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A large number of studies have found that the five genes of LDHA, F-KER, DRD4, MSTN and CRY1 in the racing pigeons had single nucleotide polymorphisms, which were associated with the homing ability, making them become the potential SNP markers for molecular assisted breeding. The current detection methods were still based on the traditional RFLP, and the application of Sanger sequencing has not been reported. A detection method based on Sanger sequencing technology was established to identify the polymorphic sites in these five genes. The results showed that: the specific primers were designed for LDHA, F-KER, DRD4, MSTN and CRY1 genes in the racing pigeons to amplify the single nucleotide polymorphism sites. The obtained PCR products had single bands, showing good specificity. Further, the amplification and Sanger sequencing were performed on the feather DNA samples from 60 racing pigeons by using these primers. And the polymorphic genotyping results for each gene locus were successfully obtained. Finally, the distribution frequency of various genotypes among these 60 racing pigeons was statistically analyzed, and it was found that the frequencies of the relevant rare genotypes were all less than 5%, which were consistent with the frequencies reported in the foreign racing pigeon populations. The study showed that the established Sanger sequencing analysis method for SNP genotyping of racing pigeon performance-related genes had important application value for the breeding of racing pigeons with excellent genotypes. [ABSTRACT FROM AUTHOR]

Background: The currently known homing pigeon is a result of a sharp one-sided selection for flight characteristics focused on speed, endurance, and spatial orientation. This has led to extremely well-adapted athletic phenotypes in racing birds. Methods: Here, we identify genes and pathways contributing to exercise adaptation in sport pigeons by applying next-generation transcriptome sequencing of m.pectoralis muscle samples, collected before and after a 300 km competition flight. Results: The analysis of differentially expressed genes pictured the central role of pathways involved in fuel selection and muscle maintenance during flight, with a set of genes, in which variations may therefore be exploited for genetic improvement of the racing pigeon population towards specific categories of competition flights. Conclusions: The presented results are a background to understanding the genetic processes in the muscles of birds during flight and also are the starting point of further selection of genetic markers associated with racing performance in carrier pigeons. [ABSTRACT FROM AUTHOR]

This is the first study in Mosul to use genetic sequencing technology to diagnose and document the type, strain, and genotype of Trichomonos gallinae in racing pigeon. It was distinguished by the geographical sequence at the Mosul Iraqi city. Thirty isolates of T. gallinae were chosen from a total of 56 that had been molecularly characterized to examine the extent to which these isolates matched in terms of genetic sequencing. The DNA- from T. gallinae parasite was extracted, and the master mix for all of the polymerization reaction components was created based on the needed quantities of the reaction components for each sample. The acquired sequences were matched to known sequences in databases to determine the trichomonos species parasite and strain responsible for the infection. The results of the DNA sequencing examination revealed that after the polymerase chain reaction amplification products were sent to Macrogen, Korea to determine the genetic variation of the local strains, the products of the small subunit rRNA-Gene and the reaction product of bp 194 of the Trichomonos gallinae parasite were sent to the National Center for Biotechnology Information NCBI Gen Bank for recording. Based on the small partial ribosomal RNA according to blast in GenBank of of NCBI, the percentage of match in the genetic sequence was 100% between the genetic sequence in Mosul and the genetic sequences in Brazil and Portugal. France, Spain, Iran, Poland, Prague, Hungary, Australia, and the United States are among the countries involved. The Trichomonas gallinae genetic sequence in racing pigeons from Mosul has been discovered for the first time in the Gen Bank database, revealing a 100% match with other countries' sequences. This discovery reveals the pathogen's worldwide dissemination and interconnection, aiding in developing effective diagnostic procedures, preventive measures, and targeted treatments. The discovery also emphasizes the need for cooperation in monitoring and regulating the spread of the infection, supporting a collaborative strategy against avian diseases.

Background: Pigeon paramyxovirus serotype 1 and other virulent NDVs are known to cause multi-systemic infection in birds. However, very little is known about its pathology in poultry species. Methods: In this study, the gross and histopathological changes in various organs of PPMV-1-infected racing pigeons were characterized and morphologically diagnosed. A total of fifteen organs, grouped into organ systems, were analyzed. Results: Clinical history revealed that all pigeons were exhibiting nervous and gastrointestinal signs such as torticollis and green-white diarrhea. Morbidity and mortality rates were spiking at 10 to 15% and 10%, respectively. Gross and in situ examination showed that the brain, heart, lungs, and gastrointestinal tract were mostly affected. The majority of the macroscopic lesions include hemorrhage and variable signs of necrosis and degeneration. Histologically, the brain, kidneys, lungs, and portion of the gastrointestinal tract had presented multiple lesions which include congestion, hemorrhage, and vasculitis. Diffuse lymphoid depletion and necrosis were also notable in all lymphatic organs and related tissues. Conclusion: The results of this investigation support the multi-systemic involvement of the infection which further validates the need for stronger preventive and control measures against PPMV-1 and other avian paramyxoviruses not only for the domestic poultry but also for the other avian species. [ABSTRACT FROM AUTHOR]

