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Viral coinfection in acute respiratory infection in Mexican children treated by the emergency service: A cross-sectional study

Italian Journal of Pediatrics volume 41, Article number: 33 (2015) Cite this article

Abstract

Background

Acute respiratory infections (ARIs) cause illness. Children under five years of age are highly vulnerable to these infections. Viral coinfection or multiple viral infection is a variable that can have a significant impact on the evolution of these diseases.

Methods

This cross-sectional study was carried out in Mexican children (under five years of age) who had an ARI and who were treated by an emergency service in a hospital in Guadalajara, Jalisco, Mexico. The viral etiology, as well as the presence of multiple viral infections, was determined. A structured questionnaire was used to obtain demographic and clinical information. Odds ratio (OR) was calculated, and univariate and multivariate analyses using logistic regression were performed.

Results

In the study population, metapneumovirus (hMPV) was the most frequent virus (22%), followed by adenovirus (hAD) (16%), respiratory syncytial virus (RSV) (14%), rhinovirus (hRV) (12%), bocavirus (hBoV) (9%), influenza virus (IF) (7%), and parainfluenza (PIF) (4%). The frequency of viral coinfections was 31.62%, and multiple logistic regression analysis revealed that hMPV, RSV, PIF, and hBoV were independently associated with multiple viral infection. No difference was found in the clinical manifestation of children with simple and multiple infections. Simple hMPV infection was associated with patients who presented with severe ARI. Using a multivariate analysis, we found that overcrowding is associated with coinfection when the viral etiology was hRV (OR = 2.56, 95% confidence interval (CI) 1.07 to 6.13), IF (OR = 2.56, 95% CI 1.07 to 6.13), PIF (OR = 2.96, 95% CI 1.15 to 7.65), hAD (OR = 2.56, 95% CI 1.07 to 6.13), and hBoV (OR = 2.9, 95% CI 1.14 to 7.34).

Conclusions

Viral coinfections are frequent in children requiring treatment by an emergency service. However, the severity of ARI is similar to that of children with a simple infection. The hMPV is common and may confer a significant disease burden in the Mexican population. Finally, overcrowding is a housing characteristic that favors the development of coinfections.

Background

Acute respiratory infections (ARIs) are a public health problem due to their high morbidity. According to the World Health Organization (WHO), of the total number of new cases of pneumonia in the world, about 7% to 13% require hospitalization [1], and pneumonia results in approximately 1.4 million deaths per year in children under five years of age, mainly in developing countries [2].

Several microorganisms can cause ARI. However, most of them are of viral etiology [3,4]; respiratory syncytial virus (RSV), rhinovirus (hRV), influenza virus (IF), adenovirus (hAD), and parainfluenza (PIF) are the most frequently involved viruses (reviewed in [4,5]). All of these viruses are of clinical importance, and RSV has been found to be one of the most common viruses in ARI. Additionally, RSV infection has been associated with a more aggressive behavior and an increased need for hospitalization [6-9]. Given the way these respiratory viruses are spread and the diversity of types and variants [3,10], it is not surprising that sometimes the same patient is infected with more than one virus. Therefore, many research groups have tried to determine the consequence of multiple infections as clinical manifestations worsen. However, the results show discrepancies, because in some studies severe ARI occurs mainly in individuals with simple infections (reviewed in [11]).

The etiologic factor is not the only one influencing ARI complications; environmental and socioeconomic factors also impact on disease progression. A meta-analysis found that low birth weight, lack of exclusive breastfeeding, and overcrowding, among other factors, are associated with severe ARI (reviewed in [12]).

The purpose of this study was to determine the prevalence of respiratory viruses in Mexican children who were under five years of age, had an ARI, and were admitted to the emergency department of a single institution in Guadalajara, Jalisco, Mexico. It also evaluates the relationship between viral coinfection with clinical manifestations and some possible risk factors related to demographic and housing characteristics.

Methods

Study design

This cross-sectional study was carried out in Mexican children with ARI from December 2012 to April 2013 in a secondary care hospital located in Guadalajara, Jalisco, Mexico. The study was approved by the research committee of the hospital. The parents of the recruited infants were informed about the characteristics of the study and provided written informed consent for a sample to be taken and analyzed. A structured questionnaire was used to obtain demographic and clinical information.

