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Many fields in the biological sciences have witnessed a shift away from organism- or taxon-focused research and teaching in favor of more conceptual and process-driven paradigms. The field of parasitology is no exception, despite the diversity of topics and taxa it encompasses. Concurrently, however, interest in disease ecology has increased dramatically, suggesting new opportunities that merit exploration, as well as the need for parasitology to promote its long history of ecological research to do so. Here we undertake a quantitative analysis of metrics relating to publications, research funding, career opportunities, and undergraduate teaching to comprehensively illustrate the rising prominence of disease ecology. While we distinguish generally between the fields of parasitology and disease ecology, we also emphasize the common interests and complementary approaches that enhanced integration could offer. To illustrate why enhanced integration between these 2 fields is increasingly critical, we highlight 2 successful areas in which parasitology and disease ecology have intersected (community assembly and scale, and the effects of natural enemies on life history traits). We conclude by identifying “frontier topics” that will benefit from greater cooperation and interaction between these currently relatively separate areas and the need for principal investigators to identify and communicate changes in their discipline to students and trainees, which will collectively result in many possible new benefits and prospects for current and future researchers.
River herring populations, including Alosa pseudoharengus and Alosa aestivalis, have significantly declined as a result of anthropogenic factors throughout their range in eastern North America. To better understand the health of the species, parasite surveys were conducted in several New Jersey rivers. A novel myxozoan parasite, Myxobolus mauriensis n. sp., is described infecting the cartilage of pleural ribs in young-of-the-year fish. The parasite forms large polysporic plasmodia forming pseudocysts within the ribs, which extend into the musculature. Pathology associated with infection includes costochondritis, breaks in the rib bones, and deformed bone growth. Rupture of large pseudocysts and release of mature spores are associated with myositis, dermatitis, and peritonitis. Phylogenetic analysis reveals that M. mauriensis n. sp. occurs in a long-branching clade basal to other myxobolids, grouping with several Myxobolus species from marine fish (Myxobolus groenlandicus, Myxobolus aeglefini, and Myxobolus albi). The closest identity is to M. groenlandicus, with 83% identity based on a 1,762-bp sequence of the SSU 18S rDNA. Similarly, spore morphology, tropism for cartilage, and association with marine/brackish environments are shared in these 4 species. Mature spores of M. mauriensis n. sp. are similar to other reported myxobolids, though spores are slightly wider (12.1 ± 0.44 μm) than long (11.4 ± 0.44 μm), with a length:width relationship of 0.94 (±0.04), a feature not commonly described for other species of Myxobolus. Prevalence was studied by histology and fresh observation. In both Blueback Herring and Alewife, the highest infection prevalence occurred in the Maurice River at around 20%, and lower prevalence was found in the Great Egg Harbor River at around 5%. In the Delaware River, prevalence was about 2% in Blueback Herring, while the parasite was not detected in Alewife samples.
In the present study, 90 coprolites from La Cueva de los Muertos Chiquitos (CMC) were subjected to enzyme-linked immunosorbent assay (ELISA) tests for 3 diarrhea-inducing protozoan parasites, Entamoeba histolytica, Giardia duodenalis, and Cryptosporidium parvum, to determine whether these parasites were present among the people who utilized this cave 1,200–1,400 yr ago. These people, the Loma San Gabriel, developed as a culture out of the Archaic Los Caracoles population and lived throughout much of present-day Durango and Zacatecas in Mexico. The Loma San Gabriel persisted through a mixed subsistence strategy of hunting-gathering and agricultural production. The results of ELISA testing were negative for both E. histolytica and G. duodenalis across all coprolites. A total of 66/90 (∼73% prevalence) coprolites tested positive or likely positive for C. parvum. The high prevalence of C. parvum among CMC coprolites contributes to our growing knowledge of the pathoecology among the Loma San Gabriel who utilized CMC. Herein, we report the successful recovery of C. parvum coproantigens from prehistoric coprolites. The recovery of these coproantigens demonstrates the existence of C. parvum in Mesoamerica before European contact in the 1400s.
Because there appeared to be no data available on serum gastrin concentrations in animals infected with Marshallagia marshalli, and considering the high prevalence of this parasite in livestock throughout many countries, we decided to perform research in the field using experimental infection. After surgical implantation of abomasal cannula into 10 male Baluchi sheep, each animal was orally infected with 5,000 M. marshalli larvae. Serum gastrin concentrations and abomasal pH were measured with a human ELISA kit and a PHM LE438 standard pH electrode, respectively. According to the results obtained from the study, serum gastrin increased after 14 and 21 days post-infection (dpi), while abomasal pH increased after 7 dpi and reached a maximal value 16 dpi. The increase in serum gastrin concentration was revealed 6 days after elevation in abomasal pH, which could be the result of reduced acid secretion. Generally, the present study pointed out that a limited number of M. marshalli could increase serum gastrin concentrations.
