Skip to content

Advertisement

  • Research article
  • Open Access
  • Open Peer Review

Adenovirus infection in children with acute lower respiratory tract infections in Beijing, China, 2007 to 2012

  • 1, 2,
  • 3,
  • 3,
  • 3,
  • 3,
  • 1, 2,
  • 1,
  • 1,
  • 1,
  • 3Email author and
  • 1Email author
BMC Infectious Diseases201515:408

https://doi.org/10.1186/s12879-015-1126-2

©  Liu et al. 2015

  • Received: 13 May 2015
  • Accepted: 17 September 2015
  • Published:
Open Peer Review reports

Abstract

Background

Human adenoviruses (HAdV) play a significant role in pediatric respiratory tract infections. To date, over 60 types of HAdV have been identified. Here, HAdV types are characterized in children in the Beijing area with acute lower respiratory tract infections (ALRTIs) and the clinical features and laboratory findings of hospitalized HAdV-infected cases are described.

Methods

Respiratory specimens were collected from pediatric patients with ALRTIs in the emergency department or from those admitted to Beijing Children’s Hospital between March 2007 and December 2012. Infections with common respiratory viruses were determined by PCR or RT-PCR. HAdV positive samples were further typed by PCR and sequencing.

Results

Among 3356 patients with ALRTIs, 194 (5.8 %) were found to have HAdV infection. HAdV infection was primarily confined to children (88.35 %) less than 5 years of age. A total of 11 different types of HAdV were detected throughout the study period, with HAdV-B7 (49.0 %) and HAdV-B3 (26.3 %) as the most prevalent types, followed by HAdV-C2 (7.7 %) and HAdVC1 (4.6 %). Newly emerging and re-emergent types or variants, HAdV-B55 (n = 5), HAdV-C57 (n = 3), and HAdV-B14p1 (n = 1), were identified. Results also included the reported first case of co-infection with HAdV-C2 and HAdV-C57. Clinical entities of patients with single HAdV infection (n = 49) were similar to those with mixed HAdV/respiratory syncytial virus (RSV) infections (n = 41). Patients with HAdV-B7 infection had longer duration of fever and higher serum levels of muscle enzymes than HAdV-B3-infected patients.

Conclusions

During the study period, HAdV-B7 and HAdV-B3 were the predominant types identified in pediatric ALRTIs. HAdV-B7 infection tends to have more severe clinical consequences. The presence of newly emerging types or variants and co-infection with different types of HAdV highlights the need for constant and close surveillance of HAdV infection.

Keywords

  • Adenovirus
  • Acute lower respiratory tract infection
  • Type
  • Children

Background

Acute lower respiratory tract infections (ALRTIs) are the leading cause of pediatric morbidity and mortality worldwide, particularly in developing countries. In infants and young children, ALRTIs are most frequently caused by respiratory viruses. One such virus, human adenovirus (HAdV), plays a significant role in pediatric respiratory tract infections, accounting for 2–5 % of the overall respiratory illnesses and 4–10 % of the pneumonias [1, 2]. Although most cases are mild and indistinguishable from other viral causes, ALRTIs caused by HAdV can be severe, or even fatal, and are associated with the highest risk of long term respiratory sequelae [3]. Thus, HAdV-associated ALRTIs are of particular interest to both clinicians and researchers.

HAdV are responsible for a wide spectrum of clinical diseases, including respiratory illness (both upper and lower respiratory tract), pharyngoconjunctival fever, conjunctivitis, cystitis, gastroenteritis, and neurologic and venereal disease [4]. HAdV were first isolated in 1953 as respiratory pathogens [5, 6]. To date, over 60 types of HAdV have been identified and classified into seven species (A to G) [7–14]. Cases of severe infection, outbreaks in closed populations, and even epidemic outbreaks have been associated with the newly emerging or re-emergent types or variants [15–17].

Interestingly, different types of HAdV display various tissue tropisms that correlate with different clinical manifestations of infection. HAdV infections of the respiratory tract are predominantly caused by HAdV-B (including subspecies B1 and B2), HAdV-C, or HAdV-E. The predominant types vary among different countries and regions and they change over time because transmission of novel strains between countries or across continents may occur [18].

Type identification is critical to epidemiological surveillance, detection of new strains, and understanding of HAdV pathogenesis. However, because most clinical laboratories do not type the isolates, there is little published information about epidemiologic and clinical features of HAdV infections by type in children with ALRTIs. To identify HAdV types and species in children with ALRTIs in Beijing area and to characterize clinical features and laboratory findings of hospitalized HAdV-infected cases, respiratory specimens were collected from hospital-admitted pediatric patients with ALRTIs and typed HAdV positive samples using PCR and sequencing.

Methods

Ethics statement

The study protocol was approved by the Ethical Review Committee of Beijing Children’s Hospital. Individual written informed consent was obtained from the parents or guardians of all participants.

Patients and clinical specimens

From March 2007 to December 2012, pediatric patients with ALRTIs who presented in emergency department or were admitted to respiratory department or intensive care unit, Beijing Children’s Hospital, were recruited for the study. The study site hospital is a tertiary comprehensive pediatric hospital with over 900 beds and more than twenty clinical departments. ALRTIs were defined as the presence of signs and symptoms of respiratory tract infection (i.e., fever, coughing, rhinorrhea, oropharyngeal hyperemia, swelling of tonsils), and lower respiratory signs (tachypnea, dyspnea, retractions, or wheezing/rales upon auscultation). The patients were diagnosed with bronchitis, bronchiolitis or pneumonia. Chest X-rays were taken for all patients and the criteria for diagnosing pneumonia are the presence of lung infiltrates indicated by chest radiography. Nasopharyngeal aspirate or throat swab specimens were collected in virus transport media from each patient. No repeated samples were collected from any patient. All samples were stored at −80 °C prior to use.

