Genetic and Linkage Studies of New Autosomal Sex-Limited Mutant Hairless Antenna in<i> Anopheles stephensi</i> Liston

Madhyastha, A. Dinesh; Shetty, N. J.

doi:https://doi.org/10.1155/2016/4792702

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Research Article | Open Access

Volume 2016 | Article ID 4792702 | https://doi.org/10.1155/2016/4792702

Genetic and Linkage Studies of New Autosomal Sex-Limited Mutant Hairless Antenna in Anopheles stephensi Liston

A. Dinesh Madhyastha¹and N. J. Shetty¹

Academic Editor: Fedai Erler

Received29 Aug 2015

Revised19 Nov 2015

Accepted23 Nov 2015

Published04 Jan 2016

Abstract

A new morphological mutant hairless antenna (hla) was induced in the mosquito Anopheles stephensi by γ-irradiation. The expression of the mutant in the male adult revealed the antennae without the hairs. The inheritance pattern from our data demonstrates that hairless antenna is essentially sex-limited to males and is autosomal and recessive. The linkage relationships studies between the hairless antenna and greyish brown larva (grb) mutant indicated independent assortment and are present on different chromosomes, while the linkage relationship studies between the hairless antenna and ruby eye (ru) mutant revealed the suppression of hla by the ru gene in heterozygous condition. These mutants can be useful in conducting basic and applied research such as construction of linkage maps and understanding biochemical pathways and in genetic control programmes.

1. Introduction

Malaria continues to be a serious threat in many parts of the world including India. Conventional control method, that is, the chemical control, causes two major problems: environmental pollution and insecticide resistance. The insecticides will become less effective due to the resistance. Genetic control is an alternative method of controlling the vectors which includes techniques like sterile insect technique (SIT) and so forth and genetic characterization especially of these species and strains will continue to be an essential component of genetic control strategies aimed at disrupting the transmission of diseases [1].

Anopheles stephensi (order Diptera; family Culicidae) is an important urban malaria vector in the Indian subcontinent and accounts for about 15% of the annual malaria incidence [2]. An. stephensi has 3 pairs of chromosomes (). Three pairs of chromosomes (linkage groups) based on their length and position of the centromere are designated as I (subtelocentric sex chromosomes), II (longest autosome pair), and III (shorter autosome pair) [2, 3].

Traditionally, morphological mutants have been used to construct special genetic load strains containing chromosomal translocations or inversions [4, 5]. Morphological mutants are extremely useful in understanding the biology, behaviour, and biochemical pathways involved in pigmentation and constructing linkage maps to respective chromosomes and in synthesizing new strains for control of the vector [2]. Genetic markers are necessary for expanding the linkage maps [6]. Mutants obtained by irradiation have been useful in conducting basic genetic research and also applied research. Several radiation induced morphological mutants including wing, eye, and antenna mutants have been reported in Culex pipiens [7–10].

Relatively few γ-irradiation induced morphological mutants have been discovered in Anopheles. Autosomal hairy (h) and sex-linked bubble head mutants were obtained in An. albimanus [11], and frizzled (f) and homochromy1 (hom1) were isolated from ⁶⁰Co-irradiated An. gambiae [12].

The present paper describes the induction and isolation of a new radiation induced morphological mutant hairless antenna (hla), genetic basis of inheritance, and its linkage relationship with the already available autosomal mutants, that is, greyish brown larvae (grb) and ruby eye (ru) in An. stephensi.

2. Materials and Methods

2.1. Mosquito Culture

The larvae and adults were reared in an insectary maintained at °C and % relative humidity according to the procedure of Shetty [13]. The adults were held in an iron cage (8′′ X 8′′ X 8′′) covered with nylon netting. The adults were fed with 10% glucose solution soaked in cotton. The gravid females were placed in a plastic cup (2.5 × 7.5 cm) lined with filter paper and clean water was placed inside the cage for oviposition. The laid eggs were kept up to 72 hours for complete hatching. The hatched larvae were transferred to water in enamel tray and fed with dried yeast powder and dog biscuits as a source of food.

2.2. Mutants

Hairless Antennae (hla). The hairless antenna mutant was isolated from the ⁶⁰Co-irradiated mosquitoes of the Subhash Nagar, Mysore (South India) strain. Two- to three-day-old 125 males were irradiated with 3700 rad of ⁶⁰Co gamma radiation (dose rate is 185 rad/min) at the Kidwai Institute of Oncology, Bangalore. These irradiated males were immediately mass mated with virgin females of the same age. The gravid females were separated individually into plastic vials (2.5 × 7.5 cm) and kept for oviposition. The lines showing less than 50% hatchability were retained and were outcrossed with wild males and females. One of the lines in the F₂ generation, that is, T₁₀, gave 130 eggs and 60 larvae with 47% hatchability. Among the 60 larvae, 30 were males and 28 were females. Out of 30 males, five were hairless antennae males. These males were outcrossed with wild type females and the resulting F₃ progeny were inbred to get F₄ generations. The hairless antenna males were observed in alternate generations, that is, F₂, F₄, F₆, F₈, and so forth, and thus the mutant was maintained in the laboratory.

