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人类巨细胞病毒毒株的多样性和动态变化表明,供体肺是移植后病毒的主要来源。

Human cytomegalovirus strain diversity and dynamics reveal the donor lung as a major contributor after transplantation.

作者信息

Külekci Büsra, Schwarz Stefan, Brait Nadja, Perkmann-Nagele Nicole, Jaksch Peter, Hoetzenecker Konrad, Puchhammer-Stöckl Elisabeth, Goerzer Irene

机构信息

Center for Virology, Medical University of Vienna, Kinderspitalgasse 15, Vienna 1090, Austria.

Department of Thoracic Surgery, Medical University of Vienna, Währinger Gürtel 18-20, Vienna 1090, Austria.

出版信息

Virus Evol. 2022 Aug 24;8(2):veac076. doi: 10.1093/ve/veac076. eCollection 2022.

Abstract

Mixed human cytomegalovirus (HCMV) strain infections are frequent in lung transplant recipients (LTRs). To date, the influence of the donor (D) and recipient (R) HCMV serostatus on intra-host HCMV strain composition and viral population dynamics after transplantation is only poorly understood. Here, we investigated ten pre-transplant lungs from HCMV-seropositive donors and 163 sequential HCMV-DNA-positive plasma and bronchoalveolar lavage samples from fifty LTRs with multiviremic episodes post-transplantation. The study cohort included D+R+ (38 per cent), D+R- (36 per cent), and D-R+ (26 per cent) patients. All samples were subjected to quantitative genotyping by short amplicon deep sequencing, and twenty-four of them were additionally PacBio long-read sequenced for genotype linkages. We find that D+R+ patients show a significantly elevated intra-host strain diversity compared to D+R- and D-R+ patients (= 0.0089). Both D+ patient groups display significantly higher viral population dynamics than D- patients (0.0061). Five out of ten pre-transplant donor lungs were HCMV DNA positive, whereof three multiple HCMV strains were detected, indicating that multi-strain transmission via lung transplantation is likely. Using long reads, we show that intra-host haplotypes can share distinctly linked genotypes, which limits overall intra-host diversity in mixed infections. Together, our findings demonstrate donor-derived strains as the main source of increased HCMV strain diversity and dynamics post-transplantation. These results foster strategies to mitigate the potential transmission of the donor strain reservoir to the allograft, such as delivery of HCMV-selective immunotoxins prior to transplantation to reduce latent HCMV.

摘要

混合人巨细胞病毒(HCMV)株感染在肺移植受者(LTRs)中很常见。迄今为止,供体(D)和受体(R)的HCMV血清学状态对移植后宿主内HCMV株组成和病毒群体动态的影响仍知之甚少。在此,我们研究了来自HCMV血清阳性供体的10个移植前肺,以及来自50名移植后发生多次病毒血症发作的LTRs的163份连续的HCMV-DNA阳性血浆和支气管肺泡灌洗样本。研究队列包括D+R+(38%)、D+R-(36%)和D-R+(26%)患者。所有样本均通过短扩增子深度测序进行定量基因分型,其中24份样本还进行了PacBio长读长测序以确定基因型连锁。我们发现,与D+R-和D-R+患者相比,D+R+患者的宿主内株多样性显著升高(=0.0089)。两个D+患者组的病毒群体动态均显著高于D-患者(0.0061)。10个移植前供体肺中有5个HCMV DNA呈阳性,其中3个检测到多种HCMV株,这表明通过肺移植进行多株传播是可能的。使用长读长,我们表明宿主内单倍型可以共享明显连锁的基因型,这限制了混合感染中整体宿主内的多样性。总之,我们的研究结果表明供体来源的毒株是移植后HCMV株多样性和动态增加的主要来源。这些结果促进了减轻供体毒株库向同种异体移植物潜在传播的策略,例如在移植前递送HCMV选择性免疫毒素以减少潜伏性HCMV。

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