Subjects

In total, 162 samples from children under five years of age were obtained from a pediatric emergency service from December 2012 to April 2013 (corresponding to winter and spring). The inclusion criteria were age of less than five years, upper or lower respiratory tract manifestations of ARI, or both. The patients were divided into two groups according to severity of ARI: mild-moderate and severe. The criterion for determining severe ARI was that the patient had at least one sign of respiratory distress according to Official Mexican Norm NOM-031-SSA2-1999, which pertains to the care of children’s health: dyspnea, apnea, wheezing, or intercostal retraction [13]. Mild-moderate ARIs were all ARIs without respiratory distress. In this study, the patients had no fatal outcome.

Definitions

ARI was defined according to the Mexican Official Norm as infectious disease caused by microorganisms that affect the respiratory system during a period of shorter than 15 days. The ARI should have been diagnosed by the attending physician [13].

Overcrowded housing was indicated when the quotient obtained by dividing the number of household members by the number of rooms available to sleep in was greater than or equal to 3 [14].

History of breastfeeding was assessed as duration in months and was divided into two groups: greater than or equal to 6 months versus less than 6 months. There was no further questioning about whether breastfeeding was exclusive.

Comorbidity was defined as the presence of one or more diseases or conditions other than those of primary interest [15].

Nutritional status was evaluated by body mass index as underweight, normal weight, and excess weight (overweight or obesity) according to Child Growth Standards, (World Health Organization) [16].

Clinical samples

The nasal swabs were collected with sterile rayon-tipped applicators (Puritan Medical Products Co. LLC, Guilford, ME, USA) in accordance with WHO recommendations [17]. The swab was placed into a tube that contained Leibovitz viral transport medium with 100 IU/mL penicillin (American Type Culture Collection, Manassas, VA, USA), 0.25 μg/mL amphotericin B, and 0.01 mg/mL streptomycin (American Type Culture Collection). The samples were maintained at 4°C and transported at this temperature from the hospital in Guadalajara, Jalisco, to the virology laboratory of the Instituto de Salud Pública, Universidad Veracruzana (Public Health Institute, University of Veracruz), where the samples were processed and analyzed.

Virus detection

Viral genomes were extracted with a PureLink viral RNA/DNA kit (Invitrogen Corporation, Carlsbad, CA, USA) in accordance with the instructions of the manufacturer. A screening for detecting bocavirus (hBoV) [18], hAD [19], RSV [20], hRV [21], metapneumovirus (hMPV) [22,23], influenza type A (IF), and PIF was carried out by reverse transcription-polymerase chain reaction (RT-PCR) or PCR by means of an AccessQuick™ RT-PCR System (Promega Corporation, Madison, WI, USA) in accordance with the instructions of the manufacturer and with previously described primers and methods; the modifications to these methods are indicated in Additional file 1. The PIF primers were designed by our group, and the IF primers were designed and provided by Susana López and her group (National Autonomous University of Mexico).

Statistical analysis

Associations between different variables were assessed by the chi-square test or Fisher test where necessary. Statistical significance was defined as a P value of less than 0.05. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated by logistic regression. Statistical analysis was performed by using SPSS software (PASW Statistics for Windows, Version 18.0; SPSS Inc., Chicago, IL, USA) and StatCalc (Epi Info 7; Centers for Disease Control and Prevention, Atlanta, GA, USA).

Results

Characteristics of the participants

One hundred sixty-two patients were included in this study. The characteristics of the participants were analyzed. The average age of the population was 18.4 months (1.87 to 34.85 months), 28.4% were not more than 6 months old, and 58.6% of participants were male.

Clinical signs of an ARI were evaluated according to the data obtained from the questionnaire. All participants had nasal discharge and cough, and 67.3% had fever.

In regard to the housing characteristics, 8% of the participants lived in houses where they cooked with firewood, 38.9% reported having lived in overcrowded conditions, and less than 2% lived in a house with a soil floor. Furthermore, 88.8% had been breastfed at least once.

Viral etiology

Of the samples tested, 57% were positive for a virus. The viruses most frequently detected were hMPV (22%), hAD (16%), RSV (14%), and hRV (12%). hBoV (9%), IF (7%), and PIF (4%) were detected at a lower frequency (Table 1).