During a long-term study on biodiversity of bats in the Yungas and Entre Ríos provinces, 1,304 specimens of bats included in the families Noctilionidae, Phyllostomidae, Vespertilionidae, and Molossidae were collected and checked for filarioids. Litomosoides molossiEsslinger, 1973 was recovered from the thoracic and abdominal cavities of Molossus molossus (prevalence [P] = 6.4%); Litomosoides chandleriEsslinger, 1973 from Artibeus planirostris (P = 6.9%), Sturnira oporaphilum (P = 66.6%), Sturnira erythromos (P = 23.8%), Sturnira lilium (P = 7.2%), and Eumops perotis (P = 50%); and Litomosoides saltensis n. sp. was collected from Eptesicus furinalis (P = 1.7%). In this paper, we emend the description of L. molossi; describe a new species, Litomosoides saltensis n. sp., on the basis of 1 female specimen; and report for the first time L. molossi and L. chandleri parasitizing Argentinean bats, expanding the host and locality records. Litomosoides molossi exhibits a slender buccal capsule, with an anterior segment transparent, and the posterior chitinous portion displays 2 thickenings in the first third; possesses 1 dorsal prominent cephalic papilla and 4 labial papillae distributed around the mouth; cuticle with lateral punctuations all along the hypodermic chords in both sexes; and male with area rugosa and tail without cloacal papillae. In L. chandleri, the lateral punctuations are distributed on the posterior extremity of the body in both sexes. Litomosoides saltensis n. sp. displays a thick buccal capsule with a posterior segment well cuticularized, possessing 2 thickenings in the anterior half; 4 labial and 2 ventral cephalic papillae; a globular vulva located anterior to the esophagus–intestine junction; cuticle with lateral punctuations in the posterior extremity of the body; and tail with salient phasmids. We also provide a taxonomic key for the identification of the Litomosoides sp. of bat dwelling. Long-term studies and large sample sizes are needed to detect the presence of Litomosoides sp. in bats, in contrast to the findings in cricetid rodents, which seem to be more frequently collected.
Baracktrema obamai n. gen., n. sp. infects the lung of geoemydid turtles (black marsh turtle, Siebenrockiella crassicollis [type host] and southeast Asian box turtle, Cuora amboinensis) in the Malaysian states of Perak, Perlis, and Selangor. Baracktrema and UnicaecumStunkard, 1925 are the only accepted turtle blood fluke genera having the combination of a single cecum, single testis, oviducal seminal receptacle, and uterine pouch. Baracktrema differs from Unicaecum by having a thread-like body approximately 30−50× longer than wide and post-cecal terminal genitalia. Unicaecum has a body approximately 8−12× longer than wide and terminal genitalia that are anterior to the distal end of the cecum. The new genus further differs from all other accepted turtle blood fluke genera by having a cecum that is highly convoluted for its entire length, a spindle-shaped ovary between the cirrus sac and testis, a uterine pouch that loops around the primary vitelline collecting duct, a Laurer's canal, and a dorsal common genital pore. Phylogenetic analysis of the D1–D3 domains of the nuclear large subunit ribosomal DNA (28S) revealed, with high nodal support and as predicted by morphology, that Baracktrema and Unicaecum share a recent common ancestor and form a clade sister to the freshwater turtle blood flukes of Spirorchis, paraphyletic Spirhapalum, and Vasotrema and that, collectively, these flukes were sister to all other tetrapod blood flukes (HapalorhynchusGriphobilharzia plus the marine turtle blood flukes and schistosomes). Pending a forthcoming emended morphological diagnosis of the family, the clade including Spirorchis spp., paraphyletic Spirhapalum, Vasotrema, Baracktrema, and Unicaecum is a likely placeholder for “Spirorchiidae Stunkard, 1921” (type genus SpirorchisMacCallum, 1918; type species Spirorchis innominatusWard, 1921). The present study comprises the 17th blood fluke known to infect geoemydid turtles and the first proposal of a new genus of turtle blood fluke in 21 yr.
Parasitism, driven by anthropogenic habitat modifications, is being increasingly recognized as a major threat to wildlife. Unfortunately, even baseline parasite data for most wildlife species are lacking in India, including the civets, which are particularly vulnerable due to their proximity to human habitations. Civet fecal samples were collected from 10 forest fragments that vary in size and disturbance level in Anamalai Hills, Western Ghats, India. These samples were screened for the presence of gastrointestinal parasites using fecal floatation and fecal sedimentation techniques. From a total of 180 civet fecal samples, 15 gastrointestinal parasite taxa were recovered, and these species are also known to infect domesticated animals. Additionally, small, disturbed forest fragments recorded higher mean gastrointestinal parasite taxa and greater prevalence when compared to large, undisturbed forest fragments, indicating a potential relationship between anthropogenic activities and gastrointestinal parasitism of civets in the Anamalai Hills.
