Fumigant toxicity of essential oils against Sitophilus zeamais (Motschulsky) (Coleoptera: Curculionidae): a systematic review and meta-analysis

Our aim was to perform a qualitative review and a meta-analysis with 57 scientific articles (108 assays) published from 1 January 2000 to 31 June 2021 dealing with fumigant toxicity of essential oils (EOs) against Sitophilus zeamais. The studies were obtained from four electronic databases: Web of Science, SCOPUS, PubMed, and Google Scholar. The survey comprised 107 plant species belonging to 26 different families. Lethal concentration values (LC₅₀) of EOs were included in a random-effect model, and two subgroups were defined: “until 24 h” and “more than 24 h”. The EOs more frequently evaluated were those belonging to Lamiaceae (20.18%), Asteraceae (17.43%), Apiaceae (9.17%), and Rutaceae (6.42%). The global mean value was 21.37 (CI₉₅ 16.84–27.12), while the summary mean values of the subgroups were 41.45 (CI₉₅ 31.10–55.26) for “until 24 h” and 8.45 (CI₉₅ 5.72–12.48) for “more than 24 h”. Most species belonging to Apiaceae, Lamiaceae, Asteraceae, and Schisandraceae reported the highest insecticidal effects with mean values that ranged from 1.31 to 27.39 for “until 24 h” and from 0.57 to 5.31 for “more than 24 h”. Additionally, the toxicity of the most effective EOs was discussed by addressing their chemical composition and their major pure compounds chemical features.

     

Comparison between haplotype-based and individual snp-based genomic predictions for beef fatty acid profile in Nelore cattle

The aim of this study was to evaluate the genomic predictions using the single-step genomic best linear unbiased predictor (ssGBLUP) method based on SNPs and haplotype markers associated with beef fatty acids (FAs) profile in Nelore cattle. The data set contained records from 963 Nelore bulls finished in feedlot (±90 days) and slaughtered with approximately 24 months of age. Meat samples from the Longissimus dorsi muscle were taken for FAs profile measurement. FAs were quantified by gas chromatography using a SP-2560 capillary column. Animals were genotyped with the high-density SNP panel (BovineHD BeadChip assay) containing 777,962 markers. SNPs with a minor allele frequency and a call rate lower than 0.05 and 0.90, respectively, monomorphic, located on sex chromosomes, and with unknown position were removed from the data set. After genomic quality control, a total of 469,981 SNPs and 892 samples were available for subsequent analyses. Missing genotypes were imputed and phased using the FImpute software. Haplotype blocks were defined based on linkage disequilibrium using the Haploview software. The model to estimate variance components and genetic parameters and to predict the genomic values included the random genetic additive effects, fixed effects of the contemporary group and the age at slaughter as a linear covariate. Accuracies using the haplotype-based approach ranged from 0.07 to 0.31, and those SNP-based ranged from 0.06 to 0.33. Regression coefficients ranged from 0.07 to 0.74 and from 0.08 to 1.45 using the haplotype- and SNP-based approaches, respectively. Despite the low to moderate accuracies for the genomic values, it is possible to obtain genetic progress trough selection using genomic information based either on SNPs or haplotype markers. The SNP-based approach allows less biased genomic evaluations, and it is more feasible when taking into account the computational and operational cost underlying the haplotypes inference.     

Conservation planning under climate change: Toward accounting for uncertainty in predicted species distributions to increase confidence in conservation investments in space and time

Climate warming challenges our approach to building systems of protected areas because it is likely to drive accelerating shifts in species distributions, and the projections of those future species distributions are uncertain. There are several important sources of uncertainty intrinsic to using species occurrence projections for reserve system design including uncertainty in the number of occurrences captured by any reserve selection solution, and uncertainty arising from the different approaches used to fit predictive models. Here we used the present and future predicted distributions of Iberian herptiles to analyze how dynamics and uncertainty in species distributions may affect decisions about resource allocation for conservation in space and time. We identified priority areas maximizing coverage of current and future (2020 and 2080) predicted distributions of 65 species, under “Mild” and “Severe” uncertainty. Next, we applied a return-on-investment analysis to quantify and make explicit trade-offs between investing in areas selected when optimizing for different times and with different uncertainty levels. Areas identified as important for conservation in every time frame and uncertainty level were the ones considered to be robust climate adaptation investments, and included chiefly already protected areas. Areas identified only under “Mild” uncertainty were considered good candidates for investment if extra resources are available and were mainly located in northern Iberia. However, areas selected only in the “Severe” uncertainty case should not be completely disregarded as they may become climatic refugia for some species. Our study provides an objective methodology to deliver “no regrets” conservation investments.     