Table 1 Viral detection by polymerase chain reaction
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Viral etiology and severity of the acute respiratory infection

The presence of each virus in mild-moderate or severe ARI was analyzed. hMPV was found to be associated with the severe ARI group (OR = 4.0, 95% CI 1.33 to 12.06). Other viruses we analyzed showed no association with any of the groups.

Viral coinfections

The presence of more than one virus was evaluated in the sample coming from the same subject. Simple infections were the most frequent, whereas multiple infections occurred in 31.62% of patients with ARI of viral etiology. hMPV was the most frequent virus in coinfections (58.8%), followed by hAD and RSV (38.2% each).

A univariate analysis showed that only four of the seven viruses studied were significantly associated with multiple infection; PIF was the highest coinfection risk (OR = 12.42, 95% CI 1.4 to 108.3), followed by hBoV (OR = 5.16, 95 % CI 1.6 to 16.6), hMPV (OR = 3.8, 95% CI 1.6 to 9.4), and RSV (OR = 3.03, 95% CI 1.15 to 8.0). hAD, IF, and hRV showed no association (Table 2).

Table 2 Comparison of viral etiology between subjects with multiple and simple infection
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In the study population, 24.18% of cases of dual infection and 7.44% of triple infection were found. In regard to dual infections, the highest combination was observed between RSV-IF (4.65%). In the triple coinfections, the most common combination was hMPV-hAD-hBoV (2.79%) (Table 3).

Table 3 Description of the coinfection type
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Association between clinical and demographic characteristics with coinfection

A univariate analysis was carried out to find the association between coinfection and the following variables: age, sex, using wood as fuel in the house, overcrowding, having a house with a soil floor, and breastfeeding. Age of less than or equal to 6 months and living in overcrowded conditions increased the risk for multiple infection (OR = 3.04, 95% CI 1.08 to 8.6 and OR = 2.6, 95% CI 1.1 to 6.1, respectively). The rest of the demographic variables showed no significant association.

In regard to clinical features, the presence of comorbidity, nutritional state, and severity of ARI were evaluated. We found no significant differences (Table 4).

Table 4 Demographic and clinical characteristics of subjects with multiple or simple infection
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Multivariate analysis of factors associated with coinfection

A multivariate analysis was conducted in order to identify the risk factors for viral coinfection by making a stratification according to the etiological agent identified. Infection with hMPV, RSV, PIF, and hBoV showed significant association in the adjusted model. Overcrowding was a variable that remained associated in the adjusted analysis in those cases of infection with hRV (OR = 2.56, 95% CI 1.07 to 6.13), IF (OR = 2.56, 95% CI 1.07 to 6.13), PIF (OR = 2.96, 95% CI 1.15 to 7.65), hAD (OR = 2.56, 95% CI 1.07 to 6.13), and hBoV (OR = 2.9, 95% CI 1.14 to 7.34). The rest of the variables that had shown no significant association in the univariate analysis did not show one in the multivariate analysis either, except for age of less than 6 months, which was associated with infection with PIF and multiple infections (OR = 3.33, 95% CI 1.07 to 10.39) (Table 5).

Table 5 Multivariate analysis of identified risk factors for coinfections
Full size table

Discussion

In Mexico, as in other parts of the world, ARIs have a high impact on morbidity, and children are highly vulnerable to these diseases [2,24].

In this study, we conducted an analysis of the viral etiology and clinical features of children admitted to the pediatric emergency service of a secondary care hospital, located in western Mexico.

In regard to viral detection, we found that hMPV was the most frequent virus in simple infections in the population we analyzed. This virus recently has been identified and has been associated with ARI in children and adults [25,26]. In Mexico, a few studies on the prevalence of hMPV have been conducted in the pediatric population, and the frequency has been reported to range from 6% to 20% [27-29]. In this study, this virus was detected in 22% of children, a value that is very similar to what has been reported in Mexico [28,29] and elsewhere (reviewed in [30]). Furthermore, our results contrast with those of other studies in which RSV ranks as the most frequent virus in the pediatric population with ARI [6,7]. The contrasts are probably due to the different temperatures (which are recorded by season) and the different geographical location of Mexico in comparison with those of other countries.

