SEARCH

SEARCH BY CITATION

Keywords:

  • Acute respiratory disease;
  • children;
  • China;
  • human adenovirus

Abstract

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

Background

Human adenovirus 55 (HAdV-55) has caused recent outbreaks of acute respiratory disease (ARD) among adults and military trainees. The active surveillance for HAdV infections was sparse in China, and current knowledge on the HAdV-type distributions and its molecular evolution is lacking.

Objectives

To acquire better understanding on the prevalence and molecular evolution of HAdV-55 strains in China, for an informed strategy for disease control and prevention.

Population/Methods

Nasopharyngeal aspirates were collected from hospitalized children with ARTI in Chongqing during 2009–2012. The genotype of HAdV isolates were determined by sequencing the partial hexon and fiber genes. Whole genome sequences of HAdV-55 were obtained for molecular evolution analysis.

Results

About 191 (8·55%) HAdV were detected in 2234 children, including 92 (48·2%) with HAdV-7, 72 (37·7%) with HAdV-3, 6 (3·1%) with HAdV-55, 5 (2·6%) with HAdV-5, 4 (2·1%) with HAdV-1, 1 (0·5%) with HAdV-2, and 11(5·8%) with untyped HAdV. Four of these children developed pneumonia, two of whom were diagnosed with severe pneumonia and/or encephalopathy. HAdV-55 isolates clustered with HAdV-11 sequences based on the hexon gene and clustered with HAdV-14 sequences based on the fiber gene and the whole genome. The overall evolutionary rates of hexon gene, fiber gene, and whole genome of HAdV-55 were estimated at 6·2 × 10−5 s/s/y, 8·0 × 10−5 s/s/y, and 1·7 × 10−5 s/s/y, respectively.

Conclusions

This study suggested HAdV-55 as an emerging infectious disease pathogen has conserved genetic structure and is closely related to each other. Further molecular investigation based on HAdV-55 of wider origin might facilitate understanding its diversity, dissemination, and transmission in China.


Background

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

Human adenoviruses (HAdV) are a common cause of acute respiratory diseases, causing sporadic infections, as well as community and institutional outbreaks.[1] Infection with HAdV rarely causes serious or fatal illness in otherwise healthy individuals, but may cause severe disease in newborn, elderly, or immunocompromised persons.[1] There are at least 69 recognized HAdV genotypes (http://hadvwg.gmu.edu/), which are assigned to seven subgroups (A–G) according to biophysical, biochemical, and genetic characteristics.[2] The spectrum of clinical disease associated with HAdV is broad and depends largely upon the infecting HAdV genotype. Clinical signs and symptoms include fever, rhinorrhea, pharyngitis, conjunctivitis, gastroenteritis, bronchitis, pneumonia, acute hemorrhagic cystitis, meningoencephalitis, and rarely life-threatening disseminated diseases.[1] New adenovirus genotypes are increasingly recognized through the use of phylogenetic analysis based on complete genomic sequences. Novel strains may arise from mutations or recombinations of two different adenovirus strains between the hexon gene and fiber genes.[3, 4] Recently, an emergent variant, HAdV-55,[5, 6] with a proposed recombination of hexon gene between HAdV-11 and HAdV-14 strains, has been described in association with multiple outbreaks of acute respiratory disease, mostly occurring in military camps.[7-10] In 2005, a large outbreak of acute respiratory disease likely from HAdV-55 occurred in a military camp in Turkey.[8] Another two HAdV-55 outbreaks occurred among military training camps in 2005 (226 patients in Singapore[9]) and in 2009 (108 patients in China[10]). Nucleotide sequence analysis showed the strains from the two outbreaks were highly similar to the QS-DLL strain, which was the first HAdV-55 in China isolated from an ARDS outbreak in Shaanxi in t 2006 that occurred in a senior high school.[7] The most recent HAdV-55 outbreak occurred in February 2012 among patients with febrile respiratory tract infection admitted to PLA 252 hospital, Hebei Province, China (unpublished data). With rare precedent circulation of HAdV-11 and HAdV-14 in China, an increasing trend of adenovirus type 55 infections was observed among both civilian and military populations, probably due to the lack of immunity herd. This concern, in combination with its higher tendency in causing severe respiratory illness than other adenovirus, posed great threats to Chinese military that it has the potential to spread widely and cause severe epidemics. The status highlights the need for improved surveillance, with extensive molecular characterization, to identify the prevalence and the genetic variants of this emerging adenovirus. Thus far, HAdV surveillance in China is sparse, and HAdV-55 infections were chiefly identified during outbreak events. The current study was sought to acquire a better understanding of the prevalence and molecular evolution of HAdV-55 strains by performing an active surveillance for HAdV infections. This knowledge might assist with targeted population for disease prevention and geographic regions where type-specific vaccines should be administered if developed.