Preparation of nucleic acids

Total nucleic acids (DNA and RNA) were extracted from 200 μl nasopharyngeal aspirate or throat swab specimens using the NucliSens easyMAG™ automated extraction system (bioMérieux, Marcy l’Etoile, France) according to the manufacturer’s instructions and eluted in 60 μl elution buffer.

Detection of respiratory viruses

The presence of common respiratory viral agents, including parainfluenza virus (PIV) type 1–4, influenza virus (IFV), respiratory syncytial virus (RSV), human rhinovirus (HRV), enterovirus (EV), human coronavirus (HCoV 229E, NL63, HKU1, and OC43), human metapneumovirus (HMPV), human bocavirus (HBoV), and HAdV was determined by multiplex RT-PCR, single RT-PCR, or PCR assays as previously described [19, 20]. Blank virus transport media here served as a negative control for nucleic acid extraction and PCR.

Molecular typing and phylogenetic analysis of HAdV

HAdV positive samples were further amplified using a nested PCR procedure that targeted hyper variable regions 1–6 of the hexon gene as described by Lu and Erdman [21]. Expected amplicons ranged from 688 bp to 821 bp (secondary amplification) in length. Sequencing was performed in both directions using the amplification primers.

Sequences were proof read and assembled using SeqMan software v7.1.0 (DNASTAR Inc., WI, U.S.). For assignment of molecular identity and identification of the closest match, sequence alignment was performed using the Basic Local Alignment Search Tool (BLAST) against NCBI GenBank database (http://www.ncbi.nlm.nih.gov).

Clinical data collection

Clinical data were retrospectively recorded by careful analysis of patient medical files in Beijing Children’s Hospital, using a predefined Microsoft Excel spreadsheet. Patients’ demographic, clinical, and radiologic findings were collected.

Statistical analyses

Continuous variables were summarized as means ± standard deviations (SD) or medians. For categorical variables, percentages of patients in each category were calculated. Differences between groups were assessed using Pearson’s Chi square test or Fisher’s exact test for categorical variables and the one way ANOVA, Independent-Samples T test, Mann–Whitney U test, and Kruskal-Wallis test for continuous variables. All analyses were performed using SPSS software, version 19.0 (IBM Corporation, NY, U.S.). All tests were calculated in a two-tailed manner and a P value of <0.05 was considered statistically significant.

Results

Frequency of HAdV in children with ALRTIs

From March 2007 through December 2012, a total of 3356 patients with ALRTIs (2766 with pneumonia, 309 with bronchitis and 281 with bronchiolitis) were enrolled in this study. The mean age of study participants was 3.87 ± 4.03 years (median 1 year; age range, 0.5 month to 17 years and 17 months). There were 2085 male participants with a male-to-female ratio of 1.64:1.

At least one respiratory virus was detected in nasopharyngeal aspirate or throat swab specimens of 2322 (69.2 %) enrolled participants. RSV (33.4 %) was the most commonly detected viral pathogen, followed by HRV (26.6 %) and PIV (13.6 %). One hundred and ninety-four patients (5.8 %, 194/3356) were found to have HAdV infection, representing 8.7 % (194/2232) of patients with positive respiratory samples. Male paticipants were more likely to be infected with HAdV (135 boys and 59 girls, male to female ratio = 2.3:1). The mean age of infection was 2.13 ± 2.68 years (median, 1 year; age range, 1 month to 15 years). Most of HAdV-infected cases (88.35 %) were under 5 years of age and the highest percentage of HAdV infections (42.47 %) occurred in infants (age group 0– < 1 year), followed by the age group 1– < 2 years (27.84 %).

Additionally, one or more other respiratory viruses were detected in 69.6 % (n = 135) of 194 HAdV-infected participants. Dual viral infection was identified in 75 cases, triple infection in 45 cases, quadruple in 13 and quintuple in 2. RSV (n = 56) was the most frequently co-detected virus, followed by HRV (n = 53) and PIV (n = 42). HBoV (n = 24), HCoV (n = 15), IFV (n = 8), EV (n = 6), and HMPV (n = 5) were also found to be co-infected with HAdV.

Typing of HAdV

One hundred and ninety-four HAdV-positive specimens were all successfully typed by hexon gene amplifying and sequencing. Throughout the study period, four species (A, B, C, E) of HAdV, including 11 different types were identified. Additionally, HAdV-B7 (n = 95; 49.0 %) and HAdV-B3 (n = 51; 26.3 %), which belong to species B, were the most prevalent HAdV types, accounting for 75.3 % of all HAdV-associated infections. HAdV-C2 (7.7 %), HAdV-C1 (4.6 %), HAdV-C5 (3.6 %), HAdV-B55 (2.6 %), HAdV-C6 (1.5 %), HAdV-C57 (1.5 %), HAdV-A31 (1.0 %), HAdV-B14 (0.5 %), and HAdV-E4 (0.5 %) were also detected.

Interestingly, sequencing results from one specimen showed superimposed peaks in the chromatograms. To confirm the possibility of multiple HAdV strains in that sample, PCR products were cloned and sequenced further. Distinct hexon genes of different types (HAdV-C2 and HAdV-C57) were verified.