ABSTRACT: Megriviruses have been identified from fecal samples in wild pigeons in Hong Kong (China) and Hungary. In this study, the genomic sequences of pigeon Megriviruses (PiMeVs) were downloaded from GenBank and compared. Based on the genetic comparison results, a pair of primers and TaqMan probe were designed based on the conserved sequences of the 3C gene (located in the P3 gene coding region), and a TaqMan real-time PCR method (TaqMan-qPCR) was established. The standard curve of the TaqMan-qPCR had an axial intercept of 39.74 and a slope of −3.2475 with a linear correlation (R2) of 1.00 and an efficiency of 103.2%. No cross-amplification signal was found from other pigeon viruses (such as avian influenza virus, pigeon paramyxovirus type I, pigeon torque teno virus, pigeon adenovirus, and pigeon circovirus). The limit of detection concentration was 53.6 copies/μL. The intra- and interassay results were less than 1.0% based on the reproducibility test. Furthermore, field samples investigation by the established TaqMan-qPCR method showed that positive signals can be found from racing pigeon fecal samples and embryos. Thus, our data suggested that this visible TaqMan-qPCR method is sensitive, specific, and reproducible. Moreover, we first confirmed the presence of pigeon Megrivirus infection in racing pigeon embryos, indicating that the virus may be vertically transmitted. This study provides a reference basis for further understanding the epidemiology of PiMeVs.

This is the first study in Mosul to use genetic sequencing technology to diagnose and document the type, strain, and genotype of Trichomonos gallinae in racing pigeons. It was distinguished by the geographical sequence of Mosul, Iraqi city. Thirty isolates of T. gallinae were chosen from a total of 56 that had been molecularly characterized to examine the extent to which these isolates matched in terms of genetic sequencing. The DNA from the T. gallinae parasite was extracted, and the master mix for all of the polymerization reaction components was created based on the needed quantities of the reaction components for each sample. The acquired sequences were matched to known sequences in databases to determine the trichomonos species parasite and strain responsible for the infection. The results of the DNA sequencing examination revealed that after the polymerase chain reaction amplification products were sent to Macrogen, Korea, to determine the genetic variation of the local strains, the products of the small subunit rRNA-Gene and the reaction product of bp 194 of the Trichomonos gallinae parasite were sent to the National Centre for Biotechnology Information, NCBI Gen Bank, for recording. Based on the small partial ribosomal RNA according to blast in GenBank of the NCBI, the percentage of match in the genetic sequence was 100% between the genetic sequence in Mosul and the genetic sequences in Brazil and Portugal. France, Spain, Iran, Poland, Prague, Hungary, Australia, and the United States are among the countries involved. The Trichomonas gallinae genetic sequence in racing pigeons from Mosul has been discovered for the first time in the GenBank database, revealing a 100% match with other countries' sequences. This discovery reveals the pathogen's worldwide dissemination and interconnection, aiding in the development of effective diagnostic procedures, preventive measures, and targeted treatments. The discovery also emphasises the need for cooperation in monitoring and regulating the spread of the infection, supporting a collaborative strategy against avian diseases. [ABSTRACT FROM AUTHOR]

SUMMARY: Pigeon paramyxovirus type 1 (PPMV-1; species Avian orthoavulavirus-1) causes a highly infectious, acute disease of Columbiformes. The objectives of this study were to estimate the occurrence of PPMV-1 in confinement-reared pigeons in California, conduct molecular characterization of PPMV-1 isolates from diagnostic cases, assess the presentation of the disease and identify epidemiological trends based on evaluation of pigeons cases submitted to the California Animal Health and Food Safety (CAHFS) laboratory system, January 1st 2010 to December 31st 2020. From 2010 to 2020, there were 230 pigeon necropsy diagnostic accessions that included a total of 679 pigeons submitted to the lab. PPMV-1 was diagnosed in 23% (53/230) of accessions involving 206/679 PPMV-1 positive pigeons submitted for necropsy. PPMV-1 was diagnosed at least once per year, with the highest percentage of diagnosed cases occurring in 2014 (41.7%, 5/12). Trichomoniasis (32.1%) was the most common comorbidity in squab cases while colibacillosis (20.0%) was most commonly detected in PPMV-1 positive racing and show pigeons. The severity of lesions in PPMV-1 cases was also highly variable and pathology was most often described in the kidneys, pancreas, brain, and spleen. Phylogenetic analysis was conducted on the matrix gene and portions of the phosphoprotein and fusion genes of 35 PPMV-1 isolates. The sequence similarities between strains ranged from 93 to 100% identity and all but one of the strains were segregated into 1 of 4 unique clades. While no temporal pattern was evident in the phylogenetic tree, there were some differences with regard to production class and geography.

Racing pigeons are potential carriers of zooanthroponic diseases, since they can travel considerable distances during their flight. The study of the formation features of the pigeon skeleton’s hematopoietic function on different levels of its structural organization with the determination of the relationship between the growth and development of hematopoietic components and the processes of osteohistogenesis is necessary to understand the immunity of pigeons, especially during the early stages of their development when young animals are in the greatest risk of disease, especially during processes of osteogenesis and haematopoiesis in chicks. The bones of the axial and peripheral skeleton of one-day-old, 5-, 10-, 15-, 20-, and 25-day-old pigeons (n = 5) were examined. The presence and degree of development of dia- and epiphyseal ossification centers (EOCs), their relative area (RA) and X-ray density in the organs of universal hematopoiesis were determined on radiographs made on an x-Ray-TW-102 x-ray machine with an Alpha 4600 receiver using the MultiVox Dicom Viewer program. It was established that in day-old pigeons the rudiments of the studied bones are completely built by cartilaginous tissue, have low radiographic density, and fuzzy contours on radiographs. On the 10th day of life, the axial skeleton of pigeon cubs has formed EOCs of head and a tubercle on the 5th rib (third «true rib»), while in the bones of the peripheral skeleton there is an enchondral EOC of the diaphysis. The spongy and compact bone structure (BS) of the bones were fuzzy. The body of the rib and the epiphyses of the limbs’ tubular bones were cartilaginous. The X-ray density of the humerus at this age remains unchanged, and the tibial-metatarsal increases by 1.5 times, reaching 12 HU. In 15-day-old chicks, the RA of the EOC in the skeleton was moderately increased due to an increase in the RA of previously formed EOCs at the age of 10 days, the appearance of individual EOCs in the body of 5th rib, and in the tubular bones of the limbs, the enchondral EOCs of the proximal and distal epiphyses. In the diaphysis of the extremities tubular bones, a strip-like compact BS was clearly distinguished, and in the epiphyses, a small-sized spongy BS. The X-ray density of the bones almost doubled, reaching 19–21 HU. In 20-day-old pigeons, the processes of osteohistogenesis in the skeleton were almost completed, in the studied bones, all the main and additional EOCs were well expressed, their RA increased sharply. X-ray density of bones did not change. For 25-day-old pigeons in the skeleton, there was a slight increase in RA of the EOC, a process of complete synostosis of the bones was characteristic. From the moment of the appearance of the EOC in 10-day-old chicks until they reach the age of 25 days, the bones of the axial skeleton and the skeleton of the limbs were formed by 95–100% of BS, and their X-ray density was increased almost 2.5 times, reaching 19–26 HU.

