2021
DOI: 10.1186/s12879-021-06318-x
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Detection of diarrhoea associated rotavirus and co-infection with diarrhoeagenic pathogens in the Littoral region of Cameroon using ELISA, RT-PCR and Luminex xTAG GPP assays

Abstract: Background Despite the global roll-out of rotavirus vaccines (RotaTeq/Rotarix / ROTAVAC/Rotasiil), mortality and morbidity due to group A rotavirus (RVA) remains high in sub-Saharan Africa, causing 104,000 deaths and 600,000 hospitalizations yearly. In Cameroon, Rotarix™ was introduced in March 2014, but, routine laboratory diagnosis of rotavirus infection is not yet a common practice, and vaccine effectiveness studies to determine the impact of vaccine introduction have not been done. Thus, st… Show more

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Cited by 5 publications
(8 citation statements)
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“…As observed with previous studies [13,14,21,22] that younger children (0-12 months of age) are more susceptible to RVA than older ones. In the present study RVA infection within the age group of 0-11 months has the highest prevalence rate (44.4%, p = 0.03) (Table 2).…”
Section: Discussionsupporting
confidence: 86%
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“…As observed with previous studies [13,14,21,22] that younger children (0-12 months of age) are more susceptible to RVA than older ones. In the present study RVA infection within the age group of 0-11 months has the highest prevalence rate (44.4%, p = 0.03) (Table 2).…”
Section: Discussionsupporting
confidence: 86%
“…It is thus evident that 37.8% constituting the remaining cases are due to other pathogens not included in the diagnostic panel. Among these, RVA is surely a prime cause, very likely with co-infections, as recently noticed in the littoral region of Cameroon [13].…”
Section: Discussionmentioning
confidence: 74%
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“…The evaluation of the protective efficiency of ETEC vaccine candidates requires a suitable animal infection model [ 11 , 18 , 19 , 20 ] that is also suitable for the development of antibiotic alternatives for in vivo anti-ETEC activities [ 21 , 22 , 23 , 24 ]. Reported ETEC infection models have typically used methods such as plate counting, quantitative PCR for unique virulence genes, and an enzyme-linked immunosorbent assay (ELISA) to detect and quantify ETEC [ 25 , 26 ]. However, ETEC is also widespread in the environment, such as in food, water, and bioaerosols [ 27 , 28 , 29 ], which renders the quantification of ETEC less specific and poorly targeted.…”
Section: Introductionmentioning
confidence: 99%