Temporal distribution of HAdV

HAdV detection rate varied through the years, ranging from 2.55 % in 2007 to 9.15 % in 2010 (Fig. 1). Additionally, Although HAdV was detected throughout the year, cases commonly peaked in winter and spring season (Fig. 2). Furthermore, different types of HAdV did not remain constant across the whole study period (Fig. 2). Specifically, HAdV-C1, −C2, −B3, and -B7 were detected throughout the study; HAdV-C5 in all years except 2007; HAdV-C6 and HAdV-C57 in years 2008, 2009, and 2012; HAdV-B55 in 2008, 2011, and 2012; and HAdV-E4, HAdV-A31, and HAdV-B14 in years 2007, 2009, and 2010, respectively.
Fig. 1
Fig. 1

Samples collected and proportion of samples with HAdV identified in each year, 2007–2012

Fig. 2
Fig. 2

Seasonal distribution of HAdV infection in children with ALRTIs from 2007 to 2012. Detection numbers of different types of HAdV are shown in each month

Clinical features of HAdV infections

Among the 194 HAdV-positive cases, 150 hospitalized cases were included in the clinical analysis, and 44 cases from the emergency department for which the details of the medical records were not available were excluded.

Pneumonia (n = 142, 94.7 %) was the most common clinical diagnosis, followed by bronchitis (n = 7) and bronchiolitis (n = 1). Additionally, almost all hospitalized HAdV-infected patients presented with fever (144/150, 96.0%) and coughing (149/150, 99.3 %) (Table 1). The mean peak body temperature was 39.53 ± 0.67 °C (n = 144, range 37.3 − 41.4 °C) and febrile seizures were noted in two febrile patients. In addition to respiratory symptoms, diarrhea, vomiting, skin rash, and conjunctivitis were noted in 21.3 %, 9.3 %, 10.0 % and 4.7 % of the patients respectively. Twenty-two patients (14.7 %) had underlying diseases, which included congenital heart disease (8 patients), airway anomaly (malacia, stenosis, 11 patients), bronchopulmonary dysplasia (1 patient), asthma (2 patients), or primary immunodeficiency (1 patient). Seventeen patients (11.3 %) required admission to the intensive care unit and 38 patients (11.3 %) received mechanical ventilation including both noninvasive (n = 31) and invasive (n = 7) modes. Analysis revealed that the mean value of white blood cell (WBC) count was 10.09 ± 4.61 × 109/L (Table 2). Leukocytosis (WBC > 12.0 × 109/L) was observed in 37 (24.7 %) patients. Eighty-one patients (54.0 %) had elevated serum C-reaction protein (CRP).
Table 1

Clinical manifestations and laboratory findings of HAdV infections in 150 hospitalized children with ALRTIs

  

Group

Variables

All cases

HAdV

HAdV/RSV

HAdV/RSV

Single infection

Dual infections

Multiple infections

(n = 150)

(n = 49)

(n = 18)

(n = 23)

Age (years)a

2.37 ± 2.89

3.68 ± 3.64

1.53 ± 2.41

1.20 ± 0.81

Male (%)

105 (70 %)

32 (65.3 %)

12 (66.7 %)

17 (73.9 %)

Symptoms and signs

    

Fever

144 (96.0 %)

48 (98.0 %)

17 (94.4 %)

23 (100 %)

T max (°C)

39.53 ± 0.68

39.73 ± 0.66

39.48 ± 0.53

39.62 ± 0.73

Duration of fever (days)

15.31 ± 13.35

18.06 ± 18.85

14.18 ± 5.86

15.17 ± 7.25

Cough

149 (99.3 %)

49 (100 %)

18 (100 %)

23 (100 %)

Rhinorrhea

24 (16.0 %)

8 (16.3 %)

2 (11.1 %)

4 (17.4 %)

Wheezing

90 (60.0 %)

25 (51.0 %)

14 (77.8 %)

17 (73.9 %)

Swelling of tonsils

44 (29.3 %)

18 (36.7 %)

2 (11.1 %)

3 (13.0 %)

Rash

15 (10.0 %)

5 (10.2 %)

7 (12.3 %)

3 (6.8 %)

Vomitting

14 (9.3 %)

5 (10.2 %)

1 (5.6 %)

4 (17.4 %)

Diarrhea

32 (21.3 %)

11 (22.4 %)

3 (16.7 %)

7 (30.4 %)

Conjunctivitis

7 (4.7 %)

2 (4.1 %)

1 (5.6 %)

0 (0 %)

Dyspnea

61 (40.7 %)

18 (36.7 %)

8 (44.4 %)

12 (52.2 %)

ICU admission

17 (11.3 %)

7 (14.3 %)

2 (11.1 %)

5 (21.7 %)

Any underlying diseases

22 (14.7 %)

10 (20.4 %)

2 (11.1 %)

2 (8.7 %)

Treatment

    

Mechanical ventilation

38 (25.3 %)

13 (26.5 %)

4 (22.2 %)

8 (34.8 %)

Coticosteriods

122 (81.3 %)

40 (81.6 %)

13 (72.2 %)

22 (95.7 %)

Inhaled Intravenous

74 (49.3 %)

22 (44.9 %)

8 (44.4 %)

14 (60.9 %)

Immunoglobulin

34 (22.7 %)

8 (16.3 %)

1 (5.6 %)

6 (26.1 %)

Length of hospital stay (days)

18.32 ± 11.31

16.19 ± 11.01

20.17 ± 10.22

20.52 ± 10.44

Laboratory findings

    

WBC (×109/L)

10.09 ± 4.61

9.34 ± 4.85

10.50 ± 3.79

9.86 ± 4.26

CRP (mg/L)