ABSTRACT Investigations into LDH-A and DR-D4 genes polymorphism, neurotransmitter values and cytogenetic indices of 3 sexed pigeon breeds; non-racing pigeons, (wild rock), racing long distances pigeons (Jan Aarden) and racing short distances pigeons (Janssen) have been performed. The long-distances pigeon showed the highest brain neurotransmitters concentration (p

Abstract Background This study was aimed to investigate the intestinal microbiota in racing pigeons with regard to Enterococcus species distribution, virulence factors and antibiotic susceptibility. Three methods (API, Multiplex sodA-PCR, 16S rRNA sequencing) were compared for Enterococcus species identification. Cloacal samples from 179 apparently healthy pigeons of 13 different flocks were tested. Results Multiplex sodA-PCR and 16S rRNA gene sequencing showed almost perfect agreement in Enterococcus species identification. Isolates were identified as Enterococcus columbae (34.5%), Enterococcus hirae (20.7%), Enterococcus faecalis (11.7%), Enterococcus faecium (11.7%), Enterococcus gallinarum (9%), Enterococcus mundtii (4.8%), Enterococcus casseliflavus (3.4%), Enterococcus cecorum (2.1%), Enterococcus durans (2.1%). More Enterococcus species were found after the race season than before. The study showed differences between Enterococcus species in relation to 68.8% (22/32) biochemical parameters. Six out of seven virulence genes were detected: gelE (43.5%), asa1 (42.1%), efaA (30.3%), ace (30.3%), cylA (27.6%), and esp (9%). None of the isolates harboured hyl gene. Overall 15.2% of Enterococcus isolates produced gelatinase, but 66.7% gelE genes were silent. Enterococcus faecalis showed the most often efaA, ace and gelatinase activity than other enterococcal species. Nearly all isolates (93.1%) were resistant to at least one antibiotic. The most frequent resistance was to enrofloxacin (80%), doxycycline with teicoplanin (73.1%), erythromycin (49.7%). The study revealed significant differences between some enterococcal species in the antibiotic susceptibility to different antibiotics. Enterococcus columbae and E. cecorum showed significantly more frequent resistance to chloramphenicol than other enterococci. The presence of VRE (19.3%), HLGR (2.8%) and no LRE were found. Overall 30.3% of isolates were positive for vancomycin resistance genes, where vanC1 (E. gallinarum), vanC2-C3 (E. hirae, E. casseliflavus), vanB (E. columbae) predominated. Conclusions We conclude, that intestinal microbiota in racing pigeons is composed by 9 different Enterococcus species. Given that racing pigeons are kept in close contact with humans and backyard animals, combined with their long-distance flight abilities, they can serve as potential source of virulent and antibiotic resistant Enterococcus spp. in the environment.

Pigeon paramyxovirus serotype 1 (PPMV-1) is a variant of the velogenic NDV that primarily infects pigeons however, the infection is not only limited to the pigeon population. Due to its ability to spill-over, PPMV-1 can potentially exacerbate economic losses due to poultry mortalities. Currently, there has not been a reported clinical case of the infection in the Philippines yet. In this investigation, suspected PPMV-1 infection in racing pigeons from Luzon, Philippines were submitted for phylomolecular characterization. The presence of the pathogen was confirmed through the use of multiplex RT-PCR and nested RT-PCR. Nucleotide sequence analysis using the hypervariable region of the fusion (F) gene revealed that the isolates were velogenic, with a proteolytic cleavage site motif of 112KRQKRF117. Phylogenetic analysis and subgenotyping further characterized the field strains as a member virus of the subgenotype VIb/2 group. Comparison of the nucleotide sequence showed that the samples share high sequence homology with the Russian, Egyptian, Iranian, Austrian, and Ukrainian isolates. The results of this molecular characterization study on PPMV-1 from the Philippines would help design better prevention and control measures for this important pathogen. [ABSTRACT FROM AUTHOR]

