Spores Research Articles

Insight into the nuclear distribution patterns of conidia and the asexual life cycle of Polyporus umbellatus

P. umbellatus sclerotium is a traditional Chinese medicine that is widely utilized in China, Korea, Japan, and other countries due to its diverse medicinal activities, such as diuretic, antitumor, anticancer, and immune system enhancement effects. Conidia, which are common asexual spores in various fungi, are not universally present in Polyporus species. In this study, the asexual life cycle of P. umbellatus was elucidated. Conidia, i.e. arthorconidia, were produced by both dikaryotic and monokaryotic strains. In the dikaryotic strain, binucleate, uninucleate, and nuclei-free conidia were identified with proportions of 67.9 %, 12.4 %, and 19.7 %, respectively. Conversely, the monokaryotic strain did not produce binucleate conidia. This discrepancy suggests that binucleate spores are heterokaryons, while uninucleate spores are homokaryons. Clamp connections were observed in dikaryotic hyphae, but were absent in monokaryotic hyphae. Monokaryotic strains were obtained from conidia of the dikaryotic strain. Additionally, mating types were determined through pairing tests, and successful crossbreeding occurred between monokaryotic strains derived from conidia and basidiospores from different strains. This study introduced the first crossbreeding strategy for P. umbellatus.

Study on the chemical composition and anti-fungi activities of anthraquinones and its glycosides from Rumex japonicus Houtt.

Fungi, such as Trichophyton rubrum (T. rubrum) and Microsporum canis Bodin Anamorph (M. canis Bodin Anamorph) are the main pathogens of dermatophysis. According to ancient books records, Rumex japonicus Houtt. (RJH) has a miraculous effect on the treatment of dermatophysis. To reveal the anti-fungi (T. rubrum and M. canis Bodin Anamorph) components and its mechanism of the Rumex japonicus Houtt. The vinegar extraction and alcohol precipitation, HPLC and nuclear magnetic resonance spectroscopy (NMR) were employed for analyzing the chemical compositions of RJH; in vitro anti-fungal experiment was investigated including test the minimum inhibitory concentration (MIC) and the minimum fungicidal concentration (MFC), spore germination rate, nucleic acid, protein leakage rate, biofilm structure, and the mechanism of anti-fungal and anti-fungal biofilms in RJH. Seven anthraquinones and their glycoside compounds were obtained in this study respectively, such as chrysophanol, physcion, aloe-emodin, emodin, rhein, emodin-8-O-β-D-glucoside and chrysophanol-8-O-β-D-glucoside. In vitro anti-fungal experiment results showed that RJH extracts have good anti-fungal activity for dermatophytic fungi. Among them, the MIC of the rhein, emodin and aloe-emodin against T. rubrum are 1.9µg/ml, 3.9µg/ml and 15.6µg/ml, respectively; the MIC of emodin and aloe-emodin against M. canis Bodin Anamorph are 7.8µg/ml and 62.5µg/ml, respectively. In addition, its active components can inhibit fungal spore germination and the formation of bud tube, change cell membrane permeability, prevent hyphal growth, destroy biofilm structure, and down-regulate the expression of agglutinin-like sequence family 1 of the adhesion phase of biofilm growth. The study shows that RJH play a fungicidal role.

Application of algal-mycelial pellets in the treatment of the mariculture wastewater

Hypersaline mariculture wastewater necessitates treatment prior to its discharge into marine environments. Algal-mycelial pellets (AMPs), known for their cost-effectiveness, energy efficiency and sustainability, have not been previously explored for their flocculation and pollutant removal capabilities in hyperhaline conditions. This work employed an orthogonal test design to investigate the effects of nine factors at three levels on the treatment efficiency of mariculture wastewater using Chlorella sp. TNBR1 and Aspergillus niger AMPs. The comprehensive optimal conditions for achieving the highest flocculation efficiency and pollutant removal are determined to be a temperature of 30 °C, light intensity of 6000 lux, a 12:0 light-dark cycle, an initial pH of 6, a microalgal density of 11.25 × 106 cell/mL, microalgal growth phase at the early logarithmic stage, a fungal spore density of 9.00 × 105 spore/mL and a fungal pellet phase of 60 h. Under such conditions, the treatment of nonsterile actual mariculture wastewater with Chlorella sp. TNBR1 and Aspergillus niger AMPs results in a 93.35 %±7.20 % reduction in chemical oxygen demand (COD), 92.83 %±7.29 % reduction in total nitrogen (TN), 100 % removal of total phosphorus (TP), and a flocculation efficiency of 69.21 %±5.36 %. These findings confirm that AMPs are a viable solution for effectively treating COD, TN and TP in real hypersaline mariculture wastewater, while also facilitating the flocculation and harvesting of microalgae.

