4.5 Article

Genome Assembly of the A-Group Wolbachia in Nasonia oneida Using Linked-Reads Technology

Journal

GENOME BIOLOGY AND EVOLUTION
Volume 11, Issue 10, Pages 3008-3013

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gbe/evz223

Keywords

Wolbachia; Nasonia; parasitoid wasp; 10 Genomics Chromium linked reads; multi-locus strain typing; pyrosequencing

Funding

  1. Auburn University Intramural Grant Program Award [AUIGP180271]
  2. Auburn University College of Veterinary Medicine
  3. Alabama Agricultural Experiment Station Enabling Grant
  4. USDA National Institute of Food and Agriculture, Hatch project [1018100]
  5. Auburn University Presidential Graduate Research Fellowship
  6. US National Science Foundation [IOS 1456233]
  7. Nathaniel and Helen Wisch Professorship

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Wolbachia are obligate intracellular bacteria which commonly infect various nematode and arthropod species. Genome sequences have been generated from arthropod samples following enrichment for the intracellular bacteria, and genomes have also been assembled from arthropod whole-genome sequencing projects. However, these methods remain challenging for infections that occur at low titers in hosts. Here we report the first Wolbachia genome assembled from host sequences using 10x Genomics linked reads technology. The high read depth attainable by this method allows for recovery of intracellular bacteria that are at low concentrations. Based on the depth differences (714x for the insect and 59x for the bacterium), we assembled the genome of a Wolbachia in the parasitoid jewel wasp species Nasonia oneida. The final draft assembly consists of 1,293, 06 bp in 47 scaffolds with 1,114 coding genes and 97.01% genome completeness assessed by checkM. Comparisons of the five Multi Locus Sequence Typing genes revealed that the sequenced Wolbachia genome is the Al strain (henceforth IniOneA 1) previously reported in N. oneida. Pyrosequencing confirms that the wasp strain lacks A2 and B types previously detected in this insect, which were likely lost during laboratory culturing. Assembling bacterial genomes from host genome projects can provide an effective method for sequencing bacterial genomes, even when the infections occur at low density in sampled tissues.

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