Interestingly, we found hAD to be the second most common virus. This virus is a cause of ARI and has been reported to have a frequency of about 3% in Mexican children from states other than Jalisco [31,32]. In this study, hAD was identified in 16% of patients, a value that is higher than what has commonly been reported in Mexican studies. In other countries, the prevalence of hAD varies from 1% to 20% [33-36]. Our results could be explained by the fact that the sample collection may have coincided with an outbreak of this virus. It is important to consider that genomic material of this virus has been found repeatedly in infants with recurrent episodes of ARI [37] and in children with asthma [38]. This is an important issue to investigate in future studies because infection with hAD may have health complications after the initial infection and this information is not known in the Mexican population.

In addition to determining the frequency of the viruses in each of the two groups in our study, we investigated whether a virus was associated with the severity of ARI. Our results showed that hMPV was associated with patients who presented with a severe ARI similar to that found in other populations [39-41]. Owing to the hMPV association with a greater severe clinical profile and its high frequency in our population, the results indicate that it is necessary to enhance surveillance for ARI in order to identify hMPV as an emerging virus, similarly to what is carried out with IF in the Mexican population.

The presence of more than one type of virus in the same patient has been an interesting topic that has led us to investigate the importance and clinical relevance of a coinfection. In some populations, coinfection with multiple respiratory viruses is a possible risk factor for complications of ARI. However, this has not occurred consistently in all of the studies [8,11,42]. The frequency of coinfection in our study was 31.62%, and according to our results, this did not create conditions for a different severity of ARI compared with those with a simple infection. Disagreements about the impact of a viral coinfection on the clinical manifestations may be due to the sample collection period, the amount and type of virus detected, viral detection technique, and the characteristics of the population.v On the other hand, we should consider that, owing to its cross-sectional design, our study did not follow the evolution of the clinical profile.

Little is known about viral coinfections and the variables influencing them. We analyzed some risk factors for infection with multiple viruses. Interestingly, by conducting a multivariate analysis, we found that certain types of viral etiology were significantly associated with the presence of coinfections: PIF, HBoV, hMPV, and RSV. Similar to what we found, RSV, hMPV, and hBoV have been reported as having a high frequency in infections with more than one virus [43-45].

Moreover, factors other than etiological agent may influence the development of ARI. In this regard, many research groups have investigated those factors that may be modifiable and that have an impact on the health of the population. Breastfeeding, exposure to smoke of wood or cigarettes, nutritional status, and variables related to housing have been reported as possible factors impacting the evolution of respiratory infections (reviewed in [12,46]). In this study, we evaluated breastfeeding, age of less than 6 months, chronic illness, floor type in the house, exposure to wood smoke, and overcrowding as possible factors related to viral coinfection. Of these, age of less than 6 months was found to be a risk factor for coinfection only when the disease is caused by PIF.

Furthermore, overcrowding, which in the univariate analysis had been identified as a factor independently associated with the presence of coinfection, kept this association in the multivariate analysis only when the ARI is caused by hRV, IF, PIF, hAD, and hBoV. Overcrowding is common in developing countries, where the presence of a large number of people in a single room used for sleeping favors the transmission of different pathogens, and children are the most vulnerable to acquire and develop the infection, and it was reported that this housing characteristic was a risk factor for ARI [47,48]. In a meta-analysis to find factors associated with severity of respiratory infections, it was found that overcrowding conferred a meta-estimated OR of 1.9 (95% CI 1.5 to 2.5) [12]. Interestingly, in a study conducted in refugee camps in Kenya, the frequency of respiratory viruses was determined, and hAD, RSV, hMPV, PIF, and IF (in descending order) were found to be the most prevalent in circumstances characterized by a great number of people in a single space [35]. It is noteworthy that most of the population in our study is located in one of the most populated metropolitan areas in Mexico, suggesting that overcrowding still occurs. Thus, the characteristics of housing continue to be a factor for health problems in the Mexican population, and overcrowding does not occur only in rural areas [14,49].

There are some limitations to our study. First, this research was conducted only from December 2012 to April 2013 (in Mexico, winter begins on December 20), and so we might be overestimating the frequency of some viruses if the study coincided with the peak incidence of any of them or we might be underestimating if it did not. Second, this study did not look for any bacteria in the samples. It has been found that some viruses bring on bacterial infections and this condition could influence these signs and symptoms present during infection [50]. This topic is very interesting and needs to be developed in future research. Third, the study included patients who went to the emergency department, which is usually required when patients develop complications of ARI. Therefore, to have a better understanding of the influence of viral etiology on the clinical spectrum of the disease, it would be interesting to study patients with different degrees of respiratory infection severity, including ambulatory patients from outpatient clinics and hospitalized patients as well as asymptomatic subjects, given that respiratory viruses have been found in children without symptoms of ARI [51]. In the future, it would also be desirable to conduct further studies that completely follow the clinical course of patients with ARI.

