Mixture model analysis reflecting dynamics of the population diversity of 2009 pandemic H1N1 influenza virus.

Q2 Medicine
Li-Ping Long, Changhe Yuan, Zhipeng Cai, Huiping Xu, Xiu-Feng Wan
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引用次数: 0

Abstract

Influenza A viruses have been responsible for large losses of lives around the world and continue to present a great public health challenge. In April 2009, a novel swine-origin H1N1 virus emerged in North America and caused the first pandemic of the 21st century. Toward the end of 2009, two waves of outbreaks occurred, and then the disease moderated. It will be critical to understand how this novel pandemic virus invaded and adapted to a human population. To understand the molecular dynamics and evolution in this pandemic H1N1 virus, we applied an Expectation-Maximization algorithm to estimate the Gaussian mixture in the genetic population of the hemagglutinin (HA) gene of these H1N1 viruses from April of 2009 to January of 2010 and compared them with the viruses that cause seasonal H1N1 influenza. Our results show that, after it was introduced to human population, the 2009 H1N1 viral HA gene changed its population structure from a single Gaussian distribution to two major Gaussian distributions. The breadths of HA genetic diversity of 2009 H1N1 virus also increased from the first wave to the second wave of this pandemic. Phylogenetic analyses demonstrated that only certain HA sublineages of 2009 H1N1 viruses were able to circulate throughout the pandemic period. In contrast, the influenza HA population structure of seasonal H1N1 virus was relatively stable, and the breadth of HA genetic diversity within a single season population remained similar. This study revealed an evolutionary mechanism for a novel pandemic virus. After the virus is introduced to human population, the influenza virus would expand their molecular diversity through both random mutations (genetic drift) and selections. Eventually, multiple levels of hierarchical Gaussian distributions will replace the earlier single distribution. An evolutionary model for pandemic H1N1 influenza A virus was proposed and demonstrated with a simulation.

Abstract Image

反映 2009 年大流行 H1N1 流感病毒种群多样性动态的混合模型分析。
甲型流感病毒在世界各地造成了巨大的生命损失,并继续对公共卫生构成巨大挑战。2009 年 4 月,一种源于猪的新型 H1N1 病毒在北美出现,并引发了 21 世纪的首次大流行。2009 年底,爆发了两波疫情,随后疫情有所缓和。了解这种新型大流行病毒是如何入侵并适应人类群体的至关重要。为了了解这种大流行 H1N1 病毒的分子动力学和进化过程,我们应用期望最大化算法估计了 2009 年 4 月至 2010 年 1 月期间这些 H1N1 病毒血凝素(HA)基因遗传群体的高斯混合物,并将其与引起季节性 H1N1 流感的病毒进行了比较。结果表明,2009 年 H1N1 病毒 HA 基因进入人类后,其种群结构从单一高斯分布变为两大高斯分布。2009 H1N1 病毒 HA 基因多样性的广度也从此次流感大流行的第一波增加到了第二波。系统发生学分析表明,2009 H1N1 病毒中只有某些 HA 亚系能够在整个大流行期间流行。相比之下,季节性 H1N1 病毒的流感 HA 群体结构相对稳定,单季群体内 HA 遗传多样性的广度保持相似。这项研究揭示了新型大流行病毒的进化机制。病毒进入人类后,流感病毒会通过随机突变(基因漂移)和选择两种方式扩大其分子多样性。最终,多层次的高斯分布将取代早期的单一分布。本文提出了甲型 H1N1 流感病毒大流行的进化模型,并进行了模拟演示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
In Silico Biology
In Silico Biology Computer Science-Computational Theory and Mathematics
CiteScore
2.20
自引率
0.00%
发文量
1
期刊介绍: The considerable "algorithmic complexity" of biological systems requires a huge amount of detailed information for their complete description. Although far from being complete, the overwhelming quantity of small pieces of information gathered for all kind of biological systems at the molecular and cellular level requires computational tools to be adequately stored and interpreted. Interpretation of data means to abstract them as much as allowed to provide a systematic, an integrative view of biology. Most of the presently available scientific journals focus either on accumulating more data from elaborate experimental approaches, or on presenting new algorithms for the interpretation of these data. Both approaches are meritorious.
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