Materials and methods

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

Sample collection

From June 2009 to January 2012, we recruited hospitalized children with ARTI at Chongqing Children's hospital, Chongqing, China. ARTI was defined as acute onset of cough, rhinorrhea, and dyspnea, with fever ≥37·5°C. Nasopharyngeal aspirates (NPAs) were collected from the recruited children within 24 hours of admission and stored in the −80°C.

A standardized questionnaire was used to gather demographic and hospitalization data such as signs, symptoms, underlying medical conditions, and laboratory test results, radiographic findings, and disease outcome. Laboratory tests included sputum culture and an array of serological assays including IgG and IgM enzyme-linked immunosorbent assays (ELISAs) for previous infection with cytomegalovirus (CMV), Epstein–Barr virus (EBV), Chlamydia pneumoniae (CP), and Mycoplasma pneumoniae (MP).

Detection of HAdV and other respiratory viruses

DNA and RNA were extracted from each specimen using the QIAamp® MinElute Virus Spin Kits (QIAGEN, Hilden, Germany). Molecular assays for HAdV were performed using pan primers as previously described.[11] Specimens were screened for human bocavirus (HBoV), and influenza A virus by real-time RT-PCR[12] as well as for respiratory syncytial virus (RSV), parainfluenza virus (PIV), human metapneumovirus (MPV), and coronavirus by nested PCR.[13] Each PCR run included virus isolates DNA or RNA as positive control and water as negative control.

Determination of HAdV genotypes

For HAdV generic PCR-positive samples, the highly variable regions of hexon gene and entire fiber gene were PCR amplified from viral DNA and then sequenced as previously described.[14, 15] Genomic sequences were assembled using CLC genomic workbench 5.1 (CLC bio, Aarhus, Denmark). Previously published GenBank sequences of HAdV, including HAdV-1, HAdV-3, HAdV-11, HAdV-14, HAdV-21, and HAdV-55, were used for comparison and determination of the HAdV genotypes. All comparison alignments were performed, and phylogenetic tree was constructed by neighbor-joining method with 1000 bootstrap replicates using CLC genomic workbench 5.1. Similarities between strains were calculated using BioEdit, version 7.13 (North Carolina State University, Raleigh, NC, USA; www.mbio.ncsu.eud/bioedit/bioedit.html).

Molecular analysis of HAdV-55

For the determined HAdV-55, the whole genome sequences were obtained using an automated DNA sequencer (3730 DNA Sequencer; Applied Biosystems, Foster City, CA, USA). Hexon and fiber gene sequences of HAdV-55 available in the GenBank were collected for the establishment of phylogenetic tree for HAdV-55.

The rate of substitutions in HAdV-55 strains, their divergence over time, and the time to the most recent common ancestor (TMRCA) were estimated using a Bayesian Markov chain Monte Carlo (MCMC) approach as implemented in the Bayesian Evolutionary Sampling Tree package, version 1.7.2.[16] The best-fit substitution model was chosen by performing a maximum likelihood analysis using the jModeltest package, version 0.1.1.[17] Relaxed lognormal molecular clocks were employed and followed by allowing substitution rate variations among branches on the trees. The Bayesian MCMC chain lengths were 1 million generations with sampling every 1000 chain and discarding 10% of the chain as burn-in. Convergence of the chains was achieved by computational run over a sufficient time with inspection of MCMC samples using TRACER, version 1.5 (http://beast.bio.ed.ac.uk/). The resulting tree of each run was summarized using Tree Annotator, and the maximum clade credibility tree was visualized with FigTree software, version 1.3.1 (http://tree.bio.ed.ac.uk/software/figtree/). All GenBank accession numbers for the sequences obtained in this study, as well as those used for comparison are listed in Table 1.