Conclusions

In conclusion, viral coinfections have a high frequency in the population of Mexican children treated in the emergency department; in this population, overcrowding is a significant risk factor that allows contact of the host with multiple pathogens, but the coinfection depends on the type of virus occurring in the infection. hMPV is a common virus in the population we studied and is significantly associated with severe ARI, a situation that seems to create conditions for an increase in medical attention in the emergency department. Therefore, this virus could represent a major health burden among Mexican children.

Abbreviations

ARI:

Acute respiratory infection

OD:

Odss ratio

hMPV:

Human metapneumovirus

hAD:

Human adenovirus

RSV:

Respiratory syncytial virus

hRV:

Human rhinovirus

hBoV:

Human bocavirus

IF:

Influenza virus

PIF:

Parainfluenza virus

CI:

Confidence interval

References

  1. Rudan I, Boschi-Pinto C, Biloglav Z, Mulholland K, Campbell H. Epidemiology and etiology of childhood pneumonia. Bull World Health Organ. 2008;86:408–16.

    Article  PubMed Central  PubMed  Google Scholar 

  2. Liu L, Johnson HL, Cousens S, Perin J, Scott S, Lawn JE, et al. Global, regional, and national causes of child mortality: an updated systematic analysis for 2010 with time trends since 2000. Lancet. 2012;379:2151–61.

    Article  PubMed  Google Scholar 

  3. Mackie PL. The classification of viruses infecting the respiratory tract. Paediatr Respir Rev. 2003;4:84–90.

    Article  CAS  PubMed  Google Scholar 

  4. Hammond S, Chenever E, Durbin JE. Respiratory virus infection in infants and children. Pediatr Dev Pathol. 2007;10:172–80.

    Article  PubMed  Google Scholar 

  5. Sinaniotis CA. Viral pneumoniae in children: incidence and aetiology. Paediatr Respir Rev. 2004;5(Suppl A):S197–200.

    Article  PubMed  Google Scholar 

  6. Dawson-Caswell M, Muncie Jr HL. Respiratory syncytial virus infection in children. Am Fam Physician. 2011;83:141–6.

    PubMed  Google Scholar 

  7. Szabo SM, Gooch KL, Bibby MM, Vo PG, Mitchell I, Bradt P, et al. The risk of mortality among young children hospitalized for severe respiratory syncytial virus infection. Paediatr Respir Rev. 2011;13 Suppl 2:S1–8.

    Google Scholar 

  8. Harada Y, Kinoshita F, Yoshida LM, Minh le N, Suzuki M, Morimoto K, et al. Does respiratory virus coinfection increases the clinical severity of acute respiratory infection among children infected with respiratory syncytial virus? Pediatr Infect Dis J. 2013;32:441–5.

    Article  PubMed  Google Scholar 

  9. Hall CB, Weinberg GA, Iwane MK, Blumkin AK, Edwards KM, Staat MA, et al. The burden of respiratory syncytial virus infection in young children. N Engl J Med. 2009;360:588–98.

    Article  CAS  PubMed  Google Scholar 

  10. Pavia AT. Viral infections of the lower respiratory tract: old viruses, new viruses, and the role of diagnosis. Clin Infect Dis. 2011;52 Suppl 4:S284–289.

    Article  PubMed Central  PubMed  Google Scholar 

  11. Sly PD, Jones CM. Viral co-detection in infants hospitalized with respiratory disease: is it important to detect? J Pediatr (Rio J). 2011;87:277–80.

    Article  Google Scholar 

  12. Jackson S, Mathews KH, Pulanic D, Falconer R, Rudan I, Campbell H, et al. Risk factors for severe acute lower respiratory infections in children: a systematic review and meta-analysis. Croat Med J. 2013;54:110–21.

