Chromosome-level genome assemblies of the malaria vectors Anopheles coluzzii and Anopheles arabiensis

Author:

Zamyatin Anton1ORCID,Avdeyev Pavel23ORCID,Liang Jiangtao45ORCID,Sharma Atashi56ORCID,Chen Chujia56,Lukyanchikova Varvara457ORCID,Alexeev Nikita1ORCID,Tu Zhijian56ORCID,Alekseyev Max A23ORCID,Sharakhov Igor V45ORCID

Affiliation:

1. Computer Technologies Laboratory, ITMO University, Kronverkskiy Prospekt 49-A, Saint Petersburg 197101, Russia

2. Department of Mathematics, The George Washington University, 801 22nd Street NW, Washington, DC 20052, USA

3. Computational Biology Institute, Milken Institute School of Public Health, The George Washington University, 800 22nd Street NW, Washington, DC 20052, USA

4. Department of Entomology, Virginia Polytechnic Institute and State University, 170 Drillfield Drive, Blacksburg, VA 24061, USA

5. Fralin Life Sciences Institute, Virginia Polytechnic Institute and State University, 360 West Campus Drive, Blacksburg, VA 24061, USA

6. Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA

7. Institute of Cytology and Genetics the Siberian Division of the Russian Academy of Sciences, Prospekt Lavrentyeva 10, Novosibirsk 630090, Russia

Abstract

Abstract Background Anopheles coluzzii and Anopheles arabiensis belong to the Anopheles gambiae complex and are among the major malaria vectors in sub-Saharan Africa. However, chromosome-level reference genome assemblies are still lacking for these medically important mosquito species. Findings In this study, we produced de novo chromosome-level genome assemblies for A. coluzzii and A. arabiensis using the long-read Oxford Nanopore sequencing technology and the Hi-C scaffolding approach. We obtained 273.4 and 256.8 Mb of the total assemblies for A. coluzzii and A. arabiensis, respectively. Each assembly consists of 3 chromosome-scale scaffolds (X, 2, 3), complete mitochondrion, and unordered contigs identified as autosomal pericentromeric DNA, X pericentromeric DNA, and Y sequences. Comparison of these assemblies with the existing assemblies for these species demonstrated that we obtained improved reference-quality genomes. The new assemblies allowed us to identify genomic coordinates for the breakpoint regions of fixed and polymorphic chromosomal inversions in A. coluzzii and A. arabiensis. Conclusion The new chromosome-level assemblies will facilitate functional and population genomic studies in A. coluzzii and A. arabiensis. The presented assembly pipeline will accelerate progress toward creating high-quality genome references for other disease vectors.

Funder

National Institutes of Health

National Institute of Food and Agriculture Hatch

Publisher

Oxford University Press (OUP)

Subject

Computer Science Applications,Health Informatics

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