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Up to now, four coccidian species have been identified in Rallidae (Aves: Gruiformes): Eimeria mongolica, E. alakuli, E. paludosa and E. porphyrulae. Here, we described an Eimeria species, E. paludosa, from a common gallinule (Gallinula galeata) in Mexico. Oocysts were ovoid and wall pitted single-layered. A prominent micropyle was present, the oocyst residuum absent and the polar granule was present. On histological examination of tissues, endogenous stages (meronts, microgametocytes and macrogametocytes) were seen in the epithelial cells of the small intestine (upper and lower intestine). In addition to a new locality, this is the first description of E. paludosa from G. galeata and is the third description of a coccidian infecting Rallidae in the Americas.

This is the first extensive report on the identification and characterization of Avibacterium paragallinarum (AVP) isolates obtained from outbreaks of infectious coryza (IC) in IC-vaccinated layer flocks from Sonora State in Mexico. Isolates obtained from IC outbreaks during the years 2007, 2014, 2015, 2017, and 2019 were identified by conventional PCR test and 16S rRNA gene analysis, serotyped by Page serotyping and genotyped by the recently described partial sequence analysis of the HPG2 region. Furthermore, antimicrobial susceptibility profiles were determined by a recently improved minimal inhibitory concentration (MIC) test. The conventional PCR test and the 16S rRNA analyses confirmed the isolates as AVP. Serotyping results showed the involvement of isolates belonging to serotypes A, B, and C in the IC outbreaks. Genotyping of the HPG2 region revealed the presence of sequence type (ST)1, ST4, and ST11, of which the latter has also been identified in Europe. The MIC susceptibility test showed that all tested isolates were susceptible for the majority of tested antimicrobials, including erythromycin and tetracycline, which are important antibiotics for the treatment of IC. The IC situation in Sonora State, Mexico, is complex because of the presence of serotypes A, B, and C. This finding emphasizes the importance of biosecurity in combination with the application of the most optimal vaccination programs in the control of IC in Sonora State, Mexico.

Resumen La pandemia global por COVID-19 ha generado un sin número de alertas y cambios en las formas de habitar y de consumo. La triada medio ambiente-salud-individuo vuelve a ser protagonista en este escenario, en donde se aprecian graves fracturas en los sistemas de salud pública, hábitat y seguridad alimentaria. Como factor transversal a esos elementos, la contaminación ambiental se convirtió en un efecto facilitador de la pandemia pues la transmisión por contacto entre humanos a través de aerosoles representa la vía de contagio. Esta situación obligó al distanciamiento y confinamiento preventivo, medida que logró hacer evidente la pobreza, la inequidad y la desigualdad que se vive globalmente. Por otro lado, los cambios en la movilidad y la frecuencia de producción en industrias de manufactura trajo una reducción en los gases de efecto invernadero. Abstract The global pandemic due to COVID-19 has generated countless alerts and changes in the ways of living and consuming, the environment, health and individual triad is once again the protagonist in this scenario where serious fractures in the public health systems, habitat and food security are seen. As a transverse factor to these elements, environmental contamination became a facilitating effect of the pandemic and transmission by contact between humans through aerosols represents the route of contagion, this situation forced the distancing and preventive confinement, this measure to makes evident the poverty, inequality and inequity that is experienced globally, on the other hand the changes in mobility and the frequency of production in manufacturing industries brought a reduction in greenhouse gases.

This study reports the results of diagnostic and molecular typing methods for 18 Avibacterium paragallinarum isolates obtained from outbreaks of infectious coryza in commercial layer flocks in the Netherlands. Isolation, biochemical identification, species-specific PCR tests and classical serotyping were performed. In addition, molecular typing by Enterobacterial Repetitive Intergenic Consensus-Based Polymerase Chain Reaction (ERIC-PCR) and sequence analysis of the partial HPG2 region of A. paragallinarum were applied and results of both techniques were compared. Moreover, the pathogenicity of an isolate of the most common genotype detected in the Netherlands was determined in an animal experiment. All 18 Avibacterium isolates were nicotinamide adenine dinucleotide-dependent. All isolates were detected by the species-specific conventional PCR while 33% of the isolates were missed by the species-specific real-time PCR. Sequence analysis showed a probe mismatch as a result of a single nucleotide polymorphism (G1516A). Modification of the probe of the real-time PCR was necessary to overcome false negative results. Molecular typing showed that sequence analysis of the partial HPG2 region was in concordance with ERIC-PCR results and indicated the presence of two major genotypes. Serotyping showed the presence of serovars A-1, A-2 and B-1. There was no correlation between genotyping results and serotyping results. Inoculation of an isolate of the most prevalent genotype, and belonging to serovar A-1, into brown layer hens demonstrated the pathogenicity of this isolate.

El objetivo de este estudio fue caracterizar los hallazgos patológicos y su relación con los resultados clínicos y serológicos en carneros infectados experimentalmente (IE) con Brucella ovis. Se utilizaron 18 carneros de 1 a 4 años y libres de B. ovis; que se distribuyeron en tres grupos: Grupo 1 (n= 6): inoculación en mucosas (B. ovis); Grupo 2 (n= 6), inoculación vía intravenosa y Grupo 3 (n= 6) Control. Se llevó a cabo el seguimiento de un carnero -1 grupo -1 durante 189 días (d) post-IE. Se obtuvieron muestras de 2 mL de suero sanguíneo y semen entre los días 0 y 189 post-IE para realizar pruebas serológicas de Inmunodifusión en Gel de Agar (IGDA) y ELISA. El semen se procesó por la técnica de reacción en cadena de la polimerasa PCR. El análisis estadístico se realizó mediante modelos categóricos y mediciones repetidas. ELISA mostró mayor sensibilidad (P