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

被引:3
|
作者
Ghapoutsa, Rahinatou N. [1 ]
Boda, Maurice [2 ]
Gautam, Rashi [3 ]
Ndze, Valantine Ngum [4 ]
Mugyia, Akongnwi E. [5 ]
Etoa, Francois-Xavier [2 ]
Bowen, Michael D. [3 ]
Esona, Mathew D. [3 ]
机构
[1] Univ Yaounde I, Fac Sci, Dept Biochem, Yaounde, Cameroon
[2] Univ Yaounde I, Fac Sci, Dept Microbiol, Yaounde, Cameroon
[3] Ctr Dis Control & Prevent, Natl Ctr Immunizat & Resp Dis, Div Viral Dis, Atlanta, GA USA
[4] Univ Buea, Fac Hlth Sci, Buea, Cameroon
[5] Univ Buea, Dept Microbiol & Parasitol, Fac Sci, Buea, Cameroon
关键词
Cameroon; Rotavirus; Childhood diarrhoea; RT-PCR; Co-infection; Rotarix; xTAG GPP; INFECTIOUS DIARRHEA; CHILDREN; STRAINS; MORTALITY; GENOTYPE; VACCINE; IMPACT;
D O I
10.1186/s12879-021-06318-x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 (TM) 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, studies examining RVA prevalence post vaccine introduction are needed. The study aim was to determine RVA prevalence in severe diarrhoea cases in Littoral region, Cameroon and investigate the role of other diarrheagenic pathogens in RVA-positive cases. Methods We carried out a study among hospitalized children < 5 years of age, presenting with acute gastroenteritis in selected hospitals of the Littoral region of Cameroon, from May 2015 to April 2016. Diarrheic stool samples and socio-demographic data including immunization and breastfeeding status were collected from these participating children. Samples were screened by ELISA (ProSpecT (TM) Rotavirus) for detection of RVA antigen and by gel-based RT-PCR for detection of the VP6 gene. Co-infection was assessed by multiplexed molecular detection of diarrheal pathogens using the Luminex xTAG GPP assay. Results The ELISA assay detected RVA antigen in 54.6% (71/130) of specimens, with 45, positive by VP6 RT-PCR and 54, positive using Luminex xTAG GPP. Luminex GPP was able to detect all 45 VP6 RT-PCR positive samples. Co-infections were found in 63.0% (34/54) of Luminex positive RVA infections, with Shigella (35.3%; 12/34) and ETEC (29.4%; 10/34) detected frequently. Of the 71 ELISA positive RVA cases, 57.8% (41/71) were fully vaccinated, receiving two doses of Rotarix. Conclusion This study provides insight on RVA prevalence in Cameroon, which could be useful for post-vaccine epidemiological studies, highlights higher than expected RVA prevalence in vaccinated children hospitalized for diarrhoea and provides the trend of RVA co-infection with other enteric pathogens. RVA genotyping is needed to determine circulating rotavirus genotypes in Cameroon, including those causing disease in vaccinated children.
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