A Preliminary Survey of Airborne Fungal Spores of Vittaleshwar Temples at Sironcha (M.S.)

A Preliminary Survey of Airborne Fungal Spores of Vittaleshwar Temples at Sironcha (M.S.)

Fungal spore air pollution in selected environments in Nairobi, Kenya

ABSTRACT Fungal spores constitute major bioaerosols and are important indicators of bio-pollution. The rural–urban migration has increased human activity, causing air pollution concerns globally. This study explored the seasonal load, distribution, and diversity of fungal spores at different strategic sites in Nairobi, Kenya. The fungal air spores were systematically collected from markets, roads, and recreational, and dumping sites within Nairobi City County. Briefly, Sabouraud Dextrose Agar (SDA) plates were exposed on site for 5 minutes, and transported for incubation at 28°C for 7 days. Temperature, humidity, and wind speed data were recorded using the AccuWeather mobile app. Fungal cultures were identified using standard macro and micro-phenotypic features. The relationship between the fungal concentration and meteorological parameters was analyzed using multiple regression and PNiger. The wet season had the highest number of fungal spores (5318.88 CFU m− 3) compared to the dry season (1929.58 CFU m− 3.) We identified 502 isolates across two seasons; 16 genera and 38 species comprising Ascomycota 426 (89.31%), Basidiomycota 21 (4.40%), Deuteromycota 17 (3.56%), Muromycota 7(1.47%) and Zycomycota 6(1.26%). The most isolated fungal genera included Candida (17.13%), followed by Penicillium 66 (13.15%), Fusarium 62 (12.35%), Aspergillus 61 (12.15%) and Cladosporium 60 (11.95%). Temperature, humidity and windspeed significantly affected airborne fungal concentration (p = .000), (p = .0280) and (p = .000), respectively. Pearson correlation analysis showed that the temperature negatively correlated with the fungal concentration significantly (p = .000), humidity positively correlated with the fungal concentration significantly (p = .001), and wind speed negatively correlated with the fungal concentration significantly (p = .000). Our findings highlight the significance of fungal air pollution and the possible risks of human mycoses. The significance of fungal spore pollutants and human mycoses to climate change needs to be explored.

Functional Characterization of Ao4g24: An Uncharacterized Gene Involved in Conidiation, Trap Formation, Stress Response, and Secondary Metabolism in Arthrobotrys oligospora.

Arthrobotrys oligospora is a typical nematode-trapping (NT) fungus, which can secrete food cues to lure, capture, and digest nematodes by triggering the production of adhesive networks (traps). Based on genomic and proteomic analyses, multiple pathogenic genes and proteins involved in trap formation have been characterized; however, there are numerous uncharacterized genes that play important roles in trap formation. The functional studies of these unknown genes are helpful in systematically elucidating the complex interactions between A. oligospora and nematode hosts. In this study, we screened the gene AOL_s00004g24 (Ao4g24). This gene is similar to the SWI/SNF chromatin remodeling complex, which was found to play a potential role in trap formation in our previous transcriptome analysis. Here, we characterized the function of Ao4g24 by gene disruption, phenotypic analysis, and metabolomics. The deletion of Ao4g24 led to a remarkable decrease in conidia yield, trap formation, and secondary metabolites. Meanwhile, the absence of Ao4g24 influenced the mitochondrial membrane potential, ATP content, autophagy, ROS level, and stress response. These results indicate that Ao4g24 has crucial functions in sporulation, trap formation, and pathogenicity in NT fungi. Our study provides a reference for understanding the role of unidentified genes in mycelium growth and trap formation in NT fungi.

Unlocking the Transcriptional Reprogramming Repertoire between Variety-Dependent Responses of Grapevine Berries to Infection by Aspergillus carbonarius.

