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Innate immunity in asthma may be influenced by alterations in lung microbiota, potentially affecting disease severity. This study investigates the differences in lung inflammation and microbiome between asthma-ovalbumin (OVA) administered with and without fluconazole treatment in C57BL/6 mice. Additionally, the role of inflammation was examined in an in vitro study using a pulmonary cell line. At 30 days post-OVA administration, allergic asthma mice exhibited increased levels of IgE and IL-4 in serum and lung tissue, higher pathological scores, and elevated eosinophils in bronchoalveolar lavage fluid (BALF) compared to control mice. Asthma inflammation was characterized by elevated serum IL-6, increased lung cytokines (TNF-α, IL-6, IL-10), and higher fungal abundance confirmed by polymerase chain reaction (PCR). Fluconazole-treated asthma mice displayed higher levels of cytokines in serum and lung tissue (TNF-α and IL-6), increased pathological scores, and a higher number of mononuclear cells in BALF, with undetectable fungal levels compared to untreated mice. Lung microbiome analysis revealed similarities between control and asthma mice; however, fluconazole-treated asthma mice exhibited higher Bacteroidota levels, lower Firmicutes, and reduced bacterial abundance. Pro-inflammatory cytokine production was increased in supernatants of the pulmonary cell line (NCI-H292) after co-stimulation with LPS and beta-glucan (BG) compared to LPS alone. Fluconazole treatment in OVA-induced asthma mice exacerbated inflammation, partially due to fungi and Gram-negative bacteria, as demonstrated by LPS+BG-activated pulmonary cells. Therefore, fluconazole should be reserved for treating fungal asthma rather than asthma caused by other etiologies., Competing Interests: The authors declare that they have no competing interests., (© 2024 Worasilchai et al.)

Zaglyptogastra Ashmead, 1900 was erected for a large, distinctive Braconinae wasp, Z. abbotti, collected in Lower Siam (Thailand) (Ashmead 1900). Although nine species are known from the Indo-Australian region, only three are recorded from mainland Indochina: Z. abbotti Ashmead, 1990 (Thailand), Z. vitalisi (Turner, 1919) (Thailand, Laos) and Z. vietnamica Long & Mai, 2015 (Vietnam) (El-Heneidy & Quicke, 1991; Long & Mai, 2015). In 2021, two further Asia species, Z. exilis Li, van Achterberg & Chen, 2021 and Z. tricolor Li, van Achterberg & Chen, 2021 were described from China (Li et al. 2021).

Four new species of the genus Physaraia Shenefelt, 1978 (Hymenoptera: Braconidae) from Thailand are described and illustrated based on female specimens collected from the Malaise traps and aerial net, increasing the total number of Physaraia species of Indo-Australian region to six species; P. nanensis Chansri, Quicke Butcher, sp. nov., P. panhai Chansri, Quicke Butcher, sp. nov., P. sakaeratensis Chansri, Quicke Butcher, sp. nov., P. sinensis Quicke et al., 1997, P. sumatrana, Enderlein, 1905 and P. tigeri Chansri, Quicke Butcher, sp. nov. A checklist to the species known of Physaraia with their distribution and dichotomous key to accommodate the new species are provided.

To assess the estrogenic activities of synthetic estrogen, synthetic phytoestrogen, Pueraria lobata and three distinct cultivars of Pueraria mirifica, a phytoestrogen-rich herb, a vaginal cytology assay in ovariectomized rats were used. Rats were ovariectomized and treated with DW, estradiol valerate (1 mg/kg BW), genistein (0.25-2.5 mg/kg BW), Pueraria lobata and Pueraria mirifica (10-1,000 mg/kg BW) for 14 days. The vaginal cytology was checked daily and the uteri were dissected and weighed at the end of treatment or post-treatment periods. The treatments of DW, genistein and Pueraria lobata did not influence the vaginal epithelium, but the injection of estradiol valerate induced a vaginal cornification from day-3 of treatment to day-14 of post-treatment period. The occurrence of vaginal cornification after treatment and the recovery after the cessation was dependent on dosages and cultivars of Pueraria mirifica. The increments of uterus weight in all rats agreed with the cornification of vaginal epithelium. Although both uterotropic and vaginal cytology assays can be used to assess the estrogenic activity of phytoestrogen-rich herb, however, using vaginal cytology assay has two advantages: (1) we do not need to kill the animals and (2) we can follow up the recovery after the cessation of treatment.