Background: This study was aimed to investigate the intestinal microbiota in racing pigeons with regard to Enterococcus species distribution, virulence factors and antibiotic susceptibility. Three methods (API, Multiplex sodA-PCR, 16S rRNA sequencing) were compared for Enterococcus species identification. Cloacal samples from 179 apparently healthy pigeons of 13 different flocks were tested. Results: Multiplex sodA-PCR and 16S rRNA gene sequencing showed almost perfect agreement in Enterococcus species identification. Isolates were identified as Enterococcus columbae (34.5%), Enterococcus hirae (20.7%), Enterococcus faecalis (11.7%), Enterococcus faecium (11.7%), Enterococcus gallinarum (9%), Enterococcus mundtii (4.8%), Enterococcus casseliflavus (3.4%), Enterococcus cecorum (2.1%), Enterococcus durans (2.1%). More Enterococcus species were found after the race season than before. The study showed differences between Enterococcus species in relation to 68.8% (22/32) biochemical parameters. Six out of seven virulence genes were detected: gelE (43.5%), asa1 (42.1%), efaA (30.3%), ace (30.3%), cylA (27.6%), and esp (9%). None of the isolates harboured hyl gene. Overall 15.2% of Enterococcus isolates produced gelatinase, but 66.7% gelE genes were silent. Enterococcus faecalis showed the most often efaA, ace and gelatinase activity than other enterococcal species. Nearly all isolates (93.1%) were resistant to at least one antibiotic. The most frequent resistance was to enrofloxacin (80%), doxycycline with teicoplanin (73.1%), erythromycin (49.7%). The study revealed significant differences between some enterococcal species in the antibiotic susceptibility to different antibiotics. Enterococcus columbae and E. cecorum showed significantly more frequent resistance to chloramphenicol than other enterococci. The presence of VRE (19.3%), HLGR (2.8%) and no LRE were found. Overall 30.3% of isolates were positive for vancomycin resistance genes, where vanC1 (E. gallinarum), vanC2-C3 (E. hirae, E. casseliflavus), vanB (E. columbae) predominated. Conclusions: We conclude, that intestinal microbiota in racing pigeons is composed by 9 different Enterococcus species. Given that racing pigeons are kept in close contact with humans and backyard animals, combined with their long-distance flight abilities, they can serve as potential source of virulent and antibiotic resistant Enterococcus spp. in the environment. [ABSTRACT FROM AUTHOR]

The ventricular filling velocities during diastole and the influence of isoflurane anesthesia on these blood flow velocities of the racing pigeon (n = 43) are evaluated by pulsed-wave (PW) Doppler sonography. Sonographic examination demonstrates an early passive ventricular (E wave) and late active (A wave) ventricular filling. The results indicate differences between the two heart ventricles. Especially, the E wave velocity of the right heart is significantly lower than in the left heart, which is explained by the crescent-shaped cavity of the right ventricle around the left ventricle. The faster active filling velocities are significantly influenced by heart rate in conscious birds. Anesthesia with isoflurane leads to a significant decrease of the diastolic blood flowvelocities, and the Awave velocities of both ventricles are especially influenced. Anesthesia with isoflurane induces a high incidence of insufficiencies of the left atrioventricular valve in the preejection period. These observations indicate that a contraction of the left ventricle myocardium is important for a complete valvular closure and for normal functioning of this heart valve. The effective closure of the right atrioventricular muscle valve in anesthetized pigeons supports the observation of the fast innervation of this muscle valve via a direct connection to the right atrium. [ABSTRACT FROM AUTHOR]

Copyright of Avian Diseases is the property of American Association of Avian Pathologists, Inc. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The development of accurate and reliable analytical methodologies to detect the abuse of doping agents in sport animals is crucial to ensure their welfare, as well as to support continuing social acceptance of these sports. The detection of doping agents in racing pigeons is difficult, especially owing to the disadvantages and limitations of obtaining samples from conventional matrices. The present study aimed to develop and validate an analytical methodology combining a two-step extraction procedure (liquid–liquid extraction and solid-phase extraction) in feathers from racing pigeons with analysis by liquid chromatography tandem mass spectrometry (LC–MS-MS) that enabled the simultaneous detection of a beta-agonist drug (clenbuterol) and three corticosteroids (prednisolone, betamethasone and budesonide). The method was validated concerning linearity (with coefficients of determination always higher than 0.99), accuracy (87.3–112.4%), precision (repeatability and intermediate precision coefficient of variation (CV%) always below 15%), recovery (71.6–98.2%), limits of detection (0.24–0.52 ng/g) and quantification (0.79 and 0. 1.74 ng/g) and specificity. The applicability of the method was performed using feathers from pigeons administered orally with a daily dose of 0.075 mg of betamethasone. The drug was administered during 60 days and successive analyses of feathers were performed, at the end of the administration protocol and also after ceasing the oral administration of the drug, for a three weeks period. [ABSTRACT FROM AUTHOR]

Megriviruses have been identified from fecal samples in wild pigeons in Hong Kong (China) and Hungary. In this study, the genomic sequences of pigeon Megriviruses (PiMeVs) were downloaded from GenBank and compared. Based on the genetic comparison results, a pair of primers and TaqMan probe were designed based on the conserved sequences of the 3C gene (located in the P3 gene coding region), and a TaqMan real-time PCR method (TaqMan-qPCR) was established. The standard curve of the TaqMan-qPCR had an axial intercept of 39.74 and a slope of −3.2475 with a linear correlation (R 2) of 1.00 and an efficiency of 103.2%. No cross-amplification signal was found from other pigeon viruses (such as avian influenza virus, pigeon paramyxovirus type I, pigeon torque teno virus, pigeon adenovirus, and pigeon circovirus). The limit of detection concentration was 53.6 copies/μL. The intra- and interassay results were less than 1.0% based on the reproducibility test. Furthermore, field samples investigation by the established TaqMan-qPCR method showed that positive signals can be found from racing pigeon fecal samples and embryos. Thus, our data suggested that this visible TaqMan-qPCR method is sensitive, specific, and reproducible. Moreover, we first confirmed the presence of pigeon Megrivirus infection in racing pigeon embryos, indicating that the virus may be vertically transmitted. This study provides a reference basis for further understanding the epidemiology of PiMeVs. [ABSTRACT FROM AUTHOR]