Contrary to the wild type male, which has bushy antennae, the mutant has hairless antennae. However, in both cases, the length and mouthparts are similar (Figure 1).

(a)

(b)

Greyish Brown (grb). The mutant greyish brown (grb) was established in An. stephensi in our laboratory. The colour is expressed in the late 1st instar larvae and persists throughout the larval and pupal stages. The mutant colony is vigorous requiring no more care than wild type. The gene “grb” is an autosomal recessive with uniform expression and complete penetrance.

Ruby Eye (ru). The mutant ruby eye was spontaneous in origin. The ruby colour of the eye is expressed in all the developmental stages and adults. The gene “ru” is monofactorial in nature and is autosomal. This is a good marker for An. stephensi. The said mutant is maintained in large population cages in our laboratory [14].

2.3. Crosses

Testing the mode of inheritance of hairless antenna involved five crosses. For all crosses, 25 males and 25 females were mass mated. Cross 1 involved the crosses between the males and females of the wild type. Cross 2 involved the crosses between the hairless antenna males and wild type females. Cross 3 involved the F₁ heterozygote mated inter se. Cross 4 involved the F₁ heterozygote females being backcrossed to the hairless antenna males. Cross 5 involved the crosses between the F₁ heterozygote females with wild type males.

2.4. Linkage Studies

To study the linkage relationship between hairless antenna and greyish brown larva mutant, pure laboratory strains of the mutants were used. The hairless antenna males having the wild type larva body were crossed with greyish brown larva females. A total of 6 crosses were carried out to study the linkage relationship. The F₁ progeny were inbred to yield F₂ generation and the F₂ progeny were analyzed for wild type, hairless antennae, greyish brown larva, and double mutant (hairless antenna and greyish brown larva) individuals. The same procedure was followed to study the linkage relationship between the hairless antenna and ruby eye mutant.

3. Results and Discussion

We have presented the genetic studies on inheritance of hairless antenna and wild type (Table 1). Cross 1 was carried out to establish the pure-bred wild type in the laboratory. Cross 2 involved the cross between the hairless antenna and wild type female. All the males and females were normal in the F₁ progeny. In cross 3, part of the F₁ progeny was inbred to get F₂ progeny. The wild type male and hairless antenna mutant occurred in 3 : 1 ratio of the male progeny of the F₂ progeny, indicating the recessive nature of the gene hla. All the females of the F₂ progeny were of wild type, and no significant values were obtained for cross 3. Part of the F₁ heterozygote female progeny were backcrossed to the hairless antenna (cross 4): no larva hatched out from the eggs of cross 4. The microscopic dissection revealed no embryonic development in the eggs. In cross 5, the F₁ heterozygote male progeny was crossed to wild type females in which no hairless antenna males were observed among the F₂ progeny. The heterogametic male progeny of cross 2 involving the hairless antenna and wild type female were of wild type and, therefore, the gene hla is autosomal.

Since the mutation affects only the male individuals, the gene hla is sex-limited gene. The progeny of the backcross involving the F₁ heterogametic female and hairless antenna revealed only the nonembryonated eggs. The exact mechanism of the lethality of the embryo is not clearly understood. However, the lethality may be due to immobility of male gamete to fuse with an egg or incompatibility of the egg cytoplasm.

Seawright et al. [15] have reported bald antenna (ba) in An. albimanus, which was sex-limited, autosomal, and recessive. In bald antenna, the remains of the hairs of antennae were presented in the pupal moult, which is not seen in the pupal moult of hairless antenna of An. stephensi in the present study indicating that both mutants are different.

The results of the linkage studies between the hairless antenna and the greyish brown larva are presented in Table 2. Cross 1 establishes the pure breed of greyish brown larva. The F₁ progeny of cross 2 involving the hairless antenna and wild type females were only wild type. The F₁ progeny of cross 3 involving the hairless antenna and greyish brown larva parents were of wild type. The results of the cross 4 involving F₁ progeny mated inter se showed a near 9 : 3 : 3 : 1 ratio of wild type, greyish brown larva, hairless antenna, and double mutant (greyish brown larva and hairless antennae) among the total male progeny in the F₂ generation indicating independent assortment. The female progeny of the F₂ generation showed 3 : 1 ratio of wild type and greyish brown larva. All the F₂ progeny of cross 5 resembled wild type and no significant () value was obtained for cross 4 (Table 2). No progeny were obtained from cross 6. It is pertinent to mention here that the backcross carried out between the F₁ heterozygote females with double mutant male (hairless antenna and greyish brown larva) did not produce any eggs indicating sterility or incompatibility. The genes grb and hla are both autosomal and the present study revealed the nonlinkage between the two genes. Therefore, these two genes are present on different linkage groups.

