ABSTRACT
Abstract The poultry sector in Pakistan is contributing mainly in bridging gap between demand and supply for protein. Mycoplasma gallisepticum is an emerging bacterium causing serious problems in poultry industry of Pakistan. A cross-sectional study was conducted to evaluate the M. gallisepticum load in poultry populated regions of Pakistan. Total 600 serum and 600 swab samples were collected, 200 from each broiler, layers and breeders poultry in Rawalpindi and Abbottabad districts. Serum samples were analyzed through ELISA for seroprevalence. Swabs were cultured on Frey's medium followed by PCR and partial mgc2 gene sequencing. Results of seroprevalence of M. gallisepticum showed that layers (75%, n=150) are more positive as compared to breeders (70%, n=140) and broilers (50%, n=100). Typical colonies of the M. gallisepticum were observed in breeder (26.5%), followed by layer (21%) and broilers (9%). A total of 37.1% (n=42) samples were identified positive through PCR out of total 113 cultured based positive samples. A total of six M. gallisepticum isolates of current study showed 98-99 percent similarity with previously reported isolates on the basis of mgc2 gene partial sequencing. The M. gallisepticum was found highly prevalent in different poultry breads. Results of this study would add into basic data and provide a direction for livestock sector to strengthen a control strategy for mycoplasmosis in poultry farms.
Resumo O setor avícola do Paquistão está contribuindo principalmente para preencher a lacuna entre a demanda e a oferta de proteína. Mycoplasma gallisepticum é uma bactéria emergente que causa sérios problemas na indústria avícola do Paquistão. Um estudo transversal foi conduzido para avaliar a carga de M. gallisepticum em regiões de avicultura do Paquistão. Um total de 600 amostras de soro e 600 amostras de esfregaço foi coletado, 200 de cada frango de corte, poedeiras e aves reprodutoras nos distritos de Rawalpindi e Abbottabad. Amostras de soro foram analisadas por ELISA para soroprevalência. As zaragatoas foram cultivadas em meio Frey, seguido de PCR e sequenciação parcial do gene mgc2. Os resultados da soroprevalência de M. gallisepticum mostraram que as poedeiras (75%, n = 150) são mais positivas em comparação com matrizes (70%, n = 140) e frangos de corte (50%, n = 100). Colônias típicas de M. gallisepticum foram observadas em reprodutoras (26,5%), seguidas de poedeiras (21%) e frangos de corte (9%). Um total de 37,1% (n = 42) das amostras foi identificado como positivas por PCR de um total de 113 amostras positivas baseadas em cultura. Um total de seis isolados de M. gallisepticum do estudo atual mostrou 98-99% de similaridade com isolados relatados anteriormente com base no sequenciamento parcial do gene mgc2. O M. gallisepticum foi encontrado com alta prevalência em diferentes pães de aves. Os resultados deste estudo acrescentariam dados básicos e forneceriam orientação para o setor pecuário fortalecer uma estratégia de controle da micoplasmose em granjas avícolas.
Subject(s)
Animals , Poultry Diseases/epidemiology , Mycoplasma gallisepticum/genetics , Pakistan/epidemiology , Poultry , Seroepidemiologic Studies , Chickens , Cross-Sectional StudiesABSTRACT
Mycoplasma gallisepticum (MS) and Mycoplasma synoviae (MS) are important avian pathogens and cause economic losses to the poultry industry. Molecular biology techniques are currently used for a rapid detection of these pathogens and the adoption of control measures of the diseases. The aim of this study was to develop and validate a technique for simultaneous detection of MG and MS by multiplex real time polymerase chain reaction (PCR). The complete assay (Multiplex MGMS) was designed with primers and probes specific for each pathogen and developed to be carried out in a single tube reaction. Vaccines, MG and MS isolates and DNA from other Mycoplasma species were used for the development and validation of the method. Further, 78 pooled clinical samples from different poultry flocks in Brazil were obtained and used to determine the sensitivity and specificity of the technique in comparison to 2 real time PCR assays specific for MG (MG PCR) and MS (MS PCR). The results demonstrated an agreement of 100% (23 positive and 44 negative samples) between Multiplex MGMS and MG PCR in the analysis of 67 samples from MG positive and negative poultry flocks, and an agreement of 96.9% between Multiplex MGMS and MS PCR in the analysis of 64 samples from MS positive and negative poultry flocks. Considering the single amplification tests as the gold standard, the Multiplex MGMS showed 100% of specificity and sensitivity in the MG analysis and 94.7% sensitivity and 100% specificity in the MS analysis. This new assay could be used for rapid analysis of MG and MS in the poultry industry laboratories.
Subject(s)
Animals , Molecular Diagnostic Techniques/methods , Mycoplasma Infections/veterinary , Mycoplasma gallisepticum/isolation & purification , Mycoplasma synoviae/isolation & purification , Poultry Diseases/diagnosis , Real-Time Polymerase Chain Reaction/methods , Veterinary Medicine/methods , Brazil , Bacteriological Techniques/methods , Multiplex Polymerase Chain Reaction/methods , Mycoplasma Infections/diagnosis , Mycoplasma Infections/microbiology , Mycoplasma gallisepticum/genetics , Mycoplasma synoviae/genetics , Poultry , Poultry Diseases/microbiology , Sensitivity and SpecificityABSTRACT
Mycoplasma gallisepticum [MG] infection in chicken and turkey is still one of the important reasons causing economic losses in poultry. The current study concerned with rapid detection and molecular characterization of MG isolates. The all samples positive by culture were positive by PCR and rt- PCR. Five isolated [four from chicken and one from turkey] were sequenced for mgc2 gene. The present molecular study proved that four wild-type MG strains. [Eis 3- C-10, Eis 4- C-10, Eis 5- C-10 were recovered from chicken and one [Eis 6-T-10] was recovered from turkey. While Eis 7-C-10 [vaccinal F-strain] was isolated from commercial layer flock vaccinated with F- strain vaccine. We concluded that mgc2 gene was able to distinguish between MG wild - type and vaccinal strains
Subject(s)
Chickens , Turkeys , Mycoplasma gallisepticum/genetics , Polymerase Chain Reaction/methods , Amino Acids/analysisABSTRACT
Cepas vacinais de Mycoplasma gallisepticum, F e TS-11, foram examinadas quanto às suas variacões fenotípicas e antigênicas, por SDS-PAGE e através de dois métodos sorológicos (inibicão da hemaglutinacão e imunoeletroforese). A análise densitométrica das bandas obtidas nos géis de poliacrilamida mostrou pequena variabilidade fenotípica entre as amostras, sendo a banda peptidica de 75 kDa detectada apenas na amostra vacinal F. Anticorpos policlonais produzidos em galinha foram utilizados nos ensaios sorológicos para estudar a variabilidade antigênica das amostras. Houve elevada reatividade cruzada entre as amostras e os anticorpos homólogos e heterólogos. A característica mais evidente foi a resposta específica da banda peptídica de 75 kDa da vacina F ao anticorpo homólogo.