The racing season is considered a critical period for racing pigeons due to the susceptibility to stress and weakening of the birds. One of the ways how to support their health and avoid problems involves supplementation of mineral-vitamin preparations based on selenium and vitamin E, which act as important antioxidants and protect cells against damage. This study investigated the influence of peroral supplementation of selenium at a dose of 0.3 mg Se.kg−1 feed dry matter (DM) in the form of Na2SeO3 and vitamin E 300 mg.ml−1 added to water at a rate of 4 ml.l−1 during 60 days. The supplemented group comprised 14 pigeons and their results were compared with a control group of 14 pigeons fed non-supplemented commercial feed. Blood samples were collected and examined at the beginning of the supplementation period, one day before a 300 km race and after the race. Pigeons from the supplemented group exhibited increased plasma levels of Se and vitamin E, as well as the activity of glutathione peroxidase (GSH-Px) before and after the 300 km race in comparison with the controls. Comparison of the activity of the enzymes: alanine aminotransferase (ALT), aspartate aminotransferase (ASP), alkaline phosphatase (ALP), and creatinine kinase (CK) at the beginning of the supplementation and one day before the race showed no changes. A significant (P < 0.05) increase in the activity of all investigated enzymes were observed after the race in both groups.

Copyright of Acta Scientiarum Polonorum seria Zootechnica is the property of West Pomeranian University of Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Acta Scientiarum Polonorum seria Zootechnica is the property of West Pomeranian University of Technology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Oropharyngeal swab samples were collected from 438 live racing pigeons ( Columba livia), with and without signs of respiratory disease, that were housed in 220 lofts in 3 provinces in the western part of the Netherlands. Polymerase chain reaction (PCR) was used to identify Mycoplasma species and pigeon herpesvirus-1 (PHV-1) from the samples. In 8.6% of the pigeon lofts tested, signs of respiratory disease were present in pigeons at sampling, and in 30.9% of the sampled pigeon lofts, respiratory signs were observed in pigeons during the 6-month period immediately before sampling. A total of 39.8% of tested pigeons (54.5% of tested lofts) were positive for Mycoplasma species, and 30.6% of tested pigeons (48.6% of tested lofts) were positive for PHV-1. In 15.8% of the tested pigeons (26.8% of tested pigeon lofts), coinfection by Mycoplasma species and PHV-1 was identified. The number of pigeon lofts having pigeons coinfected by Mycoplasma species and PHV-1 was higher than that where only one of the infections was identified. Neither the presence of Mycoplasma species, PHV-1, nor the co-occurrence of both infections was significantly associated with signs of respiratory disease. [ABSTRACT FROM AUTHOR]

Extensive diversity has been described within the avian oropharyngeal trichomonad complex in recent years. In this study we developed clonal cultures from four isolates selected by their different ITS1/5.8S/ITS2 (ITS) genotype and their association with gross lesions of avian trichomonosis. Isolates were obtained from an adult racing pigeon and a nestling of Eurasian eagle owl with macroscopic lesions, and from a juvenile wood pigeon and an European turtle dove without clinical signs. Multi-locus sequence typing analysis of the ITS, small subunit of ribosomal rRNA (SSUrRNA) and Fe-hydrogenase (Fe-hyd) genes together with a morphological study by optical and scanning electron microscopy was performed. No significant differences in the structures were observed with scanning electron microscopy. However, the genetic characterisation revealed novel sequence types for the SSUrRNA region and Fe-hyd gene. Two clones were identified as Trichomonas gallinae in the MLST analysis, but the clones from the racing pigeon and European turtle dove showed higher similarity with Trichomonas tenax and Trichomonas canistomae than with T. gallinae at their ITS region, respectively. SSUrRNA sequences grouped all the clones in a clade that includes T. gallinae , T. tenax and T. canistomae . Further diversity was detected within the Fe-hyd locus, with a clear separation from T. gallinae of the clones obtained from the racing pigeon and the European turtle dove. In addition, morphometric comparison by optical microscopy with clonal cultures of T. gallinae revealed significant statistical differences on axostyle projection length in the clone from the European turtle dove. Morphometric and genetic data indicate that possible new species within the Trichomonas genus were detected. Taking in consideration the diversity in Trichomonas species present in the oral cavity of birds, a proper genetic analysis is highly recommended when outbreaks occur. [ABSTRACT FROM AUTHOR]

A very small size radio frequency identification (RFID) tag antenna specifically designed for racing pigeon ring applications is proposed. The structure of this UHF tag is a closed-loop type printed on a 30 × 8 mm2 polyimide film of thickness 0.063 mm. Thus, it can be wrapped into a double layer plastic cylindrical ring of size similar to those used for racing pigeon. By simply tuning the inner width of the loop, good conjugate matching between the tag chip input impedance and the tag antenna can be achieved. When mounted onto a real preserved dried pigeon feet specimen, the measured impedance bandwidth of the tag antenna was 901-929 MHz. Further experimental results have also shown that the proposed antenna has a maximum reading range of up to 50 cm. [ABSTRACT FROM AUTHOR]