31.64 ± 35.93

36.01 ± 39.67

36.78 ± 30.25

32.42 ± 43.52

AST, median (IQR) (U/L)

33 (45–71.5)

45 (34–81.8)

38.5 (33–56.3)

57 (33–83)

ALT, median (IQR) (U/L)

21 (16–36)

18.1 (15–33)

21 (18–36.5)

22 (19–46)

LDH, median (IQR) (U/L)

360 (262.5-668.5)

369.5 (285.7-899.5)

326.5 (260–584.5)

439 (288–747)

CK, median (IQR) (U/L)

83 (45–192)

87.5 (46.8-264)

84 (42.5-221.8)

88 (38–137)

HBDH, median (IQR) (U/L)

274 (200.5-508.5)

275 (203.3-562.3)

258 (203–447.9)

355 (221.5–524)

ICU intensive care unit, WBC white blood cell, CRP C-reaction protein, AST aspartate aminotransferase, ALT alanine aminotransferase, LDH, lactate dehydrogenase, CK creatinine kinase, HBDH hydroxybutyrate dehydrogenase, IQR interquartile range

aone way ANOVA: single infection vs dual infections vs multiple infections, p = 0.001

Table 2

Clinical information for HAdV-B7 and HAdV-B3 infected children

 

HAdV-B7

HAdV-B3

Variables

Single infection

Coinfection

Single infection

Coinfection

(n = 30)

(n = 52)

(n = 15)

(n = 27)

Age (years)a

3.47 ± 3.08

1.20 ± 1.26

4.91 ± 4.63

2.62 ± 2.99

Male (%)

19 (63.3 %)

41 (56.2 %)

9 (60.0 %)

17 (63.0 %)

Symptoms and signs

    

Fever

29 (96.7 %)

51 (98.1 %)

15 (100 %)

24 (88.9 %)

T max (°C)

39.84 ± 0.71

39.50 ± 0.57

39.55 ± 0.53

39.78 ± 0.67

Duration of fever (days)b

22.07 ± 21.52

14.02 ± 6.36

9.73 ± 7.31

15.38 ± 14.36

Cough

30 (100 %)

52 (100 %)

15 (100 %)

26 (96.3 %)

Rhinorrhea

4 (13.3 %)

7 (13.5 %)

3 (20 %)

5 (18.5 %)

Wheezing

17 (56.7 %)

37 (71.2 %)

7 (46.7 %)

13 (48.1 %)

Swelling of tonsils

11 (36.7 %)

9 (17.3 %)

7 (46.7 %)

9 (33.3 %)

Rash

3 (10.0 %)

5 (9.6 %)

0

3 (11.1 %)

Vomitting

3 (10.0 %)

5 (9.6 %)

2 (13.3 %)

3 (11.1 %)

Diarrhea

9 (30.0 %)

13 (25.0 %)

1 (6.7 %)

7 (25.9 %)

Conjunctivitis

1 (3.3 %)

3 (5.8 %)

0

1 (3.7 %)

Dyspnea

13 (43.3 %)

26 (50.0 %)

4 (26.7 %)

9 (33.3 %)

ICU admission

6 (20.0 %)

7 (13.5 %)

0

2 (7.4 %)

Any underlying diseases

5 (16.7 %)

6 (11.5 %)

4 (26.7 %)

4 (14.8 %)

Treatment

    

Mechanical ventilation

8 (26.7 %)

19 (36.5%)

4 (26.7 %)

4 (14.8 %)

Coticosteriods

26 (86.7 %)

45 (86.5%)

12 (80.0 %)

24 (88.9 %)

Inhaled

16 (53.3 %)

29 (55.8%)

5 (33.3 %)

14 (51.9 %)

Intravenous

    

Immunoglobulinc

8 (26.7 %)

20 (38.5 %)

0

4 (14.8 %)

Length of hospital stay (days)

18.50 ± 12.87

22.44 ± 11.67

12.33 ± 4.95

16.89 ± 10.88

Laboratory findings

    

WBC (×109/L)

8.75 ± 4.63

9.96 ± 4.95

10.34 ± 5.23

10.87 ± 3.91

CRP (mg/L)

34.68 ± 42.70

33.95 ± 39.30

41.96 ± 36.84

31.54 ± 27.96

AST, median (IQR) (U/L)d

67 (38.8–100)

60 (38.3–94.3)

33 (27–45)

38 (26–51)

ALT, median (IQR) (U/L)e

20 (16–36)

25 (19–42.8)

15 (12–21)

17 (13–26)

LDH, median (IQR) (U/L)f

565 (341.8–1232.8)

470.5 (305.3–922.8)

297 (207–397)

311 (245–462)

CK, median (IQR) (U/L)

125.5 (48–499.8)

87 (45.5–187.5)

77 (46–99)

6 (43–115)

HBDH, median (IQR) (U/L)g

408 (242.8–803)

356.5 (225.9–647.5)

219 (162–313)

210 (199–374)

ICU intensive care unit, WBC white blood cell, CRP C-reaction protein, AST aspartate aminotransferase, ALT alanine aminotransferase, LDH lactate dehydrogenase, CK creatinine kinase, HBDH hydroxybutyrate dehydrogenase, IQR interquartile range

aIndependent-Samples T test: HAdV-B7 single infection vs HAdV-B7 coinfection, p = 0.001

bIndependent-Samples T test: HAdV-B7 single infection vs HAdV-B3 single infection, p = 0.038

cFisher exact test: HAdV-B7 single infection vs HAdV-B3 single infecion, p = 0.038

dMann–Whitney U test: HAdV-B7 single infection vs HAdV-B3 single infection, p < 0.001

eMann–Whitney U test: HAdV-B7 single infection vs HAdV-B3 single infection, p = 0.029

fMann–Whitney U test: HAdV-B7 single infection vs HAdV-B3 single infection, p = 0.001

gMann–Whitney U test: HAdV-B7 single infection vs HAdV-B3 single infection, p = 0.001