Aspergillus carbonarius causes severe decays on berries in vineyards and is among the main fungal species responsible for grape contamination by ochratoxin A (OTA), which is the foremost mycotoxin produced by this fungus. The main goal of this study was to investigate at the transcriptome level the comparative profiles between two table grape varieties (Victoria and Fraoula, the white and red variety, respectively) after their inoculation with a virulent OTA-producing A. carbonarius strain. The two varieties revealed quite different transcriptomic signatures and the expression profiles of the differential expressed genes (DEGs) highlighted distinct and variety-specific responses during the infection period. The significant enrichment of pathways related to the modulation of transcriptional dynamics towards the activation of defence responses, the triggering of the metabolic shunt for the biosynthesis of secondary metabolites, mainly phenylpropanoids, and the upregulation of DEGs encoding phytoalexins, transcription factors, and genes involved in plant-pathogen interaction and immune signaling transduction was revealed in an early time point in Fraoula, whereas, in Victoria, any transcriptional reprogramming was observed after a delay. However, both varieties, to some extent, also showed common expression dynamics for specific DEG families, such as those encoding for laccases and stilbene synthases. Jasmonate (JA) may play a critical modulator role in the defence machinery as various JA-biosynthetic DEGs were upregulated. Along with the broader modulation of the transcriptome that was observed in white grape, expression profiles of specific A. carbonarius genes related to pathogenesis, fungal sporulation, and conidiation highlight the higher susceptibility of Victoria. Furthermore, the A. carbonarius transcriptional patterns directly associated with the regulation of the pathogen OTA-biosynthesis gene cluster were more highly induced in Victoria than in Fraoula. The latter was less contaminated by OTA and showed substantially lower sporulation. These findings contribute to uncovering the interplay beyond this plant-microbe interaction.

X-ray Irradiation Reduces Live Aspergillus flavus Viability but Not Aflatoxin B1 in Naturally Contaminated Maize.

Food crops around the world are commonly contaminated with Aspergillus flavus, which can produce the carcinogenic mycotoxin aflatoxin B1 (AFB1). The objective of this study is to test an X-ray irradiation sterilization method for studying AFB1 in contaminated maize samples in the laboratory. Maize that had been naturally contaminated with 300 ppb AFB1 by the growth of aflatoxigenic A. flavus was ground and then irradiated at 0.0, 1.0, 1.5, 2.0, 2.5, and 3.0 kGy. A. flavus was quantified by dilution plating on potato dextrose agar (PDA) and modified Rose Bengal media (MDRB) for viability and qPCR for gene presence. AFB1 was quantified by HPLC and ELISA. A. flavus viability, but not gene copies, significantly decreased with increasing doses of radiation (PDA: p < 0.001; MDRB: p < 0.001; qPCR: p = 0.026). AFB1 concentration did not significantly change with increasing doses of radiation (HPLC: p = 0.153; ELISA: p = 0.567). Our results imply that X-ray irradiation is an effective means of reducing viable A. flavus without affecting AFB1 concentrations. Reducing the hazard of fungal spores and halting AFB1 production at the targeted dose are important steps to safely and reproducibly move forward research on the global mycotoxin challenge.

Solar/ClO2 system inactivates fungal spores in drinking water: Synergy, efficiency and mechanisms

The risk of fungal pollution in drinking water has been paid attention. Solar/chlorine dioxide (ClO2) combined system is an environment-friendly, economical and efficient disinfection method, especially for countries and regions that are economically backward and still exposed to unsafe drinking water. In this paper, the kinetics, influencing factors, mechanism and regrowth potential of inactivated Aspergillus niger (A. niger) spores by solar/ClO2 were reported for the first time. The inactivation curve can be divided into three stages: instant inactivation within 1–2 min, slow linear inactivation and finally a tail. The synergistic factors produced by solar/ClO2 in terms of log reduction and maximum inactivation rate were 1.194 and 1.112, respectively. The inhibitory effect on the regrowth of A. niger spores inactivated by solar/ClO2 was also stronger than that by ClO2 alone. Strongly oxidizing reactive species produced by solar/ClO2 accelerated the accumulation of endogenic reactive oxygen species (ROS) caused by oxidation stress of A. niger spores, improving the inactivation ability of the system. The inactivation order of A. niger spores was: loss of culturability, accumulation of intracellular ROS, loss of membrane integrity, leakage of intracellular species and change of morphology. The inactivation performance of solar/ClO2 was better than solar/chlor(am)ine according to the comparison of inactivation efficiency and regrowth potential. Results also suggested that solar/ClO2 process was more suitable for the treatment of ground water sources.

