Rapid detection and quantification of cell free cytomegalovirus by a high-speed centrifugation-based microculture assay: comparison to longitudinally analyzed viral DNA load and pp67 late transcript during lactation

被引:54
作者
Hamprecht, K
Witzel, S
Maschmann, J
Dietz, K
Baumeister, A
Mikeler, E
Goelz, R
Speer, CP
Jahn, G
机构
[1] Univ Tubingen Hosp, Inst Med Virol & Epidemiol Viral Dis, D-72076 Tubingen, Germany
[2] Univ Wurzburg, Childrens Hosp, D-97080 Wurzburg, Germany
[3] Univ Hosp Tubingen, Dept Med Biometry, D-72076 Tubingen, Germany
[4] Childrens Univ Hosp Tubingen, Dept Neonatol, D-72076 Tubingen, Germany
关键词
CMV; breast milk; breastfeeding; microculture; quantitative PCR; NASBA;
D O I
10.1016/S1386-6532(03)00074-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Human cytomegalovirus (HCMV) is reactivated in nearly every seropositive breastfeeding mother during lactation [Lancet 357 (2001) 513]. Conventional tissue culture (TC) and low-speed centrifugation-enhanced microtiter culture methods are not able to detect HCMV from milk during all stages of lactation. Objectives: Development of a sensitive and quantitative microculture technique to describe the dynamics of HCMV reactivation in different milk compartments during lactation. Study design: Milk samples were collected longitudinally from seropositive breastfeeding mothers of preterm infants. Native milk samples were separated into fraction 1 (aqueous extract of milk fat), fraction 2 (cell and fat free milk whey) and fraction 3 (milk cells). Each of these fractions was screened qualitatively (TC, nPCR, pp67 late mRNA) and quantitatively (high-speed centrifugation-based microculture, quantiative PCR). Results: Prior to low-speed centrifugation-enhanced inoculation, virus particles were concentrated by high-speed centrifugation (60 min at 50 000 x g, 4 degreesC). Using fraction 2 we were able to describe the dynamics of viral reactivation during lactation. We present the course of the quantitative virolactia and DNAlactia and qualitative detection of HCMV pp67 late mRNA in milk whey of four mothers (three transmitters and one non-transmitter). In all these cases virolactia described an unimodal and self limited course. Peak levels of virolactia for transmitters (T-1: day 44; T-2: day 43; T-3: day 50) were closely related the onset of viruria of the corresponding preterm infants (U-1: day 39; U-2a/U-2b: day 44/57; U-3: day 60). The courses of viral load coincidence with the courses of DNA load. Conclusions: We present a rapid and highly sensitive microculture method for the quantification of cell free HCMV from milk whey and aqueous extracts from milk fat. Viral reactivation during lactation describes an unimodal course. Our findings have strong implications for quality control of any virus inactivation procedure. (C) 2003 Elsevier Science B.V. All rights reserved.
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收藏
页码:303 / 316
页数:14
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