Disease In Pigeons Research Articles

Comparative Analysis of Newcastle Disease Seroprevalence in Different Breeds of Pigeon Populations in Chattogram Bangladesh

This study was performed to determine the antibody against Newcastle disease and serum protein level in pigeons of Chattogram, Bangladesh. The results were evaluated in pigeons of different groups of age, sex, and breed by applying the hemagglutination inhibition (HI) test. A total of 90 pigeons were selected for this research. Antibody titer against Newcastle Disease virus was analyzed according to the different age groups, sex, breeds and clinical signs of ND infection of pigeons by X2 test. Incase of less than 6 month age pigeons 73% (n=22) were HI titer positive whereas more than 6 months but less than 1 year 56% (n=32) were HI negative. There was no significant variation among different sex. In both male and female pigeon groups, the percentage of HI titer-positive pigeons in females and males was 51.7% and 57.4% respectively. There was significant variation among the different breeds and equal percentages of HI titer positive and negative pigeons were found in Giribaj and local breeds whereas 100% were found in King and Owl breeds and 80% were found in the Siraji breed. There was significant variation among NDV-infected and non-infected pigeons and equal percentage of HI titer negative and positive pigeons were found in ND non- infected, whereas (80.8%) were found in ND infected pigeons. A paired test was done between HI titer and total serum protein. There was a significant (t<0.0) difference among the group. In the case of HI titer mean was about 23 titer and the standard error was 0.28. In the case of total serum protein mean was 4.45 and the standard error was 0.19.

Comparative Analysis of Newcastle Disease Seroprevalence in Different Breeds of Pigeon Populations in Chattogram, Bangladesh

This study was performed to determine the antibody against Newcastle disease and serum protein level in pigeons of Chattogram, Bangladesh. The results were evaluated in pigeons of different groups of age, sex, and breed by applying the hemagglutination inhibition (HI) test. A total of 90 pigeons were selected for this research. Antibody titer against Newcastle Disease virus was analyzed according to the different age groups, sex, breeds, and clinical signs of ND infection of pigeons by X2 test. In the case of fewer than 6 months of age pigeons, 73% (n=22) were HI titer positive whereas more than 6 months but less than 1 year 56% (n=32) were HI negative. There was no significant variation among the different sexes. In both male and female pigeon groups, the percentage of HI titer-positive pigeons in females and males was 51.7% and 57.4% respectively. There was significant variation among the different breeds and equal percentages of HI titer positive and negative pigeons were found in Giribaj and local breeds whereas 100% were found in King and Owl breeds and 80% were found in the Siraji breeds. There was significant variation among NDV-infected and non-infected pigeons and an equal percentage of HI titer negative and positive pigeons were found in ND non-infected, whereas (80.8%) were found in ND-infected pigeons. A paired test was done between HI titer and total serum protein. There was a significant (t<0.0) difference among the groups. In the case of HI titer mean was about 23 titer and the standard error was 0.28. In the case of total serum protein mean was 4.45 and the standard error was 0.19.

RAA-CRISPR/Cas12a-Mediated Rapid, Sensitive, and Onsite Detection of Newcastle Disease in Pigeons.

Pigeon Newcastle disease, caused by pigeon paramyxovirus type 1 (PPMV-1), is a significant infectious disease in pigeons that can result in substantial mortality and poses a severe threat to the pigeon industry. The rapid and accurate onsite diagnosis of pigeon disease is crucial for timely diagnosis and the implementation of effective prevention and control measures. In this study, we established a rapid detection method for PPMV-1 based on recombinase-aided amplification (RAA) and CRISPR/Cas12a. The RAA primers target the conserved regions of the L gene for preamplification in clinical nucleic acid samples, followed by CRISPR/Cas12a detection of the target gene. Visualization could be achieved by combination with a lateral flow dipstick (LFD). This method demonstrated high specificity, showing no cross-reactivity with non-PPMV-1 samples. The sensitivity of the method assessed by fluorescence analysis reached 100 copies/µL, and when it was combined with an LFD, the sensitivity was 103 copies/µL. The constructed RAA-CRISPR/Cas12a-LFD visual detection method was applied to clinical sample testing and was found to enable the rapid and accurate detection of swab samples and tissue specimens. Its sensitivity was consistent with the current gold standard, quantitative real-time PCR results. The RAA-CRISPR/Cas12a-LFD detection method we developed provides a novel approach for the rapid, simple, precise, and specific onsite diagnosis of pigeon Newcastle disease.