The C2H2 Transcription Factor Con7 Regulates Vegetative Growth, Cell Wall Integrity, Oxidative Stress, Asexual Sporulation, Appressorium and Hyphopodium Formation, and Pathogenicity in Colletotrichum graminicola and Colletotrichum siamense.

The Colletotrichum genus is listed as one of the top 10 important plant pathogens, causing significant economic losses worldwide. The C2H2 zinc finger protein serves as a crucial transcription factor regulating growth and development in fungi. In this study, we identified two C2H2 transcription factors, CgrCon7 and CsCon7, in Colletotrichum graminicola and Colletotrichum siamense, as the orthologs of Con7p in Magnaporthe oryzae. Both CgrCon7 and CsCon7 have a typical C2H2 zinc finger domain and exhibit visible nuclear localization. Disrupting Cgrcon7 or Cscon7 led to a decreased growth rate, changes in cell wall integrity, and low tolerance to H2O2. Moreover, the deletion of Cgrcon7 or Cscon7 dramatically decreased conidial production, and their knockout mutants also lost the ability to produce appressoria and hyphopodia. Pathogenicity assays displayed that deleting Cgrcon7 or Cscon7 resulted in a complete loss of virulence. Transcriptome analysis showed that CgrCon7 and CsCon7 were involved in regulating many genes related to ROS detoxification, chitin synthesis, and cell wall degradation, etc. In conclusion, CgrCon7 and CsCon7 act as master transcription factors coordinating vegetative growth, oxidative stress response, cell wall integrity, asexual sporulation, appressorium formation, and pathogenicity in C. graminicola and C. siamense.

Estimating coccidioidomycosis endemicity while accounting for imperfect detection using spatio - temporal occupancy modeling.

Coccidioidomycosis, or Valley fever, is an infectious disease caused by inhaling Coccidioides fungal spores. Incidence has risen in recent years, and it is believed the endemic region for Coccidioides is expanding in response to climate change. While Valley fever case data can help us understand trends in disease risk, using case data as a proxy for Coccidioides endemicity is not ideal because case data suffers from imperfect detection, including false positives (e.g., travel-related cases reported outside of endemic area) and false negatives (e.g., misdiagnosis or underreporting). We proposed a Bayesian, spatio-temporal occupancy model to relate monthly, county-level presence/absence data on Valley fever cases to latent endemicity of Coccidioides, accounting for imperfect detection. We used our model to estimate endemicity in the western United States. We estimated high probability of endemicity in southern California, Arizona, and New Mexico, but also in regions without mandated reporting, including western Texas, eastern Colorado, and southeastern Washington. We also quantified spatio-temporal variability in detectability of Valley fever, given an area is endemic to Coccidioides. We estimated an inverse relationship between lagged 3- and 9-month precipitation and case detection, and a positive association with agriculture. This work can help inform public health surveillance needs and identify areas that would benefit from mandatory case reporting.

Evaluation of antifungal activity of cerium oxide nanoparticles and associated cellular responses.

Cerium oxide nanoparticles (CeO2), as a metal oxide nanomaterial, are increasingly used for various industrial and biomedical applications. Although their cytotoxicity to bacteria and the associated mechanisms have attracted particular attention, the mechanisms behind their antifungal effects have remained unclear. This study investigated the antifungal properties of CeO2, focusing on Aspergillus oryzae. CeO2 inhibited fungal spore germination on solid substrates, and the effect was fungistatic rather than fungicidal. CeO2 inhibited fungal growth, especially under UV irradiation, and induced reactive oxygen species (ROS) production. Tocopherol reduced the intracellular ROS levels and the growth-inhibitory effects of CeO2, suggesting that ROS are involved in these growth-inhibitory effects. Transcriptomic analysis revealed upregulated expression of genes related to phospholipases and phosphate metabolism. CeO2 affected phosphate ion concentration in the medium, potentially influencing cellular responses. This research provided valuable insights into the antifungal effects of CeO2 application, which differ from those of conventional photocatalysts like TiO2.