The results of the crosses between the hairless antenna and ruby eye are given in Table 3. Cross 1 was for establishing pure breed of ruby eye mutant. The F₁ progeny of cross 2 involving the hairless antenna and wild type females were wild type. All the F₁ progeny of cross 3 involving the hairless antenna and ruby eye parents were wild type. Cross 4 involving F₁ progeny being mated inter se did not reveal the normal dihybrid ratio of 9 : 3 : 3 : 1 of the wild type, hairless antenna, ruby eye, double mutant (hairless antenna and ruby eye) among the F₂ male progeny. The actual numbers of males obtained were 52 : 20 : 5 : 5, respectively, for the wild type, hairless antenna, ruby eye, double mutant (hairless antenna and ruby eye). The expected numbers were 46.125 : 15.375 : 15.375 : 5.125. Though the wild type, hairless antenna and double mutant (hairless antenna and ruby eye) occurrence was in the expected ratio, the ruby eye expected ratio varied with observed number. Similarly, the observed female individual ratio of the wild type and ruby eye (97 : 9) also deviated from the expected ratio (79.5 : 26.5). These variations may be due to the suppressive nature of the hla gene over the ru gene. This may be in the heterozygous condition of hla gene and homozygous condition of ru gene (hla/+ ru/ru) individuals. In both deviations, the ruby eye individuals had 1 : 2 ratio of homozygous population (+/+ ru/ru) and heterozygous population (h1a/+ ru/ru). In the present study, observed suppression of gene activity in the progeny of F₂ generation correlates with the expected 5 : 10 (15.375) and 9 : 18 (26.5) of homozygotes: heterozygotes individuals of male and female ruby eye individuals of F₂ progeny, respectively. The progeny of cross 5 were wild type. No larvae hatched out from the eggs of cross 6. For the first time such gene interaction was observed in An. stephensi and no such observations are reported so far in other mosquito species.

Genes were tentatively assigned to the linkage groups based on genetic markers in An. stephensi. A preliminary report suggested that white eye locus was on the X chromosome (linkage group I), brown palpi, beaked proboscis, wart, and reduced antennae on linkage group II, and 4th costal spot on linkage group III [16]. Assignment of red eye (r) to linkage group I, colourless eye (c) to linkage group II, and green larva (g) and greenish brown larva (gb) to linkage group III was tentatively made [17]. Golden-yellow (gy) and black larva (Bl) mutants were linked with a map distance of and assigned to linkage group III [18]. Sequence of the genes, short palpi (sp), diamond palpi (dp), black larva (Bl), and dieldrin resistance (Dl) was shown to be as sp-dp-Bl-Dl and they were assigned to linkage group III [19]. Spotless wings (sl) and 2nd-3rd costal spots fused (2-3f) have been mapped onto linkage group II, approximately 79.5 map units apart [6]. Three new eye colour mutants, scarlet (wsca), red-spotted (prs), and pigmentless (p), were found to be sex-linked (linkage group I) [20].

Larval body and eye colour mutants have been studied in our laboratory in An. stephensi. The eye colour mutants isolated include white (w) [2], ruby (ru) [14], and sienna (si) [21]. Larval body colour mutants include yellow (y) [2], dark (da) [21], brown (b) [22], green (g) [2], greyish brown (grb) [23], grey (gy) [21], greyish black (gyb) [24], and green thorax (gt) [25].

Linkage studies from our laboratory showed that ruby (ru) was nonlinked with greyish brown (grb) [23], dark body colour (da) [2], and green thorax (gt) [25]. Sienna eye (si) was found to be closely linked ( cM) to grb [21]. From the present study, the genes hla and grb were found to be nonlinked and also suppressive nature of hla gene over the ru was observed.

Our allelic studies showed that brown and green larvae (g) [2], grey (gy) and greenish black (gbl) and dark (da), and grey (ge) and greenish black (gbl) belong to allelic series [21, 26].

All these studies indicate that white eye is present on the sex chromosome, and green thorax, greyish brown, dark body, grey body, greenish black body, and sienna eye are present on one autosome (linkage group), while ruby eye is present on the other autosome (linkage group). Yellow, green, brown larva and hairless antennae could be on either of the autosomes (Table 4).

4. Conclusion

For the first time, the hairless antenna (hla) mutant has been established in An. stephensi. The genetic studies of inheritance of hla clearly showed that it was autosomal, recessive, and sex-limited. The gene hla was expressed in males and all the females were normal. The viability of the mutant is good and can be identified very easily from the wild type without the aid of microscope. Hence, the gene hla is also considered to be an excellent marker for An. stephensi. Linkage analysis between hairless antenna and greyish brown larvae revealed that the genes hla and grb are nonlinked and could be present on different autosomes, while the data from the crosses between hla and ru revealed that the mutants segregate in non-Mendelian ratio, indicating that hla prevents the expression of ru in hemizygous condition.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgment

This work was supported by financial assistance from Department of Science and Technology (DST), New Delhi, to Professor N. J. Shetty.

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Copyright

Copyright © 2016 A. Dinesh Madhyastha and N. J. Shetty. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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