The course of Rotavirus A (RVA) infection in young racing pigeons during the racing season

BackgroundPigeon Rotavirus A (RVA) infection has been confirmed in pigeons in the last decade as a cause of Young Pigeon Disease (YPD). Although YPD has been known for many years to date, no studies have been conducted to track the spread of RVA infection in pigeons during the racing season. The presented research aims to determine the course of RVA infection during the flights of young racing pigeons in the summer season, in one of the districts in the Mazovian Voivodeship in Poland.ResultsFaecal samples of pigeons collected from transport baskets in vehicles transporting pigeons to the starting point were tested. The quantitative RT-PCR (qRT-PCR) was used to detect the genetic material of RVA. Samples taken during 6 flights were analysed. The study showed a percentage increase in infections up to the fourth flight of pigeons, and then their decrease. With Cq values below 20, breeders did not participate in the next flight and/or reported disease in the flock. With positive Cq values of 20 to 30, clinical signs of disease were not reported. Of the 76 breeders participating in the races, at least one positive result was found in 46 (60.5%). Including the occurrence of the disease during the racing season was reported by 11 breeders (14.4%). The main clinical signs in sick pigeons were vomiting, diarrhea and stowed crop. The tested pigeons were not vaccinated against RVA.ConclusionsDuring training and racing of pigeons, it is not possible to avoid exposing them to pathogens, including RVA, regardless of whether pigeons from different breeders are placed in the same baskets or are in separate baskets. However, after four flights the number of new cases of the disease decreases which indicates the development of immunity. The qRT-PCR test is useful in the diagnosis and differentiation of clinical (Cq below 20) and subclinical RVA infections in racing pigeons.

The first confirmed cases of pigeon rotavirus A (RVA) infection in domestic pigeons (Columba livia) in Poland

Abstract Introduction Although the presence of rotaviruses in pigeon samples has been reported since the 1980s, its importance as an aetiological agent of the “classical” young pigeon disease (YPD) was not proven until 2020, when the Henle–Koch postulates were confirmed for pigeon-type rotavirus A (RVA) genotype G18P(17). Material and Methods From 2011 to 2020, archived liver samples from 117 pigeons submitted by 74 individual lofts were tested for the presence of pigeon-type RVA using a VP6-specific RT-qPCR test. For four positive racing pigeons, a more detailed necropsy and histopathological analysis was performed. Results Indicators of an acute RVA infection were found in 24 out of 117 (20.5%) samples tested, the earliest in 2014. Necropsies of the four selected RVA-positive pigeons showed changes mainly in the liver, spleen and kidneys similar to those described by other researchers. The histopathological examination revealed mainly hyperaemia and necrosis in the liver, as well as mononuclear cell infiltrates in these organs. Conclusion Pigeon-type RVA is also a cause of YPD in Poland and is a serious challenge for racing pigeon breeders and veterinarians, especially during the training and flights of young pigeons.

Drug resistance patterns and genotype associations of Trichomonas gallinae in meat pigeons (Columba livia): insights from Guangdong Province, China.

Avian trichomoniasis, caused by the protozoan parasite Trichomonas gallinae, is a prevalent and economically significant disease in pigeons. This study investigated the drug resistance of T. gallinae isolates in Guangdong Province, China. The results revealed that 25.3% (20/79) of the isolates were resistant to one or more of the four nitroimidazole drugs tested, namely, metronidazole, dimetridazole, secnidazole, and tinidazole. Secnidazole elicited the highest resistance rate (19.0%; 15/79), followed by tinidazole (17.7%; 14/79), metronidazole (17.7%; 14/79), and dimetridazole (13.9%; 11/79). An enormous majority of the resistant isolates (70.0%; 14/20) exhibited resistance to multiple drugs. Additionally, the resistance rate was significantly higher in isolates from birds aged < 30 days (53.3%; 8/15) than in those from older birds (23.1%; 12/52). Moreover, no drug resistance was detected in female pigeons. The genotype of the isolated strain was also associated with drug resistance. Specifically, 50.0% (15/30) of ITS-B genotypes exhibited resistance to drugs, while only 10.2% (5/49) of ITS-A genotypes demonstrated resistance. This study also found the growth characteristics of different Trichomonas isolates to be influenced by their genotypes and initial inoculum concentrations. These findings underscore the urgent need for effective measures to control and prevent drug-resistant T. gallinae infections in pigeons, thus ensuring the stable development of the pigeon industry.

