Risk factors associated with Streptococcus pneumonia carriage in children under five years old with acute respiratory infection in Niger

Risk factors associated with Streptococcus pneumonia carriage in children under five years old with acute respiratory infection in Niger

Ibrahim Dan Dano^1,&, Sani Ousmane¹, Kamaye Moumouni², Adamou Lagare¹, Idi Issa¹, Jean Testa¹

 

¹Centre de Recherche Médicale et Sanitaire (CERMES), 634 Boulevard de la Nation, Niamey, Niger, ²Hôpital National de Niamey (HNN), Service de Pédiatrie A, Niamey, Niger

 

 

^&Corresponding author
Ibrahim Dan Dano, Centre de Recherche Médicale et Sanitaire (CERMES), 634 Boulevard de la Nation, Niamey, Niger

 

 

 

 

streptococcus pneumonia is a significant human pathogen and a leading cause of bacterial pneumonia, meningitis, and sepsis in children [1]. S. pneumonia causes an estimated 11% (8-12%) of all deaths in children aged 1-59 months [1]. S. pneumonia is a commensal of the human respiratory tract that is carried by many people without becoming ill. An important feature is that pneumococcal diseases will not occur without preceding nasopharyngeal (NP) colonization with a homologous strain [2]. Cross-sectional studies have shown that, at any given time, approximately 20 - 50% of healthy children harbour at least one serotype of this bacterium in the rhinopharynx, whereas longitudinal studies have shown that almost all children can carry this bacterial species [3, 4]. Pneumococcal carriage is an important source of horizontal spread of these pathogens within the community [5]. Such pneumococcal NP carriage studies are important because carriage has a key role in pneumococcal disease and pneumococcal spread. We assessed risk factors associated with the carriage of S. pneumonia in children under five with signs of respiratory infection.

 

 

Study design: this cross-sectional study was conducted in the paediatric departments of the National Hospital of Niamey and that of Lamordé (Niger). Children aged 1 to 59 months with signs of respiratory infection (severe cough or tachypnea with axillary temperature above 38°C) who were hospitalized in one of the paediatric departments of the two hospitals were enrolled from January 2015 to June 2016. Children under the age of one month or over the age of five years and children suffering from heart disease or chronic respiratory infection were excluded. NP samples were obtained for molecular identification. Data on potential risk factors were gathered by confidential interview based on a questionnaire.

 

Ethical considerations: this study was approved by the National Consultative Ethics Committee of Niger by decision No 0016/2013/CCNE on 30 October 2013; approved consent from the parents of the children was requested before inclusion.

 

Nasopharyngeal swabbing: nasopharyngeal swabbing was performed with the nasopharyngeal flocked swabs kit, UTM^TM 350C, Copan Diagnostics. The swabs were inserted along the nasal septum just above the floor of the passage to the nasopharynx until resistance was met; the swab was rotated gently against the NP mucosa for 10 - 15 seconds and then gently removed. After the swab removed from the patient, it was placed into the tube of UTM^TM transport medium all the way to the bottom of the tube.

 

Serum procalcitonin (PCT) level dosage: the serum PCT level was determined for the diagnosis of bacterial infection with the BRAHMS PCT kit (reference 30450) on a VIDAS machine (BioMérieux SA, France). A PCT level below 0.1 µg/L was considered normal, 0.1 to 2 µg/L was considered moderate and above 2 µg/L was considered high.

 

RT- PCR for the detection of viral and bacterial NP colonization: NP carriage of S. pneumonia was determined by a multiplex real-time PCR with the FTD Respiratory pathogens 21 plus (Ref: FTD-2+.1-32. Fast-Track Diagnostics Luxembourg Sarl). This test enables the detection of the following respiratory pathogens: influenza A (Flu A), influenza A (H1N1) swl, influenza B (Flu B); coronaviruses NL63 (Cor63), 229E (Cor229), OC43 (Cor43) and HKU1 (CorHKU1); parainfluenza 1, 2, 3 and 4 (Para1, Para2, Para3, Para4); human metapneumovirus A and B (HMPVA and B); rhinovirus (Rhino); respiratory syncytial viruses A and B (RSV A and B); adenovirus (AV); enterovirus (EV); parechovirus (PV); bocavirus (HboV); Mycoplasma pneumonia (Mpneu); Chlamydia pneumonia (Cpneu); Streptococcus pneumonia (Spneu); Haemophilus influenza B (HIB); and Staphylococcus aureus (Saur).

