2021
DOI: 10.1186/s13071-021-04988-9
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Triatoma sordida (Hemiptera, Triatominae) from La Paz, Bolivia: an incipient species or an intraspecific chromosomal polymorphism?

Abstract: Background Triatoma sordida is one of the main Chagas disease vectors in Brazil. In addition to Brazil, this species has already been reported in Bolivia, Argentina, Paraguay, and Uruguay. It is hypothesized that the insects currently identified as T. sordida are a species subcomplex formed by three cytotypes (T. sordida sensu stricto [s.s.], T. sordida La Paz, and T. sordida Argentina). With the recent description of T. rosai from the Argentinean specimens, it became necessary to assess the ta… Show more

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“…The generation of hybrids is relatively common between the species of this subfamily, with the main evolutionary events responsible for the decline of the hybrid lineage (postzygotic barriers) being inviability (offspring mortality before reaching adulthood) [ 8 ], sterility (partially or completely infertile offspring) [ 9 , 10 ] and the collapse of the hybrid (high offspring mortality from the second generation) [ 11 , 12 ]. Several studies involving experimental crosses have already been carried out among the triatomines, focusing mainly on taxonomic [ 8 , 11 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 ] and epidemiological aspects [ 24 , 25 , 26 , 27 ]. On the other hand, although prezygotic barriers are less frequent and, generally, are present in only one direction of the crossings, as observed between Rhodnius colombiensis Mejia, Galvão and Jurberg, 1999 and R. pallescens Barber, 1932 [ 28 ], Triatoma pseudomaculata Corrêa and Espínola, 1964 and T. infestans (Klug, 1834) [ 29 ], T. delpontei Romaña and Abalos, 1947 and T. platensis Neiva, 1913 [ 30 ] and T. longipennis Usinger, 1939 and T. mopan Dorn et al, 2018 [ 17 ], they may be present between species that are very distant from the phylogenetic point of view [ 29 , 31 ] and between species of different genera ( Triatoma Laporte, 1832 × Panstrongylus Berg, 1879, Triatoma × Rhodnius Stål, 1859 and Rhodnius × Psammolestes Bergroth, 1911 [ 18 , 23 , 31 ]).…”
Section: Introductionmentioning
confidence: 99%
“…The generation of hybrids is relatively common between the species of this subfamily, with the main evolutionary events responsible for the decline of the hybrid lineage (postzygotic barriers) being inviability (offspring mortality before reaching adulthood) [ 8 ], sterility (partially or completely infertile offspring) [ 9 , 10 ] and the collapse of the hybrid (high offspring mortality from the second generation) [ 11 , 12 ]. Several studies involving experimental crosses have already been carried out among the triatomines, focusing mainly on taxonomic [ 8 , 11 , 13 , 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 ] and epidemiological aspects [ 24 , 25 , 26 , 27 ]. On the other hand, although prezygotic barriers are less frequent and, generally, are present in only one direction of the crossings, as observed between Rhodnius colombiensis Mejia, Galvão and Jurberg, 1999 and R. pallescens Barber, 1932 [ 28 ], Triatoma pseudomaculata Corrêa and Espínola, 1964 and T. infestans (Klug, 1834) [ 29 ], T. delpontei Romaña and Abalos, 1947 and T. platensis Neiva, 1913 [ 30 ] and T. longipennis Usinger, 1939 and T. mopan Dorn et al, 2018 [ 17 ], they may be present between species that are very distant from the phylogenetic point of view [ 29 , 31 ] and between species of different genera ( Triatoma Laporte, 1832 × Panstrongylus Berg, 1879, Triatoma × Rhodnius Stål, 1859 and Rhodnius × Psammolestes Bergroth, 1911 [ 18 , 23 , 31 ]).…”
Section: Introductionmentioning
confidence: 99%