Literature DB >> 8314997

Detection, typing, and subtyping of enteric adenoviruses 40 and 41 from fecal samples and observation of changing incidences of infections with these types and subtypes.

J C de Jong1, K Bijlsma, A G Wermenbol, M W Verweij-Uijterwaal, H G van der Avoort, D J Wood, A S Bailey, A D Osterhaus.   

Abstract

Monoclonal antibody (MAb) preparations specific for the enteric adenoviruses of subgenus F (AdF) were generated and evaluated as typing reagents in virus neutralization tests and enzyme-linked immunosorbent assays (ELISAs). A panel of 11 genome types of adenovirus 40 (Ad40), 24 genome types of Ad41, and 47 adenovirus prototype strains was used to determine the specificities of the MAbs in the two assays. In this way two MAbs, MAb 40-1 (anti-Ad40) and MAb 41-1 (anti-Ad41) were selected. These two MAbs showed strict type specificity in both assays. A third MAb reacted in an ELISA with all 47 human adenovirus types. With two other MAbs, three antigenic subtypes of Ad41 could be distinguished by their reactivities in virus neutralization tests and ELISAs. On the basis of the five selected MAbs, a sensitive ELISA system was developed for the direct detection and simultaneous typing and subtyping of Ad40 and Ad41 present in stool specimens. The five MAbs were also used to study the epidemiology of infections with Ad40 and Ad41 in The Netherlands in the period 1981 through 1989. It was shown that there were no significant fluctuations in the annual incidence of the cluster of enteric adenoviruses as a whole. This cluster should therefore be considered to belong to the "endemic" rather than the "epidemic" adenoviruses. The relative incidence of Ad40 infections compared with that of Ad41 infections changed considerably during the period studied; the proportion of Ad41 infections rose from about 30% in 1981 to about 95% in 1986, after which it stabilized at 90 to 95%. The proportion of one of the subtypes of Ad41 (Ad41 subtype M3) increased from about 40 to 80% in the same period.

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Year:  1993        PMID: 8314997      PMCID: PMC265578          DOI: 10.1128/jcm.31.6.1562-1569.1993

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  37 in total

1.  Genome variants of adenovirus 41 (subgroup G) from children with diarrhoea in South Africa.

Authors:  A H Kidd
Journal:  J Med Virol       Date:  1984       Impact factor: 2.327

2.  Monoclonal antibodies to polioviruses. Production of specific monoclonal antibodies to the Sabin vaccine strains.

Authors:  A D Osterhaus; A L van Wezel; B van Steenis; G A Drost; T G Hazendonk
Journal:  Intervirology       Date:  1981       Impact factor: 1.763

3.  Recombination in adenovirus: crossover sites in intertypic recombinants are located in regions of homology.

Authors:  M E Boursnell; V Mautner
Journal:  Virology       Date:  1981-07-15       Impact factor: 3.616

4.  Antigen detection with monoclonal antibodies for the diagnosis of adenovirus gastroenteritis.

Authors:  J E Herrmann; D M Perron-Henry; N R Blacklow
Journal:  J Infect Dis       Date:  1987-06       Impact factor: 5.226

5.  Comparative epidemiology of two rotavirus serotypes and other viral agents associated with pediatric gastroenteritis.

Authors:  C D Brandt; H W Kim; R H Yolken; A Z Kapikian; J O Arrobio; W J Rodriguez; R G Wyatt; R M Chanock; R H Parrott
Journal:  Am J Epidemiol       Date:  1979-09       Impact factor: 4.897

6.  Adenovirus 37: identification and characterization of a medically important new adenovirus type of subgroup D.

Authors:  J C de Jong; R Wigand; G Wadell; D Keller; C J Muzerie; A G Wermenbol; G J Schaap
Journal:  J Med Virol       Date:  1981       Impact factor: 2.327

7.  Importance of enteric adenoviruses 40 and 41 in acute gastroenteritis in infants and young children.

Authors:  I Uhnoo; G Wadell; L Svensson; M E Johansson
Journal:  J Clin Microbiol       Date:  1984-09       Impact factor: 5.948

