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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1997 Oct;35(10):2458–2463. doi: 10.1128/jcm.35.10.2458-2463.1997

Identification of Abiotrophia adiacens and Abiotrophia defectiva by 16S rRNA gene PCR and restriction fragment length polymorphism analysis.

Y Ohara-Nemoto 1, S Tajika 1, M Sasaki 1, M Kaneko 1
PMCID: PMC229992  PMID: 9316889

Abstract

Abiotrophia adiacens and Abiotrophia defectiva, previously referred to as nutritionally variant streptococci, Streptococcus adjacens and Streptococcus defectivus, respectively, are causes of infective endocarditis. We describe a method of identifying these two species and also of distinguishing them from 15 other major etiological pathogens of infective endocarditis by means of 16S rRNA gene PCR amplification followed by restriction fragment length polymorphism analysis (PCR-RFLP). The 16S rRNA genes were successfully amplified with a set of universal primers from all 17 species of bacteria examined, including viridans group streptococci. The RFLP patterns of A. adiacens and A. defectiva obtained by HaeIII or MspI digestion were readily distinguished from each other and from those of other bacteria. When PCR analysis was performed with the supernatant of a suspension of a boiled colony, the 16S rRNA genes of 80 of 82 isolates (97%) of A. adiacens and all isolates (11 of 11) of A. defectiva were amplified. The HaeIII RFLP patterns of the isolates were the same as those of the corresponding type strains, although 28% of A. adiacens isolates revealed intraspecies polymorphism. The detection limit of this method was 0.1 pg of genomic DNA, as assessed by using the digoxigenin-labeling DNA detection system. Thus, the PCR-RFLP analysis that we developed is applicable for the routine detection of Abiotrophia from clinical specimens.

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Selected References

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  1. Beighton D., Homer K. A., Bouvet A., Storey A. R. Analysis of enzymatic activities for differentiation of two species of nutritionally variant streptococci, Streptococcus defectivus and Streptococcus adjacens. J Clin Microbiol. 1995 Jun;33(6):1584–1587. doi: 10.1128/jcm.33.6.1584-1587.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bottone E. J., Thomas C. A., Lindquist D., Janda J. M. Difficulties encountered in identification of a nutritionally deficient streptococcus on the basis of its failure to revert to streptococcal morphology. J Clin Microbiol. 1995 Apr;33(4):1022–1024. doi: 10.1128/jcm.33.4.1022-1024.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bouvet A. Human endocarditis due to nutritionally variant streptococci: streptococcus adjacens and Streptococcus defectivus. Eur Heart J. 1995 Apr;16 (Suppl B):24–27. doi: 10.1093/eurheartj/16.suppl_b.24. [DOI] [PubMed] [Google Scholar]
  4. Carey R. B., Gross K. C., Roberts R. B. Vitamin B6-dependent Streptococcus mitior (mitis) isolated from patients with systemic infections. J Infect Dis. 1975 Jun;131(6):722–726. doi: 10.1093/infdis/131.6.722. [DOI] [PubMed] [Google Scholar]
  5. Cayeux P., Acar J. F., Chabbert Y. A. Bacterial persistence in streptococcal endocarditis due to thiol-requiring mutants. J Infect Dis. 1971 Sep;124(3):247–254. doi: 10.1093/infdis/124.3.247. [DOI] [PubMed] [Google Scholar]
  6. FRENKEL A., HIRSCH W. Spontaneous development of L forms of streptococci requiring secretions of other bacteria or sulphydryl compounds for normal growth. Nature. 1961 Aug 12;191:728–730. doi: 10.1038/191728a0. [DOI] [PubMed] [Google Scholar]
  7. George R. H. The isolation of symbiotic streptococci. J Med Microbiol. 1974 Feb;7(1):77–83. doi: 10.1099/00222615-7-1-77. [DOI] [PubMed] [Google Scholar]
  8. Kawamura Y., Hou X. G., Sultana F., Liu S., Yamamoto H., Ezaki T. Transfer of Streptococcus adjacens and Streptococcus defectivus to Abiotrophia gen. nov. as Abiotrophia adiacens comb. nov. and Abiotrophia defectiva comb. nov., respectively. Int J Syst Bacteriol. 1995 Oct;45(4):798–803. doi: 10.1099/00207713-45-4-798. [DOI] [PubMed] [Google Scholar]
  9. Kawamura Y., Hou X. G., Sultana F., Miura H., Ezaki T. Determination of 16S rRNA sequences of Streptococcus mitis and Streptococcus gordonii and phylogenetic relationships among members of the genus Streptococcus. Int J Syst Bacteriol. 1995 Apr;45(2):406–408. doi: 10.1099/00207713-45-2-406. [DOI] [PubMed] [Google Scholar]
  10. Liu S. L., Hessel A., Sanderson K. E. Genomic mapping with I-Ceu I, an intron-encoded endonuclease specific for genes for ribosomal RNA, in Salmonella spp., Escherichia coli, and other bacteria. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6874–6878. doi: 10.1073/pnas.90.14.6874. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. McCarthy L. R., Bottone E. J. Bacteremia and endocarditis caused by satelliting streptococci. Am J Clin Pathol. 1974 May;61(5):585–591. doi: 10.1093/ajcp/61.5.585. [DOI] [PubMed] [Google Scholar]
  12. Peter J. B. The polymerase chain reaction: amplifying our options. Rev Infect Dis. 1991 Jan-Feb;13(1):166–171. doi: 10.1093/clinids/12.5.166. [DOI] [PubMed] [Google Scholar]
  13. Pompei R., Caredda E., Piras V., Serra C., Pintus L. Production of bacteriolytic activity in the oral cavity by nutritionally variant streptococci. J Clin Microbiol. 1990 Jul;28(7):1623–1627. doi: 10.1128/jcm.28.7.1623-1627.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Roberts R. B., Krieger A. G., Schiller N. L., Gross K. C. Viridans streptococcal endocarditis: the role of various species, including pyridoxal-dependent streptococci. Rev Infect Dis. 1979 Nov-Dec;1(6):955–966. doi: 10.1093/clinids/1.6.955. [DOI] [PubMed] [Google Scholar]
  15. Ruoff K. L. Nutritionally variant streptococci. Clin Microbiol Rev. 1991 Apr;4(2):184–190. doi: 10.1128/cmr.4.2.184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wada A., Ohta H., Kulthanan K., Hiramatsu K. Molecular cloning and mapping of 16S-23S rRNA gene complexes of Staphylococcus aureus. J Bacteriol. 1993 Nov;175(22):7483–7487. doi: 10.1128/jb.175.22.7483-7487.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Weisburg W. G., Barns S. M., Pelletier D. A., Lane D. J. 16S ribosomal DNA amplification for phylogenetic study. J Bacteriol. 1991 Jan;173(2):697–703. doi: 10.1128/jb.173.2.697-703.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Whiley R. A., Fraser H. Y., Douglas C. W., Hardie J. M., Williams A. M., Collins M. D. Streptococcus parasanguis sp. nov., an atypical viridans Streptococcus from human clinical specimens. FEMS Microbiol Lett. 1990 Mar 1;56(1-2):115–121. doi: 10.1111/j.1574-6968.1990.tb04133.x. [DOI] [PubMed] [Google Scholar]
  19. Zhang Y., Isaacman D. J., Wadowsky R. M., Rydquist-White J., Post J. C., Ehrlich G. D. Detection of Streptococcus pneumoniae in whole blood by PCR. J Clin Microbiol. 1995 Mar;33(3):596–601. doi: 10.1128/jcm.33.3.596-601.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]

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