After-sealing life in urban soils: Experimental evidence of resilience and efficiency of ectomycorrhizal inoculation

The restoration of urban sealed soils is a major stake for urban planners. In particular, characterizing their resilience from a biotic perspective is of primary importance for remobilizing these artificialized substrates in urban green spaces. Using Marseille (France) as a case study, we implemented a metabarcoding next generation sequencing approach to characterize the diversity and the composition of ectomycorrhizal (EM) fungal communities present in soils sealed for 60 years. Based on an inoculation experiment, we tested the ability of the remaining spore bank to establish EM interactions with plants. Altogether, we aimed at assessing the potential of peri-urban natural habitats to provide an efficient soil EM inoculum for the restoration of urban soils. We found that: (i) long-term sealing drastically reduced the diversity of EM fungi in urban soils, (ii) long-leaved spores of hypogeous gastroid fungi were efficient to establish EM symbioses with plants, and (iii) the efficiency of EM fungal inoculation depended on the natural habitat used as an inoculum source. Oak forests provided species-rich but poorly efficient inoculum. Contrastingly, soils collected in disturbed shrublands (garrigues) hosted moderately-rich EM communities containing droughtadapted species with high ability to colonize urban soils. Our findings highlight that peri-urban landscapes are promising candidates to feed local systems of urban soil restoration. In this perspective, poorly-considered habitats such as shrublands can be considered as valuable sources of soil biota to prevent the over-exploitation of agricultural areas.

Palynostratigraphy and Paleoenvironment of Afikpo Well_3, Afikpo Syncline, Nigeria

The Afikpo Syncline constitutes the western segment of the southern part of the Benue Trough. The syncline orients in the northeast-southwest direction and unconformably overlies the pre-Santonian strata of the Benue Trough. This study investigates the sediments of Afikpo Well_3, drilled within the syncline, identifies its different palynozones, and interprets their paleoenvironments of deposition. Forty-two ditch-cutting samples recovered from the well at a 150 ft interval consist of mudstones, calcareous mudstones, carbonaceous shales, and calcareous shales. These samples were subjected to palynological analysis following the conventional acid maceration technique. A total of 637 palynomorph counts were recovered. These comprise 316 pollen grains, which make up 49.61%; 129 spores, which make up 20.25%; 9 fungi spores, which make up 1.41%; 17 microforaminifera wall linings, which make up 2.67%; and 166 dinoflagellate cysts, which make up 26.06%. Two palynozones were identified within the well. These include zone AF-01 (Monocolpites marginatus assemblage zone), which ranges from depths of 1500–1320 ft and is Campanian in age; and zone AF-2 (Dinogymnium sp. assemblage zone), which extends from depths of 50 ft–1320 ft and dates back to the Maastrichtian period. Based on the predominance of palmae pollen, together with the subordinate occurrence of dinoflagellate cysts, and the fair representations of spores (Cyathidite minor), the environment of deposition of the sediments ranges from a nearshore brackish water to a shallow marine environment. The shallow environment is further confirmed by the frequent occurrence of microforaminifera wall lining and the dominance of the peridinoid dinoflagellate cysts over the gonyaulacinoids.

In Vitro Evaluation of Selenium Against Some Plant Pathogenic Fungi

Objective: Selenium (Se) is garnering interest as a promising environmentally friendly element for controlling fungal pathogens in agricultural production. This study evaluated the impact of Se treatments, comprising sodium selenite (selenite) and sodium selenate (selenate) forms, on the growth of 10 plant pathogenic fungi. Materials and Methods: The impact of Se treatments on the mycelial growth and sporulation of fungi was assessed in in vitro conditions. Probit analysis was used to determine the concentrations of salts that induced a 50% reduction (EC50) in both mycelial growth and sporulation of fungi. Results: At the highest concentration (120 ppm), selenite demonstrated inhibitory effects on mycelial growth across various species, with a reduction in growth ranging from 6.82% to 62.46%. In contrast, selenate exhibited a broader spectrum of inhibition, affecting mycelial growth from 0% to 87.14%. Across different concentrations, Fusarium pseudograminearum displayed the highest sensitivity to selenite (EC50

First Report of Fruit Rot Disease on melon (Cucumis melo L.) Caused by Fusarium ipomoeae in China.

