John T J, Nambiar A, Samuel B U, Rajasingh J
Department of Virology and Immunology, Christian Medical College Hospital, Vellore, India.
Vaccine. 1992;10(8):529-32. doi: 10.1016/0264-410x(92)90352-k.
A new monkey model of poliovirus neurovirulence has been developed avoiding the currently used intraspinal injection route which traumatizes the spinal cord. Poliovirus type 1 (0.1 ml) was inoculated into the ulnar nerve of bonnet monkeys (Macaca radiata) at the right elbow. Five monkeys were inoculated with 10(7) TCID of LSc/2ab (Sabin vaccine strain); none developed any illness. Limb paralysis, clinically resembling spinal poliomyelitis in children, developed in all four monkeys given greater than or equal to 10(5) TCID50 of Mahoney strain, and in three of four monkeys given 10(4) or 10(3) TCID50. Higher functions and cranial nerves were not affected. Paralysis occurred more frequently in the lower limbs (11 limbs in seven monkeys) than in upper limbs (six limbs in seven monkeys). The incubation period, from inoculation to onset of paralysis, ranged from 5 to 12 days. Further progression of paralysis to other limbs occurred within 2 to 6 days. No illness developed in two monkeys given 10(2) TCID50 of Mahoney virus. All monkeys given LSc/2ab and those given greater than 10(2) TCID50 Mahoney virus developed humoral antibody response; however, infection of the gastrointestinal tract was detected by virus isolation from throat swabs and stools only in monkeys given Mahoney virus, but not in those given LSc/2ab. Thus, intraneural spread of Mahoney virus to the spinal cord, neurovirulence of Mahoney but not of LSc/2ab and retrograde gastrointestinal infection with Mahoney but not with LSc/2ab are the features of this experimental model.
一种新的脊髓灰质炎病毒神经毒力猴模型已被开发出来,避免了目前使用的会损伤脊髓的脊髓内注射途径。将1型脊髓灰质炎病毒(0.1毫升)接种到帽猴(食蟹猴)右肘的尺神经中。五只猴子接种了10⁷组织培养感染剂量(TCID)的LSc/2ab(萨宾疫苗株);没有一只出现任何疾病。在接种了大于或等于10⁵半数组织培养感染剂量(TCID₅₀)马奥尼株的所有四只猴子以及接种了10⁴或10³ TCID₅₀的四只猴子中的三只中,出现了临床上类似于儿童脊髓灰质炎的肢体麻痹。高级功能和颅神经未受影响。下肢麻痹(七只猴子中的11条肢体)比上肢麻痹(七只猴子中的六条肢体)更频繁发生。从接种到麻痹发作的潜伏期为5至12天。麻痹进一步发展到其他肢体在2至6天内发生。接种10² TCID₅₀马奥尼病毒的两只猴子未发病。所有接种LSc/2ab的猴子以及接种大于10² TCID₅₀马奥尼病毒的猴子都产生了体液抗体反应;然而,仅在接种马奥尼病毒的猴子中通过从咽拭子和粪便中分离病毒检测到胃肠道感染,而接种LSc/2ab的猴子中未检测到。因此,马奥尼病毒向脊髓的神经内传播、马奥尼株的神经毒力而非LSc/2ab的神经毒力以及马奥尼株而非LSc/2ab的逆行性胃肠道感染是该实验模型的特征。