Moniliformis ibunami n. sp., is described from the intestine of the transvolcanic deermouse Peromyscus hylocetes Merriam 1898 (Cricetidae) from Parque Nacional Nevado de Colima "El Floripondio", Jalisco, Mexico. The new species can be distinguished morphologically from the other 18 congeneric species of Moniliformis by a combination of morphological and molecular characters including the number of hooks on the proboscis (12 longitudinal rows, each one with six to eight transversally arranged unrooted hooks), the proboscis length (230-270 μm), the female trunk length (159-186 mm) and egg size (40-70 × 20-40). For molecular distinction, nearly complete sequences of the small subunit (SSU) and large subunit (LSU) of the nuclear ribosomal DNA and cytochrome oxidase subunit 1 (cox 1) of the mitochondrial DNA of the new species were obtained and compared with available sequences downloaded from GenBank. Phylogenetic analyses inferred with the three molecular markers consistently showed that Moniliformis ibunami n. sp. is sister to other congeneric species of Moniliformis. The genetic distance with cox 1 gene among Moniliformis ibunami n. sp., M. saudi, M. cryptosaudi, M. kalahariensis, M. necromysi and M. moniliformis ranged from 20 to 27%. Morphological evidence and high genetic distance, plus the phylogenetic analyses, indicate that acanthocephalans collected from the intestines of transvolcanic deer mice represent a new species which constitutes the seventh species of the genus Moniliformis in the Americas.
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http://dx.doi.org/10.1016/j.parint.2021.102315 | DOI Listing |
Stud Mycol
December 2024
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
is a species-rich and cosmopolitan fungal family including species of plant pathogens, endophytes or saprobes, and parasites of humans and animals. The taxonomy of has recently been revised using a polyphasic approach. However, much remains unknown about the diversity of species and their host associations.
View Article and Find Full Text PDFParasite
November 2024
Parasitology and Mediterranean Ecoepidemiology Research Group, University of the Balearic Islands, 07122 Palma, Spain - CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, C/Monforte de Lemos 3-5, Pabellón 11, Planta 0, 28029 Madrid, Spain.
Parasitology
July 2024
Department of Eco-Epidemiology of Parasitic Diseases, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Miecznikowa 1, 02-096 Warsaw, Poland.
Environ Sci Pollut Res Int
September 2024
Department of Biology, Faculty of Science, Herat University, Herat, Afghanistan.
It is essential to determine the dominant/indicator species and their ecological preferences to develop a comprehensive bioassessment strategy for rivers. The objective of this work was to provide dependable ecological evaluation techniques for ecosystems that experience significant human-induced disruptions, with the Hari Rud River (a transboundary water resource) serving as a case study during the May (wet) and July (dry) periods of 2023. Canonical correspondence analysis revealed that electrical conductivity (EC), dissolved oxygen, ortho-phosphate (P ), and nitrate (N ) had substantial impacts on the spatial distribution of diatom species in the basin.
View Article and Find Full Text PDFAnn Parasitol
July 2024
Brest State University, Boulevard of Cosmonauts 21, 224665 Brest, Belarus.
Shrews and small rodents inhabit the drainage channel banks in reclai med areas and have their own helminth complex. The aim of the study is to conduct the 3rd research period during 2015-2019 the helminth fauna of these animals living on the drainage channel banks of model reclamation systems in Brest Polesie (south-western part of Belarus), to establish the species composition of helminths and the animal infection by these, and to compare the data obtained with previous research periods. 4,000 trap-days were worked out.
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