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The ongoing global spread of Newcastle disease underscores the crucial need for continued research on the efficacy of current vaccines against various circulating strains of Newcastle disease virus (NDV). The fusion gene of a representative Egyptian genotype VII.1.1 strain was used to substitute its corresponding gene in the K148/08 vaccinal strain after site directly mutating its cleavage site from 112RRQKRF117 to 112GKQGRL117. Fusion gene exchange between GVII and GI did not affect the thermostability of GI K148/08. Attenuation of the rescued virus was confirmed by mean death time 144 h with an intracerebral pathogenicity index of 0.00. Survival analysis after the challenge experiment confirmed that 107 EID50 was the protective dose of rK148/GVII-F. The haemagglutination inhibition level of antibodies required for full clinical protection was > 3.3 log2 for rK148/GVII-F and > 4.1 log2 for both K148/08 and LaSota. Oropharyngeal viral shedding was reduced on the 5th and 7th days post-challenge in the rK148/GVII-F vaccinated group. Replication and tropism investigations confirmed the respirotropic nature of LaSota, enterotropic nature of K148/08, and further attenuation of rK148/GVII-F. Altogether, rK148/GVII-F is a thermostable, safe, effective, and genetically stable vaccine candidate that could be adequate for use in countries that encounter GVII.1.1 and in those with tropical climate, such as most Middle Eastern countries. A thermostable, safe, and effective NDV GVII recombinant vaccine was generated. Fusion gene replacement with GVII did not affect GI K148/08 virus thermostability. Strain rK148/GVII-F provided adequate protection against a lethal NDV challenge. Oropharyngeal shedding was significantly reduced on post-challenge days 5 and 7. [ABSTRACT FROM AUTHOR]