Ventilator-associated pneumonia caused by a new-found opportunistic fungal pathogen-Myceliophthora heterothallica: a case report.

BACKGROUND: Myceliophthora heterothallica belonging to Myceliophthora is considered as an environmental fungus and has not been reported to be pathogenic or colonizing in recent literature. The present case firstly reports a ventilation-associated pneumonia caused by Myceliophthora heterothallica among the aged adult. CASE PRESENTATION: A 67-years-old Asian female patient suffering from a sudden disturbance of consciousness for 3 h was admitted to our hospital. Cardiac arrest occurred during emergency transport, and sinus rhythm was restored after cardiopulmonary resuscitation. Invasive mechanical ventilation was given to this patient for respiratory failure. After mechanical ventilation, the lung CT images showed multiple cuneiform nodules arranging subpleural accompanying with ground-glass opacity. On the 5th day of mechanical ventilation, Myceliophthora heterothallica was cultured from endotracheal aspirates. Two methods, namely automatic microbial identification system and internal transcribed spacer sequencing were employed to identify this fungus. The present case firstly uncovered the colonization ability and pathogenicity of Myceliophthora heterothallica in the respiratory tract. After 28d of treatment with piperacillin-tazobactam, this patient weaned from the ventilator and recovered from consciousness with lung infection disappearance. CONCLUSIONS: This is the first case report of ventilation-associated pneumonia in the aged patient caused by Myceliophthora heterothallica. This current case is worth for the clinical diagnosis and treatment of Myceliophthora heterothallica infection, and also enriches new pathogenic species found of thermothelomyces species.

Production and characterization of a thermostable ß-glucosidase from Myceliophthora heterothallica / Produção e caracterização de uma ß-glicosidase termoestável de Myceliophthora heterothallica

The conversion of biomass from agro-industrial residues into bioproducts is of great interest, especially to Brazil, where bioenergy has a huge potential for development. Enzymes involved in biodegradation of lignocellulosic biomass are those of the cellulase system, of which ß-glucosidase is a constituent. The production and characterization of ß-glucosidase by the thermophilic fungus Myceliophthora heterothallica by solid-state cultivation on different agro-industrial residues (sugarcane bagasse, sugarcane straw, wheat bran and a mixture of these three materials (1:1:1 w/w) was evaluated. Solid-state cultivation were conducted in 250 mL Erlenmeyer flasks, with 5 g of each substrate. Different culture parameters, such as supplementary nutrient solution to the substrate, supplementary nutrient solution pH, initial substrate moisture and fungus incubation temperature, were evaluated to establish conditions of higher enzyme production by the fungus The greatest production of enzymes occurred in a mixture of wheat bran, sugarcane bagasse and straw bagasse (1:1:1). The activity of ß-glucosidase was greater under the following conditions: nutrient solution composed of NH4NO3, MgSO4.7H2O and (NH4)2SO4 (0.1%), at pH 4.5 or 6.0, fungus incubation at 40°C or 45°C, initial moisture of substrate at 80%. Enzyme presented optimum pH at pH 5.0 and good pH stability. Best temperature was 65°C and enzyme showed 100% stability for 1h, up to 60°C. The use of agro-industrial residues provided good production of ß-glucosidase by fungus, with enzyme having the characteristics desirable from the industrial application.

A conversão da biomassa vegetal proveniente de resíduos agroindustriais em bioprodutos é de grande interesse, principalmente para o Brasil, onde a agroenergia possui grande potencial de desenvolvimento. Enzimas envolvidas na biodegradação da biomassa lignocelulósica fazem parte do grupo das celulases, no qual a 훽-glucosidase é um constituinte. O presente estudo avaliou a produção e caracterização de uma ß-glicosidase pelo fungo termofílico Myceliophthora heterothallica por cultivo em estado sólido de diferentes resíduos agroindustriais (bagaço de cana-de-açúcar, palha de cana-de-açúcar, farelo de trigo e em uma mistura dos três materiais (1:1: 1 p/p). O cultivo em estado sólido foi realizado em frascos Erlenmeyer de 250 mL, contendo 5 g de cada substrato. Diferentes parâmetros de cultivo, como solução nutriente suplementar ao substrato, pH da solução nutriente suplementar, umidade inicial do substrato e temperatura de incubação do fungo foram avaliados, visando estabelecer condições para maior produção da enzima pelo fungo. A maior produção da enzima ocorreu na mistura de farelo de trigo, e bagaço e palha de cana-de-açúcar (1:1:1). A atividade da ß-glicosidase foi maior nas seguintes condições: solução nutriente composta por NH4NO3, MgSO4.7H2O e (NH4)2SO4 (0,1%) com pH 4,5 e 6,0, temperatura de incubação do fungo a 40°C e 45°C, com umidade inicial do substrato em 80%. A enzima apresentou pH ótimo de 5,0, e boa estabilidade ao pH. A temperatura ótima foi de 65°C, e a enzima apresentou 100% de estabilidade por 1h, até 60°C. A utilização de resíduos agroindustriais proporcionou boa produção de ß-glicosidase pelo fungo, com a enzima apresentando características desejáveis para aplicação industrial.

Heterologous expression, purification and biochemical characterization of a new xylanase from Myceliophthora heterothallica F.2.1.4.

