Abstract

BackgroundThe occurrence of a genetic bottleneck in HIV sexual or mother-to-infant transmission has been well documented. This results in a majority of new infections being homogeneous, i.e., initiated by a single genetic strain. Early after infection, prior to the onset of the host immune response, the viral population grows exponentially. In this simple setting, an approach for estimating evolutionary and demographic parameters based on comparison of diversity measures is a feasible alternative to the existing Bayesian methods (e.g., BEAST), which are instead based on the simulation of genealogies.ResultsWe have devised a web tool that analyzes genetic diversity in acutely infected HIV-1 patients by comparing it to a model of neutral growth. More specifically, we consider a homogeneous infection (i.e., initiated by a unique genetic strain) prior to the onset of host-induced selection, where we can assume a random accumulation of mutations. Previously, we have shown that such a model successfully describes about 80% of sexual HIV-1 transmissions provided the samples are drawn early enough in the infection. Violation of the model is an indicator of either heterogeneous infections or the initiation of selection.ConclusionsWhen the underlying assumptions of our model (homogeneous infection prior to selection and fast exponential growth) are met, we are under a very particular scenario for which we can use a forward approach (instead of backwards in time as provided by coalescent methods). This allows for more computationally efficient methods to derive the time since the most recent common ancestor. Furthermore, the tool performs statistical tests on the Hamming distance frequency distribution, and outputs summary statistics (mean of the best fitting Poisson distribution, goodness of fit p-value, etc). The tool runs within minutes and can readily accommodate the tens of thousands of sequences generated through new ultradeep pyrosequencing technologies. The tool is available on the LANL website.

Highlights

  • The occurrence of a genetic bottleneck in HIV sexual or mother-to-infant transmission has been well documented

  • The tool is available on the LANL website [8]

  • All the parameters explained in the previous section are computed and included in the output table called “Log Likelihood - Estimated Parameters.”. This comprises, for each sample: the number of sequences in the sample, the mean and maximum pairwise Hamming distances (HD), the mean of the best fitting Poisson distribution, the corresponding time since the most recent common ancestor (MRCA), and the goodness of fit P-value It is important to notice that when the sample meets our model’s assumptions, the mean of the best fitting Poisson distribution is the mean pairwise HD of the sample

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Summary

Introduction

The occurrence of a genetic bottleneck in HIV sexual or mother-to-infant transmission has been well documented This results in a majority of new infections being homogeneous, i.e., initiated by a single genetic strain. Prior to the onset of the host immune response, the viral population grows exponentially In this simple setting, an approach for estimating evolutionary and demographic parameters based on comparison of diversity measures is a feasible alternative to the existing Bayesian methods (e.g., BEAST), which are instead based on the simulation of genealogies. The occurrence of a genetic bottleneck in HIV sexual or mother-to-infant transmissions has been well documented [1,2] This results in about 80% of new infections being homogeneous, i.e., initiated by a single genetic strain [3]. An extensive explanation of how the tool works and how to format the input data is provided in the Poisson Fitter Explanation link available on the tool website [8]

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