Introduction
In Nigeria, deaths from diarrhoea among children below the age of 5 years decreased by just over 20% between 2005 and 2015, but nevertheless remained substantial at 327.6 per 100 000 children; in contrast, the global mortality from diarrhoea in children in this age group is estimated at 74.3 per 100 000 [1]. Among the aetiologies associated with mortality due to diarrhoea in Nigeria in children under 5 years, rotaviral enteritis had the highest impact (45%), with cryptosporidiosis considered responsible for 14.3% [1]. In the global enteric multicentre study (GEMS) in which the under-5 years age group was stratified into three age groups (under 11 months, 12–23 months, and 24–59 months), it was noticed that at most study sites included, Cryptosporidium tended to be unimportant as a diarrhoeal pathogen in the oldest age stratum, with the greatest burden found in the youngest age groups [Reference Kotloff2]. An extended analysis has shown that: (1) diarrhoeal diseases in general in children under 5-years has a greater impact regarding long-term health burden than previously estimated [Reference Troeger3], and (2) the considerable short-term impact of acute cryptosporidiosis on morbidity in this age group underestimates the true burden by 153% [Reference Khalil4].
Another intestinal protozoan parasite that is often considered together with Cryptosporidium, is Giardia duodenalis. Although infection with Giardia is known to cause diarrhoea, its role in childhood diarrhoea is less certain and it tends not to be associated with increased mortality. One study estimated that in the World Health Organization AFRO region (which includes Nigeria), in the under 5-years age group, around 4-times more cases of diarrhoea were due to Giardia infection than due to Cryptosporidium infection [Reference Pires5]. However, the GEMS study found that there was no significant association between Giardia and symptoms of moderate-to-severe diarrhoea in the cohorts of children under 5-years included in the study and, indeed, in univariate analyses of the oldest age stratum (12–59 months) there was a significantly higher probability of identifying Giardia in controls than in patients in most of the study sites, including those in Africa [Reference Kotloff2]. A previous meta-analysis of published data had also concluded that although Giardia is associated with persistent diarrhoea in children in developing countries, it does not generally cause acute paediatric diarrhoea among infants and children in those countries [Reference Muhsen and Levine6]. A follow-up study of Israeli-Arab children aged 2.3–4.7 years indicated that infection with Giardia may even lower the risk of acute diarrhoea within this age group [Reference Muhsen, Cohen and Levine7].
Our study provides further data on the role of both Cryptosporidium and Giardia in paediatric diarrhoea in Nigeria. Furthermore, efforts were made to identify any risk factors for infection with either of these parasites and information regarding symptoms and any home treatment prior to admission was also collected.
Methods
Study design and setting
This was a cross-sectional study carried out at the two large healthcare centres within Abakaliki, Nigeria. Abakaliki is the capital city of Ebonyi State, SE Nigeria, approximately 650 km east of Lagos; in 2006 the population of Abakaliki was around 152 000 persons.
Stool samples were collected between the months of December 2016 and March 2017, which coincided with the dry season of the year. Caregivers (parents/guardians) of all the diarrhoeic children fulfilling the inclusion criteria for the study and admitted to the healthcare centres during this period were invited to have their children enrolled in our study. Participation was initiated on receipt of written, informed consent from the caregivers. A Strobe checklist was completed for this study and is included as Supplementary Material, which is available via the Cambridge Core website.
Study population
Children included in the study were 5-years-old or younger and had been diagnosed with acute watery diarrhoea by the managing paediatricians. Children co-infected with malaria, respiratory tract infections, or other disease conditions were excluded.
Ethical considerations
Approval for the study was given by the Review and Ethics Committee of the Federal Teaching Hospital, Abakaliki. An informed consent form was signed by parents/guardians prior to enrolment in the study; information in the form made clear that participation in the study was voluntary and participants could opt out of the study at any time without prejudice to the quality of treatment received by their children. Questionnaires designed for data collection were coded to be anonymous such that it was not possible to identify individual patients. Information was collected using the language that the caregivers felt most comfortable using.
Questionnaire
Data collected by questionnaire include sociodemographic details as well as information regarding the particular episode of diarrhoea.
Sample collection and analysis
In addition to routine diagnostics conducted at the healthcare centres, stool samples were collected from 200 cases and 37 age-matched controls (children attending the routine immunization clinics at the same healthcare centres treating the diarrhoea case-patients, with no diarrhoea and apparently healthy; all control children were 5-years or younger, with over 50% younger than 11-months old). Samples were preserved in absolute ethanol and transported to the Parasitology Laboratory of the Norwegian University of Life Sciences. Here, each sample was homogenised, washed twice in laboratory-grade water and concentrated by centrifugation. Detection of Cryptosporidium oocysts and Giardia cysts was conducted by standard immunofluorescent antibody test (IFAT) on 10 µl subsamples that were air-dried, methanol-fixed and stained with FITC-labelled monoclonal antibody (Mab: Aqua-glo, Waterborne Inc., New Orleans, USA) and 4′,6-diamidino-2-phenylindole (DAPI). Prepared slides were examined by fluorescence microscopy, using the appropriate filters, at magnifications of 200 × and 400 × and Cryptosporidium oocysts and/or Giardia cysts enumerated and DAPI inclusion recorded.