8.  Adenovirus hexon monoclonal antibody that is group specific and potentially useful as a diagnostic reagent.

Authors:  C L Cepko; C A Whetstone; P A Sharp
Journal:  J Clin Microbiol       Date:  1983-02       Impact factor: 5.948

9.  Candidate adenoviruses 40 and 41: fastidious adenoviruses from human infant stool.

Authors:  J C de Jong; R Wigand; A H Kidd; G Wadell; J G Kapsenberg; C J Muzerie; A G Wermenbol; R G Firtzlaff
Journal:  J Med Virol       Date:  1983       Impact factor: 2.327

10.  In vitro growth of some fastidious adenoviruses from stool specimens.

Authors:  A H Kidd; C R Madeley
Journal:  J Clin Pathol       Date:  1981-02       Impact factor: 3.411

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  17 in total

1.  Relevance of commercial diagnostic tests to detection of enteric adenovirus infections in South Africa.

Authors:  P L Moore; A D Steele; J J Alexander
Journal:  J Clin Microbiol       Date:  2000-04       Impact factor: 5.948

2.  Rapid subgenus identification of human adenovirus isolates by a general PCR.

Authors:  A H Kidd; M Jonsson; D Garwicz; A E Kajon; A G Wermenbol; M W Verweij; J C De Jong
Journal:  J Clin Microbiol       Date:  1996-03       Impact factor: 5.948

3.  Recognition of adenovirus types in faecal samples by southern hybridization in South Australia.

Authors:  L D Mickan; T W Kok
Journal:  Epidemiol Infect       Date:  1994-06       Impact factor: 2.451

4.  Adenoviruses isolated in the Stockholm area during 1987-1992: restriction endonuclease analysis and molecular epidemiology.

Authors:  M E Johansson; M A Andersson; P A Thörner
Journal:  Arch Virol       Date:  1994       Impact factor: 2.574

5.  Rapid shell vial culture technique for detection of enteroviruses and adenoviruses in fecal specimens: comparison with conventional virus isolation method.

Authors:  G J Van Doornum; J C De Jong
Journal:  J Clin Microbiol       Date:  1998-10       Impact factor: 5.948

6.  Adenoviruses from human immunodeficiency virus-infected individuals, including two strains that represent new candidate serotypes Ad50 and Ad51 of species B1 and D, respectively.

Authors:  J C De Jong; A G Wermenbol; M W Verweij-Uijterwaal; K W Slaterus; P Wertheim-Van Dillen; G J Van Doornum; S H Khoo; J C Hierholzer
Journal:  J Clin Microbiol       Date:  1999-12       Impact factor: 5.948

7.  Etiology of acute gastroenteritis in hospitalized children in Melbourne, Australia, from April 1980 to March 1993.

Authors:  G L Barnes; E Uren; K B Stevens; R F Bishop
Journal:  J Clin Microbiol       Date:  1998-01       Impact factor: 5.948

8.  Patients with enteric adenovirus gastroenteritis admitted to an Australian pediatric teaching hospital from 1981 to 1992.

Authors:  K Grimwood; R Carzino; G L Barnes; R F Bishop
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

9.  Coherence among different microbial source tracking markers in a small agricultural stream with or without livestock exclusion practices.

Authors:  Graham Wilkes; Julie Brassard; Thomas A Edge; Victor Gannon; Cassandra C Jokinen; Tineke H Jones; Romain Marti; Norman F Neumann; Norma J Ruecker; Mark Sunohara; Edward Topp; David R Lapen
Journal:  Appl Environ Microbiol       Date:  2013-08-02       Impact factor: 4.792

10.  Characterizations of adenovirus type 41 isolates from children with acute gastroenteritis in Japan, Vietnam, and Korea.

Authors:  Lei Li; Hideaki Shimizu; Lan Thi Phuong Doan; Phan Gia Tung; Shoko Okitsu; Osamu Nishio; Eiko Suzuki; Jeong Kee Seo; Kyo Sun Kim; Werner E G Müller; Hiroshi Ushijima
Journal:  J Clin Microbiol       Date:  2004-09       Impact factor: 5.948

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