Iwasenko J M, Scott G M, Naing Z, Glanville A R, Rawlinson W D
Virology, Department of Microbiology, South Eastern Area Laboratory Services (SEALS), Prince of Wales Hospital, Randwick, New South Wales, Australia.
Transpl Infect Dis. 2011 Apr;13(2):145-53. doi: 10.1111/j.1399-3062.2010.00584.x. Epub 2010 Nov 10.
Immunocompromised transplant recipients are at high risk for human cytomegalovirus (CMV)-related infection and disease. Antiviral prophylaxis and treatment have reduced CMV morbidity and mortality, but at times promote development of antiviral-resistant CMV strains that can significantly contribute to adverse clinical outcomes in transplant recipients. We have investigated CMV genotypes in transplant recipients (bone marrow, stem cell, kidney, heart, lung, and liver) receiving antiviral prophylaxis or preemptive therapy or treatment, to determine the viral characteristics and clinical impact of antiviral-resistant CMV in these different groups. Antiviral-resistant CMV strains were detected by polymerase chain reaction sequencing of the CMV protein kinase (UL97) and viral DNA polymerase (UL54) genes from clinical specimens. A trend toward more frequent detection of multidrug resistance and co-circulation of multiple resistant strains was seen in heart and lung transplant recipients compared with other transplantation types. A greater diversity and number of UL97 and UL54 mutations were observed in heart and lung transplant recipients; whereas antiviral-resistant CMV infections in other transplant recipients were predominantly the result of a single mutant genotype. Furthermore, 43% (6/14) of CMV-positive heart and lung transplant recipients were infected with CMV strains containing UL54 mutations conferring multidrug resistance compared with only 6% (1/18) of CMV-positive recipients of other transplanted organs or stem cells. Emergence of CMV strains containing previously unrecognized UL54 mutations (F412S and D485N) also occurred in 1 lung and 1 heart transplant recipient. The development of these mutations under antiviral selective pressure, and clinical outcome of infection suggests these mutations are likely to confer antiviral resistance. Emergence of CMV antiviral resistance remains a significant issue in immunocompromised patients treated with antiviral agents, and emphasizes the relevance of regular antiviral resistance testing when designing optimal patient-management strategies.
免疫功能低下的移植受者面临着与人类巨细胞病毒(CMV)相关感染和疾病的高风险。抗病毒预防和治疗降低了CMV的发病率和死亡率,但有时会促使抗病毒耐药CMV毒株的出现,这可能对移植受者的不良临床结局产生重大影响。我们调查了接受抗病毒预防、抢先治疗或治疗的移植受者(骨髓、干细胞、肾脏、心脏、肺和肝脏移植)中的CMV基因型,以确定这些不同组中抗病毒耐药CMV的病毒特征和临床影响。通过对临床标本中CMV蛋白激酶(UL97)和病毒DNA聚合酶(UL54)基因进行聚合酶链反应测序来检测抗病毒耐药CMV毒株。与其他移植类型相比,心脏和肺移植受者中检测到多药耐药和多种耐药毒株共同循环的频率有增加趋势。在心脏和肺移植受者中观察到UL97和UL54突变的多样性和数量更多;而其他移植受者中的抗病毒耐药CMV感染主要是单一突变基因型的结果。此外,43%(6/14)的CMV阳性心脏和肺移植受者感染了含有赋予多药耐药性的UL54突变的CMV毒株,而其他移植器官或干细胞的CMV阳性受者中只有6%(1/18)感染了此类毒株。1例肺移植受者和1例心脏移植受者中还出现了含有以前未识别的UL54突变(F412S和D485N)的CMV毒株。这些突变在抗病毒选择压力下的出现以及感染的临床结局表明这些突变可能赋予抗病毒耐药性。CMV抗病毒耐药性的出现仍然是接受抗病毒药物治疗的免疫功能低下患者中的一个重要问题,并强调在设计最佳患者管理策略时进行定期抗病毒耐药性检测的重要性。