High prevalence of Plasmodium malariae and Plasmodium ovale in malaria patients along the Thai-Myanmar border, as revealed by acridine orange staining and PCR-based diagnoses

被引:81
作者
Zhou, M
Liu, Q
Wongsrichanalai, C
Suwonkerd, W
Panart, K
Prajakwong, S
Pensiri, A
Kimura, M
Matsuoka, H
Ferreira, MU
Isomura, S
Kawamoto, F [1 ]
机构
[1] Nagoya Univ, Sch Med, Dept Med Zool, Nagoya, Aichi 466, Japan
[2] Armed Forces Res Inst Med Sci, Dept Immunol & Parasitol, Bangkok 10400, Thailand
[3] Vector Borne Dis Control Ctr 2, Chiang Mai, Thailand
[4] Prov Hlth Dept, Ranong, Thailand
[5] Osaka City Univ, Sch Med, Biophys Lab, Osaka 545, Japan
[6] Jichi Med Coll, Dept Med Zool, Minami Kawachi, Tochigi, Japan
关键词
Plasmodium malariae; Plasmodium ovale; Thailand; Myanmar; acridine orange staining; PCR diagnosis;
D O I
10.1046/j.1365-3156.1998.00223.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The prevalence of the four human malaria parasites was investigated among malaria patients at northern, central and southern towns in Thailand along the border with Myanmar between September 1995 and May 1996. Thin smears obtained from 548 Thai and Burmese patients were reviewed by an acridine orange staining method, and many mixed infections with two to four species, including P. malariae and P. ovale, were detected. These diagnostic results were compared with those by two PCR-based diagnoses, microtitre plate hybridization (MPH) and a nested PCR method, both of which targets the same, species-specific regions in the 18S rRNA genes. In both PCR diagnoses, many P. malariae and P. ovale infections were also detected. Detection sensitivity of P. malariae infection was higher in nested PCR than MPH, and a total prevalence of P. malariae infection estimated by nested PCR reached 24.3% (133/548). In 16 of them, the size of PCR products amplified by the P. malariae-specific primer was about 20-bp shorter than the expected size of 115-bp. Four of 16 possessed two different bands with normal and shorter sizes, suggesting that P. malariae isolates may be separated into two types, and that those with shorter products may be new variant form (s) with a nucleotide deletion in the target region. On the other hand, 21 P. ovale infections (3.8%) were detected by nested PCR, but four of them were MPH-negative because of the sequence variation at the probe region. These results indicated that the prevalence of P. malariae and P. ovale along the Thai-Myanmar border may be substantially higher than previously reported.
引用
收藏
页码:304 / 312
页数:9
相关论文
共 24 条
[1]   A colorimetric DNA diagnostic method for falciparum malaria and vivax malaria: A field trial in the Solomon Islands [J].
Arai, M ;
Kunisada, K ;
Kim, HS ;
Miyake, H ;
Mizukoshi, C ;
Kakutani, T ;
Yamane, A ;
Nakagami, S ;
Kawai, S ;
Nakano, H ;
Kawamoto, F ;
Wataya, Y .
NUCLEOSIDES & NUCLEOTIDES, 1996, 15 (1-3) :719-731
[2]   DNA DIAGNOSIS OF OVALE MALARIA AND MALARIAE MALARIA USING MICROTITER PLATE-HYBRIDIZATION [J].
ARAI, M ;
KUNISADA, K ;
KAWAI, S ;
KIMURA, M ;
WATAYA, Y .
NUCLEOSIDES & NUCLEOTIDES, 1994, 13 (6-7) :1363-1374
[3]   DEMONSTRATION BY THE POLYMERASE CHAIN-REACTION OF MIXED PLASMODIUM-FALCIPARUM AND PLASMODIUM-VIVAX INFECTIONS UNDETECTED BY CONVENTIONAL MICROSCOPY [J].
BROWN, AE ;
KAIN, KC ;
PIPITHKUL, J ;
WEBSTER, HK .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1992, 86 (06) :609-612
[4]  
CADIGAN FC, 1969, T ROY SOC TROP MED H, V63, P681, DOI 10.1016/0035-9203(69)90194-1
[5]  
*DEP HLTH MYANM, 1996, VECT BORN DIS CONTR, P1
[6]  
GARNHAM PCC, 1966, MALARIA PARASITES OT, P257
[7]   Direct acridine orange fluorescence examination of blood slides compared to current techniques for malaria diagnosis [J].
Gay, F ;
Traore, B ;
Zanoni, J ;
Danis, M ;
FribourgBlanc, A .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1996, 90 (05) :516-518
[8]  
Haworth J., 1988, P1379
[9]   Sequence variation in the 18S rRNA gene, a target for PCR-based malaria diagnosis, in Plasmodium ovale from southern Vietnam [J].
Kawamoto, F ;
Miyake, H ;
Kaneko, O ;
Kimura, M ;
Dung, NT ;
Dung, NT ;
Liu, Q ;
Zhou, M ;
Dao, LD ;
Kawai, S ;
Isomura, S ;
Wataya, W .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (09) :2287-2289
[10]   RAPID DIAGNOSIS OF MALARIA BY FLUORESCENCE MICROSCOPY WITH LIGHT-MICROSCOPE AND INTERFERENCE FILTER [J].
KAWAMOTO, F .
LANCET, 1991, 337 (8735) :200-202