背景:鸡对维持农村社区经济和生计的影响怎么强调都不为过。近年来,支原体病已成为影响南非鸡肉生产成功的疾病之一。肺炎支原体(MG)和滑膜支原体(MS)是南非最普遍的支原体菌株。MG和MS是影响鸡生产力的重要呼吸道病原体。本研究旨在使用qPCR进行分子检测,并使用系统发育分析表征MG和MS的存在。系统发育分析用于阐明在南非鸡品种的气管拭子中观察到的不同MG和MS的相关分类群之间的一般进化关系。
方法:45个LohmannBrown气管拭子(n=9),罗德岛红(n=9),Ovambo(n=9),供应商(n=9),和PotchefstroomKoekoek(n=9)品种是从商业农场中存在的有症状的鸡中收集的。为了检测MG和MS,从气管拭子和粪便样本中提取DNA,用16srRNA(310bp)和vlhA(400bp)基因片段进行qPCR。在对所有扩增子进行测序后,MG,和MS树状图显示了五个南非鸡品种与GeneBank参考种群之间的进化关系。
结果:qPCR显示仅在罗德岛红色品种中测试MS的气管拭子样品中有22%(2/9)存在MG和MS;在Ovambo品种中测试样品的66.6%(6/9)和33%(3/9);以及测试样品的Vendin品种的11.1%(1/9)和44.4%(4/9)。在LohmannBrown或PotchefstroomKoekoek品种中未检测到MG或MS。此外,qPCR显示,来自LohmannBrown和Ovambo品种的合并粪便样品中存在MG。从两个样品中识别出八种不同的细菌分离物。4个分离株是鸡支原体的16s核糖体核糖核酸(rRNA)基因(命名为PT/MG51/ck/00、PT/MG48/ck/00、PT/MG41/ck/00和PT/MG71/ck/00),另一种是支原体滑膜可变脂蛋白血凝素A(vlhA)基因(命名为PT/MSA22/ck/01,PT/MS41/ck/01,PT/MS74/ck/01和PT/MS46/ck/01),可在GenBank中获得。成功地对这些分离株进行了测序,其与来自基因库的分离株具有95-100%的相似性。
结论:该研究揭示了在取样的鸡品种中同时存在MG和MS。此外,在强化或商业管理系统下,发现不同品种的鸡容易感染。因此,鼓励持续监测,以防止MG和MS在南非家禽业的传播和爆发。
BACKGROUND: The impact of chickens on maintaining the economy and livelihood of rural communities cannot be overemphasized. In recent years, mycoplasmosis has become one of the diseases that affect the success of South African chicken production. Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) are the most prevalent strains of Mycoplasma in South Africa. MG and MS are significant respiratory pathogens affecting the productivity of chickens. The present study aimed to molecularly detect using qPCR and characterize the presence of MG and MS using phylogenetic analysis. The phylogenetic analysis was utilized to clarify general evolutionary relationships between related taxa of different MG and MS observed in tracheal swabs from South African chicken breeds.
METHODS: Forty-five tracheal swabs of the Lohmann Brown (n = 9), Rhode Island Red (n = 9), Ovambo (n = 9), Venda (n = 9), and Potchefstroom Koekoek (n = 9) breeds were collected from symptomatic chickens present in the commercial farm. To detect MG and MS, DNA was extracted from tracheal swabs and faecal samples, and qPCR was performed with a 16 s rRNA (310 bp) and vlhA (400 bp) gene fragment. Following the sequencing of all the amplicons, MG, and MS dendrograms showing the evolutionary relationships among the five South African chicken breeds and the GeneBank reference population were constructed.
RESULTS: The qPCR revealed the presence of MG and MS in 22% (2/9) of the tracheal swab samples tested for MS only in Rhode Island Red breeds; 66.6% (6/9) and 33% (3/9) of the tested samples in Ovambo breeds; and 11.1% (1/9) and 44.4% (4/9) of the tested samples in Venda breeds. No MG or MS were detected in the Lohmann Brown or Potchefstroom Koekoek breed. Furthermore, qPCR revealed the presence of MG in pooled faecal samples from Lohmann Brown and Ovambo breeds. Eight different bacterial isolates were recognized from both samples. Four isolates were of the 16 s ribosomal ribonucleic acid (rRNA) gene (named PT/MG51/ck/00, PT/MG48/ck/00, PT/MG41/ck/00 and PT/MG71/ck/00) gene of Mycoplasma gallisepticum, and the other was Mycoplasma Synoviae variable lipoprotein hemagglutinin A (vlhA) gene (named PT/MSA22/ck/01, PT/MS41/ck/01, PT/MS74/ck/01 and PT/MS46/ck/01) which were available in GenBank. These isolates were successfully sequenced with 95-100% similarity to the isolates from the gene bank.
CONCLUSIONS: The study revealed the presence of both MG and MS in the chicken breeds sampled. Furthermore, the different breeds of chicken were found to be susceptible to infection under the intensive or commercial management system. Therefore, continuous surveillance is encouraged to prevent the spread and outbreak of MG and MS in the poultry industry in South Africa.