Zinnah Mohammad Ali, Uddin Md Bashir, Hasan Tanjila, Das Shobhan, Khatun Fahima, Hasan Md Hasibul, Udonsom Ruenruetai, Rahman Md Masudur, Ashour Hossam M
Department of Microbiology and Public Health, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur 1706, Bangladesh.
Department of Medicine, Faculty of Veterinary, Animal and Biomedical Sciences, Sylhet Agricultural University, Sylhet 3100, Bangladesh.
Biomedicines. 2024 Jul 1;12(7):1457. doi: 10.3390/biomedicines12071457.
The Mpox virus (MPXV) is known to cause zoonotic disease in humans. The virus belongs to the genus Orthopoxvirus, of the family Poxviridae, and was first reported in monkeys in 1959 in Denmark and in humans in 1970 in the Congo. MPXV first appeared in the U.S. in 2003, re-emerged in 2017, and spread globally within a few years. Wild African rodents are thought to be the reservoir of MPXV. The exotic trade of animals and international travel can contribute to the spread of the Mpox virus. A phylogenetic analysis of MPXV revealed two distinct clades (Central African clade and West African clade). The smallpox vaccine shows cross-protection against MPXV infections in humans. Those who have not previously been exposed to Orthopoxvirus infections are more vulnerable to MPXV infections. Clinical manifestations in humans include fever, muscle pain, headache, and vesicle formation on the skin of infected individuals. Pathognomonic lesions include ballooning degenerations with Guarnieri-like inclusions in vesicular epithelial cells. Alterations in viral genome through genetic mutations might favor the re-emergence of a version of MPXV with enhanced virulence. As of November 2023, 92,783 cases and 171 deaths have been reported in 116 countries, representing a global public health concern. Here, we provide insights on the re-emergence of MPXV in humans. This review covers the origin, emergence, re-emergence, transmission, pathology, diagnosis, control measures, and immunomodulation of the virus, as well as clinical manifestations. Concerted efforts of health professionals and scientists are needed to prevent the disease and stop its transmission in vulnerable populations.
已知猴痘病毒(MPXV)可导致人类人畜共患病。该病毒属于痘病毒科正痘病毒属,1959年在丹麦首次在猴子中被报道,1970年在刚果首次在人类中被报道。MPXV于2003年首次出现在美国,2017年再次出现,并在几年内传播到全球。野生非洲啮齿动物被认为是MPXV的宿主。动物的外来贸易和国际旅行可能有助于猴痘病毒的传播。对MPXV的系统发育分析揭示了两个不同的分支(中非分支和西非分支)。天花疫苗对人类MPXV感染具有交叉保护作用。那些以前未接触过正痘病毒感染的人更容易受到MPXV感染。人类的临床表现包括发热、肌肉疼痛、头痛以及受感染个体皮肤上出现水疱。特征性病变包括水疱上皮细胞中的气球样变性和瓜尔尼耶样包涵体。通过基因突变导致的病毒基因组改变可能有利于毒力增强的MPXV毒株再次出现。截至2023年11月,116个国家已报告92783例病例和171例死亡,这是一个全球公共卫生问题。在此,我们提供了关于MPXV在人类中再次出现的见解。本综述涵盖了该病毒的起源、出现、再次出现、传播、病理学、诊断、控制措施和免疫调节以及临床表现。需要卫生专业人员和科学家共同努力来预防该疾病并阻止其在脆弱人群中的传播。