 

Statistical analysis: statistical analyses were performed with Epi info 7. We used logistic regression models to examine independent associations between pneumococcal carriage and potential risk factors. All associations with a p-value of < 0.25 in the bivariate regression analyses were subsequently entered in the multivariate regression model. Odd ratios and adjusted odd ratios with their 95% confidence intervals were computed. P-values ≤ 0.05 were considered statistically significant.

 

 

A total of 637 children aged 1 to 59 months admitted for acute respiratory infection were included in this study. The mean age of the children was 13.2 ± 12.65 months, and the female to male ratio was 0.8. The rate of respiratory virus carriage was 76%, that of bacteria carriage was 47% and that of bacteria-virus co-colonization was 42%. The most detected bacteria was S. pneumonia (39.6%), and the most detected virus was respiratory syncytial viruses A and B (23.7%), followed by rhinovirus (9.9%) and influenza A (7.1%). Details of the NP carriage rate of the respiratory pathogens detected are summarized in Figure 1, and the distribution according to age of the main pathogens detected is shown in Figure 2. In the bivariate analysis, age older than 3 months (except for 24-36 months), house flooring material of tile, mother's profession of civil servant, non-attendance at a day care centre and co-carriage with another bacteria or virus were risk factors for S. pneumonia carriage (Table 1,Table 2). No association was found with regard to sex, duration of breast feeding, educational level, father's profession, type of house and electric lightning type of house, number of children less than 15 years old in the family, vaccination status, infection and prior antibiotic treatment. Risk factors for S. pneumonia carriage in the multivariate logistic analysis were age older than 3 months (except for 24-36 months), house flooring material of tile, mother's profession of civil servant and co-carriage with another bacteria or virus (Table 3). In the simple logistic regression analysis, attendance at a day care centre was inversely related to S. pneumoniacarriage, but the association was not significant in the multivariate model.

 

 

The nasopharynx is known to be the main ecological reservoir of S. pneumonia and is where the bacteria give rise to disease after extending to other areas of the respiratory tract or penetrating normally sterile body fluids [6]. Although NP isolates are not useful for predicting the causative agent of invasive disease in individuals, they reflect epidemiological aspects of pneumococcal disease in the community [7]. In developing countries, particularly in Niger, there are few studies describing the epidemiology of NP carriage of S. pneumonia. This study focused on children under five years old with signs of respiratory infection. Most NP pneumococcal carriage studies enrolled children [8] or younger children [9-12]. Several studies have included healthy children [13] whereas others included children with concomitant respiratory infection [11]. This study described the epidemiology of NP carriage of S. pneumonia. The bacterial carriage rate obtained in this study was comparable to those in previous studies in younger children [3, 4]; likewise, the viral carriage rate was also comparable [14-16]. Carriage of S. pneumonia was associated with age; the peak incidence of carriage in children is observed during the first 3 years of life [2], and the lowest carriage rate is observed in infants younger than 2 months of age [17]. The mean age of first acquisition of S. pneumonia was reported to be 6 months with a range of 1-30 months [18-20]. Therefore, age is an important risk factor for pneumococcal colonization, and its influence varies with the phase of growth [21]. A positive association between the carriage of other pathogens and the NP carriage of S. pneumonia was found in this study. Bacterial carriage is known to be influenced by bacterial and viral intra-and inter-species interactions (commensal and pathogenic) [22]. These interactions can be synergistic or antagonistic. In general, the risk of S. pneumonia seemed to increase in the presence of particular respiratory viruses [14]. The carriage of S. aureus has been reported to be inversely related to S. pneumonia carriage [23] likely due to bacterial interference [14]; however, this study failed to show such a negative association. It is unknown whether this association is direct or dependent on other determinants [14] such as age [23] and season [24]. Environmental features are risks factors for S. pneumonia carriage [17]. Low socio-economic status was also reported as a risk factor for the colonization and carriage of respiratory pathogens, likely due to cramped and poor housing [22].

