Eimeria erythrorhynchosi n. sp. (Apicomplexa: Eimeriidae) from the American white pelican Pelecanus erythrorhynchos Gmelin, 1789 (Pelecaniformes: Pelecanidae) in Toluca, Mexico.

A new coccidian species, Eimeria erythrorhynchosi n. sp. (Apicomplexa: Eimeriidae) collected from the American white pelican Pelecanus erythrorhynchos Gmelin 1789, is reported from Toluca city, Mexico. Sporulated oocysts of the new species are ovoidal, 17.5-19.6 × 14.1-14.8 (18.5 × 14.5) µm, with a length/width (L/W) ratio of 1.0-1.5 (1.25); micropyle present, robust and protruding, W: 4.5-5.5, and polar body (1 or 2), L × W: 2.5 (2-3), associated with the micropyle; oocyst residuum absent. Sporocysts are ovoidal, 10.1-11.2 × 6.4-7.1 (10.7 × 6.8) µm, with a length/width (L/W) ratio of 1.0-1.6 (1.3); Stieda and sub-Stieda bodies are both present, but para-Stieda body is absent; sporocyst residuum of diffuse granules. Sporozoites are vermiform, 9.6 × 2.4 µm. The new species is the seventh species of Eimeria recorded in Pelecaniformes and the third in Pelecanidae.

The canary Serinus canaria (Passeriformes: Fringillidae) as a new host for Isospora bioccai in Mexico.

Isospora bioccai (Cringoli and Quesada 1991) (Protozoa, Apicomplexa, Eimeriidae) is reported and described from captive canaries Serinus canaria forma domestica (Linnaeus 1758) in Mexico. The oöcysts are subspherical, 25.5 × 23.5 µm, with smooth, bilayered wall, ∼1.3 µm thick. Micropyle absent, oöcyst residuum absent, and polar granule present, 4-8 rice-grain-shaped. Sporocysts are ovoidal, 16.7 × 10.5 µm. Stieda body knob-like and substieda body trapezoidal of irregular base. Sporocyst residuum is composed of granules of different sizes. Sporozoites are vermiform with one refractile body and a nucleus. Gamogony was seen in the duodenum. In addition to new locality, this is the first description of I. bioccai from S. canaria.

Phenotypic and genotypic profile of clinical and animal multidrug-resistant Salmonella enterica isolates from Mexico.

AIMS: The objective of this study was to obtain a phenotypic and genotypic profile of Salmonella enterica including multidrug-resistant (MDR) isolates from food-producing animals and clinical isolates, as well as their genetic relatedness in two different States of Mexico (Jalisco and State of Mexico). METHODS AND RESULTS: A total of 243 isolates were evaluated in terms of antimicrobial resistance (AMR) and related genes through a disk diffusion method and PCR respectively; we found 16 MDR isolates, all of them harbouring the blaCMY gene but not qnr genes, these isolates represent less than 10% of the collection. The pulsed-field gel electrophoresis revealed a higher genotypic similitude within isolates of State of Mexico than Jalisco. CONCLUSIONS: A low percentage of Salmonella isolates were resistant to relevant antibiotics in human health, nevertheless, the AMR and involved genes were similar despite the different serovars and origin of the isolates. SIGNIFICANCE AND IMPACT OF THE STUDY: This investigation provided an insight of the current status of AMR of Salmonella isolates in two States of Mexico and pinpoint the genes involved in AMR and their epidemiological relationship, the information could help to determine an adequate therapy in human and veterinary medicine.

Caryospora neofalconis and other enteroparasites in raptors from Mexico.

A coprological survey of enteroparasites in raptors (60 Falconiformes) from Central Mexico is reported. Three samples contained coccidian unsporulated oocysts, one contained Eimeria sp., one contained trematode eggs and one contained capillarid and trematode eggs and Eimeria sp. After sporulation at the laboratory, oocysts from a Falco peregrinus were identified as Caryospora neofalconis. The phylogenetic analysis of the C. neofalconis (GenBank accession number KT037081) showed a close relationship to the Australian strain RY 2014 isolate 16710 (GenBank accession number KJ634019) of Caryospora daceloe, with 99.2% similarity. As far as we are aware, this is the first report of C. neofalconis in raptors from Mexico and the Americas.

ERIC-PCR genotyping of emergent serovar C-1 isolates of Avibacterium paragallinarum from Mexico.

Between 2008 and 2010, 14 isolates of Avibacterium paragallinarum were identified as serovar C-1 in Mexico. All isolates were obtained from commercial laying hens suffering infectious coryza despite a history of vaccination. The enterobacterial repetitive intergenic consensus-based PCR genotyping showed that all isolates had a common pattern. Until recently, serovars A-1, A-2, B-1, and C-2 were the serovars prevalent in Mexico. Serovar C-1 has been identified in Japan and recently in the Americas in Ecuador. Our current study suggests that Av. paragallinarum serovar C-1 is an emerging serovar in Mexico. Our results also indicate that the Mexican isolates of Av. paragallinarum serovar C-1 may have a clonal relationship. Knowledge of the genetic diversity of Av. paragallinarum may be of value in understanding vaccine performance and identifying the best combination to achieve broader protection.

Identification of Avibacterium paragallinarum serovar B-1 from severe infectious coryza outbreaks in Panama.

The isolation and identification of Avibacterium paragallinarum serovar B-1 from severe infectious coryza outbreaks in broiler breeders in Panama is reported for the first time. Infectious coryza was absent for over a decade in the breeder farms area. Disease outbreaks were characterized by an up to 45% drop in egg production and increased mortality. Use of a commercial trivalent bacterin and a strengthened biosecurity program prevented outbreaks in susceptible flocks in the farm.

Typing of Haemophilus paragallinarum strains by using enterobacterial repetitive intergenic consensus-based polymerase chain reaction.

The enterobacterial repetitive intergenic consensus polymerase chain reaction (ERIC-PCR) technique was used for fingerprinting of reference strains and Mexican isolates of Haemophilus paragallinarum. A total of nine ERIC patterns were given by the nine serovar reference strains of this bacteria. Two Modesto (C-2) reference strains from different sources showed the same ERIC pattern. Seventeen ERIC patterns were obtained among 29 Mexican isolates included in the study, belonging to serovars prevalent in Mexico (A-1, A-2, B-1, and C-2). Obtained results indicate that the ERIC-PCR technique could be used as a molecular laboratory tool for subtyping of H. paragallinarum.