Given RSV was the virus most frequently co-detected with HAdV, differences among patients with single HAdV infection (n = 49) and those with HAdV/RSV co-infections, including both dual infections (n = 18) and multiple infections (HAdV/RSV with one or more other respiratory viruses, n = 23), were assessed (Table 1). The mean age of patients with multiple infections (1.20 ± 0.81) and dual infections (1.53 ± 2.41) was significantly younger than those with single HAdV infection (3.68 ± 3.64) (P = 0.001). However clinical characteristics and laboratory findings showed no significant differences among different groups.

Because HAdV-B7 and HAdV-B3 were the most predominant type among patients with HAdV infection, the clinical entities of patients with single HAdV-B7 infection (n = 30) and those with single HAdV-B3 infection (n = 15) were also compared to exclude the possible effect of other respiratory virus infection (Table 2). Patients with single HAdV-B7 infection showed longer duration of fever (22.07 ± 21.52 vs 9.73 ± 7.31, P = 0.038) than patients with HAdV-B3 alone. Immunoglobulin was more frequently used in single HAdV-B7 infected patients than in single HAdV-B3 group (P = 0.038). Patients with HAdV-B7 alone also tend to require longer hospital stay (18.50 ± 12.87 vs 12.33 ± 4.95, P = 0.082) than those with single HAdV-B3 infection, although no significant difference was found. Biochemical tests demonstrated aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH) and hydroxybutyrate dehydrogenase (HBDH) levels were significantly higher in the single HAdV-B7 infected group.

Two patients died in-hospital. Both of them required ICU admission and died of multiple organ failure. One was a 17 month-old boy with multiple underlying conditions of complex congenital heart disease and tracheobronchial malformation. The other was a previously healthy 18 month-old boy. Analysis indicated that both fatal patients were infected with HAdV-B7 but no other respiratory viruses.

Discussion

HAdV is a significant causative agent of respiratory tract illnesses in both children and adults. Here, the molecular epidemiology and clinical features of HAdV associated pediatric ALRTIs in Beijing Children’s Hospital from March 2007 to December 2012 were described. Results showed that the HAdV infection rate in the current study population was 5.8 %, which was consistent with previous reports from China and other countries [22–24]. Results showed that most patients with HAdV infection were younger than 5 years (88.35 %), which is similar to numbers reported in previous studies [1, 22, 23, 25–27]. This may because the immune systems of young children are not well developed, which leaves them prone to more severe HAdV disease. This may also suggest that school-age children are exposed to the most common endemic types of HAdV early in life, thereby establishing a protective immunity resulting only in mild clinical symptoms, such that upper respiratory tract infection does not require care in an emergency department or hospital in this age group.

Over a period of 6 years, 11 different types of HAdV belonging to 4 species (HAdV-A, B, C, E) were identified in respiratory specimens from children with ALRTIs. HAdV-7 and HAdV-3 of species B comprised the most prevalent types and presented throughout the duration of the study. Although these results were consistent with previous reports from Korea and Argentina [22, 28, 29], investigations from Croatia, Peru, Canada, France showed that species C predominated [1, 25, 26, 30]. This difference in type prevalence may be attributed to difference in regions, year of study, and population recruited.

Notably, some newly emerging or re-emergent types or variants were here identified, although only in rare cases. Five patients were found to have HAdV-B55 (formerly named HAdV-11a), which is an uncommon re-emergent type that once caused an outbreak of respiratory tract infection in a senior high school in Shanxi Province, China in 2006, including one fatal case [15]. Subsequently, HAdV-B55 has been associated with several outbreaks of respiratory disease in other provinces in China [31]. An emerging variant, HAdV-B14p1 (formerly known as 14a), was also found. Recently, HAdV-B14p1 has been associated with several large outbreaks of acute respiratory infection, which included severe and even fatal cases in the United States and Europe [16, 32]. Additionally, in 2011, an outbreak of febrile respiratory illness that affected 43 students in Gansu Province, China was reported to be caused by HAdV-B14p1 [33]. One HAdV-B14 infected patient who presented with bronchopneumonia and required hospitalization in April 2010 was identified. By further sequencing the fiber gene (data not shown), this strain was confirmed to be HAdV-B14p1 because it contained a unique characteristic 6-nuleotid deletion in fiber knob region as reported by Kajon et al. [32]. Last, this is the first report of detection of HAdV-C57 in respiratory samples collected from pediatric patients with ALRTIs and the first of co-detection of HAdV-C57 with HAdVC-2. HAdV-C57 (formerly designated strain 16700) was first isolated from the feces of a healthy child as part of an acute flaccid paralysis surveillance program. Computational genomic and bioinformatic analysis showed HAdV-C57 to be a recombinant virus with fiber gene nearly identical to HAdV-C6 and a unique hexon distinct from all viruses in species HAdV-C [34, 35]. Out of the three HAdV-C57-infected cases identified here, one was a previously healthy 9-month-old male who presented with bronchopneumonia and conjunctivitis requiring hospitalization. Because only a small number of HAdV-C57 positive cases were found here and all were co-infected with other respiratory viruses, the pathogenic role of HAdV-C57 in respiratory infections will require further investigation.