Table 1. Reference sequences for the hexon/fiber genes and complete genomes from GenBank
StrainAccession No. (Hexon/Fiber)StrainAccession No. (Complete genome)
South Dakota/6380/1997FJ841899/FJ841907HAdV-14 AY803294
Spain/273/1969FJ841900/FJ841908HAdV-11 AF532578
Taiwan/760/2002FJ841905/FJ841913HAdV-3 AY599834
Taiwan/2474/2001FJ841906/FJ841914HAdV-7 AY594255
Singapore/1218/2005FJ607010/FJ603105QS-DLL FJ643676
Singapore/1223/2005FJ607012/FJ603104SGN1222 FJ597732
CQ-814JX120175/JX120166CQ-814 JX123027
CQ-1657JX120175/JX120170CQ-1657 JX123028
CQ-1674JX120177/JX120167CQ-2903 JX123029
CQ-1741JX120172/JX120168China/P14/2011 JX491639
CQ-1747JX120173/JX120169HAdV-16 AY601636
CQ-2903JX120176/JX120171HAdV-21 AY601633
HAdV-14pFJ841903/FJ841911HAdV-4 AY594253
HAdV-26 EF153474
HAdV-12 AC_000005
HAdV-40 NC_001454
HAdV-34 AY737797
HAdV-35 AY128640
HAdV-5 AY601635
HAdV-52 DQ923122

Results

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

Altogether 2234 hospitalized children were recruited in the study, their ages ranged from 1 month to 14 years (median 8 months) and 66·6% were male. Among all the tested children, 191 (8·55%) were infected with HAdV. Further genotyping revealed 92 (48·17%) infection with HAdV-7, 72 (37·70%) with HAdV-3, 6 (3·14%) with HAdV-55, 5 (2·62%) with HAdV-5, 4 (2·09%) with HAdV-1, 1 (0·52%) with HAdV-2, and 11(5·76%) with untyped HAdV (not sequenced due to running out of the samples).

Genetic characterization of HAdV-55

The partial hexon gene covering hypervariation regions 1–7 (nt 18353-20956, corresponding to the QS-DLL strain) and fiber gene (nt 30817-31752) were successfully amplified from all the six samples, yielding 2604-bp and 954-bp amplicon, respectively. The sequence homologies of the six HAdV-55 strains were 99·8–100% for the hexon gene and 99·9–100% for the fiber gene, respectively. Phylogenetic analyses based on hexon gene and fiber gene revealed the HAdV strains in Chongqing clustered with HAdV-55 (Figure 1). Figure 1A shows that all these hexon genes obtained in this study clustered with HAdV-11 and exhibit the highest degree of nucleotide sequence identity with the strains in Singapore and USA, but different from the strains in Spain and Taiwan with the 1000 bootstraps supporting. Figure 1B demonstrates all these fiber strains from the mainland of China strains clustered with HAdV-14 strain as the expected appearance and form a separate branch, different from Taiwan and Singapore strains with the 897 bootstraps supporting. The phylogenetic trees based on hexon and fiber gene at amino acid level were also demonstrated in Figure S1, which were the same to those at nucleic acid level.

image

Figure 1. Phylogenetic analysis of human adenovirus based on partial hexon gene covering hypervariation regions 1–7 (nt 18353-20956, corresponding to the QS-DLL strain) and fiber gene (nt 30817-31752) was constructed using neighbor-joining method with 1000 bootstrap replicates. A, the hexon gene; B, the fiber gene. The strains in our study are labeled with the black solid circle.

Download figure to PowerPoint

The homology analysis demonstrated all the determined nucleotide acid sequences and deduced amino acid sequences exhibited high homology to the QS-DLL strain for both hexon gene (99·9–100%) and fiber gene (99·8–100%). While lower homologies (90·7%) were revealed in hexon gene between the six strains and the HAdV-14 strain (GenBank Accession No.: AY803294) and in fiber gene (91·9%) between the six strains and the HAdV-11 strain (GenBank Accession No.: AF532578).