    Article  PubMed Central  PubMed  Google Scholar 

  13. Mexican Official Norm: NOM-031-SSA2-1999. Ministry of Health of Mexico To care for the child’s health. 2001.

  14. National Population Council. Appendix C: Methodology for Stimating Urban Marginalization Index. [http://www.conapo.gob.mx/es/CONAPO/Indice_de_marginacion_urbana_2010]

  15. Valderas JM, Starfield B, Sibbald B, Salisbury C, Roland M. Defining comorbidity: implications for understanding health and health services. Ann Fam Med. 2009;7:357–63.

    Article  PubMed Central  PubMed  Google Scholar 

  16. World Health Organization. Child Growth Standards. [http://www.who.int/childgrowth/standards/imc_para_edad/es/]

  17. World Health Organization. Guidelines for the collection of human specimens for laboratory diagnosis of avian influenza infection [http://www.who.int/influenza/human_animal_interface/virology_laboratories_and_vaccines/guidelines_collection_h5n1_humans/en/index.html#]

  18. Smuts H, Hardie D. Human bocavirus in hospitalized children, South Africa. Emerg Infect Dis. 2006;12:1457–8.

    Article  PubMed Central  PubMed  Google Scholar 

  19. Osiowy C. Direct detection of respiratory syncytial virus, parainfluenza virus, and adenovirus in clinical respiratory specimens by a multiplex reverse transcription-PCR assay. J Clin Microbiol. 1998;36:3149–54.

    PubMed Central  CAS  PubMed  Google Scholar 

  20. Al-Majhdi FN, Al-Jarallah A, Elaeed M, Latif A, Gissmann L, Amer HM. Prevalence of respiratory syncytial virus infection in Riyadh during the winter season 2007–2008 and different risk factors impact. Int J Virol. 2009;5:154–63.

    Article  CAS  Google Scholar 

  21. Landa-Cardena A, Morales-Romero J, Garcia-Roman R, Cobian-Guemes AG, Mendez E, Ortiz-Leon C, et al. Clinical characteristics and genetic variability of human rhinovirus in Mexico. Viruses. 2012;4:200–10.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  22. Peret TC, Boivin G, Li Y, Couillard M, Humphrey C, Osterhaus AD, et al. Characterization of human metapneumoviruses isolated from patients in North America. J Infect Dis. 2002;185:1660–3.

    Article  PubMed  Google Scholar 

  23. Smuts HE, Kannemeyer J, Smit L, Smith T. Human metapneumovirus infection in South African children hospitalised with respiratory tract disease. S Afr Med J. 2004;94:359–61.

    PubMed  Google Scholar 

  24. National Health Information System. [http://sinais.salud.gob.mx/index.html]

  25. Principi N, Esposito S. Paediatric human metapneumovirus infection: epidemiology, prevention and therapy. J Clin Virol. 2014;59:141–7.

    Article  PubMed  Google Scholar 

  26. Panda S, Mohakud NK, Pena L, Kumar S. Human metapneumovirus: review of an important respiratory pathogen. Int J Infect Dis. 2014;25C:45–52.

    Article  Google Scholar 

  27. Talavera GA, Mezquita NE. Human metapneumovirus in children with influenza-like illness in Yucatan, Mexico. Am J Trop Med Hyg. 2007;76:182–3.

    PubMed  Google Scholar 

  28. Noyola DE, Alpuche-Solis AG, Herrera-Diaz A, Soria-Guerra RE, Sanchez-Alvarado J, Lopez-Revilla R. Human metapneumovirus infections in Mexico: epidemiological and clinical characteristics. J Med Microbiol. 2005;54:969–74.

    Article  PubMed  Google Scholar 

  29. Montejano-Elias L, Alpuche-Solis AG, Zarate-Chavez V, Sanchez-Alvarado J, Hernandez-Salinas AE, Noyola DE. Human metapneumovirus and other respiratory viral infections in children attending a day care center. Pediatr Infect Dis J. 2009;28:1024–6.

    Article  PubMed  Google Scholar 

  30. Milder E, Arnold JC. Human metapneumovirus and human bocavirus in children. Pediatr Res. 2009;65:78R–83R.

    Article  PubMed  Google Scholar 

  31. Rodriguez-Auad JP, Nava-Frias M, Casasola-Flores J, Johnson KM, Nava-Ruiz A, Perez-Robles V, et al. The epidemiology and clinical characteristics of respiratory syncytial virus infection in children at a public pediatric referral hospital in Mexico. Int J Infect Dis. 2012;16:e508–513.

