Taxonomic revision of species of Haematoloechus Looss, 1899 (Digenea: Plagiorchioidea), with molecular phylogenetic analysis and the description of three new species from Mexico
Abstract:Lung flukes of the genus Haematoloechus Looss, 1899 are common parasites of anurans worldwide, but the taxonomy of the group has been confusing. In this taxonomic revision, 89 species of Haematoloechus (
“…The taxonomic history and species composition of the genus Haematoloechus has been controversial because the reliable characters for species differentiation are difficult to observe and characterize; also, some species are morphologically like H. complexus , and in most of the cases it is very difficult to achieve the species delimitation only based on morphological grounds. Furthermore, the molecular data have corroborated the reliability of some characters for the differentiation of species, such as the length and width suckers’ ratio, shape of ovary and testes, and the distribution of vitellaria and uterus (León Regágnon & Topan, 2018). Haematoloechus complexus has a Nearctic distribution.…”
Section: Discussionmentioning
confidence: 76%
“…The specimens collected from the lungs of L. vaillanti were morphologically very similar to three congeneric species, that is, H. complexus , Haematoloechus caballeroi (Skrjabin & Antipin, 1962) and Haematoloechus veracruzanus León-Règagnon and Topan (2018). Our specimens share some traits with these species, such as the oral/ventral sucker ratio, ovary and testes shape, and the diagonal arrangement of uterine loops.…”
Section: Resultsmentioning
confidence: 85%
“…In the case of Haematoloechus spp., the morphological and molecular evidence unequivocally suggest that specimens of Haematoloechus from Nahá belong to H. complexus ; therefore, this is the first record of H. complexus for Chiapas state, and the second for Mexico since the species was reported in Los Tuxtlas tropical rain forest in Veracruz, a record based on the finding of the metacercariae obtained from the dragonfly Agriogomphus tumens (Velázquez-Urrieta & Pérez-Ponce de León, 2022). Previously, H. complexus had been reported in frogs distributed in Mexico, particularly in Lithobates tlaloci from Xochimilco, Lithobates montezumae from Estado de México, Lithobates forreri from Colima, and Lithobates vaillanti from Veracruz; however, in the study by León-Règagnon & Topan (2018), these authors argued that the species identification was incorrect, and they actually described these specimens as new species, namely H. caballeroi , H. occidentalis and H. veracruzanus , respectively. The taxonomic history and species composition of the genus Haematoloechus has been controversial because the reliable characters for species differentiation are difficult to observe and characterize; also, some species are morphologically like H. complexus , and in most of the cases it is very difficult to achieve the species delimitation only based on morphological grounds.…”
Section: Discussionmentioning
confidence: 99%
“…In Mexico, two species of the genus Langeronia have been previously recorded, namely Langeronia macrocirra Caballero and Bravo-Hollis, 1949, and Langeronia jimenezi Iruegas-Buentello & Salinas-López, 1989. For the genus Haematoloechus , 16 species have been reported, 12 of which are endemic (Pérez-Ponce de León et al , 2000; León-Règagnon, 2010; León-Règagnon & Topan, 2018; Velazquez-Urrieta et al , 2019; Velazquez-Urrieta & Pérez-Ponce de León, 2022). Two of these have been recorded in Chiapas, Haematoloechus floedae Harwood, 1932 and Haematoloechus sp.…”
Mexico possesses a large diversity of amphibians partly due to its complex topography and transitional position between the Nearctic and Neotropical biogeographical regions. However, its helminth parasite fauna has been relatively poorly studied. Specimens of the Vaillant's frog, Lithobates vaillanti (Brocchi) were sampled in the tropical rain forest of Nahá, in the Chiapas Highlands, and examined for parasites. Two trematode species were collected from their hosts; morphologically, specimens were allocated to the genera Langeronia Caballero and Bravo-Hollis, 1949 and Haematoloechus Looss, 1899, respectively. Individuals were sequenced for two molecular markers (the mitochondrial cytochrome c oxidase gene, and the ribosomal gene 28S), and processed for morphological analyses, including scanning electron microscopy. The new evidence was not enough to accomplish the identification at species level of Langeronia sp. due to the lack of sequence data from the type localities of Langeronia parva Christian, 1970 and Langeronia macrocirra Caballero and Bravo-Hollis, 1949. Likewise, the newly generated data were useful to properly identify the adult specimens of lung flukes as Haematoloechus complexus Seely, 1906.
