| Literature DB >> 32300276 |
Hong-Jun Li1, Juan Du2, Yan-Na Yang1, Yan Cui1, Lu Xi1, Shuai Wang2, Ya-Qiong Liu2, Guo-Feng Zhang1, Fuqiang Cui2, Qing-Bin Lu2.
Abstract
Objective We reported an outbreak of human parainfluenza virus type 1 (HPIV1) in a kindergarten and explored the genetic characteristics of HPIV1 hemagglutinin-neuraminidase (HN) and fusion (F) genes to provide more evidence about HPIV1 outbreaks. Methods Suspected cases were the children with an influenza-like illness during June 20 to 26, 2018. Nasopharyngeal swabs were collected and screened to determine the presence of respiratory pathogens by real-time fluorescent quantitative polymerase chain reaction. The HN and F gene sequences of HPIV-positive samples were further amplified and sequenced to confirm the HPIV genotype and identify genetic characteristics. A phylogenetic tree, based on the HN and F genes, was reconstructed by maximum likelihood method. Results Fourteen children in the outbreak were diagnosed as upper respiratory tract infection. The most common symptom was cough (10/14), followed by rhinorrhea (5/14), sore throat (4/14), headache (1/14), and abdominal pain (1/14). Eight patients were positive for HPIV1 and negative for other pathogens. Phylogenetic tree demonstrated that the eight strains from the year 2018 in our study located in the clade 2.3. Two specific substitutions (N333S and I509M) in the amino acids of the F protein and two substitutions (V19A and L436I) in the HN protein were different from other strains in the clade 2. Conclusion HPIV1 was attributed to the outbreak, which may be related to the genetic variations of HPIV1.Entities:
Keywords: children; outbreak; parainfluenza virus
Year: 2019 PMID: 32300276 PMCID: PMC7117075 DOI: 10.1055/s-0039-1695039
Source DB: PubMed Journal: J Pediatr Infect Dis ISSN: 1305-7707 Impact factor: 0.293
Detailed information on the children affected by the outbreak during June 2018, Beijing, China
| S.No | Sex | Age (y) | Diagnosis | Onset date (in 2018) | Highest temperature (°C) | Cough | Pharyngalgia | Rhinorrhea | Headache | Abdominal pain | WBC (×10 9 /L) |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Male | 4 | Otitis media, URTI | June 20 | 39.5 | Yes | Yes | Yes | No | No | 3.51 |
| 2 | Female | 4 | URTI | June 22 | 38.3 | Yes | No | No | No | No | – |
| 3 | Male | 4 | URTI | June 22 | 40 | Yes | Yes | Yes | No | No | 6.8 |
| 4 | Male | 4 | URTI | June 22 | 40 | Yes | No | No | Yes | No | 3.98 |
| 5 | Male | 4 | URTI | June 23 | 39 | Yes | No | No | No | No | 7.5 |
| 6 | Female | 4 | URTI | June 23 | 38.8 | Yes | Yes | No | No | No | – |
| 7 | Female | 4 | Tonsillitis, URTI | June 23 | 39.1 | Yes | No | No | No | Yes | 10.67 |
| 8 | Female | 4 | URTI | June 24 | 38 | Yes | No | Yes | No | No | – |
| 9 | Female | 4 | URTI | June 22 | 39 | Yes | No | Yes | No | No | 12.19 |
| 10 | Female | 4 | URTI | June 22 | 38.5 | Yes | Yes | No | No | No | 10 |
| 11 | Female | 4 | URTI | June 23 | 38.5 | Yes | No | Yes | No | No | 6.51 |
| 12 | Male | 4 | URTI | June 23 | 38.3 | Yes | No | No | No | No | 5.97 |
| 13 | Male | 4 | URTI | June 26 | 37.7 | Yes | No | No | No | No | – |
| 14 | Female | 4 | URTI | June 26 | 37.8 | Yes | No | No | No | No | 8.14 |
Abbreviations: URTI, upper respiratory tract infection; WBC, white blood cell.
Fig. 1Phylogenetic analysis of HPIV1 based on F gene constructed using a 2030 nucleotide sequence corresponding to nucleotide 4813–6842 in the Washington_1964 strain from the USA (GenBank accession no: NC_003461). A tree with 1,000 bootstrap replicates was reconstructed using maximum likelihood method with the MEGA 7.0 based on nucleotide sequences. The location and year of collection are shown. The strains detected in this study are in black solid circle.
Fig. 2Phylogenetic analysis of HPIV1 based on HN gene constructed using a 1894 nucleotide sequence corresponding to nucleotide 6847–8740 in the Washington_1964 strain from the USA (GenBank accession no: NC_003461). A tree with 1,000 bootstrap replicates was reconstructed using maximum likelihood method with the MEGA 7.0 based on nucleotide sequences. The location and year of collection are shown. The strains detected in this study are in black solid circle.