Summary of Common Intestinal Diseases in Pigeons and Related Pharmacological Prevention

Summary of Common Intestinal Diseases in Pigeons and Related Pharmacological Prevention

Current challenges in addressing invasive diseases in domestic pigeons: insights from our research

The current study aims to highlight the ongoing challenges in addressing invasive diseases within pigeon flocks in the Lublin region. The study material comprised bird faecal samples from 69 flocks (39 fancy pigeon flocks and 30 racing pigeon flocks) with a total estimated bird count of 7,490, as declared by the owners. Parasite forms were confirmed in samples from 56/69 flocks, indicating a prevalence of 81.2% across the study, 87.2% in fancy pigeon flocks and 73.3% in racing pigeon flocks. The identified parasites included protozoa of the genus Eimeria, roundworms Ascaridia columbae, nematodes Capillariidae, Ornithostrongylus quadriradiatus, and Syngamus trachea, cestodes and Trichomonas gallinae. The analysis revealed that coccidiosis was the predominant invasion in both racing and fancy pigeon flocks. Comparing the two types of breeding (racing pigeons and fancy pigeons), fancy pigeon flocks were more susceptible to parasitic invasions.

Sequencing of pigeon circovirus and the first report of identification of beak and feather disease virus in clinical specimens of domestic pigeons.

An internationally recognized syndrome that leads to deaths among domestic and ornamental pigeons, particularly after racing, is young pigeon disease syndrome (YPDS). Pigeon circovirus (PiCV) is regarded as one of the potential factors contributing to the occurrence of YPDS. This survey was conducted to determine the prevalence of PiCV infection and molecularly characterize the PiCV in pigeons suspected of YPDS. Eighty fecal samples were collected from 80 diseased pigeons (exhibiting symptoms such as lethargy, weight loss, crop stasis, vomiting and diarrhea) from 20 lofts in different areas of Ahvaz, Iran. Also, 20 fecal samples were obtained from 20 clinically healthy pigeons. The nested broad spectrum polymerase chain reaction test was done to identify the circovirus, using primers targeting part of the replication-associated protein gene with 350 bp, and several positive samples were sequenced. This study showed that PiCV was detected in 86 out of the 100 samples (86.00%). Two types of circoviruses were determined in the samples. One type of the detected circoviruses was PiCV which based on phylogenetic analysis had high genetic similarity with A, B, G and H genotypes of PiCV. The other type of detected circoviruses was closely related to beak and feather disease virus (BFDV) which causes one of the most significant viral diseases in psittacine birds. This is the first report of BFDV identification in pigeons.

Isolation, full sequence analysis, and in situ hybridization of pigeon paramyxovirus-1 genotype VI.2.1.1.2.2 from oriental turtle doves (Streptopelia orientalis)

Pigeon paramyxovirus-1 (PPMV-1), a genetic variant of avian paramyxovirus-1 (APMV-1), has been identified in Columbiformes and is the primary cause of diseases in captive and free-ranging pigeons. However, it has also been reported that PPMV-1 can infect chickens naturally and experimentally, thus posing a potential threat to the poultry industry. This study investigated a lethal outbreak of paramyxovirus infection that occurred among 16 oriental turtle doves (Streptopelia orientalis) in a walk-in aviary at a zoo from March to April 2021. Necropsies were performed, and histopathological findings revealed mild to moderate lymphoplasmacytic infiltration in several organs, such as the pancreas, liver, kidneys, and lungs. Reverse transcription polymerase chain reaction (RT-PCR) using formalin-fixed paraffin-embedded tissue blocks, virus isolation from fresh tissue, and in situ hybridization against the fusion (F) protein confirmed the diagnosis for PPMV-1 infection. The isolated strain NTU/C239/21 was fully sequenced by next-generation sequencing, and the results of phylogenetic analyses revealed that the F protein of NTU/C239/21 shared 98.8% nucleotide sequence identity with Pigeon/Taiwan/AHRI121/2017, which was isolated from a feral pigeon in Taiwan. The present study is the first to identify PPMV-1 infection in Streptopelia orientalis and suggests that Streptopelia orientalis may also play an important role in spreading the infection, similar to pigeons in APMV-1 spreading.

