal samples; diagnostic and clinical implications. J. Med. Virol. 84: 536-542.
7 Novikova NA, Al'tova EE, Noskova NV, Epifanova NV, Tamoikina NA. 1991. The detection of rotavirus RNA in nasopharyngeal smears by molecular hybridization. Zh. Mikrobiol. Epidemiol. Immunobiol. 1991: 23-25.
8 Ma SH. 2005. Acute infectious diarrhea in pediatric patients. Korean J. Pediatr. 48: 235-250.
9 So CW, Kim DS, Yu ST, Cho JH, Kim JD. 2013. Acute viral gastroenteritis in children hospitalized in Iksan, Korea during December 2010-June 2011. Korean J. Pediatr. 56: 383-388.   DOI
10 Dabilla N, Nunes Vieira Almeida T, Carvalho Reboucas Oliveira A, Kipnis A, Neres Silva T, Souza Fiaccadori F, et al. 2017. Norovirus in feces and nasopharyngeal swab of children with and without acute gastroenteritis symptoms: first report of GI.5 in Brazil and GI.3 in nasopharyngeal swab. J. Clin. Virol. 87: 60-66.
11 Sata T, Roth J, Zuber C, Stamm B, Heitz PU. 1991. Expression of alpha 2,6-linked sialic acid residues in neoplastic but not in normal human colonic mucosa. A lectin-gold cytochemical study with Sambucus nigra and Maackia amurensis lectins. Am. J. Pathol. 139: 1435-1448.
12 Okimoto S, Hyodo S, Yamamoto M, Nakamura K, Kobayashi M. 2011. Association of viral isolates from stool samples with intussusception in children. Int. J. Infect. Dis. 15: e641-e645.   DOI
13 Hayase Y, Tobita K, Sato H. 2002. Detection of type B influenza virus genes from biopsied gastric mucosa. J. Gastroenterol. 37: 101-105.   DOI
14 Avila MM, Carballal G, Rovaletti H, Ebekian B, Cusminsky M, Weissenbacher M. 1989. Viral etiology in acute lower respiratory infections in children from a closed community. Am. Rev. Respir. Dis. 140: 634-637.   DOI
15 Beigel JH, Farrar J, Han AM, Hayden FG, Hyer R, de Jong MD, et al., and Writing Committee of the World Health Organization (WHO) Consultation on Human Influenza A/H5. 2005. Avian influenza A (H5N1) infection in humans. N. Engl. J. Med. 353: 1374-1385.   DOI
16 Yao L, Korteweg C, Hsueh W, Gu J. 2008. Avian influenza receptor expression in H5N1-infected and noninfected human tissues. FASEB J. 22: 733-740.
17 Whiley DM, Sloots TP. 2005. Comparison of three in-house multiplex PCR assays for the detection of Neisseria gonorrhoeae and Chlamydia trachomatis using real-time and conventional detection methodologies. Pathology. 37: 364-370.   DOI
18 Kosters K, Reischl U, Schmetz J, Riffelmann M, Wirsing von Konig CH. 2002. Real-time LightCycler PCR for detection and discrimination of Bordetella pertussis and Bordetella parapertussis. J. Clin. Microbiol. 40: 1719-1722.   DOI