Multivalvulid myxosporeans of the genera Kudoa Meglitsch, 1947 and Unicapsula Davis, 1924 (Cnidaria: Myxozoa) are often the cause of unsightly cyst formation or postmortem myoliquefaction in the trunk muscle of commercial marine fish, which reduces the market value of infected individuals. Twenty species (18 Kudoa spp. and two Unicapsula spp.) have been recorded from carangid fish, although the majority of them, excluding polyxenous species, such as K. amamiensis Egusa et Nakajima, 1980, K. iwatai Egusa et Shiomitsu, 1983, K. nova Naidenova, 1975, K. quadratum (Thélohan, 1895) and K. yasunagai (Hsieh et Chen, 1984), are limited to a single or a few fish species. We report the occurrence of macroscopic cysts of Kudoa trachuri Matsukane, Sato, Tanaka, Kamata et Sugita-Konishi, 2011 in the trunk muscle of four new host fish species, i.e., Pseudocaranx dentex (Bloch et Schneider), Decapterus akaadsi Abe, D. muroadsi (Temminck et Schlegel) and Decapterus tabl Berry, fished from the Philippine Sea (Northwest Pacific Ocean), off southwestern of Japan. Myxospore morphology and genetic characteristics of the ribosomal RNA gene (rDNA) of these isolates were consistent with previous records of K. trachuri from Trachurus japonicus (Temminck et Schlegel) from around Japan. In addition, a new species of Kudoa that forms long filamentous pseudocysts in trunk myofibres was found in four of the six D. tabl collected in this study. We describe Kudoa longichorda sp. n. for this new isolate, based on its morphology of subquadrate myxospores with four shell valves and polar capsules and with small dimensions (length 4.3-5.5 µm, width 6.0-6.8 µm, thickness 4.8-6.3 µm, polar capsule length 2.3-3.1 µm, polar capsule width 1.1-1.7 µm), as well as 18S and 28S rDNA sequences distinct from those of known species.
Morphological examination of novel specimens of paruterinid cestodes from passerine birds from Brazil and Chile and of museum specimens from Paraguay revealed two new species: Anonchotaenia prolixa sp. n. from Elaenia albiceps chilensis Hellmayr from Chile, and Anonchotaenia vaslata sp. n. from Tyrannus melancholicus (Vieillot) (type host) and Myiodynastes maculatus (Statius Muller) from Paraguay. The generic diagnosis of Anonchotaenia Conn, 1900 is amended, prompted by the presence of the armed cirrus and the elongated cirrus sac of A. prolixa. Two species were redescribed: Anonchotaenia brasiliensis Fuhrmann, 1908 from Tachyphonus coronatus (Vieillot) and Thraupis cyanoptera (Vieillot) (new host records) from Brazil, and Thraupis sayaca (Linnaeus) and Volatinia jacarina (Linnaeus) from Paraguay (new host and geographic records); and Anonchotaenia macrocephala Fuhrmann, 1908 from Tachycineta leucorrhoa (Vieillot) (new host record) from Brazil, Tachycineta meyeni (Cabanis) from Chile (new host and geographic record) and Stelgidopteryx ruficollis (Vieillot) from Paraguay (new host and geographic record). Scanning electron microscopy of A. brasiliensis and A. macrocephala revealed less microthrix variation than has been reported for other cyclophyllidean taxa. Sequence data were generated for nuclear ssr- and lsr-DNA and mitochondrial rrnL and cox1 for A. prolixa, A. brasiliensis, and A. macrocephala. Maximum likelihood and Bayesian inference analyses supported each species as distinct, but revealed cryptic diversity among A. brasiliensis specimens from different host families. New host records of A. brasiliensis and A. macrocephala prompted a formal assessment of host specificity. Anonchotaenia prolixa was found to be oioxenous (HSS = 0), A. vaslata and A. macrocephala were found to be metastenoxenous (HSS = 3.000 and 3.302, respectively), whereas A. brasiliensis was found to be euryxenous (HSS = 5.876). Anonchotaenia brasiliensis has been found parasitising several species of different passerine families that participate in mixed-species foraging flocks in the Atlantic Forest. A diversity of species of other families join these flocks and are among the substantial number of South American passerine species yet to be examined for cestodes.