From the above results, three strains were sequenced for the whole genome sequences with the homology of 99·8%. The recombination analysis indicated that the HAdV-55 strain (CQ2903) shows a hexon recombination between HAdV-11 and HAdV-14 (Figure S2).

Phylogenetic tree for the whole genome sequences of HAdV-55 demonstrated that all previous HAdV-55 strains and our HAdV-55 strains clustered together with previously reported HAdV-14 strains (Figure 2). And the current viral strain, CQ-814 (Chongqing 2010 strain), was most closely related to P14 (Beijing 2011 strain), followed by CQ-1657 (Chongqing 2011 strain) and CQ-2903 (Chongqing 2012 strain). Surprisingly, the closest genetic relationship existed between CQ-2903 and QS-DLL (Shaanxi 2006 strain). The comparisons of variations for all the HAdV-55 whole genome sequences were shown in Figure 3. Most variations were missense mutations and silent mutations. The indels occurred frequently in the ends and 10 000–180 000 bases. The detailed variations among the whole genome sequences of HAdV-55 are listed in Table S1.

image

Figure 2. Phylogenetic tree of human adenovirus based on the whole genome sequence constructed by neighbor-joining method with 1000 bootstrap replicates. The strains in our study are labeled with the black solid circle.

Download figure to PowerPoint

image

Figure 3. Variation sites based on the SGN1222 strain. The black line represents the mutation, the red up arrow represents base deletion, and the blue down arrow represents base insertion.

Download figure to PowerPoint

The overall evolutionary rates of hexon gene and fiber gene of HAdV-55 were estimated at 6·2 × 10−5 nucleotide substitutions per site per year (s/s/y) (95% HPD: 5·5 × 10−6–1·5 × 10−4 s/s/y) and 8·0 × 10−5 s/s/y (95% HPD: 6·6 × 10−6–1·8 × 10−4 s/s/y), respectively. The evolutionary rates were lower (1·7 × 10−5 s/s/y, 95% HPD: 2·2 × 10−9–3·5 × 10−5 s/s/y) when based on whole genome. The HAdV-55 strains from mainland China seems to have diverged from their TMRCA with other strains from Taiwan Province/Singapore/South Dakota around 15 years ago considering the hexon gene (Figure S3A), 10 years ago considering the fiber gene (Figure S3B), and 35 years ago considering the whole genome (Figure S3C), respectively.

Clinical and laboratory characteristics of HAdV-55 infection

All the six patients with HAdV-55 infection were boys, and their ages ranged from 1 through 4 years old. All the patients occurred from August 2010 to January 2012. Three were diagnosed with severe pneumonia and/or toxic encephalopathy with their disease onset occurring in May 2011 (Table 2). The length of their hospitalization stay ranged from 4 to 12 days (median 7·5 days). Three patients had underlying medical conditions. In comparison with patients with HAdV-3 and HAdV-7 infection, patients with HAdV-55 infection presented with similar clinical manifestations (Table S2). All patients had fever of ≥38·5° with duration from 6 to 14 days, pharyngeal congestion, and swollen tonsils. The routine blood tests of all six patients were within normal ranges. Four patients had abnormal chest radiograph findings, which included increase in lung markings, interstitial change, or overinflation. The patients all recovered without sequela.

Table 2. The characteristics of the six hospitalized children infected with HAdV-55
PatientAgeSexSample Onset dateClinical diagnosisUnderlying conditionsCoinfection
  1. y, year; mo, month; CQ, Chongqing; URTI, upper respiratory tract infection; CP, chlamydia pneumonia; MPV, metapneumovirus; PIV, parainfluenza virus; HBoV, human bocavirus; CMV, cytomegalovirus.