HAdV type is traditionally determined by virus isolation and subsequently serum neutralization tests, in which antibodies raised against specific type are used to suppress cytopathic effects in tissue culture assays. By nature of its design, this test can only reveal the dominant type. By applying PCR-based identification targeting hexon or fiber genes, co-infections with multiple HAdV types (types from same or different species) have been reported in both immunocompromised and immunocompetent patients [28, 29, 36–38]. In current study, results showed that one specimen contained both HAdV-C2 and HAdV-C57 by cloned sequencing the PCR products. These were amplified directly from respiratory samples using universal primers of hexon gene. This co-infected phenomenon was confirmed using the fiber gene sequencing results with type-specific primers (data not shown). The specimen was collected from a previously healthy 2.7-year old boy, presenting with fever, coughing and seizure at emergency department on December 10, 2009. Co-infection of different HAdV types has never been reported in any previous studies of Mainland China. The clinical implications of such co-infection remain unclear, and its role in HAdV pathogenesis and evolution will require further study.

Consistent with the report from Guangzhou, Southern China [24], results here showed that 69.6% of HAdV-infected participants were co-infected with one or more other respiratory tract viruses and that RSV was the most frequently co-detected virus. However, no significant differences in clinical characteristics and laboratory findings were found between patients with single HAdV infection and those co-infected with RSV except that co-infections were more frequently observed in younger children. Similarly, a study from Peru also did found no higher prevalence of any clinical manifestations in co-infected patients than in those infected with HAdV alone [26]. The results of another report from Chile showed the clinical severity to be the same in patients with single HAdV infection and those with mixed RSV-HAdV infections [39]. These data demonstrate that, as more sensitive molecular methods become more frequently used to identify pathogens, co-detection of different viruses in the same specimen may also become more common. However, the clinical role of such co-infections will still require independent investigations.

Both HAdV-B7 and HAdV-B3 may cause severe or even fatal pneumonia in even immunocompetent children. Several previous studies showed that patients infected with HAdV-B7 tend to have higher case-fatality rates than those with HAdV-B3 [40, 41]. Two fatal cases were recorded during the study period, and both of these patients were infected with HAdV-B7 alone. Analysis revealed that patients with HAdV-B7 infection had longer duration of fever and higher serum levels of muscle enzymes than HAdV-B3-infected patients. Patients with HAdV-B7 infection also tended to require longer hospital stays although no significant difference was found. These differences have excluded the possible interference by any other co-infected respiratory viruses since this work only evaluated the patients with HAdV infection alone. Such results may suggest that HAdV-B7 infection tended to cause more extrapulmonary tissue damage (such as liver and heart) and may have more severe clinical consequence.

This is a cross-sectional study. Only one respiratory sample was collected from each patient and no viral load analysis was performed. Although HAdV is a pathogen that for long has been known to cause respiratory tract infection, asymptomatic carriage of the virus may persist for weeks [18]. The detection of HAdV in nasopharyngeal aspirate or throat swab with the use of a PCR assay could represent convalescent-phase shedding, so detection may not suggest the current infection.

Conclusions

In summary, a total of 11 different types of HAdV were identified in children with ALRTIs and HAdV-B7 and HAdV-B3 were the most predominant types. Clinical entities of patients with single HAdV infection were similar to those with mixed HAdV/RSV infections. HAdV-B7 infection tends to have more severe clinical consequences. The presence of newly emerging types or variants and co-infection with different types of HAdV highlights the need for constant and close surveillance of adenovirus infection.

Abbreviations

HAdV: 

Human adenoviruses

ALRTIs: 

Acute lower respiratory tract infections

PIV: 

Parainfluenza virus

IFV: 

Influenza virus

RSV: 

Respiratory syncytial virus

HRV: 

Human rhinovirus

EV: 

Enterovirus

HCoV: 

Human coronavirus

HMPV: 

Human metapneumovirus

HBoV: 

Human bocavirus

WBC: 

White blood cell

CRP: 

C-reaction protein

AST: 

Aspartate aminotransferase

ALT: 

Alanine aminotransferase

LDH: 

Lactate dehydrogenase

HBDH: 

Hydroxybutyrate dehydrogenase

Declarations

Acknowledgements

We would like to thank all participating physicians and nurses of Beijing Children’s Hospital for their assistance and collaboration in the sample and clinical data collection. This study was supported by grants from the National Major S & T Research Projects for the Control and Prevention of Major Infectious Diseases in China (2012ZX10004–206) and National Science and Technology Supported Projects (2013BAI09B11).

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Beijing Children’s Hospital, Capital Medical University, Beijing, 100045, P. R. China
(2)
Beijing Pediatric Research Institute, Beijing, 100045, P. R. China
(3)
MOH Key Laboratory of Systems Biology of Pathogens and Dr. Christophe Mérieux Laboratory, IPB, CAMS-Fondation Mérieux, Institute of Pathogen Biology (IPB), Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College, Beijing, 100730, P. R. China