Management of Phytophthora Blight of Pigeon Pea (Cajanus cajan L. Hugh) Through the Use of Neem (Azadirachta indica) Plant Parts Aqueous Extracts

This study is focused on the management of phytophthora blight, a fungal disease of “pigeon pea” by the application of some aqueous extracts of neem plant parts. The aim of the study was to manage the phytophthora blight of pigeon pea using the plant parts extract of neem. The study was conducted in the year, 2021, at the Demonstration Farms (both field and laboratory) of the Department of Crop Science and Technology, School of Agriculture and Agricultural Technology, Federal University of Technology, Owerri, Imo State, Nigeria. The experiment was designed as Randomized Complete Block Design (RCBD) with five replications. Data on pigeon pea growth parameters and disease incidence and severity, were statistically analyzed by the use of Analysis of Variance (ANOVA) software as outlined by Wahua. The means were separated for difference using the Fisher’s Least Significant Difference (FLSD). Results indicated that aqueous extract of neem seed application caused the tallest Pigeon pea height (103.30 cm), the highest number of pigeon pea leaves (99.40), the lowest phytophthora blight disease incidence (11.00%) and also the lowest phytophthora blight disease severity (1.00).

Lesions and viral loads in racing pigeons naturally coinfected with pigeon circovirus and columbid alphaherpesvirus 1 in Australia.

Columbid alphaherpesvirus 1 (CoHV1) is associated with oral or upper respiratory tract lesions, encephalitis, and occasional fatal systemic disease in naive or immunosuppressed pigeons. Clinical disease is often reported with CoHV1 and coinfecting viruses, including pigeon circovirus (PiCV), which may cause host immunosuppression and augment lesion development. A natural outbreak of CoHV1 and PiCV coinfection occurred in a flock of 60 racing rock pigeons (Columba livia), in which 4 pigeons succumbed within 7 d of clinical onset. Lesions included suppurative stomatitis, pharyngitis, cloacitis, meningitis, and tympanitis, with eosinophilic intranuclear inclusion bodies consistent with herpesviral infection. In addition, large numbers of botryoid intracytoplasmic inclusion bodies were present in the skin, oral mucosa, and bursa of Fabricius, suggestive of circoviral infection, which was confirmed by immunohistochemistry. The concurrent viral load of CoHV1 and PiCV was high in liver, oropharynx, and bursa of Fabricius. We found PiCV in oro-cloacal swabs from 44 of 46 additional birds of variable clinical status, PiCV alone in 23 birds, and coinfection with CoHV1 in 21 birds. Viral copy numbers were significantly higher (p < 0.0001) for both viruses in clinically affected pigeons than in subclinical qPCR-positive birds. The CoHV1-induced lesions might have been exacerbated by concomitant PiCV infection.

Correct interpretation of carrier pigeon diseases – Part 1: Ornithosis complex

The most fundamental and important topics for carrier pigeon fanciers are health and form of their competitors. It does not matter how good a pigeon is or how well fed it is, an unhealthy pigeon will never be able to win a race. One of the most common diseases of carrier pigeons during the racing season is a respiratory illness named "Ornithosis Complex". Also known as "Ornithose", "Coryza" and "One-eyed Colds" it is caused most often by a combination of Chlamydia psittaci, Pasteurella, Mycoplasma, Herpes virus and many other common bacteria such as Yersinia, Enterobacter, Streptococci and Staphylococci. Once both old and young birds have started their training and racing program, they are likely to develop an ornithosis complex, showing symptoms of swollen or puffed feathers around the ears, dry plumage, blue flesh and a disruption to moulting. Pigeons that arrive home showing signs of extreme fatigue and typical ornithosis symptoms should be treated directly with a combination of prescribed treatments, isolated from healthy birds and should not be flown to avoid spreading the disease. The study points to the fact that ornithosis complex is not a difficult problem when carrier pigeons do not overflow. It will become a big problem only after the start of the racing season, which will take away the success of many breeders.