111 y 1 moboyCQ-814August 15, 2010URTINoMPV
21 y 4 moboyCQ-1657April 22, 2011Interstitial pneumonia

Wheezing

eczema

MPV, PIV-1, Haemophilus influenza
31 y 4 moboyCQ-1674May 1, 2011

Protracted pneumonia

Toxic encephalopathy

Bronchial asthma

No HBoV, Staphyloccocus aureus
41 y 2 moboyCQ-1741May 9, 2011

Severe pneumonia

Respiratory failure

WheezingHBoV, PIV-1, CMV-IgM (+), Klebsiella pneumonia
54 y 0 moboyCQ-1747May 17, 2011

Severe pneumonia

Toxic encephalopathy

NoPIV-1, CP-IgM (+)
63 y 4 moboyCQ-2903January 8, 2012BronchitisUrticarial No

Microbiological investigation

Coinfections were frequent among the 6 hospitalized boys infected with HAdV-55. Three were coinfected with one other virus (one with MPV, one with HBoV, and one with PIV-1). Two were coinfected with two other viruses (both with HBoV and PIV-1). Three were coinfected with bacteria (Haemophilus influenzae, Staphyloccocus aureus, and Klebsiella pneumoniae, respectively). Patient-4 also had evidence of recent CMV infection (IgM assay). Patient-5 was similarly positive for recent CP infection (IGM assay).

Discussion

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

In the United States, HAdV strains of low type number are highly prevalent among children with HAdV-3, and HAdV-7, a frequent cause of outbreaks.[18, 19] Recently, novel recombination strains, including HAdV-55 and HAdV-14p1, have been evolved from a recombination of HAdV-11 and HAdV-14 ancestral strains.[20]

In Asia, the prevalence of HAdV has ranged from 0·8% to 11·30% among patients with ARTI.[21, 22] In the past, HAdV-3 and HAdV-7 strains have been the most prevalent HAdV types.[1, 23] However, recent outbreaks have also documented high prevalence of HAdV-5[24-27] and HAdV-55.[7-10] Our study provides further evidence that HAdV-55 is likely routinely circulating among Chinese children. In this hospital surveillance study, we documented six hospitalized patients with HAdV-55 infection. Our whole genome sequence data confirm the relatedness of our HAdV-55 isolates with HAdV-14, which classically has caused outbreaks (sometimes with severe disease) in various regions of North America,[18] Europe,[28], and Asia.[10] Our HAdV-55-infected patients had severe or protracted pneumonia as well as toxic encephalopathy.[20-26, 28, 27] However, whether HAdV-55 was responsible for the clinical manifestation cannot be determined, because 5 of the 6 patients with human HAdV-55 infections had also been coinfected with other pathogens.

Recombination is a well-known feature in HAdV genetics and an important force driving the evolution of HAdV.[1, 2] Our study further supported the hypothesis that HAdV-55 is a recombinant between HAdV-11 and HAdV-14 strains and more HAdV-14-like than HAdV-11-like.[5] Meanwhile, Based on the phylogenetic trees for hexon gene, the Singapore strains are more closely related to the mainland China HAdV-55 strains than with Taiwan strains while the opposite to the fiber gene. These results suggested a possible recombination event occurred at a position between hexon gene and fiber gene, between mainland China strain and Taiwan strain, which resulted in the formation of the Singapore strain. All the strains in mainland of China seem to be different from other regional HAdV-55 strains. These characteristics might reflect either spatial or temporal dynamics of HAdV-55.

For phylogenetic tree of the whole genome, the closest genetic relationship was found between the 2012 Chongqing strain (CQ-2903) and the 2006 Shaanxi strain (QS-DLL). The reason of this close relationship needs to be illustrated. A possible explanation is that all these HAdV-55 strains are derived from different lineages of a common ancestor. Data from the phylogenetic tree and molecular clock analysis suggest HAdV-55 evolved with a certain evolution rate and geographic subdivision occurred during the last 35 years, as well as Chongqing HAdV-55 strains were accumulating mutations at a certain speed from 2010 to 2012. Further molecular investigation based on HAdV-55 of wider origin might facilitate to understand its dissemination and transmission in China.

Given the possible association of severe disease with HAdV-55, the possible emergence of other novel adenovirus recombinants, and our sparse understanding of HAdV epidemiology in China, we posit that more aggressive population-based surveillance for HAdV strains should be conducted such that, if warranted in the future, type-specific diagnostics,[30] new antiviral therapeutics,[31] and possibly adenovirus vaccines[19] might be developed, studied, and employed among China's populations at highest risk of severe HAdV disease.