Moment of addition of LH to the culture medium improves in vitro survival and development of secondary goat pre-antral follicles

The present study investigated the effects of time of addition of luteinizing hormone (LH) to culture medium on the in vitro development of caprine pre-antral follicles. Pre-antral follicles (≥ 150 μm) were isolated from fragments of the goat ovarian cortex and individually cultured for 18 days in the absence (control) or presence of 100 ng/ml LH, added on days 0, 6 or 12 of culture. Follicular development was assessed based on antral cavity formation, increased follicular diameter as well as follicular and fully grown oocyte (>110 μm) viability. The results showed that after 18 days of culture, the percentage of surviving follicles in the control treatment was significantly lower when compared to other treatments (p < 0.05). There were no significant differences in antrum formation, follicular diameter and oocyte viability. The addition of LH at D6 of culture significantly increased the rates of oocytes ≥ 110 μm and the resumption of meiosis (p < 0.05). In contrast, when LH was added at the onset of culture, only germinal vesicle oocytes were obtained. In conclusion, the moment of addition of LH to the culture medium affects the performance of in vitro culture of caprine pre-antral follicles. The addition of LH to the medium from day 6 of culture onward improved the rates of follicular survival, as well as the ability of oocytes to resume meiosis. However, prolonged exposure to LH (addition at the onset of culture onward) showed detrimental effects for the meiotic resumption.     

Genotyping of Cryptosporidium spp. from free-living wild birds from Brazil

In wild and domestic birds, cryptosporidiosis is often associated with infections by Cryptosporidium galli, Cryptosporidium baileyi and Cryptosporidium meleagridis. In addition to these species, a number of avian Cryptosporidium species yet to be fully characterized are commonly found among exotic and wild avian isolates. The present study aimed to detect and identify samples of Cryptosporidium spp. from free-living wild birds, in order to contribute to the knowledge of the variability of this parasite in the free-living population of Brazil. Stool samples were collected from 242 birds, with the following proportions of individuals: 50 Emberizidae (20.7%), 112 Psittacidae (46.3%), 44 Cardinalidae (18.2%), 12 Turdidae (5.0%), eight Ramphastidae (3.3%), seven Icteridae (2.9%), three Estrilididae (1.2%), two Contigidae (0.8%), two Thraupidae (0.8%) and two Fringilidae (0.8%). Among the 242 fecal samples from wild birds, 16 (6.6%) were positive for the presence of oocysts of Cryptosporidium. Molecular characterization of the 16 samples of Cryptosporidium, were performed with phylogenetic reconstructions employing 292 positions of 18S rDNA. None of the samples of birds was characterized as C. meleagridis. C. galli was identified in one rufous-bellied thrush (Turdus rufiventris), five green-winged saltators (Saltator similis), one slate-coloured seedeater (Sporophila schistacea), one goldfinch (Carduelis carduelis) and three saffron finches (Sicalis flaveola). One goldfinch isolate, one buffy-fronted seedeater (Sporophila frontalis), one red-cowled cardinal (Paroaria dominicana) and one other saffron finch (S. flaveola) were identified as C. baileyi. Avian genotype II was found in an isolate from a white-eyed parakeet (Aratinga leucophthalma). Clinical symptoms of cryptosporidiosis in birds have already been described and the number of wild birds which were shedding parasites was high. Therefore, further epidemiological research and disease surveillance of birds in the wild is warranted.     

Efficacy of an inactivated,recombinant bovine herpesvirus type 5 (BoHV-5) vaccine

