Microscopic Identification and Determination of Total Flavonoid Content of Moringa Leaves Extract and Ethyl Acetate Fraction (Moringa oleifera L.)

This research was conducted to identify simplicia microscopically, phytochemical screening and determination of total flavonoid content of extract and ethyl acetate fraction from Moringa (Moringa oleifera L.) leaves using UV-Visible Spectrophotometry method. The experimental design used in this study was to perform microscopic identification of Moringa leaf powder simplicia, make 96% and 70% ethanol extract and ethyl acetate fraction of Moringa leaves from 70% ethanol extract, then carry out phytochemical screening and determination of total flavonoid content with quercetin standards. Phytochemical screening on the ethyl acetate fraction of Moringa leaves included tests for the content of flavonoids, saponins, tannins and alkaloids. The results of microscopic identification of Moringa leaf simplicia showed the presence of calcium oxalate crystals in the form of rosettes, mesophyll and stomata. The result of determination of total flavonoid content in 96% ethanol extract was 16.69 ± 0.74% (w/w), 70% ethanol extract was 10.84 ± 0.49% (w/w), Moringa leaf ethyl acetate fraction 14 .45 ± 0.90% (w/w). The highest total flavonoid content was found in the 96% ethanol extract of Moringa leaves in accordance with the 2017 Indonesian Herbal Pharmacopoeia, that the thick extract of Moringa leaves containing no less than 6.30% (w/w) total flavonoids was calculated as quercetin.

Materials and methods.

Large numbers of dacine specimens were collected throughout Papua New Guinea by trapping and host fruit sampling. Steinertype fruit fly traps, baited with cue lure, methyl eugenol or vanillylacetone (zingerone), were set in many localities over a wide range of ecosystems. In most cases, the traps were serviced on 2-week cycles for at least 1 year. Samples of rainforest and cultivated fruits were collected in some provinces. All specimens collected were preserved in a dry state and sent to R.A.I. Drew at Griffith University, Brisbane, Australia, for microscopic identification and curation. Data and photographs of Bactrocera longicornis were received from the Museum Nationale d'Histoire Naturelle, Paris, France. The subgeneric classification used herein follows Drew and Hancock (2016) and Hancock and Drew (2006, 2015, 2016, 2017a,b,c,d,e, 2018a,b,c, 2019).

Practical guide for microscopic identification of infectious gastrointestinal nematode larvae in sheep from Sardinia, Italy, backed by molecular analysis

Background Gastrointestinal nematodes (GIN) are ubiquitous in small ruminant farming, representing a major health and production concern. Given their differences in pathogenicity and the current problems regarding anthelmintic resistance, specific diagnosis of GIN is of significant importance. At present, the most widely applied method for this entails culture and microscopic analysis of third-stage larvae, allowing for identification at least to the genus level. Overall, a variety of keys for microscopic analysis have been published, showing substantial variation. Given this fact, this study aimed to produce a practical and updated guide for the identification of infective ovine GIN larvae. Methods Using existing keys and protocols, a total of 173larvae of the most common species/genera of ovine GIN from pooled faecal samples from Sardinia (Italy) were identified and extracted, and further individual molecular identification was performed. Morphometric and morphological data as well as high-quality photographs were collected and combined to produce the final guide. Results GIN microscopically and molecularly identified during this research include Trichostrongylus spp., Teladorsagia circumcincta, Haemonchus contortus, Cooperia curticei, and Chabertia ovina. Based on microscopic analysis, 73.5% of the larvae were correctly identified. Based on sheathed tail length, 91.8% were correctly classified into their respective preliminary groups. Conclusions It is crucial for the microscopic identification of infectious GIN larvae to examine each larva in its entirety and thus to take multiple characteristics into account to obtain an accurate diagnosis. However, a preliminary classification based on sheathed tail length (resulting in three groups: A, short; B, medium; C, long) was found to be effective. Further identification within group A can be achieved based on the presence of a cranial inflexion, caudal tubercles and full body measurements (Trichostrongylus spp. < 720 µm, T. circumcincta ≥ 720 µm). Larvae within group B can be differentiated based on sheathed tail morphometry (H. contortus > 65 µm, C. curticei ≤ 65 µm), the presence of cranial refractile bodies, total body length measurements (H. contortus ≤ 790 µm, C. curticei > 790 µm) and shape of the cranial extremity. Finally, all characteristics proposed for the differentiation between Oesophagostomum spp. and C. ovina larvae (group C) were found to have considerable restrictions. Graphical abstract

