دورية أكاديمية
Sequence variability of human erythroviruses present in bone marrow of Brazilian patients with various parvovirus B19-related hematological symptoms.
| العنوان: | Sequence variability of human erythroviruses present in bone marrow of Brazilian patients with various parvovirus B19-related hematological symptoms. |
|---|---|
| المؤلفون: | Sanabani S; Molecular Biology Laboratory, Fundação Pró-Sangue, Hemocentro de São Paulo, Brazil, São Paulo, Brazil. sabinoec@uol.com.br, Neto WK, Pereira J, Sabino EC |
| المصدر: | Journal of clinical microbiology [J Clin Microbiol] 2006 Feb; Vol. 44 (2), pp. 604-6. |
| نوع المنشور: | Journal Article; Research Support, Non-U.S. Gov't |
| اللغة: | English |
| بيانات الدورية: | Publisher: American Society for Microbiology Country of Publication: United States NLM ID: 7505564 Publication Model: Print Cited Medium: Print ISSN: 0095-1137 (Print) Linking ISSN: 00951137 NLM ISO Abbreviation: J Clin Microbiol Subsets: MEDLINE |
| أسماء مطبوعة: | Original Publication: Washington, American Society for Microbiology. |
| مواضيع طبية MeSH: | Genetic Variation* , Sequence Analysis, DNA*, Bone Marrow/*virology , Erythrovirus/*classification , Hematologic Diseases/*virology , Parvoviridae Infections/*virology , Parvovirus B19, Human/*pathogenicity, Adolescent ; Adult ; Aged ; Brazil ; Child ; DNA, Viral/analysis ; DNA, Viral/isolation & purification ; Erythrovirus/genetics ; Erythrovirus/isolation & purification ; Female ; Genotype ; Humans ; Male ; Middle Aged ; Molecular Sequence Data |
| مستخلص: | The presence of erythrovirus infections was investigated by PCR with bone marrow samples of patients with various parvovirus B19-related hematological symptoms. Erythrovirus DNA was found in 17.3% (12/69) of patients. Phylogenetic analysis revealed that five strains cluster with genotype 1, one clusters with genotype 2, and six cluster with genotype 3. Our study is the first to document the presence of the three erythrovirus genotypes in Brazil. |
| References: | N Engl J Med. 2004 Feb 5;350(6):586-97. (PMID: 14762186) J Clin Microbiol. 2004 May;42(5):2013-9. (PMID: 15131163) J Virol. 2004 Nov;78(22):12169-78. (PMID: 15507603) J Virol. 1986 Jun;58(3):921-36. (PMID: 3701931) J Virol. 1987 Aug;61(8):2395-406. (PMID: 3599180) Virology. 2002 Oct 25;302(2):224-8. (PMID: 12441066) Lancet. 1997 Apr 12;349(9058):1063-5. (PMID: 9107245) J Med Virol. 2001 Oct;65(2):362-7. (PMID: 11536245) J Med Virol. 1997 Nov;53(3):229-32. (PMID: 9365887) J Clin Microbiol. 1999 Aug;37(8):2483-7. (PMID: 10405389) J Virol. 2002 Sep;76(18):9124-34. (PMID: 12186896) Ann Intern Med. 1990 Dec 15;113(12):926-33. (PMID: 2173460) |
| سلسلة جزيئية: | GENBANK DQ229350; DQ229351; DQ229352; DQ229353; DQ229354; DQ229355; DQ229356; DQ229357; DQ229358; DQ229359; DQ229360; DQ229361 |
| المشرفين على المادة: | 0 (DNA, Viral) |
| تواريخ الأحداث: | Date Created: 20060204 Date Completed: 20060418 Latest Revision: 20220311 |
| رمز التحديث: | 20240628 |
| مُعرف محوري في PubMed: | PMC1392653 |
| DOI: | 10.1128/JCM.44.2.604-606.2006 |
| PMID: | 16455922 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 0095-1137 |
|---|---|
| DOI: | 10.1128/JCM.44.2.604-606.2006 |