References

  1. Alharbi S, Van Caeseele P, Consunji-Araneta R, Zoubeidi T, Fanella S, Souid AK, et al. Epidemiology of severe pediatric adenovirus lower respiratory tract infections in Manitoba, Canada, 1991–2005. BMC Infect Dis. 2012;12:55.View ArticlePubMedPubMed CentralGoogle Scholar
  2. Jain S, Williams DJ, Arnold SR, Ampofo K, Bramley AM, Reed C, et al. Community-acquired pneumonia requiring hospitalization among U.S. children. N Engl J Med. 2015;372(9):835–45.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Edmond K, Scott S, Korczak V, Ward C, Sanderson C, Theodoratou E, et al. Long term sequelae from childhood pneumonia; systematic review and meta-analysis. PLoS One. 2012;7(2), e31239.View ArticlePubMedPubMed CentralGoogle Scholar
  4. Hierholzer JC. Adenoviruses. In: Schmidt NJ, Emmons RW, editors. Diagnostic procedures for viral, richettsial and chlamydial infections. 6th ed. Washington DC: American public health association; 1989. p. 21–229.Google Scholar
  5. Rowe WP, Huebner RJ, Gilmore LK, Parrott RH, Ward TG. Isolation of a cytopathogenic agent from human adenoids undergoing spontaneous degeneration in tissue culture. Proc Soc Exp Biol Med. 1953;84(3):570–3.View ArticlePubMedGoogle Scholar
  6. Hilleman MR, Werner JH. Recovery of new agent from patients with acute respiratory illness. Proc Soc Exp Biol Med. 1954;85(1):183–8.View ArticlePubMedGoogle Scholar
  7. Hiroi S, Furubayashi K, Kawahata T, Morikawa S, Kase T. A case of urethritis caused by human adenovirus type 56. Jpn J Infect Dis. 2012;65(3):273–4.View ArticlePubMedGoogle Scholar
  8. Hiroi S, Izumi M, Takahashi K, Morikawa S, Kase T. Isolation and characterization of a novel recombinant human adenovirus species D. J Med Microbiol. 2012;61(Pt 8):1097–102.View ArticlePubMedGoogle Scholar
  9. Matsushima Y, Shimizu H, Kano A, Nakajima E, Ishimaru Y, Dey SK, et al. Novel human adenovirus strain, Bangladesh. Emerg Infect Dis. 2012;18(5):846–8.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Liu EB, Wadford DA, Seto J, Vu M, Hudson NR, Thrasher L, et al. Computational and serologic analysis of novel and known viruses in species human adenovirus D in which serology and genomics do not correlate. PLoS One. 2012;7(3), e33212.View ArticlePubMedPubMed CentralGoogle Scholar
  11. Dehghan S, Liu EB, Seto J, Torres SF, Hudson NR, Kajon AE, et al. Five genome sequences of subspecies B1 human adenoviruses associated with acute respiratory disease. J Virol. 2012;86(1):635–6.View ArticlePubMedPubMed CentralGoogle Scholar
  12. Jones MN, Harrach B, Ganac RD, Gozum MM, Dela CW, Riedel B, et al. New adenovirus species found in a patient presenting with gastroenteritis. J Virol. 2007;81(11):5978–84.View ArticlePubMedPubMed CentralGoogle Scholar
  13. Walsh MP, Chintakuntlawar A, Robinson CM, Madisch I, Harrach B, Hudson NR, et al. Evidence of molecular evolution driven by recombination events influencing tropism in a novel human adenovirus that causes epidemic keratoconjunctivitis. PLoS One. 2009;4(6), e5635.View ArticlePubMedPubMed CentralGoogle Scholar
  14. 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(22):12441–2.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Zhu Z, Zhang Y, Xu S, Yu P, Tian X, Wang L, et al. Outbreak of acute respiratory disease in China caused by B2 species of adenovirus type 11. J Clin Microbiol. 2009;47(3):697–703.View ArticlePubMedGoogle Scholar
  16. Carr MJ, Kajon AE, Lu X, Dunford L, O’Reilly P, Holder P, et al. Deaths associated with human adenovirus-14p1 infections, Europe, 2009–2010. Emerg Infect Dis. 2011;17(8):1402–8.View ArticlePubMedPubMed CentralGoogle Scholar
  17. CentersforDiseaseControlandPrevention(CDC). Acute respiratory disease associated with adenovirus serotype 14–four states, 2006–2007. MMWR Morb Mortal Wkly Rep 2007. 2007;56(45):1181–4.Google Scholar
  18. Lynch JR, Fishbein M, Echavarria M. Adenovirus. Semin Respir Crit Care Med. 2011;32(4):494–511.View ArticlePubMedGoogle Scholar
  19. Ren L, Gonzalez R, Wang Z, Xiang Z, Wang Y, Zhou H, et al. Prevalence of human respiratory viruses in adults with acute respiratory tract infections in Beijing, 2005–2007. Clin Microbiol Infect. 2009;15(12):1146–53.View ArticlePubMedGoogle Scholar
  20. Guo L, Gonzalez R, Xie Z, Zhou H, Liu C, Wu C, et al. Bocavirus in children with respiratory tract infections. Emerg Infect Dis. 2011;17(9):1775–7.View ArticlePubMedPubMed CentralGoogle Scholar
  21. Lu X, Erdman DD. Molecular typing of human adenoviruses by PCR and sequencing of a partial region of the hexon gene. Arch Virol. 2006;151(8):1587–602.View ArticlePubMedGoogle Scholar
  22. Hong JY, Lee HJ, Piedra PA, Choi EH, Park KH, Koh YY, et al. Lower respiratory tract infections due to adenovirus in hospitalized Korean children: epidemiology, clinical features, and prognosis. Clin Infect Dis. 2001;32(10):1423–9.View ArticlePubMedGoogle Scholar