Isolation Of Dermatophytes From Infected Stray Cats In Selangor

Background: Dermatophytosis is the most prevalent fungal infection found in cats and one of the most serious infectious skin diseases that affect this species. Dermatophytosis can be endemic in cats, particularly in poor environments, and it is difficult to eradicate in such cases. Purpose: The aim of this research was to determine the macroscopic and microscopic identification of various types of dermatophytes present in stray cats. Methods: The research was designed as a laboratory-based study. The sample was determined through physical examination of stray cats infected with fungi and was selected based on the infection site (nail, hair, and skin) of infected cats. A total of 125 samples were collected from infected stray cats through skin scraping, haircutting, and nail clipping. The collected samples were then cultured in Sabouraud Dextrose Agar (SDA) medium and incubated for two weeks at 26°C. Following incubation, fungi were stained using Lacto-phenol Cotton Blue (LPCB) for microscopic identification. Results: The identification showed that Trichophyton spp. is the most common isolated fungal species on the hair, nails, and skin of stray cats. This is followed by Aspergillus spp. and Microsporum spp. The least common dermatophytes include Curvularia spp., Absidia spp., Epidermophyton spp., Neosytallidium spp., Alternaria spp., Scopulariopsis spp., Mucor spp., and Penicillium spp. Conclusion: The research focussed exclusively on stray cats with clinical evidence of mycotic lesions and confirmed the role of stray cats in transmitting dermatophytosis through their hair, nails, and skin. The prevalence of dermatophytes on stray cats was identified in the Selangor region.

Diversity of Filamentous Molds Producing Mycotoxins in Rice Called "Deni Kachia" Sold on the Markets of Daloa (Côte d’Ivoire)

Filamentous fungi are frequent contaminants of many plant substrates and certain animal products. Their presence can improve the organoleptic quality of the product or alter it and lead to the accumulation of toxic secondary metabolites, such as mycotoxins. The objective of this work is to characterize the filamentous fungi isolated from the rice "deni kachia" stored and sold on public markets in the city of Daloa. A count and isolation of filamentous fungi, followed by macroscopic and microscopic identification was carried out. Several genera of filamentous fungi was identified. These are the genera Aspergillus, Penicillium and others. The different species of molds identified by conventional biochemical techniques were confirmed by the API 50 CH freezer.The genera Aspergillus and Penicillium are the most predominant in the samples analyzed. The presence of these species with their ability to produce mycotoxins suggests that contaminated rice poses a risk to the health of consumers.

Snapshot picture of microplastic pollution in Halifax Regional Municipality

Microplastic pollution is a pervasive problem. Many species have been found to ingest microplastics and this poses a risk to biodiversity (Fauna and Flora International, 2013). In Nova Scotia, there are few quantitative data on microplastic pollution. As quantifying microplastic pollution has only recently attained attention in Nova Scotia, no standardized methods for collection and analysis have been established. This project, although limited in scope, identified and quantified microplastic pollution on McNabs Island and Lake Banook beaches using established sampling and processing methods. The samples were evaluated using a combination of density separation, microscopic identification and RamanTM spectroscopy. This provided information to compare with other research. Keywords: Biodiversity, Microplastic Filtration SystemTM, Microplastic pollution, Nova Scotia

Potential Analysis Of Toxoplasmosis Distribution In Wild Cats (Felis silvestris) In Some Markets Of Sidoarjo District Through Microscopic Identification Of Toxoplasma gondii

There are many diseases caused by parasitic infection, one of them is toxoplasmosis which is a zoonotic disease. This study was to determine the potential spread of wild cat toxoplasmosis in several markets. The sample used in this study were 24 stray cats taken from the Larangan market, Suko market and Sukodono market in Sidorajo district, using a method of determining the size of the sample based on incidental sampling. Sample were examined using the floating method.The prevalence result obtained from Larangan market (37,5%), Suko market (37,5%) and Sukodono market (12,5%). Prevalence result in Larangan market and Suko market greater than in Sukodono market, this is due to environmental factors in Sukodono market cleaner and better sanitation. Human can become infected with oocyst if they consume food or inhale particle contaminated with T.gondii parasites. High number of cat with oocyst T.gondii can be caused by a dirty environment.