Newcastle disease in pigeon review article

Newcastle disease (ND) is a viral disease of poultry and other bird species like pigeon (Columbi livia), it characterizes as devastating and contagious and it has been distributed worldwide. ND in pigeons is caused by pigeon paramyxovirus type 1(PPMV-1) which is an antigenic and host variant of the avian paramyxovirus serotype 1 (APMV-1), the disease in pigeons is termed paramyxovirosis and cause nervous signs with high mortality usually in the bird with kidneys infected with viscerotropic strains, and neural signs appeared individually. PPMV-1 was initially detected by hemagglutination activity (HA) and confirmed with hemagglutination inhibition assay (HI), and molecular-based techniques. Serological diagnosis of paramyxovirosis is necessary because of the similarity of the PPMV-1 infection with sodium chloride poisoning, pigeon herpes virus infection (PHV), and ornidazole overdose that cause same neurological signs. PPMV-1 infection can be controlled effectively by vaccination by specific vaccines associated with good biosecurity aspect

Phylogenetic analysis of pigeon adenovirus 1 in clinical specimens of domestic pigeons (Columba livia domestica) in Iran.

An internationally identified syndrome that leads to deaths between domestic and ornamental pigeons, particularly after racing is young pigeon disease syndrome (YPDS). This study was conducted to determine the status of pigeon adenoviral infection and molecularly characterize the pigeon adenovirus in Ahvaz pigeons. Sixty stool samples of healthy pigeons (young pigeons and adult pigeons) and 60 stool samples of diseased pigeons (young and adults) with symptoms of lethargy, weight loss, crop stasis, vomiting and diarrhea were examined. Samples were screened for aviadenoviruses by polymerase chain reaction (PCR) assay and degenerated primers set to target the aviadenovirus polymerase (pol) gene were used which was designed in this study. Screening for pigeon adenovirus 1 (PiAdV-1) was performed using a primer pair that targeted the fiber gene of PiAdV-1. Out of 120 stool samples, six samples (5.00%) were positive for aviadenovirus. The results showed that independent from pigeons' age status, 5.00 and 3.33% of sick and of healthy pigeons were positive for PiAdV-1, respectively. Genomic sequencing revealed that the viruses detected in Ahvaz pigeons belonged to the PiAdV-1 genotype. The results in pigeons revealed a 98.10 - 99.53% nucleotide similarity when compared to other strains ofPiAdV-1 (TR/SKPA20, P18-05523-6 and strain IDA4) formerly deposited in GenBank® in Türkiye, Australia and The Netherlands. As far as the authors know, this was the first record of phylogenetic analysis of PiAdV-1 in Iran.

Correct interpretation of carrier pigeon diseases - Collibacillosis

Despite the breeder’s efforts to minimize stress factors during the racing season, disease can occur even in the best lofts. Among the specific diseases caused by high performance, immunosuppression of the organism, imbalance of gastrointestinal micro flora of carrier pigeons and non-observance of hygienic conditions is included collibacillosis. Collibacillosis is localized or systemic infection caused entirely or partly by avian pathogenic Escherichia coli (APEC). Although some strains of APEC cannot cause disease by themselves, their pathogenic lifestyle, suggesting that infections might always be opportunistic or secondary to some most frequently predisposing diseases such as coccidiosis, adenovirosis, canker, intestinal worms and others. The disease causes reduction in performance or loss of infected pigeons, vomiting, diarrhoea, enteritis, dehydration, depressed feed intake or decreased growth rate in young pigeons. An outbreak of collibacillosis during the racing season is often the result of a combination of several factors that cannot be completely eliminated. It is therefore useful to develop a prophylactic plan in which the breeder focuses not only on the elimination of the main predisposing diseases, but also notices the factors that can stress the pigeons and thus cause an outbreak of APEC.

Prevalence and diversity of Trichomonas gallinae in meat pigeons (Columba livia) in Guangdong Province, People's Republic of China.

Pigeon farming for meat has developed into an important economic industry in most countries, especially in China. Trichomoniasis, caused by the protozoan parasite Trichomonas gallinae, is a worldwide disease in pigeons. However, studies of the prevalence and distribution of T. gallinae lineages in domestic pigeons in southern China are limited. In this study, a total of 636 pigeon throat swabs samples from four regions in Guangdong Province were screened for T. gallinae by in vitro culture assays and microscopy. The results revealed an overall prevalence of T. gallinae infection in southern China of 26.6% (169/636). There were significant differences in the infection rate of T. gallinae between the four regions (χ2 = 117.948, df = 4, P = 0.000), with up to 44.6% in the Pearl River Delta region. The infection rate of young pigeons was as high as 70.8%. The rDNA sequences (18S rRNA/ITS1-5.8S rRNA-ITS2) of 153 positive samples were amplified and sequenced. Results identified 58.2% (89/153) overall as ITS-A (18S-VI) (also known as ITS-OBT-Tg-1) and 41.8% (64/153) as ITS-B (18S-IV) (also known as ITS-OBT-Tg-2). Thus, ITS-A (18S-VI) was the dominant T. gallinae genotype in southern China, especially in young pigeon (97.0%, 32/33). In conclusion, a high prevalence of T. gallinae infection in domestic pigeons was identified in southern China, particularly in the Pearl River Delta region. The ITS-A (18S-VI) was the dominant genotype highly pathogenic, which may weaken the immune system of pigeons, and cause a negative impact on the development of the pigeon industry in China.