“…The taxonomic history and species composition of the genus Haematoloechus has been controversial because the reliable characters for species differentiation are difficult to observe and characterize; also, some species are morphologically like H. complexus , and in most of the cases it is very difficult to achieve the species delimitation only based on morphological grounds. Furthermore, the molecular data have corroborated the reliability of some characters for the differentiation of species, such as the length and width suckers’ ratio, shape of ovary and testes, and the distribution of vitellaria and uterus (León Regágnon & Topan, 2018). Haematoloechus complexus has a Nearctic distribution.…”
Section: Discussionmentioning
confidence: 76%
“…The specimens collected from the lungs of L. vaillanti were morphologically very similar to three congeneric species, that is, H. complexus , Haematoloechus caballeroi (Skrjabin & Antipin, 1962) and Haematoloechus veracruzanus León-Règagnon and Topan (2018). Our specimens share some traits with these species, such as the oral/ventral sucker ratio, ovary and testes shape, and the diagonal arrangement of uterine loops.…”
Section: Resultsmentioning
confidence: 85%
“…In the case of Haematoloechus spp., the morphological and molecular evidence unequivocally suggest that specimens of Haematoloechus from Nahá belong to H. complexus ; therefore, this is the first record of H. complexus for Chiapas state, and the second for Mexico since the species was reported in Los Tuxtlas tropical rain forest in Veracruz, a record based on the finding of the metacercariae obtained from the dragonfly Agriogomphus tumens (Velázquez-Urrieta & Pérez-Ponce de León, 2022). Previously, H. complexus had been reported in frogs distributed in Mexico, particularly in Lithobates tlaloci from Xochimilco, Lithobates montezumae from Estado de México, Lithobates forreri from Colima, and Lithobates vaillanti from Veracruz; however, in the study by León-Règagnon & Topan (2018), these authors argued that the species identification was incorrect, and they actually described these specimens as new species, namely H. caballeroi , H. occidentalis and H. veracruzanus , respectively. The taxonomic history and species composition of the genus Haematoloechus has been controversial because the reliable characters for species differentiation are difficult to observe and characterize; also, some species are morphologically like H. complexus , and in most of the cases it is very difficult to achieve the species delimitation only based on morphological grounds.…”
Section: Discussionmentioning
confidence: 99%
“…In Mexico, two species of the genus Langeronia have been previously recorded, namely Langeronia macrocirra Caballero and Bravo-Hollis, 1949, and Langeronia jimenezi Iruegas-Buentello & Salinas-López, 1989. For the genus Haematoloechus , 16 species have been reported, 12 of which are endemic (Pérez-Ponce de León et al , 2000; León-Règagnon, 2010; León-Règagnon & Topan, 2018; Velazquez-Urrieta et al , 2019; Velazquez-Urrieta & Pérez-Ponce de León, 2022). Two of these have been recorded in Chiapas, Haematoloechus floedae Harwood, 1932 and Haematoloechus sp.…”
Mexico possesses a large diversity of amphibians partly due to its complex topography and transitional position between the Nearctic and Neotropical biogeographical regions. However, its helminth parasite fauna has been relatively poorly studied. Specimens of the Vaillant's frog, Lithobates vaillanti (Brocchi) were sampled in the tropical rain forest of Nahá, in the Chiapas Highlands, and examined for parasites. Two trematode species were collected from their hosts; morphologically, specimens were allocated to the genera Langeronia Caballero and Bravo-Hollis, 1949 and Haematoloechus Looss, 1899, respectively. Individuals were sequenced for two molecular markers (the mitochondrial cytochrome c oxidase gene, and the ribosomal gene 28S), and processed for morphological analyses, including scanning electron microscopy. The new evidence was not enough to accomplish the identification at species level of Langeronia sp. due to the lack of sequence data from the type localities of Langeronia parva Christian, 1970 and Langeronia macrocirra Caballero and Bravo-Hollis, 1949. Likewise, the newly generated data were useful to properly identify the adult specimens of lung flukes as Haematoloechus complexus Seely, 1906.
“…Our result showed the highest prevalence of trematodes reached by Haematoloechus sp. The species belong to Haematoloechus are known in every continent except Antarctica [11]. More than 50 species of this genus have been described around the world [12].…”
Fejervarya cancrivora is often used as raw material for food and export commodities. In 2014, it was recorded that Karawang Regency was the largest producer of frog’s legs meat in West Java. Research on trematode worms of F. cancrivora from Karawang Regency was conducted to find out the diversity of trematodes worms and its infection patterns. The observation was carried out on 120 frogs. The lungs, stomach, intestine, and caecum were examined for trematodes. The results showed that the F. cancrivora infected by four species of trematodes i.e., Glypthelmins sp., Pleurogenoides sp., Haematoloechus sp., and Diplodiscus sp. with a prevalence of 25.8%, 18.3%, 35.8%, and 23.3%, respectively, and parasite index 1 -25, 1-268, 1-19, and 1-23 individual parasite in each host, respectively.
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