Almeida Henrique Meiroz de Souza, Sonalio Karina, Mechler-Dreibi Marina Lopes, Petri Fernando Antônio Moreira, Storino Gabriel Yuri, Maes Dominiek, de Oliveira Luís Guilherme
School of Agricultural and Veterinarian Sciences, São Paulo State University (Unesp), Jaboticabal 14884-900, São Paul, Brazil.
Unit of Porcine Health Management, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
Vet Sci. 2022 Dec 5;9(12):674. doi: 10.3390/vetsci9120674.
, the etiological agent of swine enzootic pneumonia, has been reported to increase the susceptibility to secondary infections and modulate the respiratory microbiota in infected pigs. However, no studies have assessed the influence of on the respiratory microbiota diversity under experimental conditions. Therefore, this study evaluated the impact of infection on the respiratory microbiota of experimentally infected swine over time. To accomplish this, 12 weaned pigs from a . -free farm were divided into two groups: strain 232 infected (n = 8) and non-infected (n = 4). The first group received 10 mL of Friis medium containing 10 CCU/mL of while the control group received 10 mL of sterile Friis medium. Inoculation of both groups was performed intratracheally when the animals were 35 days old (d0). At 28 days post-inoculation (dpi) and 56 dpi, 4 infected animals plus 2 controls were humanely euthanized, and biopsy samples of nasal turbinates (NT) and bronchus-alveolar lavage fluid (BALF) samples were collected. The DNA was extracted from the individual samples, and each group had the samples pooled and submitted to next-generation sequencing. Taxonomic analysis, alpha and beta diversity indexes, weighted unifrac, and unweighted unifrac distances were calculated. A high relative frequency (99%) of in BALF samples from infected animals was observed with no significant variation between time points. The infection did not seem to alter the diversity and evenness of bacterial communities in NT, thus, relative frequency was low in NT pools from infected animals (28 dpi-0.83%; 56 dpi-0.89%). PCoA diagrams showed that BALF samples from infected pigs were grouped and far from the control samples, whereas NT from infected animals were not separated from the control. Under the present coditions, infection influenced the lower respiratory microbiota, which could contribute to the increased susceptibility of infected animals to respiratory infections.
猪地方流行性肺炎的病原体已被报道会增加感染猪对继发感染的易感性并调节其呼吸道微生物群。然而,尚无研究评估在实验条件下该病原体对呼吸道微生物群多样性的影响。因此,本研究评估了该病原体感染随时间对实验感染猪呼吸道微生物群的影响。为实现这一目的,从一个无该病原体的猪场选取12头断奶仔猪,分为两组:感染232株菌株组(n = 8)和未感染组(n = 4)。第一组接受10 mL含10 CCU/mL该病原体的弗里斯培养基,而对照组接受10 mL无菌弗里斯培养基。两组动物在35日龄(d0)时经气管内接种。在接种后28天(dpi)和56 dpi,对4头感染动物加2头对照动物实施安乐死,并采集鼻甲(NT)活检样本和支气管肺泡灌洗液(BALF)样本。从各个样本中提取DNA,每组将样本合并并进行下一代测序。计算分类分析、α和β多样性指数、加权UniFrac和非加权UniFrac距离。在感染动物的BALF样本中观察到该病原体的相对频率较高(99%),各时间点之间无显著差异。感染似乎并未改变NT中细菌群落的多样性和均匀度,因此,感染动物的NT样本池中的该病原体相对频率较低(28 dpi - 0.83%;56 dpi - 0.89%)。主坐标分析(PCoA)图显示,感染猪的BALF样本聚集在一起且远离对照样本,而感染动物的NT样本与对照样本未分离。在当前条件下,该病原体感染影响下呼吸道微生物群,这可能导致感染动物对呼吸道感染的易感性增加。