    Article  PubMed  Google Scholar 

  32. Wong-Chew RM, Farfan-Quiroz R, Sanchez-Huerta JL, Nava-Frias M, Casasola-Flores J, Santos-Preciado JI. Frequency of respiratory viruses and clinical characteristics in children attending a care center in Mexico City. Salud Publica Mex. 2010;52:528–32.

    PubMed  Google Scholar 

  33. Lu Y, Wang S, Zhang L, Xu C, Bian C, Wang Z, et al. Epidemiology of human respiratory viruses in children with acute respiratory tract infections in Jinan. China Clin Dev Immunol. 2013;2013:210490.

    Google Scholar 

  34. Rocholl C, Gerber K, Daly J, Pavia AT, Byington CL. Adenoviral infections in children: the impact of rapid diagnosis. Pediatrics. 2004;113:e51–56.

    Article  PubMed  Google Scholar 

  35. Ahmed JA, Katz MA, Auko E, Njenga MK, Weinberg M, Kapella BK, et al. Epidemiology of respiratory viral infections in two long-term refugee camps in Kenya, 2007–2010. BMC Infect Dis. 2012;12:7.

    Article  PubMed Central  PubMed  Google Scholar 

  36. Videla C, Carballal G, Misirlian A, Aguilar M. Acute lower respiratory infections due to respiratory syncytial virus and adenovirus among hospitalized children from Argentina. Clin Diagn Virol. 1998;10:17–23.

    Article  CAS  PubMed  Google Scholar 

  37. Kalu SU, Loeffelholz M, Beck E, Patel JA, Revai K, Fan J, et al. Persistence of adenovirus nucleic acids in nasopharyngeal secretions: a diagnostic conundrum. Pediatr Infect Dis J. 2010;29:746–50.

    Article  PubMed Central  PubMed  Google Scholar 

  38. Marin J, Jeler-Kacar D, Levstek V, Macek V. Persistence of viruses in upper respiratory tract of children with asthma. J Infect. 2000;41:69–72.

    Article  CAS  PubMed  Google Scholar 

  39. Wilkesmann A, Schildgen O, Eis-Hubinger AM, Geikowski T, Glatzel T, Lentze MJ, et al. Human metapneumovirus infections cause similar symptoms and clinical severity as respiratory syncytial virus infections. Eur J Pediatr. 2006;165:467–75.

    Article  PubMed  Google Scholar 

  40. Debiaggi M, Canducci F, Ceresola ER, Clementi M. The role of infections and coinfections with newly identified and emerging respiratory viruses in children. Virol J. 2012;9:247.

    Article  PubMed Central  PubMed  Google Scholar 

  41. Jartti T, Jartti L, Ruuskanen O, Soderlund-Venermo M. New respiratory viral infections. Curr Opin Pulm Med. 2012;18:271–8.

    Article  PubMed  Google Scholar 

  42. Paranhos-Baccala G, Komurian-Pradel F, Richard N, Vernet G, Lina B, Floret D. Mixed respiratory virus infections. J Clin Virol. 2008;43:407–10.

    Article  PubMed  Google Scholar 

  43. Stempel HE, Martin ET, Kuypers J, Englund JA, Zerr DM. Multiple viral respiratory pathogens in children with bronchiolitis. Acta Paediatr. 2009;98:123–6.

    Article  PubMed Central  PubMed  Google Scholar 

  44. Cilla G, Onate E, Perez-Yarza EG, Montes M, Vicente D, Perez-Trallero E. Viruses in community-acquired pneumonia in children aged less than 3 years old: High rate of viral coinfection. J Med Virol. 2008;80:1843–9.

    Article  PubMed  Google Scholar 

  45. da Silva ER, Pitrez MC, Arruda E, Mattiello R, Sarria EE, de Paula FE, et al. Severe lower respiratory tract infection in infants and toddlers from a non-affluent population: viral etiology and co-detection as risk factors. BMC Infect Dis. 2013;13:41.

    Article  PubMed Central  PubMed  Google Scholar 

  46. Braubach M, Jacobs DE, Ormandy D. Environmental burden of disease associated with inadequate housing. World Health Organization. 2011. www.euro.who.int/__data/assets/pdf_file/0003/142077/e95004.pdf.