Myceliophthora heterothallica is a thermophilic fungus potentially relevant for the production of enzymes involved in the degradation of plant biomass. A xylanase encoding gene of this species was identified by means of RT-PCR using primers designed based on a xylanase coding sequence (GH11) of the fungus M. thermophila. The obtained gene was ligated to the vector pET28a(+) and the construct was transformed into Escherichia coli cells. The recombinant xylanase (r-ec-XylMh) was heterologously expressed, and the highest activity was observed at 55 °C and pH 6. The enzyme stability was greater than 70% between pH 4.5 and 9.5 and the inclusion of glycerol (50%) resulted in a significant increase in thermostability. Under these conditions, the enzyme retained more than 50% residual activity when incubated at 65 °C for 1 h, and approximately 30% activity when incubated at 70 °C for the same period. The tested cations did not increase xylanolytic activity, and the enzyme indicated significant tolerance to several phenolic compounds after 24 h, as well as high specificity for xylan, with no activity for other substrates such as CMC (carboxymethylcellulose), Avicel, pNPX (p-nitrophenyl-ß-D-xylopyranoside) and pNPA (p-nitrophenyl-α-L-arabinofuranoside), and is thus, of potential relevance in pulp bleaching.

Sexual crossing of thermophilic fungus Myceliophthora heterothallica improved enzymatic degradation of sugar beet pulp.

BACKGROUND: Enzymatic degradation of plant biomass requires a complex mixture of many different enzymes. Like most fungi, thermophilic Myceliophthora species therefore have a large set of enzymes targeting different linkages in plant polysaccharides. The majority of these enzymes have not been functionally characterized, and their role in plant biomass degradation is unknown. The biotechnological challenge is to select the right set of enzymes to efficiently degrade a particular biomass. This study describes a strategy using sexual crossing and screening with the thermophilic fungus Myceliophthora heterothallica to identify specific enzymes associated with improved sugar beet pulp saccharification. RESULTS: Two genetically diverse M. heterothallica strains CBS 203.75 and CBS 663.74 were used to generate progenies with improved growth on sugar beet pulp. One progeny, named SBP.F1.2.11, had a different genetic pattern from the parental strains and had improved saccharification activity after the growth on 3 % sugar beet pulp. The improved SBP saccharification was not explained by altered activities of the major (hemi-)cellulases. Exo-proteome analysis of progeny and parental strains after 7-day growth on sugar beet pulp showed that only 17 of the 133 secreted CAZy enzymes were more abundant in progeny SBP.F1.2.11. Particularly one enzyme belonging to the carbohydrate esterase family 5 (CE5) was more abundant in SBP.F1.2.11. This CE5-CBM1 enzyme, named as Axe1, was phylogenetically related to acetyl xylan esterases. Biochemical characterization of Axe1 confirmed de-acetylation activity with optimal activities at 75-85 °C and pH 5.5-6.0. Supplementing Axe1 to CBS 203.75 enzyme set improved release of xylose and glucose from sugar beet pulp. CONCLUSIONS: This study identified beneficial enzymes for sugar beet pulp saccharification by selecting progeny with improved growth on this particular substrate. Saccharification of sugar beet pulp was improved by supplementing enzyme mixtures with a previously uncharacterized CE5-CBM1 acetyl xylan esterase. This shows that sexual crossing and selection of M. heterothallica are the successful strategy to improve the composition of enzyme mixtures for efficient plant biomass degradation.

Genetics of mating in members of the Chaetomiaceae as revealed by experimental and genomic characterization of reproduction in Myceliophthora heterothallica.

Members of the Chaetomiaceae are among the most studied fungi in industry and among the most reported in investigations of biomass degradation in both natural and laboratory settings. The family is recognized for production of carbohydrate-active enzymes and antibiotics. Thermophilic species are of special interest for their abilities to produce thermally stable enzymes and to be grown under conditions that are unsuitable for potential contaminant microorganisms. Such interests led to the recent acquisition of genome sequences from several members of the family, including thermophilic species, several of which are reported here for the first time. To date, however, thermophilic fungi in industry have served primarily as parts reservoirs and there has been no good genetic model for species in the family Chaetomiaceae or for thermophiles in general. We report here on the reproductive biology of the thermophile Myceliophthora heterothallica, which is heterothallic, unlike most described species in the family. We confirmed heterothallism genetically by following the segregation of mating type idiomorphs and other markers. We have expanded the number of known sexually-compatible individuals from the original isolates from Indiana and Germany to include several isolates from New Mexico. An interesting aspect of development in M. heterothallica is that ascocarp formation is optimal at approximately 30 °C, whereas vegetative growth is optimal at 45 °C. Genome sequences obtained from several strains, including isolates of each mating type, revealed mating-type regions whose genes are organized similarly to those of other members of the Sordariales, except for the presence of a truncated version of the mat A-1 (MAT1-1-1) gene in mating-type a (MAT1-2) strains. In M. heterothallica and other Chaetomiaceae, mating-type A (MAT1-1) strains have the full-length version of mat A-1 that is typical of mating-type A strains of diverse Ascomycota, whereas a strains have only the truncated version. This truncated mat A-1 has an intact open reading frame and a derived start codon that is not present in mat A-1 from A strains. The predicted protein contains a region that is conserved across diverse mat A-1 genes, but it lacks the major alpha1 domain, which characterizes proteins in this family and is known to be required for fertility in A strains from other Ascomycota. Finally, we have used genes from M. heterothallica to probe for mating genes in other homothallic and heterothallic members of the Chaetomiaceae. The majority of homothallic species examined have a typical mat A-1,2,3 (MAT1-1-1,2,3) region in addition to an unlinked mat a-1 (MAT1-2-1) gene, reflecting one type of homothallism commonly observed in diverse Ascomycota.