A retrospective molecular investigation of selected pigeon viruses between 2018-2021 in Turkey.

A recent first detection of pigeon aviadenovirus-1 and pigeon circovirus co-infection associated with Young Pigeon Disease Syndrome (YPDS) in a pigeon flock in Turkey, prompted a study focused on documenting the distribution of Pigeon aviadenovirus (PiAdV-1 and PiAdV-2), Pigeon circovirus (PiCV), Columbid alphaherpesvirus 1 (pigeon herpesvirus (PiHV)) and Fowl aviadenovirus (FAdV) in the country. These viruses were selected as they are associated with severe disease in pigeons across the world. A total of 192 cloacal swabs were collected from young (<1 year old) pigeons from 16 different private pigeon flocks across Turkey, between 2018 and 2021 as part of routine diagnostic sampling. PiCV genetic material was the most frequently detected 4/16 (25%), PiAdV-1 and CoHV-1 DNA were both found in one flock each, while neither PiAdV-2 and FAdV were detected in any of the studied pigeon flocks. PiCV and PiHV genetic material were both detected in the same pigeon flock’s cloacal samples as a co-infection with the identification of PiHV being a first in Turkey.

Pigeon Rotavirus A as the cause of systemic infection in juvenile pigeons (young pigeon disease).

Recent investigations suggested pigeon associated Rotavirus Typ A genotype G18P[17] (RVA) as a causative agent of the classical 'young pigeon disease' (YPD). YPD was first described in the late 1980 s as an acute, mainly seasonally recurring disorder of mostly juvenile domestic pigeons (Columba livia) with clinical signs such as anorexia, dairrhea, vomiting, congested crops, weight loss and occasionally mortality. Various studies in the past indicated a multifactorial nature of YPD. Several pathogens, such as pigeon circovirus 1, avian adenoviruses and Escherichia coli were also suggested, but none of these could reproduce the disease experimentally. However, the impact of other pathogens on the clinical development of YPD cannot be excluded and requires further investigation. This present review summarizes available information on RVA-induced disease in pigeons, its association with YPD, the transmission, and diagnosis of the infection, and on prophylactic strategies to prevent RVA outbreaks.

A pigeon paramyxovirus type 1 isolated from racing pigeon as an inactivated vaccine candidate provides effective protection

Pigeon paramyxovirus type 1 (PPMV-1), a variant of Newcastle disease virus (NDV), causes severe Newcastle disease (ND) in pigeons. However, there is no PPMV-1 vaccine available worldwide. In this study, a strain of PPMV-1 was isolated from outbreaks in a vaccinated racing pigeon (Columbia livia) loft in China, namely, PPMV-1/pigeon/Gansu/China/02/2020 (GS02). Experimental infection with GS02 showed mortality rates of 100% and 87.50% in 4- and 12-week-old pigeons, respectively, suggesting that GS02 is virulent and more sensitive to young pigeons. The whole genome of GS02 determined the fusion (F) protein possessing virulence cleavage site 112RRQKRF117. Phylogenetic analysis indicated that GS02 was a subgenotype VI.2.1.1.2.2 (VIk) of Class II NDV and more closely related to the JS/06/20/Pi (MW271791) strain, but it was far from the genetic distance from the commercial vaccine chicken-origin La Sota strain. Using inactivated GS02 as a vaccine candidate and inactivated vaccine La Sota to immunize the pigeons, both of them provided complete protection against GS02 challenge. The GS02 vaccine candidate induced higher antibody titers than the La Sota vaccine, and cross-reactivity testing showed antigenically slight differences between GS02 and La Sota. These results indicated that the GS02 candidate could be a potential pigeon-derived vaccine for the prevention and control of PPMV-1 in pigeons.