Bovine herpesvirus type 5 (BoHV-5) is the causative agent of bovine herpetic encephalitis. In countries where BoHV-5 is prevalent, attempts to vaccinate cattle to prevent clinical signs from BoHV-5-induced disease have relied essentially on vaccination with BoHV-1 vaccines. However, such practice has been shown not to confer full protection to BoHV-5 challenge. In the present study, an inactivated, oil adjuvanted vaccine prepared with a recombinant BoHV-5 from which the genes coding for glycoprotein I (gI), glycoprotein E (gE) and membrane protein US9 were deleted (BoHV-5 gI/gE/US9⁻), was evaluated in cattle in a vaccination/challenge experiment. The vaccine was prepared from a virus suspension containing a pre-inactivation antigenic mass equivalent to 10^7.69 TCID₅₀/dose. Three mL of the inactivated vaccine were administered subcutaneously to eight calves serologically negative for BoHV-5 (vaccinated group). Four other calves were mock-vaccinated with an equivalent preparation without viral antigens (control group). Both groups were boostered 28 days later. Neither clinical signs of disease nor adverse effects were observed during or after vaccination. A specific serological response, revealed by the development of neutralizing antibodies, was detected in all vaccinated animals after the first dose of vaccine, whereas control animals remained seronegative. Calves were subsequently challenged on day 77 post-vaccination (pv) with 10^9.25 TCID₅₀ of the wild-type BoHV-5 (parental strain EVI 88/95). After challenge, vaccinated cattle displayed mild signs of respiratory disease, whereas the control group developed respiratory disease and severe encephalitis, which led to culling of 2/4 calves. Searches for viral DNA in the central nervous system (CNS) of vaccinated calves indicated that wild-type BoHV-5 did not replicate, whereas in CNS tissues of calves on the control group, viral DNA was widely distributed. BoHV-5 shedding in nasal secretions was significantly lower in vaccinated calves than in the control group on days 2, 3, 4 and 6 post-challenge (pc). In addition, the duration of virus shedding was significantly shorter in the vaccinated (7 days) than in controls (12 days). Attempts to reactivate latent infection by administration of dexamethasone at 147 days pv led to recrudescence of mild signs of respiratory disease in both vaccinated and control groups. Infectious virus shedding in nasal secretions was detected at reactivation and was significantly lower in vaccinated cattle than in controls on days 11–13 post-reactivation (pr). It is concluded that the inactivated vaccine prepared with the BoHV-5 gI/gE/US9⁻ recombinant was capable of conferring protection to encephalitis when vaccinated cattle were challenged with a large infectious dose of the parental wild type BoHV-5. However, it did not avoid the establishment of latency nor impeded dexamethasone-induced reactivation of the virus, despite a significant reduction in virus shedding after challenge and at reactivation on vaccinated calves.     

Effect of Dietary Protein Level on Apparent Heat Increment and Post-Prandial Nitrogen Excretion of Penaeus setiferus, P. schmitti, P. duorarum, and P. notialis Postlarvae

The calorigenic effect of feeding (apparent heat increment, AHI) and post-prandial nitrogen excretion (PPNE) were measured in postlarval (PL 25–30) Penaeus setiferus, P. schmitti, P. duorarum and P. notialis fed a fixed ration of 3 mg/animal using purified diets with 40, 50, 60, or 65% protein. Both AHI and PPNE increased with increasing dietary protein. The contribution of PPNE to AHI varied from 6.1 to 94%, with lesser values for P. setiferus and greater ones for P. duorarum . Also, the AHI coefficient (percentage of ingested energy) increased with increasing dietary protein. The AHI and PPNE coefficients for the four shrimp species ranged from 0.3 to 6.5% and 0.02 to 5.04% of ingested energy, respectively. These results suggest close relationships among protein requirements, the capacity to use dietary proteins as a source of energy, and adaptation by different species to different types of food. The amount of energy used for production of ammonia is proposed as an adequate measure of the part played by dietary proteins in food cost.     

Chitosan as a biocontrol agent against the pinewood nematode (Bursaphelenchus xylophilus)

The pine wilt disease (PWD) is caused by Bursaphelenchus xylophilus and poses great environmental and economic challenges. Thus, the development of sustainable techniques for the control of this epidemic disease is of major importance. This work aimed at evaluating if the application of different molecular weight (MW) chitosans as a soil amendment could be used to control the PWD in maritime pine (Pinus pinaster, very susceptible to the disease) and stone pine (Pinus pinea, less susceptible). At the end of the experimental period (24 days after inoculation), P. pinaster and P. pinea untreated plants presented ca. 3825 ± 100 and 70 ± 47 nematodes, respectively. In P. pinaster, the high‐MW chitosan prompted the most drastic results, inducing a 21.9‐fold reduction in nematodes numbers, whereas in P. pinea, the most effective was the low MW chitosan, which reduced nematodes numbers up to 7‐fold, compared with untreated plants. P. pinea seems to be highly resistant to the disease, presenting nematode numbers up to 54.6‐fold lower than P. pinaster and less severe chlorophyll loss (ca. 2‐fold).     

Diagnostics of the peach root-knot nematode,Meloidogyne floridensis using multiplex real-time PCR

European Journal of Plant Pathology - The peach root-knot nematode, Meloidogyne floridensis is an emerging pest of peach and other crops that is currently known to occur only in California,...