Severe outcome of influenza A/H1N1/09v infection associated with 222G/N polymorphisms in the haemagglutinin: a multicentre study

被引:44
作者
Baldanti, F. [1 ]
Campanini, G. [1 ]
Piralla, A. [1 ]
Rovida, F. [1 ]
Braschi, A. [2 ]
Mojoli, F. [2 ]
Iotti, G. [3 ]
Belliato, M. [3 ]
Conaldi, P. G. [4 ]
Arcadipane, A. [5 ]
Pariani, E. [6 ]
Zanetti, A. [6 ]
Minoli, L. [7 ]
Emmi, V. [3 ]
机构
[1] Fdn IRCCS Policlin San Matteo, Mol Virol Unit, I-27100 Pavia, Italy
[2] Fdn IRCCS Policlin San Matteo, Intens Care Unit 1, I-27100 Pavia, Italy
[3] Fdn IRCCS Policlin San Matteo, Intens Care Unit 2, I-27100 Pavia, Italy
[4] ISSMET, Inst Microbiol & Virol, Palermo, Italy
[5] ISSMET, Intens Care Unit, Palermo, Italy
[6] Univ Milan, Dipartimento Sanita Pubbl Microbiol Virol, Milan, Italy
[7] Univ Pavia, Fdn IRCCS Policlin San Matteo, Inst Infect Dis, Pavia, Italy
关键词
222G/N variants; bronchoalveolar lavage; intensive-care unit; influenza A/H1N1/09v; virulence; VIRUS; D222G;
D O I
10.1111/j.1469-0691.2010.03403.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In a multicentre study, influenza A/H1N1/09v 222G/N variants were more frequently detected in patients admitted to the intensive-care unit for invasive mechanical ventilation or extracorporeal membrane oxygenation (10/23; 43.5%) than in patients hospitalized in other units (2/27; 7.4%) and community patients (0/81; 0.0%) (p <0.01). A significantly higher virus load (p 0.02) in the lower vs the upper respiratory tract was observed. Predominance of 222G/N variants in the lower respiratory tract (40% of total virus population) vs the upper respiratory tract (10%) was shown by clonal analysis of haemagglutinin sequences in paired nasal swab and bronchoalveolar lavage samples. The time from illness onset to sampling was significantly longer in patients with severe infection vs community patients (p <0.001). It was concluded that the 222G/N variants showed increased virulence; mutant variants were probably selected in individual patients; and the longer duration of illness might have favoured the emergence of adaptive mutations through multiple replication cycles.
引用
收藏
页码:1166 / 1169
页数:4
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