Survivability of low pathogenic (H9N2) avian influenza virus in water in the presence of Atyopsis moluccensis (Bamboo shrimp)

被引:9
作者
Pathak, A. P. [1 ]
Murugkar, H. V. [2 ]
Nagarajan, S. [2 ]
Sood, R. [2 ]
Tosh, C. [2 ]
Kumar, M. [2 ]
Athira, C. K. [3 ]
Praveen, A. [4 ]
机构
[1] GB Pant Univ Agr & Technol, Dept Vet Publ Hlth & Epidemiol, Pantnagar, Uttarakhand, India
[2] NIHSAD, ICAR, Bhopal, Madhya Pradesh, India
[3] Indian Vet Res Inst, Div Vet Publ Hlth, Bareilly, Uttar Pradesh, India
[4] Vet Dispensary, Korukollu, Andhra Prades, India
关键词
aquatic fauna; avian influenza; bamboo shrimps; persistence; survivability; HEPATITIS-A VIRUS; NATURAL-WATER; RT-PCR; H5N1; SHELLFISH; TRANSMISSION; INACTIVATION; ACCUMULATION; INFECTION; CLAMS;
D O I
10.1111/zph.12420
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Low pathogenic avian influenza virus (LPAIV) exhibits an ecological climax with the aquatic ecosystem. The most widely prevalent subtype of LPAIV is H9N2. Wild aquatic birds being the natural reservoirs and ducks, the Trojan horses for Avian Influenza Virus (AIV), can contaminate the natural water bodies inhabited by them. The virus can persist in the contaminated water from days to years depending upon the environmental conditions. Various aquatic species other than ducks can promote the persistence and transmission of AIV; however, studies on the role of aquatic fauna in persistence and transmission of avian influenza virus are scarce. This experiment was designed to evaluate the survivability of H9N2 LPAIV in water with and without Atyopsis moluccensis (bamboo shrimp) for a period of 12days. The infectivity and amount of virus in water were calculated and were found to be significantly higher in water with A.moluccensis than in water without A.moluccensis. The study also showed that A.moluccensis can accumulate the virus mechanically which can infect chicken eggs up to 11days. The virus transmission potential of A.moluccensis requires further studies.
引用
收藏
页码:E124 / E129
页数:6
相关论文
共 33 条
[21]   Single step multiplex real-time RT-PCR for H5N1 influenza A virus detection [J].
Payungporn, S ;
Chutinimitkul, S ;
Chaisingh, A ;
Damrongwantanapokin, S ;
Buranathai, C ;
Amonsin, A ;
Theamboonlers, A ;
Poovorawan, Y .
JOURNAL OF VIROLOGICAL METHODS, 2006, 131 (02) :143-147
[22]   Human infection with influenza H9N2 [J].
Peiris, M ;
Yuen, KY ;
Leung, CW ;
Chan, KH ;
Ip, PLS ;
Lai, RWM ;
Orr, WK ;
Shortridge, KF .
LANCET, 1999, 354 (9182) :916-917
[23]  
REED L. J., 1938, AMER JOUR HYG, V27, P493
[24]   Chlorine inactivation of highly pathogenic avian influenza virus (H5N1) [J].
Rice, Eugene W. ;
Adcock, Noreen J. ;
Sivaganesan, Mano ;
Brown, Justin D. ;
Stallknecht, David E. ;
Swayne, David E. .
EMERGING INFECTIOUS DISEASES, 2007, 13 (10) :1568-1570
[25]   Distribution of norwalk virus within shellfish following bioaccumulation and subsequent depuration by detection using RT-PCR [J].
Schwab, KJ ;
Neill, FH ;
Estes, MK ;
Metcalf, TG ;
Atmar, RL .
JOURNAL OF FOOD PROTECTION, 1998, 61 (12) :1674-1680
[26]  
Shoham Dany, 2012, Influenza Res Treat, V2012, P912326, DOI 10.1155/2012/912326
[27]  
Skraber S., 2005, Biofilms, V2, P105, DOI 10.1017/S1479050505001833
[28]   Managing water quality with aquatic macrophytes [J].
Srivastava J. ;
Gupta A. ;
Chandra H. .
Reviews in Environmental Science and Bio/Technology, 2008, 7 (3) :255-266
[29]  
Stumpf P., 2010, AVIAN DIS DIGEST, V5, pe9
[30]   INTESTINAL INFLUENZA - REPLICATION AND CHARACTERIZATION OF INFLUENZA-VIRUSES IN DUCKS [J].
WEBSTER, RG ;
YAKHNO, M ;
HINSHAW, VS ;
BEAN, WJ ;
MURTI, KG .
VIROLOGY, 1978, 84 (02) :268-278