 

The mother's occupation appeared to affect S. pneumonia carriage more than the father's profession in this study. Pneumococcal carriage was reported to be associated with exposure to other children [19, 22, 24]. Frequent and close person-to-person contact favours the development and transmission of pneumococci. Attendance at a day care centre was reported to be a risk factor for pneumococcal carriage [22], particularly in developed countries [25]. In this study, attendance at a day care centre was surprisingly inversely associated with pneumococcal carriage in the bivariate analysis, but it was not significant in the multivariate analysis. This could be a consequence of a confounding effect. The high prevalence of carriage in developing countries is a possible explanation of the lack of association between pneumococcal carriage and attendance at a day care centre [26]. Close contact and poor hygienic conditions cannot explain increased pneumococcal carriage in day care centres. Additional factors are apparently associated, such as age, number of children attending the day care centre and pathogen interference. No association between pneumococcal carriage and the number of children less than 15 years old in the family was found. A study in Gambia [12] also failed to identify an association with the number of children in the house or children sleeping in the same room. The relationship between the carriage of S. pneumonia and educational level is not clear. Although some studies showed a close relationship between low educational level of the parents and higher nasopharyngeal colonization [12], other studies [13, 27, 28] such this study failed to show this association. Although reported in some studies [12, 29-31], this study did not identify any associations between the carriage of S. pneumonia, smoking habits, breast feeding and recent antibiotic use. However, the results obtained showed that when the house floor material was tile, the prevalence of carriage increased. A study performed in Gambia [26] did not identify this association, but they did not consider tile in their design. Several studies from different parts of the world [31-33] have demonstrated the ability of different pneumococcal conjugate vaccines to reduce the rate of pneumococcal carriage. It has been reported [34] that after vaccination with a conjugate vaccine, rapid replacement of pneumococci by new serotypes not included in the vaccine occurs; thus, cross protection can also occur. This might explain the lack of association between pneumococcal carriage and vaccination with PCV-13 observed in this study, which did not identify the different pneumococcal serotypes. Unlike other studies [14, 35, 36], no association between NP carriage of S. pneumonia and antibiotic pre-treatment was found, as reported by another study [37]. The differences with other studies suggest that the factors that influence colonization are multiple and not entirely clear [22]. This study included children with signs of respiratory infection who were visiting a paediatric care centre; thus, these results may not represent a healthy paediatric population.

 

 

These results can be helpful to understand the dynamics of pneumococcal nasopharyngeal colonization; they confirm the interest of vaccinating infants before the age of 3 months with appropriate vaccine to prevent nasopharyngeal colonization and pneumococcal diseases in children.

 

 

The authors declare no competing interest.

 

 

Study design: Ibrahim Dan Dano, Sani Ousmane, Kamaye Moumouni. Laboratory analysis: Ibrahim Dan Dano, Sani Ousmane, Adamou Lagare. Data analysis and interpretation: Ibrahim Dan Dano, Jean Testa. Wrote the manuscript: Ibrahim Dan Dano. Critical review and approval of manuscript: Sani Ousmane, Kamaye Moumouni Adamou Lagare Idi Issa Jean Testa. All the authors have read and agreed to the final manuscript.

 

 

We thank the total Corporate Foundation who financed this work through the department of International Affairs, Institut Pasteur International Network. We warmly thank the personnel of the Bacteriology-Virology Unit and Epidemiology Unit of CERMES, the personnel of the Pediatric Department of National Reference Hospital Niamey and National Reference Hospital of Lamordé, Niamey for their contributions.

 

 

Table 1: sociodemographic potential risk factors estimated by bivariate logistic regression for the carriage of S. pneumoniae in children under five years old with acute respiratory infection

Table 2: medical potential risk factors estimated by bivariate logistic regression for the carriage of S. pneumonia in children under five years old with acute respiratory infection

Table 3: adjusted ORs estimated by multivariate logistic regression for S. pneumoniae carriage, according to possible risk factors

Figure 1: NP bacterial and viral carriage legende: Flu A: influenza A; H1N1: influenza A swl; Flu B: influenza B; Cor63: coronaviruses NL63; Cor229: coronaviruses 229E; Cor43: coronaviruses OC43; CorHKU1: coronaviruses HKU; Para 1: parainfluenza 1; Para 2: parainfluenza 2; Para 3: parainfluenza 3; Para 4: parainfluenza 4; HMPVA and B: human metapneumovirus A and B; Rhino : rhinovirus; RSV A and B: respiratory syncytial viruses A and B; AV: adenovirus; EV: enterovirus; PV: parechovirus; HboV: bocavirus; Mpneu: Mycoplasma pneumoniae; Cpneu: Chlamydia pneumoniae; Spneu: Streptococcus pneumoniae; HIB: Haemophilus influenzae B; Saur: Staphylococcus aureus

Figure 2: NP carriage of main pathogens detected according to age

 

 

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