Literature DB >> 12164601

Characterization of rotavirus infection in a hospital neonatal unit in Pretoria, South Africa.

Duncan Steele1, Emmy Reynecke, Mariet de Beer, Pieter Bos, Izelle Smuts.   

Abstract

Rotavirus infection in neonates is common and has been reported to be generally asymptomatic. In this longitudinal study, specimens were collected from 114 newborns in the Neonatal Unit at Pretoria Academic Hospital on a daily basis between January and May 1997. The babies remained in the ward between 1 week and 4 months. The stool specimens or rectal swabs were analysed for the presence of rotavirus antigen using a commercial enzyme-linked immunosorbent assay (Dako Rotavirus EIA) or electron microscopy. In total, 80 (70 per cent) of the neonates excreted rotavirus during their stay in the unit. There was a direct correlation between the length of stay in the ward and the shedding of rotavirus. The babies excreted rotavirus on average between 2 and 7 days. Rotavirus infection tended to occur within the first 2 weeks of life and was only observed once in most babies. Polyacrylamide gel electrophoresis of the RNA revealed the presence of two strains of rotavirus, with the differences in the RNA electropherotype occurring in the RNA segment triplet 7, 8 and 9. The VP7 serotype of the virus is encoded by one of these genes, and so the VP7 serotype of the virus was determined by monoclonal antibody and RT-PCR using VP7 serotype specific primers. The VP4 genotype of the viruses was also determined using RT-PCR of the VP4 gene to determine if a new rotavirus had been introduced to the ward. The strains were all characterized as G4P[6], which is similar to the antigenic make-up of the virus recovered 10 years before. This highlights the remarkable stability of rotavirus strains in neonatal units over long periods of time.

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Year:  2002        PMID: 12164601     DOI: 10.1093/tropej/48.3.167

Source DB:  PubMed          Journal:  J Trop Pediatr        ISSN: 0142-6338            Impact factor:   1.165


  5 in total

1.  Mutated G4P[8] rotavirus associated with a nationwide outbreak of gastroenteritis in Nicaragua in 2005.

Authors:  Filemon Bucardo; Beatrice Karlsson; Johan Nordgren; Margarita Paniagua; Alcides González; Juan Jose Amador; Felix Espinoza; Lennart Svensson
Journal:  J Clin Microbiol       Date:  2007-01-17       Impact factor: 5.948

2.  The Lewis A phenotype is a restriction factor for Rotateq and Rotarix vaccine-take in Nicaraguan children.

Authors:  Filemón Bucardo; Johan Nordgren; Yaoska Reyes; Fredman Gonzalez; Sumit Sharma; Lennart Svensson
Journal:  Sci Rep       Date:  2018-01-24       Impact factor: 4.379

3.  Human milk oligosaccharides, milk microbiome and infant gut microbiome modulate neonatal rotavirus infection.

Authors:  Sasirekha Ramani; Christopher J Stewart; Daniel R Laucirica; Nadim J Ajami; Bianca Robertson; Chloe A Autran; Dhairyasheel Shinge; Sandya Rani; Sasirekha Anandan; Liya Hu; Josephine C Ferreon; Kurien A Kuruvilla; Joseph F Petrosino; B V Venkataram Prasad; Lars Bode; Gagandeep Kang; Mary K Estes
Journal:  Nat Commun       Date:  2018-11-27       Impact factor: 14.919

4.  A shift in circulating rotaviral genotypes among hospitalized neonates.

Authors:  Sudhabharathi Reju; Padma Srikanth; Sribal Selvarajan; Reuben Kuruvilla Thomas; Ramya Barani; Prakash Amboiram; Gunasekaran Palani; Gagandeep Kang
Journal:  Sci Rep       Date:  2022-02-18       Impact factor: 4.379

5.  Persistence of G10P[11] neonatal rotavirus infections in southern India.

Authors:  Sudhir Babji; Kulandaipalayam Natarajan Sindhu; Sribal Selvarajan; Sasirekha Ramani; Srinivasan Venugopal; Shainey Alokit Khakha; Priya Hemavathy; Santhosh Kumar Ganesan; Sidhartha Giri; Sudhabharathi Reju; Krithika Gopalakrishnan; Binu Ninan; Miren Iturriza-Gomara; Padma Srikanth; Gagandeep Kang
Journal:  J Clin Virol       Date:  2021-09-28       Impact factor: 3.168

  5 in total

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