Infidum similisTravassos, 1916 (Dicrocoeliidae: Leipertrematinae) was found in the gall bladder of Leptophis diplotropis Günther, 1872 from El Podrido, Acapulco, Guerrero, Mexico. A phylogenetic analysis based on partial sequences of the 28S ribosomal RNA using maximum likelihood (ML) and Bayesian inference (BI) analyses was carried out to assess its phylogenetic position within suborder Xiphidiata, alongside members of the superfamilies Gorgoderoidea and Plagiorchoidea. The phylogenetic trees showed that the genus is most-closely related to the Plagiorchoidea rather than to the Gorgoderoidea, in keeping with previous taxonomic designations. Phylogenies obtained from ML and BI analysis of the 28S rDNA gene revealed a well supported clade in which Choledocystus hepaticus (Lutz, 1928) Sullivan, 1977 is sister to I. similis. On the other hand, a tree obtained using a partial sequence of the cytochrome c oxidase subunit 1 (cox1) mtDNA gene (ML and BI analysis), with species supposed to be closely related to I. similis according to 28S, does not support this relatedness. Based on the independence of Infidum from the subfamily Leipertrematinae Yamaguti, 1958, our results clearly demonstrated that the genus corresponds to a different family and with species closely related to C. hepaticus within Plagiorchoidea. New data are presented about the tegumental surface of I. similis by scanning electron microscopy as well as the estimation of its haploid genome size using Feulgen Image Analysis Densitometry of sperm nuclei as part of the characterization of this species. This is the first genome size estimated for a member of Plagiorchiida, and these data will provide a new source of knowledge on helminth diversity and evolutionary studies. This constitutes the first host record, and new geographical distribution, for this species in Mexico.
Hemogregarines are the most-commonly reported hemoparasites in reptiles. In this work we analyzed samples from 572 individuals of 6 species of the wall gecko genus Tarentola from European and African countries adjacent to the Mediterranean Sea as well as from the Macaronesian islands. Screening was done using hemogregarine-specific primers for the 18S rRNA gene. Positive amplifications were sequenced so that the diversity of the hemogregarines from these hosts could be assessed within a phylogenetic framework. The results from the phylogenetic analysis showed that within Tarentola, the detected parasites are comprised of at least 4 distinct main lineages of Hepatozoon spp. In clades A and B, the new sequences clustered closely together with the ones previously known from individuals of the genus Tarentola and other species of geckos but also with those from other vertebrate host groups including skinks, snakes, iguanids, and rodents. Clade C included a sample from Tarentola angustimentalis of the Canary Islands. This sequence is the first molecular characterization of these hemogregarines in this archipelago. Until now, this lineage had only been found in lacertids, skinks, and snakes, so this infection extends the host range for this clade. Lastly, in the newly detected clade D, the retrieved parasite sequences form a group currently identified as exclusive of geckos. Our results show that geckos of Tarentola spp. harbor a great diversity of hemogregarines but also that further sampling and other tools, including a multi-locus approach using faster-evolving genetic markers, and identification of definitive hosts are needed to better understand the biology, diversity, and distribution of these parasites.
Almost nothing is known about the questing and dispersal behavior of immature Gulf Coast ticks (Amblyomma maculatum), a vector of both medical and veterinary concern. This experiment examined host-seeking (questing) and dispersal of marked, previously colonized, nymphal A. maculatum released in field plots in rural Oktibbeha County, Mississippi during 2015. A total of 500 (250 per replication) A. maculatum nymphs were painted and released in 5 plots (50 ticks each time). Observations were then made 5 times, approximately every 3 days, searching the plots for ticks from the release points outwards to 50 cm. Mean overall vertical questing height of ticks in Replication 1 in March (5.13 cm) was significantly higher than that of Replication 2 in April (2.57 cm) for a combined mean questing height of 3.58 cm. Ticks dispersed at a mean rate of 1.71 cm/day (Replication 1) and 0.98 cm/day (Replication 2), for an overall mean dispersal rate of 1.27 cm/day. When observation days where tick movement was impacted by adverse weather conditions were excluded, means between the replications were much closer. Only 38 of 2,500 possible total observations (1.5%) of the marked ticks were subsequently seen questing in this study, perhaps mirroring low questing rates of nymphal A. maculatum in nature. Additionally, 2 ticks were found in dense vegetation at the base of a plant. These data show that nymphs of this species disperse slowly, quest low to the ground, and can hide in very dense vegetation.
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