Pigeon paramyxovirus type 1 (PPMV-1 ; species Avian orthoavulavirus-1) causes a highly infectious, acute disease of Columbiformes. The objectives of this study were to estimate the occurrence of PPMV-1 in confinement-reared pigeons in California, conduct molecular characterization of PPMV-1 isolates from diagnostic cases, assess the presentation of the disease and identify epidemiological trends based on evaluation of pigeons cases submitted to the California Animal Health and Food Safety (CAHFS) laboratory system, January 1st 2010 to December 31st 2020. From 2010 to 2020, there were 230 pigeon necropsy diagnostic accessions that included a total of 679 pigeons submitted to the lab. PPMV-1 was diagnosed in 23% (53/230) of accessions involving 206/679 PPMV-1 positive pigeons submitted for necropsy. PPMV-1 was diagnosed at least once per year, with the highest percentage of diagnosed cases occurring in 2014 (41.7%, 5/12). Trichomoniasis (32.1%) was the most common comorbidity in squab cases while colibacillosis (20.0%) was most commonly detected in PPMV-1 positive racing and show pigeons. The severity of lesions in PPMV-1 cases was also highly variable and pathology was most often described in the kidneys, pancreas, brain, and spleen. Phylogenetic analysis was conducted on the matrix gene and portions of the phosphoprotein and fusion genes of 35 PPMV-1 isolates. The sequence similarities between strains ranged from 93 to 100% identity and all but one of the strains were segregated into 1 of 4 unique clades. While no temporal pattern was evident in the phylogenetic tree, there were some differences with regard to production class and geography. [ABSTRACT FROM AUTHOR]

Background: Recent epidemics of highly pathogenic avian influenza (HPAI) produced an unprecedented number of cases in mute swans (Cygnus olor) in European countries, which indicates that these birds are very sensitive to the H5N1 virus. The HPAI outbreaks stirred a debate on the controversial stamping-out policy in populations of protected bird species. After preventive vaccination had been approved in the European Union, several countries have introduced vaccination schemes to protect poultry, captive wild birds or exotic birds in zoos against HPAI. The aim of this study was to investigate the immune response of wild mute swans to immunization with an inactivated AI H5N2 vaccine approved for use in poultry. The serological responses of mute swans were assessed by comparison with racing pigeons (Columba livia), a species which is characterized by different susceptibility to infection with the H5N1 HPAI virus and plays a questionable role in the ecology of influenza (H5N1) viruses. Results: Swans were vaccinated once or twice at an interval of 4 weeks. The humoral immune response was evaluated by hemagglutination inhibition (HI) and NP-ELISA. The lymphocyte blast transformation test was used to determine the cell-mediated immune response. Higher values of the geometric mean titer (GMT) and 100% seroconversion (HI ≽32) were noted in double vaccinated swans (1448.2) than in single vaccinated swans (128.0) or in double vaccinated pigeons (215.3). Significant differences in HI titers were observed between swans and pigeons, but no variations in ELISA scores were noted after the booster dose. Immunization of swans had no effect on the proliferative activity of lymphocytes. Conclusions: The inactivated H5N2 vaccine was safe and immunogenic for mute swans and pigeons. Vaccination may have practical implications for swans kept in zoos, wildlife parks or rehabilitation centers. However, challenge studies are needed to prove the efficacy of the H5N2 AI vaccine. [ABSTRACT FROM AUTHOR]

Succinate dehydrogenase (SDH), Ca2+ ATPase, Lactate dehydrogenase (LDH), are involved in energy metabolism. These enzymes can be used as indicators of the energy capacity of aerobic cells. The study investigated the effects of l-carnitine supplementation on M. pectoralis superficialis, M. pectoralis profundus, M. extensor carpi radialis muscle and M. flexor carpi ulnaris. Twenty-eight racing pigeons hatched at the same time were divided randomly into three groups. Eight pigeons, which were used as the control group, were sacrificed at 92-day old. The remaining twenty pigeons continued training until they reached 157-day old, with half the pigeons getting 25 mg/head/day of l-carnitine, while the other half given the same amount of water. The pigeons were assessed by histochemical methods and reverse transcription polymerase chain reaction (RT-PCR). To assess influence of l -carnitine on muscle fibre composition and the performance of three genes' mRNA, this study applied SDH localization, SDH, Ca 2+ ATPase and LDH mRNA expression to examine the results after oral administration of l-carnitine in vivo in racing pigeons. The results showed that l-carnitine significantly elevated the amount of white muscle fibre type IIa (p < 0.05). The mRNA expression quantities of SDH and LDH gene was higher via RT-PCR method. However, the expression of Ca 2+ ATPase remains similar. In conclusion, appropriate oral administration of l-carnitine of 25 mg/pigeon/day will result in an improvement of muscles related to flying. [ABSTRACT FROM AUTHOR]

Trichomonas gallinae, the cause of avian trichomonosis, is most commonly found in the order Columbiformes. Racing pigeons are often treated preventively with nitro-imidazoles, which could result in the emergence of resistant isolates, and these isolates can be a threat to wildlife when exchanges occur. The sequence type of 16 T. gallinae isolates obtained from racing pigeons and 15 isolates from wild pigeons was determined based on the ITS1/5.8S rRNA/ITS2 region sequence. In addition, the resistance profiles of these isolates against 5 different nitro-imidazoles (metronidazole, dimetridazole, ronidazole, tinidazole, and carnidazole) were determined. Two different Trichomonas sequence types were isolated. Sequence type A isolates were recovered from racing and wild pigeons, in contrast to sequence type B, which was only isolated from wild pigeons. Isolates with sequence type B were all susceptible to the tested nitro-imidazoles, except for tinidazole resistance in 3 isolates. Resistance to the nitro-imidazoles was observed more frequently in isolates obtained from racing pigeons than from wild pigeons, with most isolates belonging to sequence type A. A higher percentage of the sequence type A isolated from racing pigeons, in comparison with those isolated from the wild pigeons, were resistant to the nitro-imidazoles and displayed higher mean lethal concentration (MLC) values. Two isolates belonging to sequence type A, 1 recovered from a racing pigeon and 1 from a wild pigeon, displayed a similar resistance pattern, suggesting a potential exchange of resistant isolates between racing pigeons and wild pigeons. [ABSTRACT FROM AUTHOR]