Funding

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

This study is supported by the China Mega-Project on Infectious Disease Prevention (No. 2013ZX10004202-002) and National Science Fund for Young Scholars (81222037).

Competing interests

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

Regarding this report, the authors do not have any commercial or other association that would be considered a conflict of interest.

Ethical approval

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information

The study protocol was reviewed and approved by the ethics review committee of Chongqing Medical University. Written informed consents were acquired from parents or guardians of all participants.

References

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information
  • 1
    Lynch JP 3rd, Fishbein M, Echavarria M. Adenovirus. Semin Respir Crit Care Med 2011; 32:494511.
  • 2
    Harrach B, Benkő M, Both GW et al. Family Adenoviridae; in King AMQ, Adams MJ, Carstens EB, Lefkowitz EJ (eds): Virus Taxonomy 9th Report of the International Committee on Taxonomy of Viruses. New York: Elsevier, 2011; 125141.
  • 3
    JonesII MS, Harrach B, Ganac RD et al. New adenovirus species found in a patient presenting with gastroenteritis. J Virol 2007; 81:59785984.
  • 4
    Lukashev AN, Ivanova OE, Eremeeva TP, Iggo RD. Evidence of frequent recombination among human adenoviruses. J Gen Virol 2008; 89:380388.
  • 5
    Walsh MP, Seto J, Jones MS, Chodosh J, Xu W, Seto D. Computational analysis identifies human adenovirus type 55 as a re-emergent acute respiratory disease pathogen. J Clin Microbiol 2010; 48:991993.
  • 6
    Zhang Q, Seto D, Cao B, Zhao S, Wan C. Genome sequence of human adenovirus type 55, a re-emergent acute respiratory disease pathogen in china. J Virol 2012; 86:1244112442.
  • 7
    Zhu Z, Zhang Y, Xu S et al. Outbreak of acute respiratory disease in China caused by B2 species of adenovirus type 11. J Clin Microbiol 2009; 47:697703.
  • 8
    Chmielewicz B, Benzler J, Pauli G, Krause G, Bergmann F, Schweiger B. Respiratory disease caused by a species B2 adenovirus in a military camp in Turkey. J Med Virol 2005; 77:232237.
  • 9
    Kajon AE, Dickson LM, Metzgar D, Houng HS, Lee V, Tan BH. Outbreak of febrile respiratory illness associated with adenovirus 11a infection in a Singapore military training cAMP. J Clin Microbiol 2010; 48:14381441.
  • 10
    Xu J, Guo J-X, Li H et al. Etiological analysis of an outbreak of respiratory infection with unknown season in a certain unit of PLA. Med J Chin PLA 2010; 3:252255.
  • 11
    Xu W-H, McDonough MC, Erdman DD. Species-specific identification of human adenoviruses by a multiplex PCR assay. J Clin Microbiol 2000; 38:41144120.
  • 12
    Gunson RN, Collins TC, Carman WF. Real-time RT-PCR detection of 12 respiratory viral infections in four triplex reaction. J Clin Virol 2005; 33:341344.
  • 13
    Tiveljung-Lindell A, Rotzén-Östlund M, Gupta S et al. Development and implementation of a molecular diagnostic platform for daily rapid detection of 15 respiratory viruses. J Med Virol 2009; 81:167175.
  • 14
    Biere B, Schweiger B. Human adenoviruses in respiratory infections: sequencing of the hexon hypervariable region reveals high sequence variability. J Clin Virol 2010; 47:366371.
  • 15
    Madisch I, Harste G, Pommer H, Heim A. Phylogenetic analysis of the main neutralization and hemagglutination determinants of all human adenovirus prototypes as a basis for molecular classification and taxonomy. J Virol 2005; 79:1526515276.
  • 16
    Drummond AJ, Rambaut A. BEAST: bayesian evolutionary analysis by sampling trees. BMC Evol Biol 2007; 7:214.
  • 17
    Guindon S, Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 2003; 52:696704.
  • 18
    Kajon AE, Lu X, Erdman DD et al. Molecular epidemiology and brief history of emerging adenovirus 14-associated respiratory disease in the United States. J Infect Dis 2010; 202:93103.
  • 19
    Gray GC. Adenovirus vaccines; in Plotkin SA, Orenstein W, Offit PA (eds): Vaccines, 6th edn. Pennsylvania: Saunders Elsevier, 2011; 113126.
  • 20
    Gray GC, Chorazy ML. Human adenovirus 14a: a new epidemic threat. J Infect Dis 2009; 199:14131415.
  • 21
    Yu X, Lu R, Wang Z et al. Etiology and clinical characterization of respiratory virus infections in adult patients attending an emergency department in Beijing. PLoS ONE 2012; 7:e32174.
  • 22
    Guo L, Gonzalez R, Zhou H et al. Detection of three human adenovirus species in adults with acute respiratory infection in China. Eur J Clin Microbiol Infect Dis 2012; 31:10511058.
  • 23
    Deng J, Qian Y, Zhao L-Q et al. Identification and typing of adenoviruses from pediatric patients with acute respiratory infections in Beijing from 2003 to 2008. Chin J Pediatr 2010; 48:739743.
  • 24
    Tang L, Wang L, Tan X, Xu W. Adenovirus serotype 7 associated with a severe lower respiratory tract disease outbreak in infants in Shaanxi Province, China. Virol J 2011; 8:23.
  • 25
    Xie L, Yu XF, Sun Z et al. Two adenovirus serotype 3 outbreaks associated with febrile respiratory disease and pharyngoconjunctival fever in children under 15 years of age in Hangzhou of China during 2011. J Clin Microbiol 2012; 50:18791888.
  • 26
    Liu X-L, Song H-B, Zhang L et al. Investigate on an outbreak of adenovirus 5 infection. Chin J Epidemiol 2003; 24:607.
  • 27
    Yu W, Xu F, Yang S-G, Zhu X-Z. Epidemiological analysis of an outbreak of respiratory tract infection caused by adenovirus. Chin J Epidemiol 2008; 29:603.
  • 28
    O'Flanagan D, O'Donnell J, Domegan L et al. First reported cases of human adenovirus serotype 14p1 infection, Ireland, October 2009 to July 2010. Euro Surveill 2011; 16:pii=19801.
  • 29
    Girouard G, Garceau R, Thibault L, Oussedik Y, Bastien N, Li Y. Adenovirus serotype 14 infection, new brunswick, Canada, 2011. Emerg Infect Dis 2013; 19:119122.
  • 30
    Bil-Lula I, De Franceschi N, Pawlik K, Wozniak M. Improved real-time PCR assay for detection and quantification of all 54 known types of human adenoviruses in clinical samples. Med Sci Monit 2012; 18:BR221BR228.
  • 31
    Dropulic LK, Cohen JI. Update on new antivirals under development for the treatment of double-stranded DNA virus infections. Clin Pharmacol Ther 2010; 88:610619.