Fusarium rot on melon fruit has become an important postharvest disease for producers worldwide, typically involving multiple Fusarium pathogens (Khuna et al. 2022; Medeiros Araújo et al. 2021). In 2022, Fusarium fruit rot of muskmelon (Cucumis melo var. conomon) occurred sporadically in a field at Huainan Academy of Agricultural Sciences (32.658193º N, 117.064922º E) with an incidence of about 10%. Among these diseased muskmelons, a fruit exhibiting a white to yellowish colony athe intersection of the diseased and healthy tissues was collected and labeled TGGF22-17. The streak plate method was employed to isolate fungal spores on Bengal Red PDA (potato dextrose agar), which were then incubated at 25℃ in darkness. Following isolation and purification, a single-spore strain, TGGF22-17, was obtained and analyzed using morphological characters on PDA, synthetic nutrient agar (SNA) and carnation leaf agar (CLA) (Leslie and Summerell 2006), along with molecular identification. Colours were rated according to the color charts of Kornerup and Wanscher (1978). Based on the colony morphology on PDA, the isolate displayed a rosy buff or buff color with a white to buff margin. The colony margin was undulate, with the reverse transitioning from amber-yellow to honey-yellow. Aerial macroconidia on SNA were thin-walled, hyaline, mostly 3-5 septate, falcate, and measured 18.5-46.4 (x̄=34.2) × 2.9-4.8 (x̄ =3.9) μm in size (n =50). Sporodochial macroconidia on CLA were mostly five-septate with long apical and basal cells, exhibiting dorsiventral curvature. They were hyaline, with the apical cell hooked to tapering and the basal cell foot-shaped, measuring 46.5-89.6 (x̄ =72.3) × 3.5-5.0 (x̄ =4.3) μm in size (n = 100). Portions of three loci (TEF-1α, RPB1 and RPB2) were amplified and sequenced as described by Wang et al. (2019). Sequences were deposited in GenBank with accession number PP196583 to PP196585. The three gene sequences (TEF-1α, RPB1 and RPB2) of strain TGGF2022-17 shared 99.5% (629/632bp), 97.9% (1508/1540 bp) and 99.9% (1608/1609 bp) identity to the ex-type strain F. ipomoeae LC12165 respectively by pairwise DNA alignments on the FUSARIOID-ID database (https://www.fusarium.org). Phylogenetic analysis of the partial TEF-1α and RPB2 sequences with PhyloSuite (Zhang et al. 2020) showed the isolated fungus clustered with F. ipomoeae. Based on the morphological and phylogenetic analyses, TGGF22-17 was identified as F. ipomoeae. Pathogenicity tests were performed on healthy melons, which were surface-sterilized with 75% alcohol and wounded using a sterilized inoculation needle. A 4-mm diameter plug from a 7-day-old SNA culture of TGGF22-17 was aseptically inserted in the middle of the wound, sealed with plastic bag after absorbent cotton was included to maintain moisture. Five melons were each inoculated at three points. Noncolonized PDA agar plugs served as the negative control. The inoculated and uninoculated plugs were removed approximately 48 hours after inoculation. The melon inoculated with TGGF22-17 exhibited water-soaked black lesions 48h post-inoculation, resulting in a 100% infection rate (15/15). After 7 days, mycelium was obseved on the inoculated melons. No disease symptoms were observed on the uninoculated melons. To fulfill Koch's postulates, fungi were isolated from the inoculated fruit and confirmed as F. ipomoeae by morphological observation. Fusarium ipomoeae has been reported to cause fruit rot on winter squash (Cucurbita maxima) in Japan (Kitabayashi et al. 2023). To our knowledge, this is the first report of fruit rot on muskmelon caused by F. ipomoeae in China and this report will be valuable for monitoring and management of fruit rot disease on muskmelons.

Clearing the Air, Breathe Easy: Intensive Care Unit Remodeling Unveils Insights into Aspergillosis Prevention