Clinically healthy racing pigeons may harbour notifiable pathogens and serve as an unnoticed reservoir. Thus, 3480 healthy racing pigeons from 172 different lofts were monitored over a period of 2 years for the presence of avian influenza virus (AIV) and avian paramyxovirus-1 (APMV-1). Pharyngeal and cloacal swabs as well as blood samples were collected from juvenile and adult pigeons. Pools of five pharyngeal swabs per loft and age group were initially screened by real-time reverse transcriptase-polymerase chain reaction (rRT-PCR). Pharyngeal and cloacal samples from lofts that were positive or suspect in the AIV rRT-PCR or the APMV-1 rRT-PCR were inoculated into embryonated chicken eggs for virus isolation. In addition, sera were examined for antibodies against AIV by enzyme-linked immunosorbent assay. The antibody levels after vaccination against APMV-1 were determined by haemagglutination inhibition assay. Of the investigated lofts, 0.0 to 1.4% were positive by rRT-PCR for APMV-1 and 0.0 to 6.7% for AIV during this 2-year period with a total of four samplings. No sample yielded replicating virus in egg culture. No antibodies against AIV were detected. Haemagglutination inhibition test of vaccinated racing pigeons indicated age-dependent APMV-1 titres. The results suggest that the examined racing pigeons may have had contact with AIV, but virus replication may have been too low to induce detectable circulating antibody levels. Only a low percentage of samples were positive for APMV-1, but two outbreaks were observed in monitored flocks, indicating ongoing circulation of APMV-1 in the racing pigeon population. These observations highlight the relevance of APMV-1 vaccination and indicate the importance of flock immunity. [ABSTRACT FROM PUBLISHER]

The diagnostic evaluation of the glomerular filtration rate by urinary clearance has significant practical limitations in birds because urine is excreted together with feces. Thus, pharmacokinetic modeling of an exogenous plasma creatinine clearance could be useful for assessing renal creatinine excretion in birds. For this study, creatinine (50 mg/kg) was administered to 2 groups of 15 pigeons (Columba livia) each; in one group by the intravenous (IV) route and in the second by the intramuscular (IM) route. The time series of the plasma creatinine concentrations were analyzed by pharmacokinetic models. Body mass-specific creatinine excretion was determined for IV and IM administration to be between 6.30 and 6.44 mL/min per kg, respectively. Body surface area-specific creatinine clearance, which is related to the metabolic rate, was calculated between 0.506 and 0.523 mL/min per dm², respectively. The results showed that IV as well as IM administration can be used for assessing renal creatinine excretion in pigeons. For practical reasons, IM administration is recommended, with the use of the Bateman function to calculate creatinine elimination. [ABSTRACT FROM AUTHOR]

The history and geography of sports in nineteenth- and twentieth-century France have been studied intensively during the last thirty years but one sport -- that of pigeon racing -- has received virtually no attention. This paper ventures into a largely unexplored field. After describing briefly the general history of homing pigeons and the specific geography of pigeon racing clubs in France in 1890, it focuses on the département of Pas-de-Calais in northern France. Pas-de-Calais and the adjacent département of Nard together accounted for more than half of the just over 400 pigeon racing clubs identified in France in 1890. Within the context of the rapid development between 1870 and 1914 of its population, society and economy (and especially its coalmining industry), Pas-de-Calais saw the creation of more than one thousand recreational societies, especially sports clubs, among them numerous pigeon racing clubs. Three hundred pigeon racing clubs in one of the département's six arrondissements -- that of Béthune -- are examined closely from surviving but fragmentary sources. The aims, names, membership and racing activities of these societies are studied from their unpublished records. They are shown to have developed in close association with the growth of coalmining communities and in particular with the role of Belgian immigrants in those communities. [ABSTRACT FROM AUTHOR]

Newcastle disease (ND) is a devastating disease of poultry that has to some extent been neglected by those working in the field in the past 10 to 15 years while attention has been focused on the emergence and spread of highly pathogenic avian influenza caused by a H5N1 subtype virus. During 2000 to 2009 in the European Union (EU) member states, ND viruses virulent for chickens have been detected in wild birds, domesticated pigeons and poultry. Based on these isolations it appears that the epizootic in racing pigeons caused by the variant viruses termed pigeon avian paramyxovirus type 1, which form the genetic group 4b(VIb) first seen in Europe in 1981, continued during 2000 to 2009, and the virus is probably enzootic in racing pigeons in some EU countries. This virus appears to have spread regularly to wild birds, especially those of the Columbidae family, and has been the cause of significant outbreaks in poultry. Other avian paramyxovirus type 1 viruses responsible for ND outbreaks in the EU during 2000 to 2009 have been those from genetic groups 5b(VIIb) and 5d(VIId). There is evidence that the former may well represent spread from a wild bird source and these viruses have also been isolated from wild birds, while the latter represents continuing spread from the East. Future legislation or recommendations aimed at the control and eradication of ND will need to encompass these three sources of virulent ND viruses. [ABSTRACT FROM PUBLISHER]

