印度尼西亚弥漫性麻风患者致病菌为麻风分枝杆菌病分析

Q2 Agricultural and Biological Sciences Biodiversitas Pub Date : 2023-09-15 DOI:10.13057/biodiv/d240854
MEDHI DENISA ALINDA, ABDUL KARIM, BAGUS H. KUSUMA PUTRA, ERY WIDAYATI, M. YULIANTO LISTIAWAN, DINAR ADRIATY, ISWAHYUDI ISWAHYUDI, PUPUT ADE WAHYUNINGTYAS, CITA ROSITA PRAKOESWA
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摘要

摘要Adriaty D, Alinda MD, Karim A, Putra BHK, Agusni RI, Iswahyudi, Wahyuningtyas PA, Wahyuni R, Widayati E, Listiawan MY, Prakoeswa CR. 2023。印度尼西亚弥漫性麻风患者致病菌为麻风分枝杆菌病分析。生物多样性24:4521-4529。除了临床症状外,目前的调查还涉及在显微镜和分子上识别,以明确区分麻风分枝杆菌病基因组与麻风分枝杆菌,以便能够适当地进行治疗。到目前为止,还没有关于印尼这一发现的报道。一名53岁的爪哇男子双腿溃疡,在过去两年中反复出现。有些溃疡之前会出现水泡,很快就会变成伤口。溃疡宽而深,被黑色结痂覆盖,边缘不规则渗出。他有反复出血史,从未接受过麻风病治疗。住院前两周,他的腿和手上出现了新的溃疡,病情迅速恶化。身体虚弱,没有发烧,皮肤有光泽,呈鱼鳞状。面部无结节,可见弥漫性浸润,也可发生骨质疏松。本研究采用BTA检查法,活检材料HE和wade -fit染色的组织病理学检查,皮肤裂隙涂片材料PCR法。BTA检查显示BI为3+,MI为7%。组织病理学显示表皮变薄,含有BTA的泡沫细胞增多,包括尾注和维管周围组织。用LERF2-MLER4引物嵌套PCR检测麻风分枝杆菌,扩增子大小为135bp,阳性。利用LPMF2-MLER4引物检测麻风分枝杆菌的高级PCR检测也显示扩增片段大小为142bp的阳性结果。DNA测序结果与麻风支原体核苷酸序列一致。临床及组织病理学结果符合弥漫性麻风及Lucio现象。DNA测序结果与墨西哥报道的麻风支原体病相符。因此,可以得出结论,在生物分子菌株中,该细菌是印度尼西亚从未报告过的麻风分枝杆菌病。
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Analysis Mycobacterium lepromatosis as the causative agent of diffuse lepromatous leprosy patient in Indonesia
Abstract. Adriaty D, Alinda MD, Karim A, Putra BHK, Agusni RI, Iswahyudi, Wahyuningtyas PA, Wahyuni R, Widayati E, Listiawan MY, Prakoeswa CR. 2023. Analysis Mycobacterium lepromatosis as the causative agent of diffuse lepromatous leprosy patient in Indonesia. Biodiversitas 24: 4521-4529. The present investigation deals with identifying, besides clinical signs, both microscopically and molecularly, to clearly differentiate the Mycobacterium lepromatosis genome against Mycobacterium leprae so that treatment can be carried out properly. To date, there has yet to be a report on this discovery in Indonesia. A 53-year-old Javanese man had ulceration on both legs that had been reoccurring in the past two years. Some of the ulcers were preceded by blisters that rapidly turned into a wound. The ulcers were described as wide and deep, covered with blackish crusts and some exudative areas with irregular edges. He had a history of recurrent epistaxis and had never been treated for leprosy. There was rapid progression and the development of new ulcers on his legs and hands for two weeks before hospitalization. There was body weakness, no fever, and the skin was shiny and ichthyosiform. On the face, diffuse infiltration will appear without nodules, and madarosis also occurs. Examination in this study used the BTA examination method, histopathological examination with HE and Wade-fite staining with biopsy material and the PCR method using skin slit smear material. The results of the BTA examination showed that BI was 3+, and MI showed 7%. Histopathology showed thinning of the epidermis with many foam cells containing BTA, including endnotes and perivascular tissues. Nested PCR examination with LERF2-MLER4 primers for detecting M. leprae showed a positive result with amplicon 135bp in size. Advanced PCR examination using LPMF2-MLER4 primers for detecting M. lepromatosis also showed a positive result with amplicons 142bp in size. The result of DNA sequencing was consistent with the order of nucleotides of M. lepromatosis. Based on the clinical and histopathological results, it was consistent with diffuse lepromatous leprosy and Lucio’s phenomenon. The DNA sequencing showed a suitable result with M. lepromatosis, which has been reported in Mexico. Thus, it can be concluded that in biomolecular strain, this bacterium is an M. lepromatosis that has never been reported in Indonesia.
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来源期刊
Biodiversitas
Biodiversitas Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
2.80
自引率
0.00%
发文量
471
审稿时长
6 weeks
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