Supporting Information

  1. Top of page
  2. Abstract
  3. Background
  4. Materials and methods
  5. Results
  6. Discussion
  7. Funding
  8. Competing interests
  9. Ethical approval
  10. References
  11. Supporting Information
FilenameFormatSizeDescription
irv12232-sup-0001-FigureS1.tifimage/tif2401KFigure S1. Phylogenetic analysis of human adenovirus based on partial hexon gene covering hypervariation regions 1–7 (nt 18353-20956, corresponding to the QS-DLL strain) and fiber gene (nt 30817-31752) at amino acid level was constructed using neighbor-joining method with 1000 bootstrap replicates.
irv12232-sup-0002-FigureS2.tifimage/tif1605KFigure S2. The recombination analysis for HAdV-55 (CQ2903) based on the whole genome sequence by RDP 3.5.1.
irv12232-sup-0003-FigureS3A.tifimage/tif827KFigure S3. Bayesian timescale phylogeny of HAdV-55 based on the hexon gene (A), fiber gene (B), and whole genome (C).
irv12232-sup-0004-FigureS3B.tifimage/tif851K 
irv12232-sup-0005-FigureS3C.tifimage/tif665K 
irv12232-sup-0006-TableS1.docxWord document27KTable S1. The variations among the whole genome sequences of HAdV-55.
irv12232-sup-0007-TableS2.docxWord document42KTable S2. Clinical manifestations and laboratory findings for the hospitalized children infected with HAdV.

Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.