Mészáros Beáta, Sápy Tamás, Gergely Lajos, Csoma Eszter
University of Debrecen Department of Medical Microbiology Debrecen Hungary.
University of Debrecen Department of Obstetrics and Gynaecology Debrecen Hungary.
Acta Microbiol Immunol Hung. 2014 Sep;61(3):309-16. doi: 10.1556/AMicr.61.2014.3.5.
The aim of the present study was to assess the frequency of human herpesvirus 6A (HHV-6A) and human herpesvirus 6B (HHV-6B) infection during pregnancy. 100-100 blood samples were collected from pregnant and non-pregnant women, then nucleic acid was isolated from both plasma and leukocytes fraction. Nested and real-time PCR were used to detect and differentiate HHV-6A and HHV-6B DNA and to determine viral loads. Reverse transcription PCR (RT-PCR) for HHV-6 U79/80 mRNA was performed in order to reveal active HHV-6 replication.HHV-6A and HHV-6B active infections were not detected in blood samples neither from pregnant nor from non-pregnant women. Frequency of HHV-6B and HHV-6A latency did not show difference between the studied groups (15% vs. 16%). HHV-6B latency was dominant in both studied groups (14/15 and 15/16). Beside these results, in leukocyte samples of one pregnant and three non-pregnant women high HHV-6A viral loads (1.28 × 10⁵ - 5.07 × 10⁵ GEq / 1.5 × 10⁶ leukocytes) were detected, and viral DNA was also found in plasma samples. Although RT-PCR did not confirm virus replication, but chromosomal integration was also not proved unequivocally, the number of 0.08-0.33 HHV-6 copy / 1 leukocyte refers more to postnatal infection.
本研究的目的是评估孕期人类疱疹病毒6A(HHV-6A)和人类疱疹病毒6B(HHV-6B)感染的频率。从孕妇和非孕妇中采集100份血液样本,然后从血浆和白细胞组分中分离核酸。采用巢式和实时PCR检测并区分HHV-6A和HHV-6B DNA,并确定病毒载量。进行HHV-6 U79/80 mRNA的逆转录PCR(RT-PCR)以揭示HHV-6的活跃复制。在孕妇和非孕妇的血液样本中均未检测到HHV-6A和HHV-6B的活跃感染。研究组之间HHV-6B和HHV-6A潜伏感染的频率没有差异(15%对16%)。HHV-6B潜伏感染在两个研究组中均占主导(14/15和15/16)。除这些结果外,在1名孕妇和3名非孕妇的白细胞样本中检测到高HHV-6A病毒载量(1.28×10⁵ - 5.07×10⁵ GEq / 1.5×10⁶白细胞),并且在血浆样本中也发现了病毒DNA。虽然RT-PCR未证实病毒复制,但也未明确证明染色体整合,0.08 - 0.33 HHV-6拷贝/1个白细胞的数量更提示产后感染。