Background: Invasive aspergillosis (IA) poses a substantial threat to morbidity and mortality, particularly among immunocompromised individuals. In 2023, a New York City Intensive Care Unit (ICU) experienced an aspergillus outbreak following a structural water leak, resulting in two patients diagnosed with Invasive Aspergillus niger in their bronchial cultures. Immediate interventions, including patient relocation and ICU reconstruction were implemented to mitigate further impacts. This study aims to assess the impact of timely relocation of patients and renovation of the ICU, on the incidence of invasive aspergillosis. Method: A quasi-experimental study design of ICU patients over a nine month period included surveillance by the Infection Prevention department from March 1 to December 1, 2023. Surveillance included review of microbiology reports, environmental cultures, and patient chart reviews. The Pre-intervention spanned March 1 to May 1, and the post-intervention from May 4 to December 1. Indoor mold assessments of pre- and post-intervention involved testing wall surfaces for moisture, air sample collection for fungal spores, and surface swabs for direct fungal analysis. The intervention included relocating all seventeen patients from the impacted ICU and comprehensive reconstruction. Reconstruction involved the removal and replacement of all sheetrock within the unit extending four feet from the floor with moisture-resistant sheetrock. Additionally, moisture resistant single sheet welded vinyl flooring and cove-bases were installed. All heating, ventilation, and air-conditioning (HVAC) systems were inspected and cleaned. Construction activities strictly adhered to Infection Control Risk Assessment (ICRA) guidelines, with emphasis on maintaining negative pressure, to ensure a safe environment. Result: Environmental swab samples from 50% of ICU rooms indicated growth of Aspergillus/Penicillium, Chaetomium, and Stachybotrys/Memnoniella type spores during the pre-intervention phase. Environmental microbiology results strongly suggest the indoor environment as the fungal spore source, with the presence of fruiting structures indicating surface mold growth. Indoor air samples, when compared to outdoor samples collected during pre-intervention, showed rare (2-6 raw count) growth of Aspergillus in 55% of the sampled rooms and subequently no growth post-intervention. Prospective surveillance revealed no further aspergillus growth in the ICU population and environment. Conclusion: Our findings highlight a potential correlation between environmental modifications and reduced IA incidence. Swift mitigation and structural interventions are crucial in averting potentially fatal outcomes, marking a significant advancement of prevention strategies for inner-city hospital settings. Although promising, study limitations include the inability to speciate environmental aspergillus for comparison to patient bronchial cultures and the absence of baseline bronchial cultures for affected patients on admission.

Phylogeny, biogeography, and host range of gall midges (Diptera: Cecidomyiidae) feeding on spores of rust fungi (Basidiomycota: Pucciniales).

Rust fungi (Pucciniales) are plant pathogens that can cause devastating yield losses to economically important crops and threaten native plants with extinction. Rusts are usually controlled with fungicides when rust-resistant plant varieties are unavailable. However, natural enemies may offer an alternative to chemicals by acting as biological controls. The larvae of Mycodiplosis Rübsaamen (49 spp.) feed on the spores of rusts and powdery mildew fungi and have been suggested as a potential biocontrol candidate for disease-causing rusts. However, little is known about the phylogenetic relationships, biogeography, and host range of this genus. We screened 5,665 rust specimens from fungarium specimens and field collections and recovered a total of 363 larvae on 315 rust specimens from 17 countries. Three mitochondrial and 2 nuclear loci were amplified and sequenced for the phylogenetic reconstruction of 129 individuals. We recovered 12 clades, of which 12 and 10 were supported with maximum likelihood and Bayesian inference, respectively. Of the 12 clades, 7 comprised species from multiple continents and climatic regions, and 5 comprised species from a single region. Individuals forming clades were collected from 2 to 18 rust species, suggesting that Mycodiplosis species have a broad host range. In total, Mycodiplosis larvae were identified on 44 different rust species collected from 18 plant families. Future studies should focus on expanding field sampling efforts, including data from additional gene regions, and incorporating morphological data to further elucidate species diversity and distribution patterns.

Effect of glyphosate on the sporulation of aquatic fungi: an in-vitro experience

Effect of glyphosate on the sporulation of aquatic fungi: an in-vitro experience

PENGARUH PEMBENAH TANAH HAYATI TERHADAP SIFAT KIMIA ENTISOL TERGENANG DAN TIDAK TERGENANG

Farmers began to implement organic systems when the quality of rice fields decreased. Indonesia has several active volcanoes so that the agricultural land was formed by generally Entisols. Several natural and synthetic soil conditioners were starting to be used to decompose the litter and increase the availability of Entisol nutrients. The research aimed to study the effect of providing biological soil amendments on the chemical properties of Entisols. The demonstration plots scale research were used a completely randomized design with a combination of treatments: (P1) Flooded dolomite control, (P2) Non-flooded dolomite control, (P3) Flooded bio soil-neutralizer, and (P4) Non-flooded bio soil-neutralizer. Parameters of soil chemical properties observed were pH, C-organic (%), N-total (%), P2O5-total (%), K2O-total (%), CEC (c mol + kg-1), total bacteria (CFU mL-1), and total fungi (spores g-1). The chemical properties of Entisols before treatment showed slightly acidic pH, low C-organic, low N-total, low K-total, low P-total, and very high CEC. After applying the soil neutralizer, there were an increase in chemical properties including pH becoming alkaline and neutral, medium C-organic, standards to moderat NPK-total, and high CEC. Flooding treatment did not increase the chemical properties of the Entisols.