Anopheles funestus (African malaria mosquito, FUMOZ) (AfunF3)

Anopheles funestus (African malaria mosquito, FUMOZ) Assembly and Gene Annotation

The Anopheles funestus data and its display on Ensembl Genomes are made possible through a joint effort by the Ensembl Genomes group and VectorBase, a component of VEuPathDB.

The assembly name may not match that from INSDC due to additional community contributions applied by VEuPathDB to the initial INSDC assembly (recorded by the assembly accession).

About Anopheles funestus

Range

Anopheles funestus has a wide geographic distribution, extending throughout Africa where is one of the most important vectors of malaria.

Habitats

A typical An. funestus larval habitat is a large, permanent or semi-permanent body of fresh water with emergent vegetation, such as swamps, large ponds and lake edges. Larvae have been found in shaded and sunlit environments where An. funestus may use emergent vegetation as refuge against predation while the shading it casts, or the presence of shade from overhanging plants, is of lesser importance. In some areas, An. funestus larvae are associated with rice cultivation (e.g. Madagascar, Mali) and replaces An. arabiensis in a successive temporal process during rice plant growth, exhibiting higher densities in older, maturing fields compared to the preceding open conditions preferred by An. arabiensis. An. funestus is a highly adaptable species, allowing it to occupy and maintain its wide distribution and utilise and conform to the many habitat types and climatic conditions contained therein.

Resting and feeding preferences

An. funestus is considered to be highly anthropophilic. Behaviourally, its late-night biting patterns potentially allows ready access to human blood without incurring undue density-dependant host avoidance. This late-night biting preference is clearly evident throughout its range, with peak biting period generally occurring after 22:00, commonly between midnight and the early hours of the morning. Endophilic resting behaviour is also commonly reported, allowing successful vector control using indoor residual spraying and insecticide-treated nets. However, insecticide exposure has resulted in selection pressure and rapid development of insecticide resistance to pyrethroids, now well established in some populations. Compared to other dominant vector species in Africa, An. funestus shows fairly consistent behaviour (generally anthropophilic and endophilic) throughout its range but some behavioural differences have been reported. For example, anthropophilic behaviour has been found in western Senegal and zoophilic behaviour in the east of the country.

Vectorial capacity

An. funestus is regarded as an important vector of malaria. The endophilic resting behaviour of An. funestus combined with a relatively high longevity, makes it as good a vector, or better in some areas, as An. gambiae. Insecticide resistance to pyrethroids, now well established in some An. funestus populations, has been implicated as the primary reason for a major resurgence of epidemic malaria reported in Kwazulu-Natal, South Africa in the late 1990s.

This text was modified from Sinka ME et al. (2010) The dominant Anopheles vectors of human malaria in Africa, Europe and the Middle East: occurrence data, distribution maps and bionomic précis Parasites & Vectors 3:117.

FUMOZ strain

Originally isolated in Mozambique. There was no isofemale subcolony selection. The strain is available from BEI resources.

Source: VectorBase

Picture credit: James Gathany, Dr. Frank Collins, University of Notre Dame, USCDCP Public domain via Wikimedia Commons (Image source)

AfunF3 assembly

The AfunF3 assembly is described in the paper 'A chromosome-scale assembly of the major African malaria vector Anopheles funestus', Ghurye et. al., GigaScience, Volume 8, Issue 6, June 2019, giz063, https://doi.org/10.1093/gigascience/giz063. The AfunF3 assembly replaces the AfunF1 assembly for the FUMOZ strain.

AfunF3 was generated using 240x coverage of long-read single-molecule sequencing for contigging, combined with 100x coverage of short-read Hi-C data for chromosome scaffolding. The assembled contigs total 446 Mbp of sequence and contain substantial duplication due to alternative alleles present in the sequenced pool of mosquitos from the FUMOZ colony. Using alignment and depth-of-coverage information, these contigs were deduplicated to a 211 Mbp.

AfunF3.2 gene set

Community annotation patch build for July 2019.

References

  1. A chromosome-scale assembly of the major African malaria vector Anopheles funestus.
    Ghurye J, Koren S, Small ST, Redmond S, Howell P, Phillippy AM, Besansky NJ. 2019. Gigascience. 8(6)
  2. The dominant Anopheles vectors of human malaria in Africa, Europe and the Middle East: occurrence data, distribution maps and bionomic prcis.
    Sinka ME, Bangs MJ, Manguin S, Coetzee M, Mbogo CM, Hemingway J, Patil AP, Temperley WH, Gething PW, Kabaria CW et al. 2010. Parasit Vectors. 3:117.

Picture credit: VectorBase.org

Statistics

Summary

AssemblyAfunF3, INSDC Assembly GCA_003951495.1,
Database version111.3
Golden Path Length210,989,154
Genebuild byVEuPathDB
Genebuild methodImport
Data sourceUniversity of Notre Dame

Gene counts

Coding genes13,094
Non coding genes1,082
Small non coding genes1,080
Long non coding genes2
Gene transcripts15,703

Other

Short Variants12,049,452