DNA was extracted from all those samples that were positive for Cryptosporidium oocysts and every fourth of the other samples (both cases and controls; a total of 59 cases samples and nine control samples) by resuspending 50% of the remaining pellet in 100 µl Tris–EDTA buffer and heating for 1 h in a heat block set at 100 °C. DNA was then isolated using a QIAmp DNA mini-kit (QIAGEN GmbH, Germany) following the manufacturer's protocol.
For those samples that were positive for Cryptosporidium, fragments of two genes were used for molecular investigations; these were the SSU rRNA gene (approximately 800 bp) and the GP60 gene (approximately 950 bp;), using published primers and protocols [Reference Xiao8, Reference Sulaiman9]. For all samples from which DNA had been extracted, PCR with primers targeting the SSU rRNA gene of Giardia was also conducted using published primers and protocols [Reference Hopkins10]. Each set of PCR included a negative (laboratory-grade water) control and a positive control.
PCR amplification products from positive samples were purified (High Pure PCR product purification kit, Roche Applied Science) according to the manufacturer's protocol and sequenced on both strands at a commercial facility (Macrogen, South Korea). Chromatograms were examined and sequences adjusted manually. Sequence searches were conducted using BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi) and, in addition, for GP60 sequences, the 5′ end was manually checked and tandem repeats of the serine-coding trinucleotides enumerated to determine subtype family.
Analysis of the samples for viral pathogens was conducted at the Institute of Virology, University of Leipzig, Germany using multiplex real-time polymerase chain reaction (PCR) standard protocol; the detailed data about viruses are intended for separate presentation.
Data handling and statistical analysis
Data were compiled in an excel database; and then exported to SPSS version 24 for analysis. Associations were investigated by contingency table analysis (Fisher's Exact Test).
Results
Study population, symptoms and case management
Of the 200 case samples collected, one was not suitable for analysis due to specimen leakage; hence 199 cases and 37 controls were included in our final analysis.
The majority of the study participants were males (60.8%) and within the age range of 0–11-months-old (68.4%). Most participants came from rural areas and were not exclusively breastfed (72.0%), (Table 1).
Table 1. Descriptive characteristics of cases and potential risk factors for infection
In most of the children, the diarrhoea was associated with fever (98.7%) and vomiting (92.5%), and although mucus in faeces was common, only 5% passed blood-stained stools (Table 2).
Table 2. Clinical features associated with the diarrhoeal cases
In the children's homes, oral rehydration solutions were commonly used (98.0%), whereas the use of zinc tablets (98%), intravenous fluids (92.5%) and antibiotics (87.0%) were the commonest hospital management practices (Table 3).
Table 3. Case management practices used for paediatric acute watery diarrhoea at home and in the hospitals
Aetiology of diarrhoea and occurrence of Cryptosporidium and Giardia
We did not detect Giardia cysts by IFAT in any of the stool samples, cases or controls and PCR directed towards the Giardia SSU rRNA gene were also negative for the nine control samples and 59 case samples tested. Thus, the prevalence of Giardia infection in this cohort was considered to be 0.00% (95% Confidence Intervals (CI) 0.00–1.89).
We did not detect Cryptosporidium oocysts in any of the control samples, but oocysts were identified in 13 of the 199 stool samples from cases (6.5%; 95% CI 3.86–10.85). Of these positive samples, five contained low numbers of oocysts (20–30 oocysts in the whole slide), seven had moderate numbers of oocysts (up to five oocysts per field of view) but five of these exhibited poor or absent DAPI staining and one sample had very high numbers of oocysts. The number of oocysts per gram of faecal sample could not be estimated due to lack of information on the quantity of stool sample preserved in ethanol.
Of the 13 Cryptosporidium-positive samples, for all of which molecular characterisation was attempted, sequences were obtained only for three (the sample with high numbers of oocysts and the two samples with moderate numbers of oocysts and good DAPI staining). All three were Cryptosporidium hominis, two were of GP60 subtype family Ia (IaA30R3 and IaA14R3) and one of GP60 subtype Id (IdA11).
No associations between Cryptosporidium infection and other variables (age, gender, rural or urban residence) were identified.
Rotavirus was found in 92.3% of the cases; other agents detected included Enterovirus (20.8%), Astrovirus (8.6%), Parechovirus (8.1%) and Sapovirus (2.7%). Ascaris eggs and Entamoeba spp. cysts were also seen in 0.5% (1/199) and 1.0% (2/199) of cases, respectively.