Abstract: The emerging Sarcocystis calchasi induces a severe and lethal central nervous disease in its intermediate host, the domestic pigeon (Columba livia f. domestica). Experimental studies have identified the Northern goshawk (Accipiter g. gentilis) as final host. Phylogenetically closely related European sparrowhawks (Accipiter n. nisus) and wood pigeons (Columba palumbus) have been found to harbor genetically closely related Sarcocystis spp. However, data on the prevalence and potential interspecies occurrence of these parasites are lacking. Here, we report that European Accipiter hawks (Accipitrinae) are highly infected with S. calchasi, S. columbae and Sarcocystis sp. ex A. nisus in their small intestine. Thirty-one of 50 (62%) Northern goshawks necropsied during 1997–2008 were positive for S. calchasi in a newly established species-specific semi-nested PCR assay based on the first internal transcribed spacer region. Unexpectedly, 14 of 20 (71.4%) European sparrowhawks tested also positive. In addition, birds of both species were found to be infested with S. columbae and an, as yet, unnamed Sarcocystis sp. recently isolated from European sparrowhawks. These findings raise new questions about the host specificity of S. calchasi and its high virulence in domestic pigeons, since sparrowhawks only rarely prey on pigeons. Notably, isolated sporocysts from both infected Accipiter spp. measured 8μm×11.9μm, precluding a preliminary identification of S. calchasi in feces of Accipiter hawks based on morphology alone. Importantly, three of four Northern goshawks used in falconry tested positive for S. calchasi. In conclusion, the results indicate that both European Accipter spp. in Germany serve as natural final hosts of S. calchasi and suggest that falconry and pigeon sport may serve as risk factors for the spread of this pathogen in domestic pigeons. [ABSTRACT FROM AUTHOR]

Selenium is a trace element of importance for animal health. It is essential for adequate functioning of many enzymes such as, the antioxidant enzyme, glutathione peroxidase, which protects the cell against free radicals. A muscular effort induces a rise in reactive oxygen species production which, in turn, can generate an oxidative stress. Two groups of eight racing pigeons were fed respectively with a diet containing 30.3 (control group) and 195.3 (selenium group) μg selenium/kg diet. The pigeons were submitted to a standardised simulation of a flying effort during 2 h. Blood was taken before and after the effort to measure antioxidant markers and blood parameters related to muscle metabolism. Plasma selenium concentration and glutathione peroxidase activity were significantly higher in the selenium group. There were no significant differences for the other measured parameters. As a consequence of the effort, the pigeons of the selenium group showed a higher increase of glutathione peroxidase activity and a smaller increase of plasma lactate concentration. Variations because of the effort in the other markers were not significantly different between the two groups. It is concluded that the selenium status was improved with the feeding of feedstuffs high in Selenium. [ABSTRACT FROM AUTHOR]

The aim of this study was to determine the basic haematological parameters in feral and racing pigeons and to compare these parameters according to age, sex and season in healthy feral pigeons as well as between Chlamydophila-serologically positive and negative feral pigeons. Red blood cells (RBC), packed cell volume (PCV), haemoglobin (Hb), mean cell volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), white blood count (WBC), thrombocyte count and differential WBC, were determined in 366 pigeons ( Columba livia forma domestica) captured in the City of Zagreb between 1999 and 2002. Of these, 232 feral (179 adult and 53 juvenile, 104 male and 75 female) and 57 racing pigeons (25 male and 32 female) were clinically healthy and bacteriologically and serologically negative, but 77 birds had antibody titres against Chlamydophila sp. Significantly lower values of RBC, PCV, Hb, MCH, WBC and thrombocyte ( P<0.05) were observed in young compared to adult pigeons, while the differences in MCV and MCH were not significant between age classes. In differential WBC of young pigeons, a significantly higher percentage of heterophils, eosinophils, basophils and monocytes and a significantly smaller percentage of lymphocytes ( P<0.01) was found than in adult pigeons. Significant sex-related differences were seen only in MCV values and in the percentage of lymphocytes (higher in females) and neutrophils (higher in males). PCV, Hb, MCV and MCH increased, while WBC decreased during wintertime ( P<0.05). In differential WBC, percentage of heterophils was low in summer and autumn. At the same time, a higher percentage of basophils was found. Low numbers of monocytes were found in summer and low values of eosinophils in winter. In racing pigeons, values of eosinophils and basophils were significantly lower than in feral pigeons. Pigeons which had antibodies against Chlamydophila sp. possessed a higher percentage of monocytes and less lymphocytes than sero-negative animals, while WBC was significant lower than in sero-negative feral pigeons. [ABSTRACT FROM AUTHOR]

An adult racing pigeon ( Columba livia ) was presented with a subcutaneous mass on the ventral aspect of the right wing. A fine-needle aspirate and radiographic study of the mass were suggestive of highly invasive sarcomatous neoplasm. Euthanasia was decided because of the poor prognosis. Necropsy confirmed the highly invasive nature of the neoplasm, which also occupied a large portion of the right breast. There also was extensive osteolysis of the sternum with neoplastic invasion of the left breast and the coelomic cavity. Histopathology revealed a highly cellular, poorly demarcated, unencapsulated invasive sarcoma. Immunohistochemistry was positive for muscle actin, and myoglobin, weakly positive for vimentin, and negative for desmin, neuron-specific enolase and S-100 protein, suggesting a diagnosis of undifferentiated rhabdomyosarcoma. [ABSTRACT FROM AUTHOR]