  47. Barua A, Tiwari VK, Kesari SP. Determinants of respiratory diseases in East Sikkim. BMC Res Notes. 2013;6:356.

    Article  PubMed Central  PubMed  Google Scholar 

  48. Savitha MR, Nandeeshwara SB, Kumar MJ, ul Haque F, Raju CK. Modifiable risk factors for acute lower respiratory tract infections. Indian J Pediatr. 2007;74:477–82.

    Article  CAS  PubMed  Google Scholar 

  49. Epidemiological Profile of Children in Mexico. [www.epidemiologia.salud.gob.mx/doctos/infoepid/publicaciones/2011/monografias/P_EPI_DE_LA_INFANCIA_EN_MEXICO_2010.pdf]

  50. Hament JM, Kimpen JL, Fleer A, Wolfs TF. Respiratory viral infection predisposing for bacterial disease: a concise review. FEMS Immunol Med Microbiol. 1999;26:189–95.

    Article  CAS  PubMed  Google Scholar 

  51. Advani S, Sengupta A, Forman M, Valsamakis A, Milstone AM. Detecting respiratory viruses in asymptomatic children. Pediatr Infect Dis J. 2012;31:1221–6.

    Article  PubMed Central  PubMed  Google Scholar 

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Acknowledgements

J.D. (#318952), G.P.-G. (#346287), and C.R.-A. (#366125) are recipients of a scholarship from the Consejo Nacional de Ciencia y Tecnología (National Council for Science and Technology). We thank Adriana Landa Cardeña for her valuable technical assistance in this study, Susana López for her advice in the IF detection and for providing the sequence of the oligonucleotides, Julio Santiago Cruz for his assistance in the detection of hRV and Programa para el Desarrollo Profesional Docente (Professional Teacher Development Program) for financial support.

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Authors and Affiliations

  1. Instituto de Salud Pública, Universidad Veracruzana, Av. Luis Castelazo Ayala s/n., Col. Industrial Ánimas, 91190, Xalapa, Veracruz, México

    Jahaziel Diaz, Jaime Morales-Romero, Gustavo Pérez-Gil, Rebeca García-Román, Omar López-López, Evelyn Bañuelos, Cristal Rizada-Antel, Roberto Zenteno-Cuevas, Clara Luz Sampieri & Hilda Montero

  2. Centro de Ciencias Biomédicas, Universidad Veracruzana, Av. Luis Castelazo Ayala s/n., Col. Industrial Ánimas, 91190, Xalapa, Veracruz, México

    Gustavo Pérez-Gil

  3. Hospital Civil de Guadalajara “Dr. Juan I. Menchaca”, Salvador Quevedo y Zubieta 750, Col. La Perla, 44100, Guadalajara, Jalisco, México

    Martín Bedolla-Barajas, Netzahualpilli Delgado-Figueroa & Luis Gustavo Orozco-Alatorre

  4. Facultad de Química Farmacéutica Biológica, Universidad Veracruzana, Lomas del Estadio s/n, Col. Zona Universitaria, 91000, Xalapa, Veracruz, México

    Omar López-López & Evelyn Bañuelos

  5. Facultad de Ciencias Químicas, Universidad Veracruzana, Prolongación de Oriente 6, 1009, Col. Rafael Alvarado, 94340, Orizaba, Veracruz, México

    Ángel Ramos-Ligonio

  6. Unidad de Procedimientos Preparativos y de acceso a servicios de Proteómica, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Av. Universidad, Col. Ciudad Universitaria, 04510, Distrito Federal, México

    Silvia I Mora

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  1. Jahaziel Diaz
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Corresponding author

Correspondence to Hilda Montero.

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Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

HM and JM-R designed the research. JD, CR-A, and HM wrote the manuscript. JD, OL-L, and EB performed the experiments. RG-R, CLS and SIM standardized the methods for viral detection. JD, GP-G, JM-R, MB-B, RZ-C, AR-L, and HM carried out data analysis. MB-B, ND-F, and LGO-A collected the samples and conducted medical-clinical interpretations. All authors contributed to the final interpretation of results and assisted in writing the manuscript. All authors read and approved the final manuscript.

Additional file

Additional file 1:

Methods PCR.

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Diaz, J., Morales-Romero, J., Pérez-Gil, G. et al. Viral coinfection in acute respiratory infection in Mexican children treated by the emergency service: A cross-sectional study. Ital J Pediatr 41, 33 (2015). https://doi.org/10.1186/s13052-015-0133-7

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