  23. Qurei L, Seto D, Salah Z, Azzeh M. A molecular epidemiology survey of respiratory adenoviruses circulating in children residing in Southern Palestine. PLoS One. 2012;7(8), e42732.View ArticlePubMedPubMed CentralGoogle Scholar
  24. Zou L, Zhou J, Li H, Wu J, Mo Y, Chen Q, et al. Human adenovirus infection in children with acute respiratory tract disease in Guangzhou, China. APMIS. 2012;120(8):683–8.View ArticlePubMedGoogle Scholar
  25. Tabain I, Ljubin-Sternak S, Cepin-Bogovic J, Markovinovic L, Knezovic I, Mlinaric-Galinovic G. Adenovirus respiratory infections in hospitalized children: clinical findings in relation to species and serotypes. Pediatr Infect Dis J. 2012;31(7):680–4.View ArticlePubMedGoogle Scholar
  26. Ampuero JS, Ocana V, Gomez J, Gamero ME, Garcia J, Halsey ES, et al. Adenovirus respiratory tract infections in Peru. PLoS One. 2012;7(10), e46898.View ArticlePubMedPubMed CentralGoogle Scholar
  27. Selvaraju SB, Kovac M, Dickson LM, Kajon AE, Selvarangan R. Molecular epidemiology and clinical presentation of human adenovirus infections in Kansas City children. J Clin Virol. 2011;51(2):126–31.View ArticlePubMedGoogle Scholar
  28. Lee J, Choi EH, Lee HJ. Comprehensive serotyping and epidemiology of human adenovirus isolated from the respiratory tract of Korean children over 17 consecutive years (1991–2007). J Med Virol. 2010;82(4):624–31.View ArticlePubMedGoogle Scholar
  29. Barrero PR, Valinotto LE, Tittarelli E, Mistchenko AS. Molecular typing of adenoviruses in pediatric respiratory infections in Buenos Aires, Argentina (1999–2010). J Clin Virol. 2012;53(2):145–50.View ArticlePubMedGoogle Scholar
  30. Berciaud S, Rayne F, Kassab S, Jubert C, Faure-Della CM, Salin F, et al. Adenovirus infections in Bordeaux University Hospital 2008–2010: clinical and virological features. J Clin Virol. 2012;54(4):302–7.View ArticlePubMedGoogle Scholar
  31. Li X, Kong M, Su X, Zou M, Guo L, Dong X, et al. An outbreak of acute respiratory disease in China caused by human adenovirus type B55 in a physical training facility. Int J Infect Dis. 2014;28:117–22.View ArticlePubMedGoogle Scholar
  32. Kajon AE, Lu X, Erdman DD, Louie J, Schnurr D, George KS, et al. Molecular epidemiology and brief history of emerging adenovirus 14-associated respiratory disease in the United States. J Infect Dis. 2010;202(1):93–103.View ArticlePubMedGoogle Scholar
  33. Huang G, Yu D, Zhu Z, Zhao H, Wang P, Gray GC, et al. Outbreak of febrile respiratory illness associated with human adenovirus type 14p1 in Gansu Province, China. Influenza Other Respir Viruses. 2013;7(6):1048–54.View ArticlePubMedPubMed CentralGoogle Scholar
  34. Walsh MP, Seto J, Liu EB, Dehghan S, Hudson NR, Lukashev AN, et al. Computational analysis of two species C human adenoviruses provides evidence of a novel virus. J Clin Microbiol. 2011;49(10):3482–90.View ArticlePubMedPubMed CentralGoogle Scholar
  35. Lukashev AN, Ivanova OE, Eremeeva TP, Iggo RD. Evidence of frequent recombination among human adenoviruses. J Gen Virol. 2008;89(Pt 2):380–8.View ArticlePubMedGoogle Scholar
  36. Metzgar D, Osuna M, Yingst S, Rakha M, Earhart K, Elyan D, et al. PCR analysis of egyptian respiratory adenovirus isolates, including identification of species, serotypes, and coinfections. J Clin Microbiol. 2005;43(11):5743–52.View ArticlePubMedPubMed CentralGoogle Scholar
  37. Wang SL, Chi CY, Kuo PH, Tsai HP, Wang SM, Liu CC, et al. High-incidence of human adenoviral co-infections in taiwan. PLoS One. 2013;8(9), e75208.View ArticlePubMedPubMed CentralGoogle Scholar
  38. McCarthy T, Lebeck MG, Capuano AW, Schnurr DP, Gray GC. Molecular typing of clinical adenovirus specimens by an algorithm which permits detection of adenovirus coinfections and intermediate adenovirus strains. J Clin Virol. 2009;46(1):80–4.View ArticlePubMedPubMed CentralGoogle Scholar
  39. Palomino MA, Larranaga C, Villagra E, Camacho J, Avendano LF. Adenovirus and respiratory syncytial virus-adenovirus mixed acute lower respiratory infections in Chilean infants. Pediatr Infect Dis J. 2004;23(4):337–41.View ArticlePubMedGoogle Scholar
  40. Kim YJ, Hong JY, Lee HJ, Shin SH, Kim YK, Inada T, et al. Genome type analysis of adenovirus types 3 and 7 isolated during successive outbreaks of lower respiratory tract infections in children. J Clin Microbiol. 2003;41(10):4594–9.View ArticlePubMedPubMed CentralGoogle Scholar
  41. Lai CY, Lee CJ, Lu CY, Lee PI, Shao PL, Wu ET, et al. Adenovirus serotype 3 and 7 infection with acute respiratory failure in children in Taiwan, 2010–2011. PLoS One. 2013;8(1), e53614.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© Liu et al. 2015

Advertisement

BMC Infectious Diseases

ISSN: 1471-2334

Contact us