Discussion
The results reported here support those of earlier studies that suggest that in countries such as Nigeria, Giardia infection is not associated with paediatric diarrhoea. Indeed, a meta-analysis of case-control and cohort studies has indicated that there is a significant inverse association between acute diarrhoea and Giardia in stools in children in non-industrialised settings [Reference Muhsen and Levine6]. Thus, these studies have also often shown that control subjects (without diarrhoea) are more frequently infected with Giardia, suggesting that Giardia may mediate a protective effect (e.g. [Reference Muhsen, Cohen and Levine7, Reference Albert11–Reference Bodhidatta14]), but this was not seen in our study. The nature of the proposed protective effect suggested from other studies is unclear, although changes in mucosal immunity or suppression of other enteric pathogens have been suggested; it is worth noting that a study from Tanzania found that the apparently protective effect of Giardia infection in children of under 6-years was abrogated when multi-nutrient supplementation was used [Reference Veenemans15]. An alternative possibility is that in profuse watery diarrhoea caused by any aetiology (bacteriological, viral, parasitological), any resident Giardia trophozoites might be ‘washed out’ before they have time to encyst, hence the lack of Giardia cysts in the samples of diarrhoeic patients, including in our study. It could then be argued that Giardia DNA could have been detected; however, as the samples were collected from children attending healthcare centres due to diarrhoeal disease, it may be likely that any resident Giardia are washed out in early bouts of diarrhoea prior to admission to the healthcare centre and collection of the faecal sample. Such a situation could also, perhaps, explain why previous studies [Reference Muhsen, Cohen and Levine7, Reference Albert11–Reference Bodhidatta14] have suggested that Giardia infection may exert a protective effect.
Thus, the apparent lack of any Giardia-positive samples in this cohort (cases and controls) may not be as surprising as first appears. Indeed, giardiasis itself is associated with fatty, rather than watery diarrhoea. Preservation in ethanol has been recommended for faecal samples possibly containing Giardia cysts, for subsequent detection by either microscopy (IFAT) or PCR [Reference Wilke and Robertson16]. Nevertheless, degradation during transport cannot be completely excluded as the reason for the lack of detection of Giardia, either cyst structures detected by IFAT, or DNA that can be amplified by targeted PCR. However, this seems unlikely given the detection of Cryptosporidium in some samples. Indeed, previous studies from Nigeria investigating infections in children under 5-years of age have tended to detect Giardia cases at a relatively low prevalences (e.g. one Giardia-positive 6-month-old with enteritis among six children below 2 years [Reference Maikai17]; one child (below 4-years of age) among 215 children with diarrhoea and no Giardia infections among 100 age-matched controls without diarrhoea [Reference Ogunsanya, Rotimi and Adenuga18]). However, investigations amongst older children (school-age children, 7–17 years) have tended to show a higher prevalence of Giardia infection, e.g., 12.3% [Reference Gyang19] and 37.2% [Reference Efunshile20]; in neither of these studies from school-age children was diarrhoea reported among the subjects.
The 6.5% prevalence of Cryptosporidium infection in our study was within the range reported by other studies from Nigeria in children aged below 5 years. For example, a 4.8% prevalence among 165 children below 5-years of age with diarrhoea was found in Jos, with C. hominis the predominant species, as we found, and subtype Id [Reference Anejo-Okopi21]; a 5.6% prevalence of Cryptosporidium was reported in children with diarrhoea below 6-years of age from Ebonyi state, with both C. hominis and C. parvum identified and, among the C. hominis isolates, four different GP60 subtypes, including two in the Ia family [Reference Ukwah22]; a prevalence of Cryptosporidium infection was found in 11.1% of 21 diarrhoeic children less than 12 months of age from Oyo state; two of the isolates were C. hominis, both subtype IaA24R3 [Reference Ayinmode, Fagbemi and Xiao23].
Our data support the higher occurrence of C. hominis species in Africa, despite just under 50% of the infected children (6 of 13) living in rural areas, where C. parvum may be more common due to associations with animal infections. However, the data provide no information regarding likely vehicles for infection and, given the low number of isolates characterised using molecular methods, our data should be treated with caution regarding extrapolation to other settings.
In conclusion, our results demonstrate that although viral infections appear to be of greatest importance in paediatric diarrhoea in this setting, Cryptosporidium infection is also of relevance. However, Giardia infection seems to be of limited importance in this age group of children, both for asymptomatic children and those with watery diarrhoea. Given that Giardia infections occur relatively frequently in older children, we speculate that our data probably reflect the differing epidemiologies and potentially differing transmission routes for these two parasites. This is important, as many studies tend to consider both Cryptosporidium and Giardia as being very similar epidemiologically, probably due to the fact that they are both intestinal protozoan parasites (albeit of widely differing phylogeny and biology) and have both been associated with waterborne outbreaks.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S0950268818003151.
Author ORCIDs
L. J. Robertson 0000-0001-5186-4421.
Acknowledgements
We would like to thank all the parents, guardians and children who participated in this study for their ready cooperation. We also acknowledge the support of Dr Nwangwu Emeka and the nurses at our study sites. In Leipzig, we are grateful for the support of Dr Arne Rodloff and we note that Dr Pikka Jokelainen at Statens Serum Institut, Copenhagen provided support from Denmark. Dr Kjersti Selstad Utaaker and Dr Kristoffer Relling Tysnes are gratefully acknowledged for some technical support at the Norwegian University of Life Sciences. This research received no specific grant from any funding agency, commercial or not-for-profit sectors.
Conflict of interest
None.
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